| Name |
|---|
InterPro Predicted Protein Domain Annotations DatasetFrom InterPro Protein domains predicted for gene products based on sequence similarity to known domain signatures |
Hub Proteins Protein-Protein Interactions DatasetFrom Hub Proteins Sets of proteins interacting with hub proteins aggregated from data |
NURSA Protein-Protein Interactions DatasetFrom Nuclear Receptor Signaling Atlas Protein-protein interactions inferred from membership in complexes |
Pathway Commons Protein-Protein Interactions DatasetFrom Pathway Commons Protein-protein interactions from low-throughput or high-throughput studies aggregated by Pathway Commons from the following databases: Reactome, NCI Pathways, PhosphoSite, HumanCyc, HPRD, PANTHER, DIP, BioGRID, IntAct, BIND, Transfac, MiRTarBase, Drugbank, Recon X, Comparative Toxicogenomics Database, and KEGG |
Virus MINT Protein-Viral Protein Interactions DatasetFrom Virus MINT Interactions between viral and human proteins manually curated from literature |
COMPARTMENTS Curated Protein Localization Evidence Scores Dataset (Archived)From COMPARTMENTS Protein subcellular localization evidence scores by manual literature curation |
COMPARTMENTS Experimental Protein Localization Evidence Scores Dataset (Archived)From COMPARTMENTS Protein subcellular localization evidence scores by integrating experimental data |
COMPARTMENTS Text-mining Protein Localization Evidence Scores Dataset (Archived)From COMPARTMENTS Gene-cellular compartment co-occurrence scores from text-mining biomedical abstracts |
CORUM Protein Complexes DatasetFrom CORUM Proteins participating in complexes by manual literature curation |
Guide to Pharmacology Protein Ligands of Receptors DatasetProtein ligand-receptor interactions curated by experts |
HPA Tissue Protein Expression Profiles DatasetFrom Human Protein Atlas Semiquantitative protein expression profiles for tissues |
HPM Cell Type and Tissue Protein Expression Profiles DatasetFrom Human Proteome Map Protein expression profiles for tissues and cell types |
LOCATE Curated Protein Localization Annotations DatasetFrom LOCATE Subcellular localization of proteins from low-throughput or high-throughput protein localization assays |
NURSA Protein Complexes DatasetFrom Nuclear Receptor Signaling Atlas Proteins identified in complexes isolated from cultured cells |
ProteomicsDB Cell Type and Tissue Protein Expression Profiles DatasetFrom Proteomics Database Protein expression profiles for tissues and cell types reprocessed from many proteomics datasets |
SILAC Phosphoproteomics Signatures of Differentially Phosphorylated Proteins for Protein Ligands DatasetPhosphorylation levels of proteins in cell lines following ligand treatment |
TISSUES Curated Tissue Protein Expression Evidence Scores Dataset (Archived)From TISSUES Protein tissue expression evidence scores by manual literature curation |
TISSUES Experimental Tissue Protein Expression Evidence Scores Dataset (Archived)From TISSUES Protein tissue expression evidence scores by integrating experimental data |
TISSUES Text-mining Tissue Protein Expression Evidence Scores Dataset (Archived)From TISSUES Gene-tissue co-occurrence scores from text-mining biomedical abstracts |
Virus MINT Protein-Virus Interactions DatasetFrom Virus MINT Interactions between viruses and human proteins manually curated from literature |
LOCATE Predicted Protein Localization Annotations DatasetFrom LOCATE Subcellular localization of proteins by sequence similarity to localization sequences |
TISSUES Curated Tissue Protein Expression Evidence Scores 2025 DatasetFrom TISSUES Protein tissue expression evidence scores by manual literature curation |
TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 DatasetFrom TISSUES Protein tissue expression evidence scores by integrating experimental data |
TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 DatasetFrom TISSUES Gene-tissue co-occurrence scores from text-mining biomedical abstracts |
COMPARTMENTS Curated Protein Localization Evidence Scores 2025 DatasetFrom COMPARTMENTS Protein subcellular localization evidence scores by manual literature curation |
COMPARTMENTS Experimental Protein Localization Evidence Scores 2025 DatasetFrom COMPARTMENTS Protein subcellular localization evidence scores by integrating experimental data |
COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 DatasetFrom COMPARTMENTS Gene-cellular compartment co-occurrence scores from text-mining biomedical abstracts |
CM4AI U2OS Cell Map Protein Localization Assemblies DatasetFrom Cell Maps for AI Protein localization assemblies constructed from integrating AP-MS biomolecular interaction and IF imaging data |
HPA Cell Line Gene Expression Profiles DatasetFrom Human Protein Atlas RNA-seq gene expression profiles for cell lines from HPA |
HPA Tissue Gene Expression Profiles DatasetFrom Human Protein Atlas RNA-seq gene expression profiles for tissues from HPA |
HPA Tissue Sample Gene Expression Profiles DatasetFrom Human Protein Atlas RNA-seq gene expression profiles for tissue samples from HPA |
TSRM Genezinc finger domain-related protein TSRM |
ZFAND6P1 Genezinc finger, AN1-type domain 6 pseudogene 1 |
ZFAND2B Genezinc finger, AN1-type domain 2B This gene encodes a protein containing AN1-type zinc-fingers and ubiquitin-interacting motifs. The encoded protein likely associates with the proteosome to stimulate the degradation of toxic or misfolded proteins. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2012] |
ZFAND2A Genezinc finger, AN1-type domain 2A Predicted to enable zinc ion binding activity. Predicted to be involved in proteasome-mediated ubiquitin-dependent protein catabolic process and protein targeting to ER. Predicted to act upstream of or within cellular response to arsenic-containing substance and positive regulation of proteasomal ubiquitin-dependent protein catabolic process. Predicted to be located in nucleus. Predicted to be part of proteasome complex. Predicted to be active in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
ZGPAT Genezinc finger, CCCH-type with G patch domain Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in negative regulation of epidermal growth factor-activated receptor activity and negative regulation of transcription by RNA polymerase II. Located in nucleoplasm and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ZFAND6 Genezinc finger, AN1-type domain 6 Predicted to enable polyubiquitin modification-dependent protein binding activity. Involved in cellular response to tumor necrosis factor; negative regulation of apoptotic process; and regulation of canonical NF-kappaB signal transduction. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
ZFAND5 Genezinc finger, AN1-type domain 5 Predicted to enable DNA binding activity and zinc ion binding activity. Predicted to act upstream of or within several processes, including face development; fibroblast migration; and platelet-derived growth factor receptor signaling pathway. Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZFAND4 Genezinc finger, AN1-type domain 4 Predicted to enable zinc ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZFAND3 Genezinc finger, AN1-type domain 3 Predicted to enable DNA binding activity and zinc ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZFAND1 Genezinc finger, AN1-type domain 1 Enables proteasome binding activity. Involved in cellular response to arsenite ion; positive regulation of intracellular protein transport; and stress granule disassembly. Located in cytoplasmic stress granule. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF185 Genezinc finger protein 185 (LIM domain) Zinc-finger proteins bind nucleic acids and play important roles in various cellular functions, including cell proliferation, differentiation, and apoptosis. This gene encodes a LIM-domain zinc finger protein. The LIM domain is composed of two contiguous zinc finger domains, separated by a two-amino acid residue hydrophobic linker. The LIM domain mediates protein:protein interactions. Multiple alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, May 2010] |
LOC100129734 Genezinc finger, AN1-type domain 1 pseudogene |
BAZ1B Genebromodomain adjacent to zinc finger domain, 1B This gene encodes a member of the bromodomain protein family. The bromodomain is a structural motif characteristic of proteins involved in chromatin-dependent regulation of transcription. This gene is deleted in Williams-Beuren syndrome, a developmental disorder caused by deletion of multiple genes at 7q11.23. [provided by RefSeq, Jul 2008] |
ZZEF1 Genezinc finger, ZZ-type with EF-hand domain 1 Enables histone reader activity; lysine-acetylated histone binding activity; and methylated histone binding activity. Predicted to be involved in chromatin organization. Predicted to act upstream of or within several processes, including glutamatergic synaptic transmission; regulation of peptidyl-tyrosine phosphorylation; and visual learning. Predicted to be located in cell surface; postsynapse; and presynaptic active zone. [provided by Alliance of Genome Resources, Mar 2025] |
ZCWPW2 Genezinc finger, CW type with PWWP domain 2 Enables methylated histone binding activity. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZCWPW1 Genezinc finger, CW type with PWWP domain 1 Enables histone reader activity; methyl-CpG binding activity; and methylated histone binding activity. Predicted to be involved in meiosis I; positive regulation of DNA metabolic process; and spermatogenesis. Predicted to act upstream of or within homologous chromosome pairing at meiosis. Predicted to be located in XY body. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
BAZ2A Genebromodomain adjacent to zinc finger domain, 2A Enables histone binding activity. Contributes to RNA polymerase I core promoter sequence-specific DNA binding activity. Predicted to be involved in DNA methylation-dependent constitutive heterochromatin formation; negative regulation of transcription by RNA polymerase I; and rDNA heterochromatin formation. Predicted to act upstream of or within heterochromatin formation. Located in cytosol and nuclear speck. [provided by Alliance of Genome Resources, Mar 2025] |
BAZ2B Genebromodomain adjacent to zinc finger domain, 2B This gene belongs to the bromodomain gene family. Members of this gene family encode proteins that are integral components of chromatin remodeling complexes. The encoded protein showed strong preference for the activating H3K14Ac mark in a histone peptide screen, suggesting a potential role in transcriptional activation. This gene may be associated with susceptibility to sudden cardiac death (SCD). [provided by RefSeq, Aug 2016] |
LOC100289500 Genezinc finger, AN1-type domain 1 pseudogene |
ZUFSP Genezinc finger with UFM1-specific peptidase domain This gene encodes a protein containing zinc finger motifs and a cysteine peptidase domain. The encoded protein functions as a K63-specific de-ubiquitinating enzyme that specifically cleaves long K63-linked polyubiquitin chains in the middle of a chain (i.e. `endo cleavage) rather than by removing the terminal ubiquitin from a chain. This enzyme is thought to be involved in the regulation of DNA repair by cleaving K63-linked ubiquitin chains at repair foci. This protein is related to proteases for the ubiquitin-like modifiers Ufm1 (ubiquitin fold modifier 1) and Atg8/Gabarapl2, but does not have any activity on these modifiers. [provided by RefSeq, Mar 2018] |
BAZ1A Genebromodomain adjacent to zinc finger domain, 1A The BAZ1A gene encodes the accessory subunit of the ATP-dependent chromatin assembly factor (ACF), a member of the ISWI ('imitation switch') family of chromatin remodeling complexes (summarized by Racki et al., 2009 [PubMed 20033039]).[supplied by OMIM, Apr 2010] |
SEMA4A Genesema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A This gene encodes a member of the semaphorin family of soluble and transmembrane proteins. Semaphorins are involved in numerous functions, including axon guidance, morphogenesis, carcinogenesis, and immunomodulation. The encoded protein is a single-pass type I membrane protein containing an immunoglobulin-like C2-type domain, a PSI domain and a sema domain. It inhibits axonal extension by providing local signals to specify territories inaccessible for growing axons. It is an activator of T-cell-mediated immunity and suppresses vascular endothelial growth factor (VEGF)-mediated endothelial cell migration and proliferation in vitro and angiogenesis in vivo. Mutations in this gene are associated with retinal degenerative diseases including retinitis pigmentosa type 35 (RP35) and cone-rod dystrophy type 10 (CORD10). Multiple alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Sep 2010] |
SEMA4B Genesema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4B Predicted to enable chemorepellent activity; neuropilin binding activity; and semaphorin receptor binding activity. Predicted to be involved in several processes, including axon guidance; neural crest cell migration; and semaphorin-plexin signaling pathway. Predicted to be located in membrane and synapse. Predicted to be active in glutamatergic synapse and postsynaptic density membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SEMA4C Genesema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C Predicted to enable chemorepellent activity; neuropilin binding activity; and semaphorin receptor binding activity. Involved in muscle cell differentiation and positive regulation of stress-activated MAPK cascade. Located in extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
SEMA4D Genesema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4D Enables identical protein binding activity; semaphorin receptor binding activity; and transmembrane signaling receptor activity. Involved in several processes, including ossification involved in bone maturation; positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction; and regulation of neuron projection development. Located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SEMA4F Genesema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4F This gene encodes a transmembrane class IV semaphorin family protein, which plays a role in neural development. This gene may be involved in neurogenesis in prostate cancer, the development of neurofibromas, and breast cancer tumorigenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012] |
SEMA4G Genesema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4G Semaphorins are a large family of conserved secreted and membrane associated proteins which possess a semaphorin (Sema) domain and a PSI domain (found in plexins, semaphorins and integrins) in the N-terminal extracellular portion. Based on sequence and structural similarities, semaphorins are put into eight classes: invertebrates contain classes 1 and 2, viruses have class V, and vertebrates contain classes 3-7. Semaphorins serve as axon guidance ligands via multimeric receptor complexes, some (if not all) containing plexin proteins. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2011] |
LOC105379427 Genezinc finger protein 717-like |
LOC442041 Genezinc finger protein 532 pseudogene |
ZNF117 Genezinc finger protein 117 This gene encodes a protein containing multiple C2H2-type zinc finger motifs. Readthrough transcription occurs between this gene and the upstream endogenous retrovirus group 3 member 1 (ERV3-1) locus, and may result in additional transcript variants encoding the zinc finger protein. [provided by RefSeq, Jan 2017] |
ZNF114 Genezinc finger protein 114 Enables identical protein binding activity. Predicted to be involved in regulation of DNA-templated transcription. Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF112 Genezinc finger protein 112 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF736P3Y Genezinc finger protein 736 pseudogene 3, Y-linked |
LOC100419801 Genezinc finger protein 532 pseudogene |
LOC100419803 Genezinc finger protein 510 pseudogene |
LOC100419802 Genezinc finger protein 184 pseudogene |
LOC100419806 Genezinc finger protein 519 pseudogene |
ZNF831 Genezinc finger protein 831 Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF830 Genezinc finger protein 830 Predicted to enable nucleic acid binding activity and zinc ion binding activity. Predicted to be involved in several processes, including mitotic DNA integrity checkpoint signaling; nuclear DNA replication; and preantral ovarian follicle growth. Predicted to act upstream of or within several processes, including blastocyst growth; chromosome organization; and intestinal epithelial structure maintenance. Predicted to be located in nucleoplasm. Predicted to be part of spliceosomal complex. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF835 Genezinc finger protein 835 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF837 Genezinc finger protein 837 Enables identical protein binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF836 Genezinc finger protein 836 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF839 Genezinc finger protein 839 Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF304 Genezinc finger protein 304 This gene encodes a member of the Krueppel C2H2-type zinc-finger family of proteins. The encoded protein functions as a transcriptional repressor that recruits a corepressor complex to stimulate promoter hypermethylation and transcriptional silencing of target genes. Expression of this gene is upregulated in colorectal, ovarian and breast cancer, and this gene may promote cancer cell survival, growth and invasion. [provided by RefSeq, Jul 2016] |
ZNF302 Genezinc finger protein 302 This gene encodes a member of the zinc-finger protein family. The encoded protein contains seven C2H2-type zinc fingers and a KRAB domain, but its function has yet to be determined. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2014] |
ZNF300 Genezinc finger protein 300 The protein encoded by this gene is a C2H2-type zinc finger DNA binding protein and likely transcriptional regulator. The function of this protein is not yet known. Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2010] |
LOC100419755 Genezinc finger protein 426 pseudogene |
ZNF848P Genezinc finger protein 848, pseudogene |
ZNF605 Genezinc finger protein 605 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
UNKL Geneunkempt family zinc finger-like This gene encodes a RING finger protein that may function in Rac signaling. It can bind to Brg/Brm-associated factor 60b and can promote its ubiquitination. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jun 2013] |
ZNF733P Genezinc finger protein 733, pseudogene |
LOC100419888 Genezinc finger protein 331 pseudogene |
ZNF213 Genezinc finger protein 213 C2H2 zinc finger proteins, such as ZNF213, have bipartite structures in which one domain binds DNA or RNA and the other modulates target gene expression.[supplied by OMIM, Apr 2004] |
ZNF419 Genezinc finger protein 419 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF418 Genezinc finger protein 418 Enables DNA-binding transcription repressor activity. Predicted to be involved in microautophagy; regulation of proteasomal ubiquitin-dependent protein catabolic process; and regulation of transcription by RNA polymerase II. Is active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF417 Genezinc finger protein 417 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF416 Genezinc finger protein 416 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in microautophagy; regulation of proteasomal ubiquitin-dependent protein catabolic process; and regulation of transcription by RNA polymerase II. Predicted to act upstream of or within cardiac muscle hypertrophy; negative regulation of cell growth involved in cardiac muscle cell development; and negative regulation of protein phosphorylation. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF415 Genezinc finger protein 415 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in fibrillar center and microtubule cytoskeleton. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF414 Genezinc finger protein 414 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF410 Genezinc finger protein 410 Enables DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in negative regulation of gene expression and positive regulation of transcription by RNA polymerase II. Predicted to be located in chromosome. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF726P1 Genezinc finger protein 726 pseudogene 1 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100130632 Genezinc finger protein 530-like |
ZNF658 Genezinc finger protein 658 Enables transcription cis-regulatory region binding activity. Involved in cellular response to zinc ion; negative regulation of DNA-templated transcription; and ribosome biogenesis. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF655 Genezinc finger protein 655 This gene encodes a zinc finger protein. The zinc finger proteins are involved in DNA binding and protein-protein interactions. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
ZNF653 Genezinc finger protein 653 Enables AF-2 domain binding activity; DNA-binding transcription factor binding activity; and transcription corepressor activity. Involved in extracellular negative regulation of signal transduction and negative regulation of transcription by RNA polymerase II. Predicted to be located in extracellular region. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF652 Genezinc finger protein 652 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF384 Genezinc finger protein 384 This gene encodes a C2H2-type zinc finger protein, which may function as a transcription factor. This gene also contains long CAG trinucleotide repeats that encode consecutive glutamine residues. The protein appears to bind and regulate the promoters of the extracellular matrix genes MMP1, MMP3, MMP7 and COL1A1. Studies in mouse suggest that nuclear matrix transcription factors (NP/NMP4) may be part of a general mechanical pathway that couples cell construction and function during extracellular matrix remodeling. Alternative splicing results in multiple transcript variants. Recurrent rearrangements of this gene with the Ewing's sarcoma gene, EWSR1 on chromosome 22, or with the TAF15 gene on chromosome 17, or with the TCF3 (E2A) gene on chromosome 19, have been observed in acute leukemia. A related pseudogene has been identified on chromosome 7. [provided by RefSeq, Apr 2011] |
ZNF383 Genezinc finger protein 383 The protein encoded by this gene is a KRAB-related zinc finger protein that inhibits the transcription of some MAPK signaling pathway genes. The repressor activity resides in the KRAB domain of the encoded protein. [provided by RefSeq, Sep 2016] |
ZFP41 GeneZFP41 zinc finger protein Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFP42 GeneZFP42 zinc finger protein Enables sequence-specific double-stranded DNA binding activity. Involved in female gonad development and male gonad development. Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419762 Genezinc finger protein 773 pseudogene |
ZFHX4 Genezinc finger homeobox 4 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100130861 Genezinc finger protein 736 pseudogene |
ZFHX3 Genezinc finger homeobox 3 This gene encodes a transcription factor with multiple homeodomains and zinc finger motifs, and regulates myogenic and neuronal differentiation. The encoded protein suppresses expression of the alpha-fetoprotein gene by binding to an AT-rich enhancer motif. The protein has also been shown to negatively regulate c-Myb, and transactivate the cell cycle inhibitor cyclin-dependent kinase inhibitor 1A (also known as p21CIP1). This gene is reported to function as a tumor suppressor in several cancers, and sequence variants of this gene are also associated with atrial fibrillation. Multiple transcript variants expressed from alternate promoters and encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009] |
ZNF192P2 Genezinc finger protein 192 pseudogene 2 |
ZNF192P1 Genezinc finger protein 192 pseudogene 1 Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF497 Genezinc finger protein 497 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF496 Genezinc finger protein 496 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in positive regulation of DNA-templated transcription and regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF493 Genezinc finger protein 493 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF490 Genezinc finger protein 490 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC646629 Genezinc finger protein 470 pseudogene |
ZNF826P Genezinc finger protein 826, pseudogene Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF519P3 Genezinc finger protein 519 pseudogene 3 |
ZIM2 Genezinc finger, imprinted 2 In human, ZIM2 and PEG3 (GeneID:5178) are two distinct genes that share a set of 5' exons and have a common promoter, and both genes are paternally expressed. Alternative splicing events connect the shared exons either with the remaining 4 exons unique to ZIM2, or with the remaining 2 exons unique to PEG3. This is in contrast to mouse and cow, where ZIM2 and PEG3 genes do not share exons in common, and the imprinting status of ZIM2 is also not conserved amongst mammals. Additional 5' alternatively spliced transcripts encoding the same protein have been found for the human ZIM2 gene. [provided by RefSeq, Oct 2010] |
ZIM3 Genezinc finger, imprinted 3 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF519 Genezinc finger protein 519 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; and chromatin binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF512 Genezinc finger protein 512 This gene encodes a protein containing four putative zinc finger motifs. Zinc finger motifs may bind to proteins or nucleic acids. Zinc finger-containing proteins are involved in a variety of processes, including regulation of transcription. Alternative splicing results in multiple transcript variants for this gene. [provided by RefSeq, Sep 2012] |
ZNF513 Genezinc finger protein 513 The protein encoded by this gene is a possible transcriptional regulator involved in retinal development. Defects in this gene can be a cause of autosomal-recessive retinitis pigmentosa. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2011] |
ZNF510 Genezinc finger protein 510 This gene encodes a krueppel C2H2-type zinc-finger protein family member. The encoded protein is expressed in several cancer cell types and may be a biomarker for early diagnosis of these cancers. [provided by RefSeq, Sep 2015] |
ZNF511 Genezinc finger protein 511 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF516 Genezinc finger protein 516 Zinc-finger proteins bind nucleic acids and play important roles in various cellular functions, including cell proliferation, differentiation, and apoptosis. This gene encodes a zinc-finger protein, and belongs to the krueppel C2H2-type zinc-finger protein family. It may be involved in transcriptional regulation. [provided by RefSeq, Sep 2012] |
ZNF514 Genezinc finger protein 514 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
CNBP GeneCCHC-type zinc finger, nucleic acid binding protein This gene encodes a nucleic-acid binding protein with seven zinc-finger domains. The protein has a preference for binding single stranded DNA and RNA. The protein functions in cap-independent translation of ornithine decarboxylase mRNA, and may also function in sterol-mediated transcriptional regulation. A CCTG expansion from <30 repeats to 75-11000 repeats in the first intron of this gene results in myotonic dystrophy type 2. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2016] |
LOC100421122 Genezinc finger protein 106 homolog (mouse) pseudogene |
ZNF75D Genezinc finger protein 75D This gene encodes a protein that likely functions as a transcription factor. The protein, which belongs to the ZNF75 family, includes an N-terminal SCAN domain, a KRAB box, and five C2H2-type zinc finger motifs. Another functional gene belonging to this family is located on chromosome 16, while pseudogenes have been identified on chromosomes 11 and 12. Alternative splicing results in multiple transcripts variants. [provided by RefSeq, Jun 2010] |
LOC100533635 Genezinc finger protein 384 pseudogene |
ZNF750 Genezinc finger protein 750 This gene encodes a protein with a nuclear localization site and a C2H2 zinc finger domain. Mutations in this gene have been associated with seborrhea-like dermatitis with psoriasiform elements. [provided by RefSeq, Jul 2008] |
LOC100533638 Genezinc finger protein 85 pseudogene |
LOC728376 Genezinc finger protein 430 pseudogene |
ZGLP1 Genezinc finger, GATA-like protein 1 ZGLP1 encodes an evolutionary conserved transcriptional regulator with GATA-like zinc fingers. In females, it is expressed in embryonic germ cells and is essential for oogenic fate determination. It acts downstream of bone morphogenetic protein (BMP) and is involved in the regulation of genes involved in RNA processing, transcription and chromatin modification, retrotransposon regulation, meiotic cell cycle, and oocyte development. In males it is not required for the germ cell sex determination but is required by the spermatogonia for efficiently completing the meiotic prophase. [provided by RefSeq, Jul 2022] |
LOC100419752 Genezinc finger protein 251 pseudogene |
DNLZ GeneDNL-type zinc finger Enables protein folding chaperone. Involved in chaperone-mediated protein complex assembly. Located in nucleoplasm. Is active in cytosol; mitochondrion; and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF273 Genezinc finger protein 273 This gene is a member of the krueppel C2H2-type zinc-finger protein family and encodes a protein with 13 C2H2-type zinc fingers and a KRAB domain. This nuclear protein is involved in transcriptional regulation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008] |
ZNF277 Genezinc finger protein 277 Predicted to enable RNA polymerase II cis-regulatory region sequence-specific DNA binding activity and metal ion binding activity. Predicted to act upstream of or within cellular response to hydrogen peroxide and regulation of cellular senescence. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF276 Genezinc finger protein 276 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in kinetochore. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF275 Genezinc finger protein 275 This gene encodes a zinc finger protein that appears to be conserved in eutheria. Its function has not yet been established. [provided by RefSeq, Jul 2010] |
ZNF274 Genezinc finger protein 274 This gene encodes a zinc finger protein containing five C2H2-type zinc finger domains, one or two Kruppel-associated box A (KRAB A) domains, and a leucine-rich domain. The encoded protein has been suggested to be a transcriptional repressor. It localizes predominantly to the nucleolus. Alternatively spliced transcript variants encoding different isoforms exist. These variants utilize alternative polyadenylation signals. [provided by RefSeq, Jul 2008] |
LOC100652813 Genezinc finger protein 138 pseudogene |
LOC100419830 Genezinc finger protein 337 pseudogene |
LOC100419834 Genezinc finger protein 134 pseudogene |
LOC100419836 Genezinc finger protein 347 pseudogene |
LOC100419838 Genezinc finger protein 860 pseudogene |
LOC100419839 Genezinc finger protein 300 pseudogene |
ZNF815P Genezinc finger protein 815, pseudogene |
LOC100131479 Genezinc finger protein 430 pseudogene |
ZNF841 Genezinc finger protein 841 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF843 Genezinc finger protein 843 Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF844 Genezinc finger protein 844 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF846 Genezinc finger protein 846 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF592 Genezinc finger protein 592 This gene is thought to play a role in a complex developmental pathway and the regulation of genes involved in cerebellar development. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia. [provided by RefSeq, Jan 2011] |
ZNF593 Genezinc finger protein 593 Enables preribosome binding activity and zinc ion binding activity. Involved in positive regulation of transcription by RNA polymerase II. Located in nucleolus and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF596 Genezinc finger protein 596 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF595 Genezinc finger protein 595 This gene encodes a protein belonging to the Cys2His2 zinc finger protein family, whose members function as transcription factors that can regulate a broad variety of developmental and cellular processes. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Oct 2013] |
ZNF598 Genezinc finger protein 598 Zinc-finger proteins bind nucleic acids and play important roles in various cellular functions, including cell proliferation, differentiation, and apoptosis. This protein and Grb10-interacting GYF protein 2 have been identified as a components of the mammalian 4EHP (m4EHP) complex. The complex is thought to function as a translation repressor in embryonic development. [provided by RefSeq, Oct 2012] |
ZNF599 Genezinc finger protein 599 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFR2 Genezinc finger RNA binding protein 2 Predicted to enable double-stranded RNA binding activity and single-stranded RNA binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF337 Genezinc finger protein 337 This gene encodes a zinc finger domain containing protein. The function of this protein has yet to be determined. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014] |
ZNF334 Genezinc finger protein 334 This gene encodes a member of the C2H2 zinc finger family. The encoded protein contains a Krueppel-associated box, fourteen C2H2 zinc finger domains, and four C2H2-type/integrase DNA-binding domains. Decreased expression of this gene may be a marker for rheumatoid arthritis. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012] |
ZNF335 Genezinc finger protein 335 The protein encoded by this gene enhances transcriptional activation by ligand-bound nuclear hormone receptors. However, it does this not by direct interaction with the receptor, but by direct interaction with the nuclear hormone receptor transcriptional coactivator NRC. The encoded protein may function by altering local chromatin structure. [provided by RefSeq, Jul 2008] |
ZNF333 Genezinc finger protein 333 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF331 Genezinc finger protein 331 This gene encodes a zinc finger protein containing a KRAB (Kruppel-associated box) domain found in transcriptional repressors. This gene may be methylated and silenced in cancer cells. This gene is located within a differentially methylated region (DMR) and shows allele-specific expression in placenta. Alternative splicing and the use of alternative promoters results in multiple transcript variants encoding the same protein. [provided by RefSeq, Nov 2015] |
LOC100419761 Genezinc finger protein 654 pseudogene |
LOC100419763 Genezinc finger with KRAB and SCAN domains 8 pseudogene |
ZNF33B Genezinc finger protein 33B This gene encodes a member of the zinc finger family of proteins. This gene shows decreased expression in cumulus cells derived from patients undergoing controlled ovarian stimulation. This gene is present in a gene cluster with several related zinc finger genes in the pericentromeric region of chromosome 10. Pseudogenes have been identified on chromosomes 7 and 10. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2015] |
ZNF33A Genezinc finger protein 33A Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFP92 GeneZFP92 zinc finger protein Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFP90 GeneZFP90 zinc finger protein This gene encodes a member of the zinc finger protein family that modulates gene expression. The encoded protein derepresses the transcription of certain fetal cardiac genes and may contribute to the genetic reprogramming that occurs during the development of heart failure. Genome wide association studies have identified this gene among ulcerative colitis risk loci. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Mar 2015] |
ZFP91 GeneZFP91 zinc finger protein The protein encoded by this gene is a member of the zinc finger family of proteins. The gene product contains C2H2-type domains, which are the classical zinc finger domains found in numerous nucleic acid-binding proteins. This protein functions as a regulator of the non-canonical NF-kappaB pathway in lymphotoxin-beta receptor signaling. Alternative splicing results in multiple transcript variants. A read-through transcript variant composed of ZFP91 and the downstream CNTF gene sequence has been identified, but it is thought to be non-coding. Read-through transcription of ZFP91 and CNTF has also been observed in mouse. A ZFP91-related pseudogene has also been identified on chromosome 2. [provided by RefSeq, Oct 2010] |
ZEB1 Genezinc finger E-box binding homeobox 1 This gene encodes a zinc finger transcription factor. The encoded protein likely plays a role in transcriptional repression of interleukin 2. Mutations in this gene have been associated with posterior polymorphous corneal dystrophy-3 and late-onset Fuchs endothelial corneal dystrophy. Alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Mar 2010] |
LOC101929991 Genezinc finger protein 93-like |
LOC100505841 Genezinc finger protein 474-like Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF83 Genezinc finger protein 83 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF81 Genezinc finger protein 81 This gene encodes a protein that likely functions as a transcription factor. The protein contains an N-terminal KRAB domain and several C2H2-type zinc finger motifs. Mutations in this gene cause an X-linked form of intellectual disability (MRX45). Microduplication of a region of chromosome X including this gene has also been associated with other forms of intellectual disability. [provided by RefSeq, Jul 2017] |
ZNF80 Genezinc finger protein 80 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within negative regulation of transcription by RNA polymerase II. Predicted to be located in cytoplasm. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF85 Genezinc finger protein 85 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF84 Genezinc finger protein 84 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF736P7Y Genezinc finger protein 736 pseudogene 7, Y-linked |
ZNF863P Genezinc finger protein 863, pseudogene |
WIZP1 Genewidely interspaced zinc finger motifs pseudogene 1 |
HELZ Genehelicase with zinc finger HELZ is a member of the superfamily I class of RNA helicases. RNA helicases alter the conformation of RNA by unwinding double-stranded regions, thereby altering the biologic activity of the RNA molecule and regulating access to other proteins (Wagner et al., 1999 [PubMed 10471385]).[supplied by OMIM, Mar 2008] |
RBAK GeneRB-associated KRAB zinc finger This gene encodes a nuclear protein which interacts with the tumor suppressor retinoblastoma 1. The two interacting proteins are thought to act as a transcriptional repressor for promoters which are activated by the E2F1 transcription factor. This protein contains a Kruppel-associated box (KRAB), which is a transcriptional repressor motif. Read-through transcripts that include exons from the downstream gene LOC389458 are expressed from this locus. [provided by RefSeq, Mar 2011] |
ZNF619P1 Genezinc finger protein 619 pseudogene 1 |
ZNF33BP1 Genezinc finger protein 33B pseudogene 1 |
VEZF1P1 Genevascular endothelial zinc finger 1 pseudogene 1 |
ZNF141 Genezinc finger protein 141 The protein encoded by this gene is a zinc finger protein that may be a tumor suppressor. Defects in this gene have been associated with autosomal recessive postaxial polydactyly type A. [provided by RefSeq, Jan 2017] |
ZNF140 Genezinc finger protein 140 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and sequence-specific double-stranded DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF143 Genezinc finger protein 143 Enables DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in positive regulation of snRNA transcription by RNA polymerase II. Predicted to be located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF142 Genezinc finger protein 142 The protein encoded by this gene belongs to the Kruppel family of C2H2-type zinc finger proteins. It contains 31 C2H2-type zinc fingers and may be involved in transcriptional regulation. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2013] |
ZNF146 Genezinc finger protein 146 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytosol and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF148 Genezinc finger protein 148 The protein encoded by this gene is a member of the Kruppel family of zinc finger DNA binding proteins. The encoded protein activates transcription of the T-cell receptor and intestinal alkaline phosphatase genes but represses transcription of the ornithine decarboxylase, vimentin, gastrin, stomelysin, and enolase genes. Increased expression of this gene results in decreased patient survival rates from colorectal cancer, while mutations in this gene have been associated with global developmental delay, hypoplastic corpus callosum, and dysmorphic facies. [provided by RefSeq, Feb 2017] |
ZNF736P4Y Genezinc finger protein 736 pseudogene 4, Y-linked |
ZNF736P12Y Genezinc finger protein 736 pseudogene 12, Y-linked |
ZNF968P Genezinc finger protein 968, pseudogene |
CTCF GeneCCCTC-binding factor (zinc finger protein) This gene is a member of the BORIS + CTCF gene family and encodes a transcriptional regulator protein with 11 highly conserved zinc finger (ZF) domains. This nuclear protein is able to use different combinations of the ZF domains to bind different DNA target sequences and proteins. Depending upon the context of the site, the protein can bind a histone acetyltransferase (HAT)-containing complex and function as a transcriptional activator or bind a histone deacetylase (HDAC)-containing complex and function as a transcriptional repressor. If the protein is bound to a transcriptional insulator element, it can block communication between enhancers and upstream promoters, thereby regulating imprinted expression. Mutations in this gene have been associated with invasive breast cancers, prostate cancers, and Wilms' tumors. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010] |
ZNF426 Genezinc finger protein 426 Kaposi's sarcoma-associated herpesvirus (KSHV) can be reactivated from latency by the viral protein RTA. The protein encoded by this gene is a zinc finger transcriptional repressor that interacts with RTA to modulate RTA-mediated reactivation of KSHV. While the encoded protein can repress KSHV reactivation, RTA can induce degradation of this protein through the ubiquitin-proteasome pathway to overcome the repression. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015] |
ZNF425 Genezinc finger protein 425 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Involved in negative regulation of DNA-templated transcription. Located in cytoplasm and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF423 Genezinc finger protein 423 The protein encoded by this gene is a nuclear protein that belongs to the family of Kruppel-like C2H2 zinc finger proteins. It functions as a DNA-binding transcription factor by using distinct zinc fingers in different signaling pathways. Thus, it is thought that this gene may have multiple roles in signal transduction during development. Mutations in this gene are associated with nephronophthisis-14 and Joubert syndrome-19. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2012] |
ZNF420 Genezinc finger protein 420 The protein encoded by this gene is a KRAB-type zinc finger protein that negatively-regulates p53-mediated apoptosis. Under stress conditions, the encoded protein is phosphorylated by ATM and dissociates from p53, which activates p53 and initiates apoptosis. [provided by RefSeq, Jul 2016] |
ZNF428 Genezinc finger protein 428 Predicted to enable metal ion binding activity. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF429 Genezinc finger protein 429 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF969P Genezinc finger protein 969, pseudogene |
ZNF884P Genezinc finger protein 884, pseudogene |
ZFP14 GeneZFP14 zinc finger protein Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within blastocyst hatching. Predicted to be located in membrane. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC728743 Genezinc finger protein pseudogene |
LOC100128713 Genezinc finger protein 816A pseudogene |
ZNF735 Genezinc finger protein 735 This gene encodes a kruppel-associated box-containing zinc finger protein (KRAB-ZFP). The encoded protein contains an N-terminal kruppel-associated box (KRAB) domain and nine C-terminal C2H2-type zinc finger domains. The KRAB-ZFPs represent the largest family of mammalian transcriptional repressors, which function through the recruitment of the nuclear co-factor KRAB-Associated Protein 1 (KAP1), to engage histone modifiers and induce heterochromatin formation. [provided by RefSeq, Jul 2017] |
ZNF92P2 Genezinc finger protein 92 pseudogene 2 |
ZNF92P3 Genezinc finger protein 92 pseudogene 3 |
ZNF219 Genezinc finger protein 219 This gene is a member of the Kruppel-like zinc finger gene family. The encoded protein functions as a transcriptional repressor of the high mobility group nucleosome binding domain 1 protein, which is associated with transcriptionally active chromatin. [provided by RefSeq, Apr 2017] |
LOC100419859 Genezinc finger, MYM-type 1 pseudogene |
LOC100419678 Genezinc finger, MYM-type 1 pseudogene |
ZFHX2 Genezinc finger homeobox 2 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in regulation of sensory perception of pain. Located in nucleus. Implicated in Marsili syndrome. [provided by Alliance of Genome Resources, Mar 2025] |
HKR1 GeneHKR1, GLI-Kruppel zinc finger family member Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100130854 Genezinc finger protein 562 pseudogene |
LOC100419686 Genezinc finger protein 256 pseudogene |
LOC100419685 Genezinc finger protein 555 pseudogene |
LOC100419684 Genezinc finger protein 114 pseudogene |
LOC100419680 Genezinc finger protein 430 pseudogene |
ZFPM2 Genezinc finger protein, FOG family member 2 The zinc finger protein encoded by this gene is a widely expressed member of the FOG family of transcription factors. The family members modulate the activity of GATA family proteins, which are important regulators of hematopoiesis and cardiogenesis in mammals. It has been demonstrated that the protein can both activate and down-regulate expression of GATA-target genes, suggesting different modulation in different promoter contexts. A related mRNA suggests an alternatively spliced product but this information is not yet fully supported by the sequence. [provided by RefSeq, Jul 2008] |
ZNF271P Genezinc finger protein 271, pseudogene Zinc finger proteins interact with nucleic acids and have diverse functions. The zinc finger domain is a conserved amino acid sequence motif containing 2 specifically positioned cysteines and 2 histidines that are involved in coordinating zinc. Kruppel-related proteins form 1 family of zinc finger proteins. See ZFP93 (MIM 604749) for additional information on zinc finger proteins.[supplied by OMIM, Apr 2004] |
ZNF519P1 Genezinc finger protein 519 pseudogene 1 |
ZNF519P2 Genezinc finger protein 519 pseudogene 2 |
ZNF355P Genezinc finger protein 355, pseudogene Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF603P Genezinc finger protein 603, pseudogene |
ZNF663P Genezinc finger protein 663, pseudogene |
ZNF252P Genezinc finger protein 252, pseudogene |
ZNF877P Genezinc finger protein 877, pseudogene |
ZNF722P Genezinc finger protein 722, pseudogene |
ZNF628 Genezinc finger protein 628 Zinc finger proteins (ZNFs), which bind nucleic acids, perform many key functions, the most important of which is regulating transcription. See ZNF91 (MIM 603971) for general information on ZNFs.[supplied by OMIM, Mar 2008] |
ZNF629 Genezinc finger protein 629 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF624 Genezinc finger protein 624 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF625 Genezinc finger protein 625 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF626 Genezinc finger protein 626 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF627 Genezinc finger protein 627 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF620 Genezinc finger protein 620 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF621 Genezinc finger protein 621 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF622 Genezinc finger protein 622 Enables preribosome binding activity. Involved in several processes, including intrinsic apoptotic signaling pathway in response to oxidative stress; positive regulation of JNK cascade; and positive regulation of kinase activity. Located in Golgi apparatus; cytosol; and nuclear lumen. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF623 Genezinc finger protein 623 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SWSAP1 GeneSWIM-type zinc finger 7 associated protein 1 Enables ATP hydrolysis activity and single-stranded DNA binding activity. Involved in double-strand break repair via homologous recombination and protein stabilization. Part of Shu complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100533643 Genezinc finger protein 91 pseudogene |
LOC100533644 Genezinc finger protein 628 pseudogene |
LOC100533646 Genezinc finger protein 135 pseudogene Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF544 Genezinc finger protein 544 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF547 Genezinc finger protein 547 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF540 Genezinc finger protein 540 Enables mRNA regulatory element binding translation repressor activity. Involved in negative regulation of DNA-templated transcription and negative regulation of translation. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF543 Genezinc finger protein 543 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF549 Genezinc finger protein 549 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF548 Genezinc finger protein 548 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFPM1 Genezinc finger protein, FOG family member 1 Enables RNA polymerase II-specific DNA-binding transcription factor binding activity and transcription corepressor activity. Involved in platelet formation; regulation of definitive erythrocyte differentiation; and regulation of gene expression. Part of transcription repressor complex. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF70P1 Genezinc finger protein 70 pseudogene 1 |
ZNF783 Genezinc finger family member 783 Enables identical protein binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF782 Genezinc finger protein 782 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF781 Genezinc finger protein 781 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF787 Genezinc finger protein 787 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF786 Genezinc finger protein 786 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF785 Genezinc finger protein 785 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF784 Genezinc finger protein 784 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within hematopoietic progenitor cell differentiation. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF789 Genezinc finger protein 789 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF788 Genezinc finger family member 788 Predicted to be involved in regulation of DNA-templated transcription. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100289416 Genezinc finger protein 793 |
ZEB2P1 Genezinc finger E-box binding homeobox 2 pseudogene 1 |
LOC100533641 Genezinc finger protein 100 pseudogene |
ZNF248 Genezinc finger protein 248 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105378242 Genezinc finger protein 705A-like |
LOC100419863 Genezinc finger protein 705A pseudogene |
ZFPL1 Genezinc finger protein-like 1 Predicted to enable DNA binding activity and zinc ion binding activity. Predicted to be involved in regulation of DNA-templated transcription. Located in Golgi apparatus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNRF4 Genezinc and ring finger 4 Enables ubiquitin protein ligase activity. Involved in negative regulation of nucleotide-binding activity oligomerization domain containing 2 signaling pathway and proteasome-mediated ubiquitin-dependent protein catabolic process. Is active in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ZNRF1 Genezinc and ring finger 1, E3 ubiquitin protein ligase This gene encodes an E3 ubiquitin-protein ligase that plays a role in neural-cell differentiation. Overexpression of this gene causes neurite-like elongation. The encoded protein contains both a zinc finger and a RING finger motif and is localized in the endosome/lysosome compartment, indicating that it may be involved in ubiquitin-mediated protein modification, and in synaptic vessicle membranes in neurons. [provided by RefSeq, Feb 2012] |
ZNRF3 Genezinc and ring finger 3 Enables frizzled binding activity and ubiquitin-protein transferase activity. Involved in negative regulation of Wnt signaling pathway; protein ubiquitination; and ubiquitin-dependent protein catabolic process. Located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ZNRF2 Genezinc and ring finger 2, E3 ubiquitin protein ligase Enables ubiquitin protein ligase activity. Involved in positive regulation of autophagosome-lysosome fusion. Located in cytoplasmic vesicle membrane; nuclear lumen; and plasma membrane. Part of protein-containing complex. Is active in intracellular membrane-bounded organelle. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF646P1 Genezinc finger protein 646 pseudogene 1 |
LOC100129391 Genezinc finger (CCCH type), RNA-binding motif and serine/arginine rich 2 pseudogene |
ZNF546 Genezinc finger protein 546 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in membrane. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF541 Genezinc finger protein 541 Predicted to enable transcription corepressor activity. Predicted to be involved in male meiotic nuclear division and regulation of DNA-templated transcription. Predicted to be located in nucleus. Predicted to be part of histone deacetylase complex and transcription regulator complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC101930552 Genezinc finger protein 717-like |
ZNF709 Genezinc finger protein 709 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF708 Genezinc finger protein 708 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in membrane and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF703 Genezinc finger protein 703 Predicted to enable DNA-binding transcription factor binding activity and metal ion binding activity. Involved in several processes, including cellular response to estradiol stimulus; positive regulation of mammary gland epithelial cell proliferation; and regulation of transforming growth factor beta receptor signaling pathway. Located in cytoplasm and nuclear matrix. Part of protein-containing complex. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF701 Genezinc finger protein 701 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF700 Genezinc finger protein 700 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF707 Genezinc finger protein 707 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF706 Genezinc finger protein 706 Predicted to enable metal ion binding activity. Predicted to be involved in negative regulation of DNA-templated transcription and negative regulation of stem cell population maintenance. Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF704 Genezinc finger protein 704 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF56 Genezinc finger protein 56 |
ZNF57 Genezinc finger protein 57 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF7 Genezinc finger protein 7 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in membrane. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF4 Genezinc finger protein-4 |
ZNF5 Genezinc finger protein-5 |
ZNF2 Genezinc finger protein 2 The protein encoded by this gene belongs to the C2H2-type zinc-finger protein family. The exact function of this gene is not known, however, zinc-finger proteins are known to interact with DNA and function as transcription regulators. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2014] |
ZNF3 Genezinc finger protein 3 Enables identical protein binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
CTCFL GeneCCCTC-binding factor (zinc finger protein)-like CCCTC-binding factor (CTCF), an 11-zinc-finger factor involved in gene regulation, utilizes different zinc fingers to bind varying DNA target sites. CTCF forms methylation-sensitive insulators that regulate X-chromosome inactivation. This gene is a paralog of CTCF and appears to be expressed primarily in the cytoplasm of spermatocytes, unlike CTCF which is expressed primarily in the nucleus of somatic cells. CTCF and the protein encoded by this gene are normally expressed in a mutually exclusive pattern that correlates with resetting of methylation marks during male germ cell differentiation. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2012] |
ZNF8 Genezinc finger protein 8 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II. Predicted to act upstream of or within BMP signaling pathway. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZKSCAN7P1 Genezinc finger with KRAB and SCAN domains 7 pseudogene 1 |
LOC643381 Genezinc finger protein 614 pseudogene |
LOC100533636 Genezinc finger protein 519 pseudogene |
ZNF138 Genezinc finger protein 138 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in membrane and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF132 Genezinc finger protein 132 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF133 Genezinc finger protein 133 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF134 Genezinc finger protein 134 Predicted to enable DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II; regulation of cytokine production; and regulation of immune system process. Predicted to be located in nucleus. Predicted to be active in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF135 Genezinc finger protein 135 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in cytoskeleton organization and regulation of cell morphogenesis. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF136 Genezinc finger protein 136 This gene encodes a zinc finger protein containing a Kruppel-associated box (KRAB) A-box domain at its N-terminus, followed by fourteen contiguous C2H2 zinc finger domains and a degenerate zinc finger. The KRAB A-box showed weak transcriptional repressor activity in a reporter gene assay. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016] |
ZNF736P1Y Genezinc finger protein 736 pseudogene 1, Y-linked |
ZNF736P11Y Genezinc finger protein 736 pseudogene 11, Y-linked |
ZNF813 Genezinc finger protein 813 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF812 Genezinc finger protein 812 |
LOC100287523 Genezinc finger protein 2-like |
ZNF362 Genezinc finger protein 362 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF365 Genezinc finger protein 365 This gene encodes a zinc finger protein that may play a role in the repair of DNA damage and maintenance of genome stability. The N-terminal C2H2 zinc finger motif is required to form a protein complex with PARP1 and MRE11, which are known to be involved in the restart of stalled DNA replication forks. A mutation in this gene may be associated with breast cancer susceptibility. [provided by RefSeq, Mar 2020] |
ZNF367 Genezinc finger protein 367 Enables DNA-binding transcription factor activity. Acts upstream of or within regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF366 Genezinc finger protein 366 Enables nuclear estrogen receptor binding activity and transcription corepressor activity. Involved in negative regulation of intracellular estrogen receptor signaling pathway; negative regulation of transcription by RNA polymerase II; and response to estrogen. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419739 Genezinc finger protein 341 pseudogene |
MORC2 GeneMORC family CW-type zinc finger 2 This gene encodes a member of the Microrchidia (MORC) protein superfamily. The encoded protein is known to regulate the condensation of heterochromatin in response to DNA damage and play a role in repressing transcription. The protein has been found to regulate the activity of ATP citrate lyase via specific interaction with this enzyme in the cytosol of lipogenic breast cancer cells. The protein also plays a role in lipogenesis and adipocyte differentiation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Feb 2016] |
MORC3 GeneMORC family CW-type zinc finger 3 This gene encodes a protein that localizes to the nuclear matrix and forms nuclear bodies via an ATP-dependent mechanism. The protein is predicted to have coiled-coil and zinc finger domains and has RNA binding activity. Alternative splicing produces multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Feb 2016] |
MORC1 GeneMORC family CW-type zinc finger 1 This gene encodes the human homolog of mouse morc and like the mouse protein it is testis-specific. Mouse studies support a testis-specific function since only male knockout mice are infertile; infertility is the only apparent defect. These studies further support a role for this protein early in spermatogenesis, possibly by affecting entry into apoptosis because testis from knockout mice show greatly increased numbers of apoptotic cells. [provided by RefSeq, Jan 2009] |
MORC4 GeneMORC family CW-type zinc finger 4 In human, the four current members of the microrchidia (morc) gene family share an N-terminal ATPase-like ATP-binding region and a CW four-cysteine zinc-finger motif. The protein encoded by this gene also has a nuclear matrix binding domain and a two-stranded coiled-coil motif near its C-terminus. This gene is widely expressed at low levels in normal tissues and has elevated expression in placenta and testis. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Jan 2010] |
LOC105379522 Genezinc finger protein 717-like |
FEZF1 GeneFEZ family zinc finger 1 This gene encodes a transcriptional repressor that belongs to the zinc finger double domain protein family. The encoded protein is thought to play a role in the embryonic migration of gonadotropin-releasing hormone neurons into the brain. Mutations in this gene are associated with hypogonadotropic hypogonadism-22 with anosmia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014] |
FEZF2 GeneFEZ family zinc finger 2 Predicted to enable several functions, including DNA-binding transcription factor activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; and chromatin binding activity. Predicted to be involved in regulation of gene expression. Predicted to act upstream of or within several processes, including negative regulation of transcription by RNA polymerase II; nervous system development; and regulation of neuron differentiation. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFRP1 Genezinc finger RNA binding protein pseudogene 1 |
ZFP69B GeneZFP69 zinc finger protein B Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Involved in Golgi organization. Located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105369285 Genezinc finger protein 813-like |
ZNF479 Genezinc finger protein 479 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF471 Genezinc finger protein 471 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF470 Genezinc finger protein 470 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nuclear body. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF473 Genezinc finger protein 473 This gene encodes a member of the Krueppel C2H2-type zinc-finger family of proteins. The encoded protein, a component of the U7 snRNP complex, plays a role in histone 3'-end pre-mRNA processing and may be required for cell cycle progression to S phase. Expression level and methylation status of this gene may be correlated with bone mineral density. [provided by RefSeq, Jul 2016] |
ZNF474 Genezinc finger protein 474 Predicted to enable metal ion binding activity. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100418554 Genezinc finger protein 93 pseudogene |
LOC100418556 Genezinc finger protein 70 pseudogene |
LOC100418550 Genezinc finger protein 93 pseudogene |
LOC100418551 Genezinc finger protein 70 pseudogene |
LOC100418552 Genezinc finger protein 93 pseudogene |
LOC100418553 Genezinc finger protein 70 pseudogene |
ZKSCAN1 Genezinc finger with KRAB and SCAN domains 1 This gene encodes a member of the Kruppel C2H2-type zinc-finger family of proteins. This encoded protein may function as a transcription factor that regulates the expression of GABA type-A receptors in the brain. Transcripts from this gene have been shown to form stable and abundant circular RNAs. Elevated expression of this gene has been observed in gastric cancer and the encoded protein may stimulate migration and invasion of human gastric cancer cells. [provided by RefSeq, Oct 2016] |
ZKSCAN3 Genezinc finger with KRAB and SCAN domains 3 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; and chromatin binding activity. Involved in lysosome organization; negative regulation of metabolic process; and regulation of DNA-templated transcription. Located in cytoplasm and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZKSCAN2 Genezinc finger with KRAB and SCAN domains 2 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZKSCAN5 Genezinc finger with KRAB and SCAN domains 5 This gene encodes a zinc finger protein of the Kruppel family. The protein contains a SCAN box and a KRAB A domain and may be involved in transcriptional regulation. A similar protein in mouse is differentially expressed in spermatogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015] |
ZKSCAN4 Genezinc finger with KRAB and SCAN domains 4 Enables identical protein binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZKSCAN7 Genezinc finger with KRAB and SCAN domains 7 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZKSCAN8 Genezinc finger with KRAB and SCAN domains 8 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF677 Genezinc finger protein 677 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF676 Genezinc finger protein 676 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF675 Genezinc finger protein 675 Enables ubiquitin protein ligase binding activity. Involved in negative regulation of osteoclast differentiation; negative regulation of signal transduction; and regulation of DNA-templated transcription. Located in nucleus and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF674 Genezinc finger protein 674 This gene encodes a zinc finger protein with an N-terminal Kruppel-associated box-containing (KRAB) domain and 11 Kruppel-type C2H2 zinc finger domains. Like other zinc finger proteins, this gene may function as a transcription factor. This gene resides on an area of chromosome X that has been implicated in nonsyndromic X-linked cognitive disabilities. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2017] |
ZNF672 Genezinc finger protein 672 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF671 Genezinc finger protein 671 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF670 Genezinc finger protein 670 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Acts upstream of or within lipid metabolic process. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF679 Genezinc finger protein 679 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF678 Genezinc finger protein 678 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFP69 GeneZFP69 zinc finger protein Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of lipid metabolic process and regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFP64 GeneZFP64 zinc finger protein Predicted to enable DNA binding activity and metal ion binding activity. Involved in mesenchymal cell differentiation. Located in cytoplasm and megasporocyte nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFP62 GeneZFP62 zinc finger protein Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF385C Genezinc finger protein 385C Predicted to enable nucleic acid binding activity and zinc ion binding activity. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF385B Genezinc finger protein 385B Enables p53 binding activity. Involved in intrinsic apoptotic signaling pathway by p53 class mediator. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF385A Genezinc finger protein 385A Zinc finger proteins, such as ZNF385A, are regulatory proteins that act as transcription factors, bind single- or double-stranded RNA, or interact with other proteins (Sharma et al., 2004 [PubMed 15527981]).[supplied by OMIM, Oct 2008] |
ZNF654 Genezinc finger protein 654 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF382 Genezinc finger protein 382 This gene encodes a KRAB domain zinc finger transcription factor (KZNF). KZNFs play critical roles in the regulation of many cellular processes including differentiation, proliferation and apoptosis. The encoded protein inhibits activating protein 1 (AP-1) and nuclear factor kappa-B (NF-kB) signaling and may function as a tumor suppressor in multiple carcinomas. This gene is found in a cluster with other zinc finger protein genes on the long arm of chromosome 19, and alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2012] |
ZNF823 Genezinc finger protein 823 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419913 Genezinc finger protein 678 pseudogene |
ZXDB Genezinc finger, X-linked, duplicated B The ZXDB gene is one of a pair of duplicated zinc finger genes on chromosome Xp11.21 (Greig et al., 1993 [PubMed 8268913]); see also ZXDA (MIM 300235).[supplied by OMIM, Jul 2010] |
ZXDC GeneZXD family zinc finger C Enables C2H2 zinc finger domain binding activity; LRR domain binding activity; and transcription coactivator activity. Involved in positive regulation of DNA-templated transcription. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZXDA Genezinc finger, X-linked, duplicated A This gene encodes one of two duplicated zinc finger genes on chromosome Xp11. This gene is the telomeric copy; GeneID 158586 ZXDB is the more centromeric copy. The two genes have 98% nucleotide sequence similarity, and the predicted proteins contain 10 tandem zinc finger motifs. [provided by RefSeq, Nov 2009] |
ZNF702P Genezinc finger protein 702, pseudogene Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105372373 Genezinc finger protein 772 |
LOC100421332 Genezinc finger with KRAB and SCAN domains 1 pseudogene |
ZNF215 Genezinc finger protein 215 This gene is imprinted in a tissue-specific manner with preferential expression in the testis, and encodes a zinc finger protein that belongs to a family of zinc finger transcription factors. The encoded protein contains an N-terminal SRE-ZBP, Ctfin51, AW-1, and Number 18 (SCAN) domain, a kruppel-associated box A (KRABA) domain, and four C-terminal zinc finger domains. This gene is located within one of three regions on chromosome 11p15 associated with Beckwith-Wiedemann syndrome, called Beckwith-Wiedemann syndrome chromosome region-2 (BWSCR2), and is thought to play a role in the etiology of this disease. [provided by RefSeq, Aug 2017] |
ZNF214 Genezinc finger protein 214 This gene is expressed predominantly in the testis and encodes a zinc finger protein that contains an N-terminal kruppel-associated box A (KRABA) domain and twelve zinc finger domains. This gene is located within one of three regions on chromosome 11p15 associated with Beckwith-Wiedemann syndrome, called Beckwith-Wiedemann syndrome chromosome region-2 (BWSCR2), and is thought to play a role in the etiology of this disease. [provided by RefSeq, Aug 2017] |
ZNF217 Genezinc finger protein 217 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II. Located in mitochondrion and nuclear speck. Part of histone deacetylase complex. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF211 Genezinc finger protein 211 This gene encodes a protein containing a Kruppel-associated box domain and multiple zinc finger domains. This protein may play a role in developmental processes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014] |
ZNF212 Genezinc finger protein 212 This gene belongs to the C2H2-type zinc finger gene family. The zinc finger proteins are involved in gene regulation and development, and are quite conserved throughout evolution. Like this gene product, a third of the zinc finger proteins containing C2H2 fingers also contain the KRAB domain, which has been found to be involved in protein-protein interactions. [provided by RefSeq, Jul 2008] |
LOC100421641 Genezinc finger CCHC-type and RNA binding motif 1 pseudogene |
ZNF534 Genezinc finger protein 534 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF536 Genezinc finger protein 536 The protein encoded by this gene is a highly conserved zinc finger protein. The encoded protein is most abundant in brain, where it negatively regulates neuronal differentiation. [provided by RefSeq, Sep 2015] |
ZNF530 Genezinc finger protein 530 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF532 Genezinc finger protein 532 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC101929206 Genezinc finger protein 708-like |
LOC100421074 GeneZFP14 zinc finger protein pseudogene |
LOC100130881 Genezinc finger protein 12 pseudogene |
ZNF732 Genezinc finger protein 732 This gene encodes a kruppel-associated box-containing zinc finger protein (KRAB-ZFP). The encoded protein contains an N-terminal kruppel-associated box (KRAB) domain and sixteen C-terminal C2H2-type zinc finger domains. The KRAB-ZFPs represent the largest family of mammalian transcriptional repressors, which function through the recruitment of the nuclear co-factor KRAB-Associated Protein 1 (KAP1), to engage histone modifiers and induce heterochromatin formation. [provided by RefSeq, Jul 2017] |
ZNF730 Genezinc finger protein 730 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF736 Genezinc finger protein 736 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF737 Genezinc finger protein 737 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF738 Genezinc finger protein 738 Predicted to enable ubiquitin-protein transferase activity. Predicted to be involved in protein polyubiquitination. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF317P1 Genezinc finger protein 317 pseudogene 1 |
LOC100419679 Genezinc finger protein 670 pseudogene |
LOC100129947 Genezinc finger protein 674 pseudogene |
ZNF69 Genezinc finger protein 69 Enables identical protein binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF66 Genezinc finger protein 66 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in membrane and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100287477 Genezinc finger protein 420-like |
ZNF29P Genezinc finger protein 29, pseudogene |
ZNF736P2Y Genezinc finger protein 736 pseudogene 2, Y-linked |
ZNF296 Genezinc finger protein 296 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in negative regulation of dendrite development; regulation of transcription by RNA polymerase II; and spermatogenesis. Predicted to act upstream of or within negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF292 Genezinc finger protein 292 This gene encodes a growth hormone-dependent, zinc finger transcription factor that functions as a tumor suppressor. Naturally occurring mutations in this gene are associated with gastric cancer, colorectal cancer, and chronic lymphocytic leukemia. [provided by RefSeq, May 2017] |
ZNF962P Genezinc finger protein 962, pseudogene |
ZNF37CP Genezinc finger protein 37C, pseudogene |
ZNF821 Genezinc finger protein 821 This gene encodes a protein with two C2H2 zinc finger motifs and a score-and-three (23)-amino acid peptide repeat (STPR) domain. The STPR domain of the encoded protein binds to double stranded DNA and may also contain a nuclear localization signal, suggesting that this protein interacts with chromosomal DNA. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011] |
ZNF827 Genezinc finger protein 827 Enables NuRD complex binding activity. Involved in several processes, including establishment of protein localization to telomere; negative regulation of shelterin complex assembly; and telomere maintenance. Located in chromatin and chromosome, telomeric region. Part of ribonucleoprotein complex. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF829 Genezinc finger protein 829 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
DBF4P1 GeneDBF4 zinc finger pseudogene 1 |
ZNF311 Genezinc finger protein 311 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF316 Genezinc finger protein 316 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF317 Genezinc finger protein 317 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF318 Genezinc finger protein 318 Predicted to enable protein heterodimerization activity and protein homodimerization activity. Predicted to be involved in negative regulation of DNA-templated transcription and positive regulation of DNA-templated transcription. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF319 Genezinc finger protein 319 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419748 Genezinc finger protein 852 pseudogene |
LOC100419741 Genezinc finger protein 772 pseudogene |
ST18 Genesuppression of tumorigenicity 18, zinc finger Enables RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in cytokine-mediated signaling pathway; negative regulation of cell population proliferation; and positive regulation of macromolecule metabolic process. Located in nucleus. Part of protein-DNA complex. [provided by Alliance of Genome Resources, Mar 2025] |
DBF4B GeneDBF4 zinc finger B This gene encodes a regulator of the cell division cycle 7 homolog (S. cerevisiae) protein, a serine-threonine kinase which links cell cycle regulation to genome duplication. This protein localizes to the nucleus and, in complex with the cell division cycle 7 homolog (S. cerevisiae) protein, may facilitate M phase progression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2010] |
ZNF818P Genezinc finger protein 818, pseudogene Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZC3HAV1L Genezinc finger CCCH-type, antiviral 1-like Located in cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF886P Genezinc finger protein 886, pseudogene |
ZNF33AP1 Genezinc finger protein 33A pseudogene 1 |
ZNF259P1 Genezinc finger protein 259 pseudogene 1 |
ZNF165 Genezinc finger protein 165 This gene encodes a member of the Kruppel family of zinc finger proteins. Members of this DNA-binding protein family act as transcriptional regulators. This gene is located within a cluster of zinc finger family members. The encoded protein may play a role in spermatogenesis. [provided by RefSeq, Jul 2008] |
LOC100131411 Genezinc finger protein 28 pseudogene |
LOC100419896 Genezinc finger protein 267 pseudogene |
LOC100419894 Genezinc finger protein 347 pseudogene |
LOC100419895 Genezinc finger protein 670 pseudogene |
LOC100419892 Genezinc finger protein 592 pseudogene |
LOC100419890 Genezinc finger, MYM-type 4 pseudogene |
LOC100419891 Genezinc finger protein 114 pseudogene |
ZNF404 Genezinc finger protein 404 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF407 Genezinc finger protein 407 This gene encodes a zinc finger protein whose exact function is not known. It may be involved in transcriptional regulation. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009] |
ZNF408 Genezinc finger protein 408 The protein encoded by this gene contains ten tandem zinc fingers and an N-terminal SET domain, so it is likely a DNA binding protein that interacts with other proteins. In adults, the encoded protein is expressed most highly in retina. Consequently, defects in this gene have been associated with familial exudative vitreoretinopathy (FEVR) and retinitis pigmentosa (RP). [provided by RefSeq, Dec 2016] |
ZNF648 Genezinc finger protein 648 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF649 Genezinc finger protein 649 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of osteoblast differentiation and regulation of transcription by RNA polymerase II. Predicted to act upstream of or within negative regulation of DNA-templated transcription. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF646 Genezinc finger protein 646 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF644 Genezinc finger protein 644 The protein encoded by this gene is a zinc finger transcription factor that may play a role in eye development. Defects in this gene have been associated with high myopia. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Aug 2011] |
ZNF645 Genezinc finger protein 645 This gene encodes a member of the zinc finger domain-containing protein family. This family member contains both a RING-type and a C2H2-type of zinc finger domain, and it may function as an E3 ubiquitin-protein ligase. Protein localization suggests a role in human sperm production and quality control. [provided by RefSeq, Aug 2011] |
ZNF641 Genezinc finger protein 641 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytosol; nucleolus; and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF398 Genezinc finger protein 398 This gene encodes a member of the Kruppel family of C2H2-type zinc-finger transcription factor proteins. The encoded protein acts as a transcriptional activator. Two transcript variants encoding distinct isoforms have been identified for this gene. Other transcript variants have been described, but their full length sequence has not been determined. [provided by RefSeq, Jul 2008] |
ZNF391 Genezinc finger protein 391 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF394 Genezinc finger protein 394 The protein encoded by this gene is a zinc finger protein that inhibits the transcription of mitogen-activated protein kinase signaling pathways. The encoded protein may be involved in cardiac function. [provided by RefSeq, Sep 2016] |
ZNF395 Genezinc finger protein 395 Enables DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in positive regulation of transcription by RNA polymerase II. Located in cytosol and nuclear speck. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF396 Genezinc finger protein 396 Enables protein heterodimerization activity; protein homodimerization activity; and sequence-specific double-stranded DNA binding activity. Involved in negative regulation of DNA-templated transcription. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF397 Genezinc finger protein 397 This gene encodes a protein with a N-terminal SCAN domain, and the longer isoform contains nine C2H2-type zinc finger repeats in the C-terminal domain. The protein localizes to centromeres during interphase and early prophase, and different isoforms can repress or activate transcription in transfection studies. Multiple transcript variants encoding different isoforms have been found for this gene. Additional variants have been described, but their biological validity has not been determined. [provided by RefSeq, Oct 2009] |
ZFP37 GeneZFP37 zinc finger protein This gene encodes a transcription factor that belongs to a large family of zinc finger proteins. A similar protein in mouse is thought to play a role in regulating the structures of the nucleolus and centromere in neurons. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013] |
ZFP30 GeneZFP30 zinc finger protein Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF774 Genezinc finger protein 774 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF542P Genezinc finger protein 542, pseudogene Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF619 Genezinc finger protein 619 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF204P Genezinc finger protein 204, pseudogene This locus represents a transcribed pseudogene, possibly of ZNF79 (GeneID 7633). The protein encoded by this locus would have significant N-terminal truncation, and would lack the KRAB domain and the C2H2 type zinc finger domain, compared to ZNF79. [provided by RefSeq, Jun 2011] |
HELZ2 Genehelicase with zinc finger 2, transcriptional coactivator The protein encoded by this gene is a nuclear transcriptional co-activator for peroxisome proliferator activated receptor alpha. The encoded protein contains a zinc finger and is a helicase that appears to be part of the peroxisome proliferator activated receptor alpha interacting complex. This gene is a member of the DNA2/NAM7 helicase gene family. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
LOC100887072 Genezinc finger protein 470 pseudogene |
LOC100887071 Genezinc finger protein 845 pseudogene |
LOC100887070 Genezinc finger protein 729 pseudogene |
LOC100419796 Genezinc finger protein 146 pseudogene |
LOC100419553 Genezinc finger protein 35 pseudogene |
LOC100419552 Genezinc finger protein 57 pseudogene |
LOC105379260 Geneputative zinc finger protein LOC441666 |
ZNF299P Genezinc finger protein 299, pseudogene |
ZNF93 Genezinc finger protein 93 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific. Involved in transposable element silencing. Predicted to be located in nucleoplasm. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF859P Genezinc finger protein 859, pseudogene |
ZFX Genezinc finger protein, X-linked This gene on the X chromosome is structurally similar to a related gene on the Y chromosome. It encodes a member of the krueppel C2H2-type zinc-finger protein family. The full-length protein contains an acidic transcriptional activation domain (AD), a nuclear localization sequence (NLS) and a DNA binding domain (DBD) consisting of 13 C2H2-type zinc fingers. Studies in mouse embryonic and adult hematopoietic stem cells showed that this gene was required as a transcriptional regulator for self-renewal of both stem cell types, but it was dispensable for growth and differentiation of their progeny. Multiple alternatively spliced transcript variants encoding different isoforms have been identified, but the full-length nature of some variants has not been determined. [provided by RefSeq, May 2010] |
ZFR Genezinc finger RNA binding protein This gene encodes an RNA-binding protein characterized by its DZF (domain associated with zinc fingers) domain. The encoded protein may play a role in the nucleocytoplasmic shuttling of another RNA-binding protein, Staufen homolog 2, in neurons. Expression of this gene is regulated through alternative polyadenylation that mediates differential microRNA targeting. Elevated expression of this gene has been observed in human patients with pancreatic cancer and knockdown of this gene may result in reduced viability and invasion of pancreatic cancer cells. [provided by RefSeq, Sep 2016] |
ZNF321P Genezinc finger protein 321, pseudogene |
ZNF891 Genezinc finger protein 891 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100287610 Genezinc finger protein 73-like |
ZNF488 Genezinc finger protein 488 Predicted to enable DNA binding activity and metal ion binding activity. Predicted to be involved in oligodendrocyte development and regulation of DNA-templated transcription. Predicted to act upstream of or within negative regulation of DNA-templated transcription and positive regulation of oligodendrocyte differentiation. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF480 Genezinc finger protein 480 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF483 Genezinc finger protein 483 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF484 Genezinc finger protein 484 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF485 Genezinc finger protein 485 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF486 Genezinc finger protein 486 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF487 Genezinc finger protein 487 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAI2 Genesnail family zinc finger 2 This gene encodes a member of the Snail family of C2H2-type zinc finger transcription factors. The encoded protein acts as a transcriptional repressor that binds to E-box motifs and is also likely to repress E-cadherin transcription in breast carcinoma. This protein is involved in epithelial-mesenchymal transitions and has antiapoptotic activity. Mutations in this gene may be associated with sporatic cases of neural tube defects. [provided by RefSeq, Jul 2008] |
SNAI3 Genesnail family zinc finger 3 SNAI3 is a member of the SNAIL gene family, named for the Drosophila snail gene, which plays roles in mesodermal formation during embryogenesis (Katoh and Katoh, 2003 [PubMed 12579345]).[supplied by OMIM, Apr 2009] |
SNAI1 Genesnail family zinc finger 1 The Drosophila embryonic protein snail is a zinc finger transcriptional repressor which downregulates the expression of ectodermal genes within the mesoderm. The nuclear protein encoded by this gene is structurally similar to the Drosophila snail protein, and is also thought to be critical for mesoderm formation in the developing embryo. At least two variants of a similar processed pseudogene have been found on chromosome 2. [provided by RefSeq, Jul 2008] |
LOC100533634 Genezinc finger protein 737 pseudogene |
DZIP3 GeneDAZ interacting zinc finger protein 3 Enables several functions, including phosphatase binding activity; polyubiquitin modification-dependent protein binding activity; and ubiquitin-protein transferase activity. Involved in protein polyubiquitination. Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
DZIP1 GeneDAZ interacting zinc finger protein 1 Enables BBSome binding activity and molecular adaptor activity. Involved in cilium organization; heart development; and protein-containing complex localization to centriolar satellite. Located in cytoplasm; microtubule organizing center; and nucleoplasm. Implicated in mitral valve prolapse and spermatogenic failure 47. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF587P1 Genezinc finger protein 587 pseudogene 1 |
ZNF569 Genezinc finger protein 569 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF568 Genezinc finger protein 568 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in embryonic placenta morphogenesis and negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF567 Genezinc finger protein 567 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF566 Genezinc finger protein 566 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in membrane. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF565 Genezinc finger protein 565 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF564 Genezinc finger protein 564 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF563 Genezinc finger protein 563 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF562 Genezinc finger protein 562 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF561 Genezinc finger protein 561 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF849P Genezinc finger protein 849, pseudogene |
ZNF169 Genezinc finger protein 169 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF286A Genezinc finger protein 286A Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in membrane. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF286B Genezinc finger protein 286B Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF160 Genezinc finger protein 160 The protein encoded by this gene is a Kruppel-related zinc finger protein which is characterized by the presence of an N-terminal repressor domain, the Kruppel-associated box (KRAB). The KRAB domain is a potent repressor of transcription; thus this protein may function in transcription regulation. Multiple transcript variants have been found for this gene. [provided by RefSeq, Apr 2016] |
ZNF768 Genezinc finger protein 768 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromosome. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF765 Genezinc finger protein 765 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF764 Genezinc finger protein 764 Enables transcription coregulator activity. Involved in cellular response to glucocorticoid stimulus. Is active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF766 Genezinc finger protein 766 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF761 Genezinc finger protein 761 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF763 Genezinc finger protein 763 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF34 Genezinc finger protein 34 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF35 Genezinc finger protein 35 Enables DNA-binding transcription factor activity and sequence-specific DNA binding activity. Predicted to be involved in cellular response to retinoic acid; regulation of transcription by RNA polymerase II; and spermatogenesis. Located in nucleus and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF32 Genezinc finger protein 32 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF30 Genezinc finger protein 30 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF804A Genezinc finger protein 804A The protein encoded by this gene is a zinc finger binding protein. Polymorphisms in this gene, especially rs1344706, are thought to confer increased susceptibility to schizophrenia, bipolar disorder, and heroin addiciton. [provided by RefSeq, Nov 2015] |
ZNF804B Genezinc finger protein 804B Predicted to enable metal ion binding activity. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF658B Genezinc finger protein 658B, pseudogene Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC441528 Genezinc finger protein 839-like |
LOC401261 Genezinc finger protein ZIC 5 |
CIZ1 GeneCDKN1A interacting zinc finger protein 1 The protein encoded by this gene is a zinc finger DNA binding protein that interacts with CIP1, part of a complex with cyclin E. The encoded protein may regulate the cellular localization of CIP1. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012] |
LOC100133252 Genezinc finger protein 131 pseudogene |
ZNF264 Genezinc finger protein 264 This gene encodes a zinc finger protein and belongs to the krueppel C2H2-type zinc-finger protein family. Zinc finger proteins are often localized in the nucleus, bind nucleic acids, and regulate transcription. [provided by RefSeq, Jan 2010] |
ZNF266 Genezinc finger protein 266 This gene encodes a protein containing many tandem zinc-finger motifs. Zinc fingers are protein or nucleic acid-binding domains, and may be involved in a variety of functions, including regulation of transcription. This gene is located in a cluster of similar genes encoding zinc finger proteins on chromosome 19. Alternative splicing results in multiple transcript variants for this gene. [provided by RefSeq, Sep 2012] |
ZNF260 Genezinc finger protein 260 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF263 Genezinc finger protein 263 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and transcription cis-regulatory region binding activity. Involved in negative regulation of transcription by RNA polymerase II and positive regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF268 Genezinc finger protein 268 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in several processes, including positive regulation of non-canonical NF-kappaB signal transduction; regulation of apoptotic process; and regulation of primary metabolic process. Located in cytosol and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
MZF1 Genemyeloid zinc finger 1 Enables DNA-binding transcription factor activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; and protein homodimerization activity. Involved in negative regulation of transcription by RNA polymerase II and positive regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419845 Genezinc finger protein 415 pseudogene |
LOC100419844 Genezinc finger protein 610 pseudogene |
LOC100419847 Genezinc finger protein 436 pseudogene |
LOC100419841 Genezinc finger protein 107 pseudogene |
LOC100419840 Genezinc finger protein 446 pseudogene |
LOC100419842 Genezinc finger protein 396 pseudogene |
LOC100128601 Genezinc finger protein 770 pseudogene |
ZRSR1 Genezinc finger (CCCH type), RNA-binding motif and serine/arginine rich 1 Predicted to enable pre-mRNA 3'-splice site binding activity. Predicted to be involved in mRNA splicing, via spliceosome. Predicted to be located in nucleus. Predicted to be part of U2AF complex and spliceosomal complex. [provided by Alliance of Genome Resources, Mar 2025] |
IKZF5 GeneIKAROS family zinc finger 5 (Pegasus) Members of the Ikaros (ZNFN1A1; MIM 603023) family of transcription factors, which includes Pegasus, are expressed in lymphocytes and are implicated in the control of lymphoid development.[supplied by OMIM, Jul 2002] |
IKZF4 GeneIKAROS family zinc finger 4 (Eos) Members of the Ikaros (ZNFN1A1; MIM 603023) family of transcription factors, which includes Eos, are expressed in lymphocytes and are implicated in the control of lymphoid development.[supplied by OMIM, Jul 2002] |
IKZF1 GeneIKAROS family zinc finger 1 (Ikaros) This gene encodes a transcription factor that belongs to the family of zinc-finger DNA-binding proteins associated with chromatin remodeling. The expression of this protein is restricted to the fetal and adult hemo-lymphopoietic system, and it functions as a regulator of lymphocyte differentiation. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene. Most isoforms share a common C-terminal domain, which contains two zinc finger motifs that are required for hetero- or homo-dimerization, and for interactions with other proteins. The isoforms, however, differ in the number of N-terminal zinc finger motifs that bind DNA and in nuclear localization signal presence, resulting in members with and without DNA-binding properties. Only a few isoforms contain the requisite three or more N-terminal zinc motifs that confer high affinity binding to a specific core DNA sequence element in the promoters of target genes. The non-DNA-binding isoforms are largely found in the cytoplasm, and are thought to function as dominant-negative factors. Overexpression of some dominant-negative isoforms have been associated with B-cell malignancies, such as acute lymphoblastic leukemia (ALL). [provided by RefSeq, May 2014] |
IKZF3 GeneIKAROS family zinc finger 3 (Aiolos) This gene encodes a member of the Ikaros family of zinc-finger proteins. Three members of this protein family (Ikaros, Aiolos and Helios) are hematopoietic-specific transcription factors involved in the regulation of lymphocyte development. This gene product is a transcription factor that is important in the regulation of B lymphocyte proliferation and differentiation. Both Ikaros and Aiolos can participate in chromatin remodeling. Regulation of gene expression in B lymphocytes by Aiolos is complex as it appears to require the sequential formation of Ikaros homodimers, Ikaros/Aiolos heterodimers, and Aiolos homodimers. Several alternative transcripts encoding different isoforms have been described, as well as some non-protein coding variants. [provided by RefSeq, Apr 2012] |
IKZF2 GeneIKAROS family zinc finger 2 (Helios) This gene encodes a member of the Ikaros family of zinc-finger proteins. Three members of this protein family (Ikaros, Aiolos and Helios) are hematopoietic-specific transcription factors involved in the regulation of lymphocyte development. This protein forms homo- or hetero-dimers with other Ikaros family members, and is thought to function predominantly in early hematopoietic development. Multiple transcript variants encoding different isoforms have been found for this gene, but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008] |
WIZ Genewidely interspaced zinc finger motifs Enables several functions, including RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; histone methyltransferase binding activity; and transcription corepressor binding activity. Involved in positive regulation of nuclear cell cycle DNA replication and protein stabilization. Located in midbody and nucleoplasm. Biomarker of atherosclerosis. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF879 Genezinc finger protein 879 This gene encodes a kruppel-associated box-containing zinc finger protein (KRAB-ZFP). The encoded protein contains an N-terminal kruppel-associated box (KRAB) domain and thirteen C-terminal C2H2-type zinc finger domains. The KRAB-ZFPs represent the largest family of mammalian transcriptional repressors, which function through the recruitment of the nuclear co-factor KRAB-Associated Protein 1 (KAP1), to engage histone modifiers and induce heterochromatin formation. [provided by RefSeq, Jul 2017] |
ZNF878 Genezinc finger protein 878 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFP82 GeneZFP82 zinc finger protein Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
TSHZ2 Geneteashirt zinc finger homeobox 2 This gene is a member of the teashirt C2H2-type zinc-finger protein family of transcription factors. This gene encodes a protein with five C2H2-type zinc fingers, a homeobox DNA-binding domain and a coiled-coil domain. This nuclear protein is predicted to act as a transcriptional repressor. This gene is thought to play a role in the development and progression of breast and other types of cancer. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016] |
TSHZ3 Geneteashirt zinc finger homeobox 3 This gene encodes a zinc-finger transcription factor that regulates smooth muscle cell differentiation in the developing urinary tract. Consistent with this role, mice in which this gene has been inactivated exhibit abnormal gene expression in urinary tract smooth muscle cell precursors and kidney defects including hydronephrosis. The encoded transcription factor comprises a gene silencing complex that inhibits caspase expression. Reduced expression of this gene and consequent caspase upregulation may be correlated with progression of Alzheimer's disease in human patients. [provided by RefSeq, Jul 2016] |
TSHZ1 Geneteashirt zinc finger homeobox 1 This gene encodes a colon cancer antigen that was defined by serological analysis of recombinant cDNA expression libraries. The encoded protein is a member of the teashirt C2H2-type zinc-finger protein family and may be involved in transcriptional regulation of developmental processes. Mutations in this gene may be associated with congenital aural atresia syndrome. [provided by RefSeq, Jan 2012] |
ZNF92P1Y Genezinc finger protein 92 pseudogene 1, Y-linked |
LOC105372810 Geneputative zinc finger protein 355P |
ZNF157 Genezinc finger protein 157 This gene product is a likely zinc finger family transcription factor. It contains KRAB-A and KRAB-B domains that act as transcriptional repressors in related proteins, and multiple zinc finger DNA binding motifs and finger linking regions characteristic of the Kruppel family. This gene is part of a gene cluster on chromosome Xp11.23. [provided by RefSeq, Jul 2008] |
ZNF154 Genezinc finger protein 154 This gene encodes a protein that belongs to the zinc finger Kruppel family of transcriptional regulators, whose members are thought to function in normal and abnormal cell growth and differentiation. Hypermethylation of this gene is associated with the recurrence of non muscle invasive bladder cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014] |
ZNF155 Genezinc finger protein 155 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105369224 Genezinc finger protein 806 pseudogene |
ZNF444P1 Genezinc finger protein 444 pseudogene 1 |
LOC344065 Genezinc finger protein 184 pseudogene Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100301990 Genezinc finger protein 610 pseudogene |
ZNF887P Genezinc finger protein 887, pseudogene |
LOC101060181 Genezinc finger protein ZnFP12 |
ZNF699 Genezinc finger protein 699 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF691 Genezinc finger protein 691 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF692 Genezinc finger protein 692 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II and regulation of gluconeogenesis. Located in nucleolus and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF695 Genezinc finger protein 695 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF697 Genezinc finger protein 697 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF696 Genezinc finger protein 696 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419712 Genezinc finger protein 12 pseudogene |
LOC100419715 Genezinc finger protein 626 pseudogene |
LOC100419716 Genezinc finger protein 709 pseudogene |
ZNF343 Genezinc finger protein 343 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF341 Genezinc finger protein 341 Enables DNA binding activity and DNA-binding transcription activator activity. Predicted to be involved in regulation of DNA-templated transcription. Located in nucleus. Implicated in hyper IgE recurrent infection syndrome 3. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF347 Genezinc finger protein 347 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF346 Genezinc finger protein 346 The protein encoded by this gene is a nucleolar, zinc finger protein that preferentially binds to double-stranded (ds) RNA or RNA/DNA hybrids, rather than DNA alone. Mutational studies indicate that the zinc finger domains are not only essential for dsRNA binding, but are also required for its nucleolar localization. The encoded protein may be involved in cell growth and survival. It plays a role in protecting neurons by inhibiting cell cycle re-entry via stimulation of p21 gene expression. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2015] |
ZNF345 Genezinc finger protein 345 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC645749 Genezinc finger protein 131 pseudogene |
LOC100419690 Genezinc finger protein 114 pseudogene |
LOC100419691 Genezinc finger protein 114 pseudogene |
LOC100419692 Genezinc finger protein 791 pseudogene |
LOC100419693 Genezinc finger protein 114 pseudogene |
DBF4 GeneDBF4 zinc finger Predicted to enable protein serine/threonine kinase activator activity. Predicted to be involved in positive regulation of nuclear cell cycle DNA replication and regulation of cell cycle phase transition. Located in nuclear body. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF75CP Genezinc finger protein 75C, pseudogene Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF354A Genezinc finger protein 354A Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytosol; nucleolus; and nucleoplasm. Biomarker of in situ carcinoma and seminoma. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF354C Genezinc finger protein 354C Enables DNA-binding transcription repressor activity, RNA polymerase II-specific. Involved in negative regulation of sprouting angiogenesis. Located in cytoplasm; nuclear membrane; and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF354B Genezinc finger protein 354B Predicted to enable several functions, including DNA-binding transcription factor activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; and transcription corepressor activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF602P Genezinc finger protein 602, pseudogene |
ZNF90P2 Genezinc finger protein 90 pseudogene 2 |
ZNF90P3 Genezinc finger protein 90 pseudogene 3 |
ZNF90P1 Genezinc finger protein 90 pseudogene 1 |
GLIS2 GeneGLIS family zinc finger 2 This gene is a member of the GLI-similar zinc finger protein family and encodes a nuclear transcription factor with five C2H2-type zinc finger domains. The protein encoded by this gene is widely expressed at low levels in the neural tube and peripheral nervous system and likely promotes neuronal differentiation. It is abundantly expressed in the kidney and may have a role in the regulation of kidney morphogenesis. p120 regulates the expression level of this protein and induces the cleavage of this protein's C-terminal zinc finger domain. This protein also promotes the nuclear translocation of p120. Mutations in this gene cause nephronophthisis (NPHP), an autosomal recessive kidney disease characterized by tubular basement membrane disruption, interstitial lymphohistiocytic cell infiltration, and development of cysts at the corticomedullary border of the kidneys.[provided by RefSeq, Jan 2010] |
GLIS3 GeneGLIS family zinc finger 3 This gene is a member of the GLI-similar zinc finger protein family and encodes a nuclear protein with five C2H2-type zinc finger domains. This protein functions as both a repressor and activator of transcription and is specifically involved in the development of pancreatic beta cells, the thyroid, eye, liver and kidney. Mutations in this gene have been associated with neonatal diabetes and congenital hypothyroidism (NDH). Alternatively spliced variants that encode different protein isoforms have been described but the full-length nature of only two have been determined. [provided by RefSeq, Jul 2008] |
GLIS1 GeneGLIS family zinc finger 1 GLIS1 is a GLI (MIM 165220)-related Kruppel-like zinc finger protein that functions as an activator and repressor of transcription (Kim et al., 2002 [PubMed 12042312]).[supplied by OMIM, Mar 2008] |
ZNF324B Genezinc finger protein 324B Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF324 Genezinc finger protein 324 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Acts upstream of or within with a positive effect on G1/S transition of mitotic cell cycle and cell population proliferation. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF320 Genezinc finger protein 320 ZNF320 encodes a Kruppel-like zinc finger protein. Members of this protein family are involved in activation or repression of transcription.[supplied by OMIM, Jul 2002] |
FLYWCH1P1 GeneFLYWCH-type zinc finger 1 pseudogene 1 |
LOC100419774 Genezinc finger protein 383 pseudogene |
ZNF451 Genezinc finger protein 451 Enables SUMO ligase activity; transcription corepressor activity; and transcription regulator inhibitor activity. Involved in negative regulation of transcription initiation by RNA polymerase II; negative regulation of transforming growth factor beta receptor signaling pathway; and protein sumoylation. Located in PML body. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF454 Genezinc finger protein 454 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
DBF4P2 GeneDBF4 zinc finger pseudogene 2 |
DZIP1L GeneDAZ interacting zinc finger protein 1-like Predicted to enable metal ion binding activity. Involved in cilium assembly and regulation of protein localization. Located in centriole and ciliary basal body. Implicated in polycystic kidney disease 5. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF723P Genezinc finger protein 723, pseudogene Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF611 Genezinc finger protein 611 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF610 Genezinc finger protein 610 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF613 Genezinc finger protein 613 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF615 Genezinc finger protein 615 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF614 Genezinc finger protein 614 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF616 Genezinc finger protein 616 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF618 Genezinc finger protein 618 Enables identical protein binding activity and transcription coregulator binding activity. Predicted to be involved in regulation of DNA-templated transcription. Located in pericentric heterochromatin. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419791 Genezinc finger protein 449 pseudogene |
LOC100419790 Genezinc finger protein 670 pseudogene |
LOC100419795 Genezinc finger, MYM-type 1 pseudogene |
LOC100419794 Genezinc finger protein 449 pseudogene |
LOC100533637 Genezinc finger protein 83 pseudogene |
LOC100533633 Genezinc finger protein 257 pseudogene |
LOC100533632 Genezinc finger protein 736 pseudogene |
ZNF518B Genezinc finger protein 518B Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF518A Genezinc finger protein 518A The protein encoded by this gene is a member of the krueppel C2H2-type zinc finger protein family. The encoded protein contains five zinc fingers and is likely a nuclear transcriptional regulator. Numerous transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Aug 2016] |
ZNF556 Genezinc finger protein 556 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF557 Genezinc finger protein 557 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF554 Genezinc finger protein 554 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleolus and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF555 Genezinc finger protein 555 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF552 Genezinc finger protein 552 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF550 Genezinc finger protein 550 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF551 Genezinc finger protein 551 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF558 Genezinc finger protein 558 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF559 Genezinc finger protein 559 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF209P Genezinc finger protein 209, pseudogene |
LOC100131832 GeneZFP91 zinc finger protein pseudogene |
LOC729532 Genezinc finger protein 207 pseudogene |
ZNF790 Genezinc finger protein 790 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF791 Genezinc finger protein 791 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF792 Genezinc finger protein 792 Enables identical protein binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF793 Genezinc finger protein 793 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. Implicated in Barrett's esophagus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF799 Genezinc finger protein 799 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF833P Genezinc finger protein 833, pseudogene Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of gene expression. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF184 Genezinc finger protein 184 The protein encoded by this gene is predicted to be a Kruppel C2H2-type zinc-finger protein family member. Sequence analysis predicts that the protein contains two Kruppel associated box (KRAB) boxes in the N-terminus and highly conserved zinc finger motifs at the C-terminus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2016] |
ZNF181 Genezinc finger protein 181 Zinc finger proteins have been shown to interact with nucleic acids and to have diverse functions. The zinc finger domain is a conserved amino acid sequence motif containing 2 specifically positioned cysteines and 2 histidines that are involved in coordinating zinc. Kruppel-related proteins form 1 family of zinc finger proteins. See MIM 604749 for additional information on zinc finger proteins.[supplied by OMIM, Jul 2003] |
ZNF180 Genezinc finger protein 180 Zinc finger proteins have been shown to interact with nucleic acids and to have diverse functions. The zinc finger domain is a conserved amino acid sequence motif containing 2 specifically positioned cysteines and 2 histidines that are involved in coordinating zinc. Kruppel-related proteins form 1 family of zinc finger proteins. See MIM 604749 for additional information on zinc finger proteins.[supplied by OMIM, Jul 2002] |
ZNF182 Genezinc finger protein 182 Zinc-finger proteins bind nucleic acids and play important roles in various cellular functions, including cell proliferation, differentiation, and apoptosis. This gene encodes a zinc finger protein, and belongs to the krueppel C2H2-type zinc-finger protein family. It may be involved in transcriptional regulation. Multiple alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, May 2010] |
ZNF189 Genezinc finger protein 189 Kruppel-like zinc finger proteins such as ZNF189 contain a conserved stretch of 7 amino acids that connects a variable number of DNA-binding zinc finger repeats of the cys(2)his(2) (C2H2) type (summarized by Odeberg et al., 1998 [PubMed 9653648]). Approximately 30% of human Kruppel-like zinc finger proteins contain an N-terminal Kruppel-associated box (KRAB) domain. The KRAB domain consists of approximately 75 amino acids that may be subdivided into an A box, which is present in every KRAB domain and is essential for transcriptional repression, and a B box, which is not always present.[supplied by OMIM, May 2010] |
ZNF239 Genezinc finger protein 239 MOK2 proteins are DNA- and RNA-binding proteins that are mainly associated with nuclear RNP components, including the nucleoli and extranucleolar structures (Arranz et al., 1997 [PubMed 9121460]).[supplied by OMIM, Mar 2008] |
ZNF236 Genezinc finger protein 236 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in cellular response to glucose stimulus. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF235 Genezinc finger protein 235 This gene product belongs to the zinc finger protein superfamily, members of which are regulatory proteins characterized by nucleic acid-binding zinc finger domains. The encoded protein is a member of the Kruppel family of zinc finger proteins, and contains Kruppel-associated box (KRAB) A and B domains and 15 tandemly arrayed C2H2-type zinc fingers. It is an ortholog of the mouse Zfp93 protein. This gene is located in a cluster of zinc finger genes on 19q13.2. [provided by RefSeq, Jul 2008] |
ZNF234 Genezinc finger protein 234 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF233 Genezinc finger protein 233 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF232 Genezinc finger protein 232 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF230 Genezinc finger protein 230 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419870 Genezinc finger protein 717 pseudogene |
LOC100419872 Genezinc finger, MYM-type 4 pseudogene |
LOC100418549 Genezinc finger protein 93 pseudogene |
ZNF880 Genezinc finger protein 880 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF883 Genezinc finger protein 883 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100132599 Genezinc finger protein 114 pseudogene |
ZNF718 Genezinc finger protein 718 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF714 Genezinc finger protein 714 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF716 Genezinc finger protein 716 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF710 Genezinc finger protein 710 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF711 Genezinc finger protein 711 This gene encodes a zinc finger protein of unknown function. It bears similarity to a zinc finger protein which acts as a transcriptional activator. This gene lies in a region of the X chromosome which has been associated with cognitive disability. [provided by RefSeq, Jul 2008] |
ZNF713 Genezinc finger protein 713 The protein encoded by this gene contains C2H2 zinc finger domains. In some individuals, a CGG-repeat expansion from 5-22 repeats to 68-450 repeats has been identified in the first intron of this gene. This mutation is thought to effect the expression of this gene and it has been proposed that it may be associated with Autistic Spectrum Disorder. [provided by RefSeq, Jul 2016] |
ZNF45 Genezinc finger protein 45 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF44 Genezinc finger protein 44 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF43 Genezinc finger protein 43 This gene belongs to the C2H2-type zinc finger gene family. The zinc finger proteins are involved in gene regulation and development, and are quite conserved throughout evolution. Like this gene product, a third of the zinc finger proteins containing C2H2 fingers also contain the KRAB domain, which has been found to be involved in protein-protein interactions. [provided by RefSeq, Jul 2008] |
ZNF41 Genezinc finger protein 41 This gene encodes a protein that contains KRAB-A and KRAB-B domains multiple zinc finger DNA binding motifs and finger linking regions characteristic of the Kruppel family. An initial study suggested that this gene may be associated with X-linked cognitive disability, but a later study has called this finding into question (PMID:23871722).[provided by RefSeq, Apr 2016] |
ZNF48 Genezinc finger protein 48 Enables identical protein binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF717 Genezinc finger protein 717 This gene encodes a Kruppel-associated box (KRAB) zinc-finger protein, which belongs to a large group of transcriptional regulators in mammals. These proteins bind nucleic acids and play important roles in various cellular functions, including cell proliferation, differentiation and apoptosis, and in regulating viral replication and transcription. A pseudogene of this gene was identified on chromosome 1. [provided by RefSeq, May 2016] |
VEZF1 Genevascular endothelial zinc finger 1 Transcriptional regulatory proteins containing tandemly repeated zinc finger domains are thought to be involved in both normal and abnormal cellular proliferation and differentiation. ZNF161 is a C2H2-type zinc finger protein (Koyano-Nakagawa et al., 1994 [PubMed 8035792]). See MIM 603971 for general information on zinc finger proteins.[supplied by OMIM, Sep 2008] |
LOC100631319 Genezinc finger protein 273 pseudogene |
LOC100631318 Genezinc finger protein 85 pseudogene |
LOC100131257 Genezinc finger protein 655 pseudogene |
ZNF734P Genezinc finger protein 734, pseudogene |
ZNF107 Genezinc finger protein 107 This gene encodes a protein containing multiple C2H2-type zinc finger regions. Proteins containing zinc fingers may act as transcriptional regulators, but may also have other cellular functions. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013] |
ZNF106 Genezinc finger protein 106 Enables RNA binding activity. Predicted to be involved in insulin receptor signaling pathway. Predicted to be located in nuclear speck and nucleolus. Predicted to be active in cytosol and membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF101 Genezinc finger protein 101 Zinc finger proteins (ZNFs), such as ZNF101, bind nucleic acids and perform many key functions, the most important of which is regulating transcription (summary by Bellefroid et al., 1993 [PubMed 8467795]). See ZNF91 (MIM 603971) for general information on ZNFs.[supplied by OMIM, Nov 2010] |
ZNF100 Genezinc finger protein 100 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFP64P1 GeneZFP64 zinc finger protein pseudogene 1 |
LOC100289569 Genezinc finger protein 736 pseudogene |
LOC645937 Genezinc finger protein 598 pseudogene |
ZNF75A Genezinc finger protein 75a Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF560 Genezinc finger protein 560 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105379617 Genezinc finger protein 430-like |
ZNF808 Genezinc finger protein 808 Enables transcription cis-regulatory region binding activity. Involved in cell differentiation; negative regulation of gene expression; and pancreas development. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF805 Genezinc finger protein 805 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF806 Genezinc finger protein 806 |
ZNF807 Genezinc finger protein 807 |
ZNF800 Genezinc finger protein 800 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to act upstream of or within acinar cell differentiation and endocrine pancreas development. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419721 Genezinc finger protein 670 pseudogene |
ZNF37A Genezinc finger protein 37A Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105372319 Geneputative zinc finger protein 56 |
ZNF816 Genezinc finger protein 816 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in membrane. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF814 Genezinc finger protein 814 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF101P2 Genezinc finger protein 101 pseudogene 2 |
ZNF101P1 Genezinc finger protein 101 pseudogene 1 |
LOC399783 Genezinc finger protein 532 pseudogene |
LOC100128948 Genezinc finger protein 607 pseudogene |
ZIK1P1 Genezinc finger protein interacting with K protein 1 pseudogene 1 |
ZNF736P8Y Genezinc finger protein 736 pseudogene 8, Y-linked |
ZFY Genezinc finger protein, Y-linked This gene encodes a zinc finger-containing protein that may function as a transcription factor. This gene was once a candidate gene for the testis-determining factor (TDF) and was erroneously referred to as TDF. [provided by RefSeq, Jul 2008] |
ZNF888 Genezinc finger protein 888 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF468 Genezinc finger protein 468 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF469 Genezinc finger protein 469 This gene encodes a zinc-finger protein. Low-percent homology to certain collagens suggests that it may function as a transcription factor or extra-nuclear regulator factor for the synthesis or organization of collagen fibers. Mutations in this gene cause brittle cornea syndrome. [provided by RefSeq, Jul 2008] |
ZNF462 Genezinc finger protein 462 The protein encoded by this gene belongs to C2H2-type zinc finger family of proteins. It contains multiple C2H2-type zinc fingers and may be involved in transcriptional regulation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016] |
ZNF461 Genezinc finger protein 461 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF467 Genezinc finger protein 467 The protein encoded by this gene is a zinc finger protein whose function has not yet been elucidated in humans. However, the mouse ortholog of this protein enhances adipocyte differentiation and suppresses osteoblast differentiation in bone marrow. The mouse protein also is a transcription factor for several genes and can help recruit histone deacetylase complexes. [provided by RefSeq, Aug 2016] |
LOC100130990 Genezinc finger protein 561-like |
ZNF668 Genezinc finger protein 668 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in DNA repair. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF669 Genezinc finger protein 669 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF660 Genezinc finger protein 660 This gene encodes a protein that contains multiple C2H2 zinc finger domains, and is located in a cluster of zinc-finger encoding genes on chromosome 3. Naturally-occurring readthrough transcription is observed between this gene and the downstream zinc finger protein 197 gene and is represented by GeneID:110354863. [provided by RefSeq, May 2017] |
ZNF662 Genezinc finger protein 662 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF664 Genezinc finger protein 664 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF665 Genezinc finger protein 665 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF667 Genezinc finger protein 667 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFP57 GeneZFP57 zinc finger protein The protein encoded by this gene is a zinc finger protein containing a KRAB domain. Studies in mouse suggest that this protein may function as a transcriptional repressor. Mutations in this gene have been associated with transient neonatal diabetes mellitus type 1 (TNDM1).[provided by RefSeq, Sep 2009] |
LOC441666 Genezinc finger protein 91 pseudogene |
ZEB2 Genezinc finger E-box binding homeobox 2 The protein encoded by this gene is a member of the Zfh1 family of 2-handed zinc finger/homeodomain proteins. It is located in the nucleus and functions as a DNA-binding transcriptional repressor that interacts with activated SMADs. Mutations in this gene are associated with Hirschsprung disease/Mowat-Wilson syndrome. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Jan 2010] |
ZNF890P Genezinc finger protein 890, pseudogene |
ZNF652P1 Genezinc finger protein 652 pseudogene 1 |
ZNF587B Genezinc finger protein 587B Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
FLYWCH1 GeneFLYWCH-type zinc finger 1 Enables transcription coactivator binding activity and transcription corepressor activity. Involved in DNA damage response and negative regulation of transcription by RNA polymerase II. Located in cytosol; nuclear body; and pericentric heterochromatin. Part of transcription regulator complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419908 Genezinc finger protein 585A pseudogene |
AZFP GeneAML-associated zinc finger protein |
ZNF415P1 Genezinc finger protein 415 pseudogene 1 |
ZNF207 Genezinc finger protein 207 Enables microtubule binding activity. Involved in mitotic spindle assembly checkpoint signaling; nuclear chromosome segregation; and protein stabilization. Located in kinetochore; nuclear lumen; and spindle matrix. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF205 Genezinc finger protein 205 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II; positive regulation of hydrogen peroxide biosynthetic process; and positive regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway. Predicted to be located in mitochondrion and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF202 Genezinc finger protein 202 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II. Located in chromosome; nuclear body; and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF200 Genezinc finger protein 200 Predicted to enable metal ion binding activity. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF208 Genezinc finger protein 208 Zinc finger proteins (ZNFs), such as ZNF208, bind DNA and, through this binding, regulate gene transcription. Most ZNFs contain conserved C2H2 motifs and are classified as Kruppel-type zinc fingers. A conserved protein motif, termed the Kruppel-associated box (KRAB) domain, mediates protein-protein interactions (Eichler et al., 1998 [PubMed 9724325]). See ZNF91 (MIM 603971) for further information on ZNFs.[supplied by OMIM, Aug 2009] |
ZNF839P1 Genezinc finger protein 839 pseudogene 1 |
ZNF114P1 Genezinc finger protein 114 pseudogene 1 |
ZNF492 Genezinc finger protein 492 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF491 Genezinc finger protein 491 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105370704 Geneputative zinc finger protein 355P |
ZNF501 Genezinc finger protein 501 Enables sequence-specific double-stranded DNA binding activity. Involved in Golgi organization. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF500 Genezinc finger protein 500 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF503 Genezinc finger protein 503 Predicted to enable metal ion binding activity. Involved in G1 to G0 transition involved in cell differentiation; negative regulation of cell population proliferation; and negative regulation of gene expression. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF502 Genezinc finger protein 502 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in positive regulation by host of viral process and viral release from host cell. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF507 Genezinc finger protein 507 Predicted to enable DNA binding activity and metal ion binding activity. Predicted to be involved in positive regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF506 Genezinc finger protein 506 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF847P Genezinc finger protein 847, pseudogene |
LOC100419831 Genezinc finger protein 420 pseudogene |
LOC100419833 Genezinc finger protein 709 pseudogene |
LOC100419835 Genezinc finger protein 160 pseudogene |
ZNF747 Genezinc finger protein 747 Predicted to enable metal ion binding activity. Predicted to be involved in regulation of DNA-templated transcription. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF746 Genezinc finger protein 746 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in protein complex oligomerization and regulation of transcription by RNA polymerase II. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF740 Genezinc finger protein 740 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF749 Genezinc finger protein 749 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419642 Genezinc finger protein 85 pseudogene |
ZNF18 Genezinc finger protein 18 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF19 Genezinc finger protein 19 The protein encoded by this gene contains a zinc finger, a nucleic acid-binding domain present in many transcription factors. This gene is located in a region next to ZNF23, a gene also encoding a zinc finger protein, on chromosome 16. [provided by RefSeq, Jul 2008] |
ZNF14 Genezinc finger protein 14 The protein encoded by this gene contains a zinc finger and a Kruppel-associated box (KRAB) domain. KRAB domain is known to be involved in the transcriptional repression of a number of zinc finger proteins. [provided by RefSeq, Jul 2008] |
ZNF16 Genezinc finger protein 16 The protein encoded by this gene contains multiple tandem zinc finger motifs. The encoded protein is involved in the differentiation of erythroid and megakaryocytic cells. This gene is located in a cluster of related genes on chromosome 8 encoding zinc finger proteins. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2012] |
ZNF17 Genezinc finger protein 17 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF10 Genezinc finger protein 10 The protein encoded by this gene contains a C2H2 zinc finger, and has been shown to function as a transcriptional repressor. The Kruppel-associated box (KRAB) domain of this protein is found to be responsible for its transcriptional repression activity. RING finger containing protein TIF1 was reported to interact with the KRAB domain, and may serve as a mediator for the repression activity of this protein. [provided by RefSeq, Jul 2008] |
ZNF12 Genezinc finger protein 12 This gene is a member of the krueppel C2H2-type zinc-finger protein family and encodes a protein with eight C2H2-type zinc fingers and a KRAB domain. This nuclear protein is involved in developmental control of gene expression. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008] |
LOC100631320 Genezinc finger protein 486 pseudogene |
LOC100631321 Genezinc finger protein 100 pseudogene |
ZNF287 Genezinc finger protein 287 This gene encodes a member of the krueppel family of zinc finger proteins, suggesting a role as a transcription factor. Its specific function has not been determined. This gene is located near the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008] |
ZNF284 Genezinc finger protein 284 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF285 Genezinc finger protein 285 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF282 Genezinc finger protein 282 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in negative regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF283 Genezinc finger protein 283 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF281 Genezinc finger protein 281 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in negative regulation of gene expression; negative regulation of transcription by RNA polymerase II; and positive regulation of DNA-templated transcription. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
SNAI1P1 Genesnail family zinc finger 1 pseudogene 1 |
ZRSR2 Genezinc finger (CCCH type), RNA-binding motif and serine/arginine rich 2 This gene encodes an essential splicing factor. The encoded protein associates with the U2 auxiliary factor heterodimer, which is required for the recognition of a functional 3' splice site in pre-mRNA splicing, and may play a role in network interactions during spliceosome assembly. [provided by RefSeq, Jul 2008] |
LOC101930105 Genezinc finger protein 839-like |
LOC100419825 Genezinc finger protein 655 pseudogene |
ZNF37BP Genezinc finger protein 37B, pseudogene |
ZNF780A Genezinc finger protein 780A Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF780B Genezinc finger protein 780B Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZMAT1 Genezinc finger, matrin-type 1 This gene encodes a protein containing Cys2-His2 (C2H2)-type zinc fingers, which are similar to those found in the nuclear matrix protein matrin 3. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012] |
ZMAT3 Genezinc finger, matrin-type 3 This gene encodes a protein containing three zinc finger domains and a nuclear localization signal. The mRNA and the protein of this gene are upregulated by wildtype p53 and overexpression of this gene inhibits tumor cell growth, suggesting that this gene may have a role in the p53-dependent growth regulatory pathway. Alternative splicing of this gene results in two transcript variants encoding two isoforms differing in only one amino acid. [provided by RefSeq, Jul 2008] |
ZMAT2 Genezinc finger, matrin-type 2 Predicted to enable DNA binding activity and zinc ion binding activity. Involved in mRNA splicing, via spliceosome. Located in nucleus. Part of U2-type precatalytic spliceosome. [provided by Alliance of Genome Resources, Mar 2025] |
ZMAT5 Genezinc finger, matrin-type 5 Predicted to enable zinc ion binding activity. Predicted to be involved in RNA splicing. Located in nucleoplasm. Part of U12-type spliceosomal complex. [provided by Alliance of Genome Resources, Mar 2025] |
ZMAT4 Genezinc finger, matrin-type 4 Enables identical protein binding activity. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF720P1 Genezinc finger protein 720 pseudogene 1 |
ZNF853 Genezinc finger protein 853 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF852 Genezinc finger protein 852 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF850 Genezinc finger protein 850 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF581 Genezinc finger protein 581 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF580 Genezinc finger protein 580 Enables sequence-specific double-stranded DNA binding activity. Involved in several processes, including cellular response to hydrogen peroxide; positive regulation of cell migration; and positive regulation of interleukin-8 production. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF583 Genezinc finger protein 583 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF582 Genezinc finger protein 582 The protein encoded by this gene is a zing finger protein and putative transcription factor that is highly methylated in cervical cancers. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016] |
ZNF584 Genezinc finger protein 584 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF587 Genezinc finger protein 587 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF586 Genezinc finger protein 586 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF589 Genezinc finger protein 589 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF326 Genezinc finger protein 326 Enables RNA polymerase II complex binding activity. Involved in regulation of DNA-templated transcription elongation and regulation of RNA splicing. Located in nucleoplasm. Part of DBIRD complex. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF322 Genezinc finger protein 322 ZNF322A is a member of the zinc-finger transcription factor family and may regulate transcriptional activation in MAPK (see MAPK1; MIM 176948) signaling pathways (Li et al., 2004 [PubMed 15555580]).[supplied by OMIM, Mar 2008] |
ZNF329 Genezinc finger protein 329 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419779 Genezinc finger protein 195 pseudogene |
LOC100419775 Genezinc finger protein 519 pseudogene |
LOC100419773 Genezinc finger protein 33B pseudogene |
ZNF517 Genezinc finger protein 517 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF123P Genezinc finger protein 123, pseudogene |
GZF1 GeneGDNF-inducible zinc finger protein 1 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II. Located in nucleolus and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100289238 Genezinc finger RNA binding protein pseudogene |
LOC100287754 Genezinc finger protein 44 pseudogene |
ZNF90 Genezinc finger protein 90 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF91 Genezinc finger protein 91 The ZNF91 gene encodes a zinc finger protein of the KRAB (Kruppel-associated box) subfamily (Bellefroid et al., 1991, 1993 [PubMed 2023909] [PubMed 8467795]).[supplied by OMIM, May 2010] |
ZNF92 Genezinc finger protein 92 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF98 Genezinc finger protein 98 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF99 Genezinc finger protein 99 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF845 Genezinc finger protein 845 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF731P Genezinc finger protein 731, pseudogene |
ZNF597 Genezinc finger protein 597 This gene encodes a protein with multiple zinc finger domains. Loss of the related gene in rodents results in defects in neural development and embryonic lethality in mutant homozygotes. This gene is adjacent to a differentially methylated region (DMR) and is imprinted and maternally expressed. [provided by RefSeq, Nov 2015] |
ZNF594 Genezinc finger protein 594 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF174 Genezinc finger protein 174 This gene encodes a protein with three Cys2-His2-type zinc fingers in the carboxy-terminus, a putative nuclear localization signal, and an amino-terminus SCAN box which forms homodimers. This protein is believed to function as a transcriptional repressor. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Dec 2016] |
ZNF175 Genezinc finger protein 175 Enables DNA-binding transcription activator activity, RNA polymerase II-specific; DNA-binding transcription repressor activity, RNA polymerase II-specific; and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II and positive regulation of transcription by RNA polymerase II. Located in cytosol and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF177 Genezinc finger protein 177 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in blood microparticle. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF436 Genezinc finger protein 436 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF431 Genezinc finger protein 431 This gene encodes a member of the Krueppel C2H2-type zinc-finger family of proteins. The encoded protein may negatively regulate transcription of target genes, including the hedgehog signaling pathway receptor patched 1, by interacting with histone deacetylases. Mutations in this gene may be associated with non-syndromic facial clefting in human patients. [provided by RefSeq, Jul 2016] |
ZNF430 Genezinc finger protein 430 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in substantia nigra development. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF433 Genezinc finger protein 433 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF432 Genezinc finger protein 432 Enables damaged DNA binding activity and protein-macromolecule adaptor activity. Involved in DNA damage response. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF439 Genezinc finger protein 439 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF438 Genezinc finger protein 438 Enables DNA-binding transcription factor activity. Involved in negative regulation of DNA-templated transcription. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC400682 Genezinc finger protein 100-like |
ZNF885P Genezinc finger protein 885, pseudogene |
LOC100631243 Genezinc finger protein 211 pseudogene |
LOC100631242 Genezinc finger protein 852 pseudogene |
LOC724084 Genezinc finger protein 706 pseudogene |
ZFP28 GeneZFP28 zinc finger protein Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF736P9Y Genezinc finger protein 736 pseudogene 9, Y-linked |
ZNF280D Genezinc finger protein 280D Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF280C Genezinc finger protein 280C This gene encodes a member of the zinc finger domain-containing protein family. This family member contains multiple Cys2-His2(C2H2)-type zinc finger domains, the most common type of zinc finger domain that self-folds to form a beta-beta-alpha structure that binds a zinc ion. [provided by RefSeq, Aug 2011] |
ZNF280B Genezinc finger protein 280B The protein encoded by this gene is a transcription factor that upregulates expression of MDM2, which negatively regulates p53 expression. This gene is highly expressed in prostate cancer cells, which leads to a reduction in p53 levels and an increase in growth of the cancer cells. Several transcript variants have been found for this gene, but only one of them is protein-coding. [provided by RefSeq, Jan 2015] |
ZNF280A Genezinc finger protein 280A This gene encodes a zinc finger protein. The encoded protein contains 4 C2H2-type zinc fingers, which are commonly found in transcription factors. A variety of functions may be performed by this type of zinc finger protein, including the binding of DNA or RNA. [provided by RefSeq, Apr 2014] |
LOC105372277 Genezinc finger protein 799-like |
LOC100419545 Genezinc finger protein 35 pseudogene |
MAZ GeneMYC-associated zinc finger protein (purine-binding transcription factor) Enables DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in several processes, including regulation of gene expression; regulation of signal transduction; and transcription by RNA polymerase II. Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
UNK Geneunkempt family zinc finger Enables mRNA CDS binding activity. Involved in cell morphogenesis involved in neuron differentiation and negative regulation of cytoplasmic translation. Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF876P Genezinc finger protein 876, pseudogene Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF137P Genezinc finger protein 137, pseudogene Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF639 Genezinc finger protein 639 This gene encodes a member of the Kruppel-like zinc finger family of proteins. Amplification and overexpression of this gene have been observed in esophageal squamous cell carcinoma. The encoded protein has been shown to bind DNA in a sequence-specific manner and may regulate HIV-1 gene expression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014] |
ZNF638 Genezinc finger protein 638 The protein encoded by this gene is a nucleoplasmic protein. It binds cytidine-rich sequences in double-stranded DNA. This protein has three types of domains: MH1, MH2 (repeated three times) and MH3. It is associated with packaging, transferring, or processing transcripts. Multiple alternatively spliced transcript variants have been found for this gene, but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008] |
ZNF630 Genezinc finger protein 630 This gene encodes a protein containing an N-terminal Kruppel-associated box-containing (KRAB) domain and 13 Kruppel-type C2H2 zinc finger domains. This gene resides on an area of chromosome X that has been implicated in nonsyndromic X-linked cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013] |
LOC100418555 Genezinc finger protein 70 pseudogene |
SCRT1 Genescratch family zinc finger 1 This gene encodes a C2H2-type zinc finger transcriptional repressor that binds to E-box motifs. The encoded protein may promote neural differention and may be involved in cancers with neuroendocrine features. [provided by RefSeq, Jul 2013] |
SCRT2 Genescratch family zinc finger 2 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in negative regulation of extrinsic apoptotic signaling pathway via death domain receptors and negative regulation of transcription by RNA polymerase II. Predicted to act upstream of or within regulation of neuron migration. Predicted to be located in chromatin. [provided by Alliance of Genome Resources, Mar 2025] |
LOC389906 Genezinc finger protein 839 pseudogene |
LOC730110 Genezinc finger protein 492 pseudogene |
LOC728587 Genezinc finger protein 736 pseudogene |
ZNF570 Genezinc finger protein 570 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF571 Genezinc finger protein 571 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF572 Genezinc finger protein 572 Enables identical protein binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II; regulation of cytokine production; and regulation of immune system process. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF573 Genezinc finger protein 573 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF574 Genezinc finger protein 574 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF575 Genezinc finger protein 575 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF576 Genezinc finger protein 576 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF577 Genezinc finger protein 577 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF578 Genezinc finger protein 578 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in cytoplasm. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF579 Genezinc finger protein 579 Enables DNA-binding transcription factor activity, RNA polymerase II-specific and transcription cis-regulatory region binding activity. Involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105376056 Geneputative zinc finger protein LOC441666 |
OVOL3 Geneovo-like zinc finger 3 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in epidermal cell differentiation and regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
JAZF1 GeneJAZF zinc finger 1 This gene encodes a nuclear protein with three C2H2-type zinc fingers, and functions as a transcriptional repressor. Chromosomal aberrations involving this gene are associated with endometrial stromal tumors. Alternatively spliced variants which encode different protein isoforms have been described; however, not all variants have been fully characterized [provided by RefSeq, Jul 2008] |
ZNF778 Genezinc finger protein 778 The protein encoded by this gene is a member of the krueppel C2H2-type zinc-finger protein family, and it contains one KRAB domain and eighteen C2H2-type zinc fingers. This gene is a candidate gene for autism and variable cognitive impairment in the 16q24.3 microdeletion syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2011] |
ZNF776 Genezinc finger protein 776 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF777 Genezinc finger protein 777 Predicted to enable DNA-binding transcription factor activity. Involved in negative regulation of DNA-templated transcription; negative regulation of cell population proliferation; and protein heterooligomerization. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF775 Genezinc finger protein 775 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF772 Genezinc finger protein 772 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF773 Genezinc finger protein 773 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF770 Genezinc finger protein 770 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF771 Genezinc finger protein 771 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleolus and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF25 Genezinc finger protein 25 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF24 Genezinc finger protein 24 Enables DNA-binding transcription activator activity, RNA polymerase II-specific; identical protein binding activity; and sequence-specific DNA binding activity. Involved in negative regulation of DNA-templated transcription and positive regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF26 Genezinc finger protein 26 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF20 Genezinc finger protein 20 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF23 Genezinc finger protein 23 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF22 Genezinc finger protein 22 Predicted to enable DNA binding activity. Predicted to be involved in odontogenesis and regulation of DNA-templated transcription. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF28 Genezinc finger protein 28 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF251 Genezinc finger protein 251 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within hematopoietic stem cell homeostasis. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF250 Genezinc finger protein 250 Enables identical protein binding activity and sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF253 Genezinc finger protein 253 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF254 Genezinc finger protein 254 Zinc finger proteins have been shown to interact with nucleic acids and to have diverse functions. The zinc finger domain is a conserved amino acid sequence motif containing 2 specifically positioned cysteines and 2 histidines that are involved in coordinating zinc. Kruppel-related proteins form 1 family of zinc finger proteins. See ZFP93 (MIM 604749) for additional information on zinc finger proteins.[supplied by OMIM, Jul 2002] |
ZNF257 Genezinc finger protein 257 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF256 Genezinc finger protein 256 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in negative regulation of DNA-templated transcription. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZIK1 Genezinc finger protein interacting with K protein 1 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF725P Genezinc finger protein 725, pseudogene |
LOC732229 GeneAN1-type zinc finger protein 5 pseudogene |
LOC100129144 Genezinc finger protein 681 pseudogene |
OVOL2 Geneovo-like zinc finger 2 This gene encodes a member of the evolutionarily conserved ovo-like protein family. Mammalian members of this family contain a single zinc finger domain composed of a tetrad of C2H2 zinc fingers with variable N- and C-terminal extensions that contain intrinsically disordered domains. Members of this family are involved in epithelial development and differentiation. Knockout of this gene in mouse results in early embryonic lethality with phenotypes that include neurectoderm expansion, impaired vascularization, and heart anomalies. In humans, allelic variants of this gene have been associated with posterior polymorphous corneal dystrophy. [provided by RefSeq, Apr 2016] |
OVOL1 Geneovo-like zinc finger 1 This gene encodes a putative zinc finger containing transcription factor that is highly similar to homologous protein in Drosophila and mouse. Based on known functions in these species, this protein is likely involved in hair formation and spermatogenesis in human as well. [provided by RefSeq, Aug 2011] |
ZNF865 Genezinc finger protein 865 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF862 Genezinc finger protein 862 Predicted to enable metal ion binding activity and protein dimerization activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF860 Genezinc finger protein 860 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF512B Genezinc finger protein 512B Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Involved in negative regulation of miRNA transcription. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZFP1 GeneZFP1 zinc finger protein This gene belongs to the zinc finger protein family. Some members of this family bind to DNA by zinc-mediated secondary structures called zinc fingers, and are involved in transcriptional regulation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016] |
ZFP2 GeneZFP2 zinc finger protein Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZFP3 GeneZFP3 zinc finger protein Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419706 Genezinc finger protein 84 pseudogene |
ZNF840P Genezinc finger protein 840, pseudogene |
GLI2 GeneGLI family zinc finger 2 This gene encodes a protein which belongs to the C2H2-type zinc finger protein subclass of the Gli family. Members of this subclass are characterized as transcription factors which bind DNA through zinc finger motifs. These motifs contain conserved H-C links. Gli family zinc finger proteins are mediators of Sonic hedgehog (Shh) signaling and they are implicated as potent oncogenes in the embryonal carcinoma cell. The protein encoded by this gene localizes to the cytoplasm and activates patched Drosophila homolog (PTCH) gene expression. It is also thought to play a role during embryogenesis. The encoded protein is associated with several phenotypes- Greig cephalopolysyndactyly syndrome, Pallister-Hall syndrome, preaxial polydactyly type IV, postaxial polydactyly types A1 and B. [provided by RefSeq, Jul 2008] |
GLI3 GeneGLI family zinc finger 3 This gene encodes a protein which belongs to the C2H2-type zinc finger proteins subclass of the Gli family. They are characterized as DNA-binding transcription factors and are mediators of Sonic hedgehog (Shh) signaling. The protein encoded by this gene localizes in the cytoplasm and activates patched Drosophila homolog (PTCH) gene expression. It is also thought to play a role during embryogenesis. Mutations in this gene have been associated with several diseases, including Greig cephalopolysyndactyly syndrome, Pallister-Hall syndrome, preaxial polydactyly type IV, and postaxial polydactyly types A1 and B. [provided by RefSeq, Jul 2008] |
GLI1 GeneGLI family zinc finger 1 This gene encodes a member of the Kruppel family of zinc finger proteins. The encoded transcription factor is activated by the sonic hedgehog signal transduction cascade and regulates stem cell proliferation. The activity and nuclear localization of this protein is negatively regulated by p53 in an inhibitory loop. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009] |
GLI4 GeneGLI family zinc finger 4 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF970P Genezinc finger protein 970, pseudogene |
FIZ1 GeneFLT3-interacting zinc finger 1 This gene encodes zinc finger protein, which interacts with a receptor tyrosine kinase involved in the regulation of hematopoietic and lymphoid cells. This gene product also interacts with a transcription factor that regulates the expression of rod-specific genes in retina. [provided by RefSeq, Jul 2008] |
ZNF402P Genezinc finger protein 402, pseudogene |
ZNF861P Genezinc finger protein 861, pseudogene Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF460 Genezinc finger protein 460 Zinc finger proteins, such as ZNF272, interact with nucleic acids and have diverse functions. The zinc finger domain is a conserved amino acid sequence motif containing 2 specifically positioned cysteines and 2 histidines that are involved in coordinating zinc. Kruppel-related proteins form 1 family of zinc finger proteins. See ZFP93 (MIM 604749) for additional information on zinc finger proteins.[supplied by OMIM, May 2004] |
ZNF124 Genezinc finger protein 124 This gene encodes a protein with an amino-terminal KRAB-A box and multiple repeated Kruppel-type (C2H2) zinc finger motifs at its carboxy terminus. The encoded protein may function as a transcription factor. Expression of this gene is increased after vascular endothelial growth factor (VEGF) stimulation in human leukemia cell lines and results in inhibition of apoptotic cell death induced by irradiation or exposure to etoposide. Alternative splicing results in multiple transcript variants encoding distinct proteins. [provided by RefSeq, Jul 2014] |
ZNF121 Genezinc finger protein 121 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF736P6Y Genezinc finger protein 736 pseudogene 6, Y-linked |
LOC101928592 Genezinc finger protein OZF-like |
ZNF736P10Y Genezinc finger protein 736 pseudogene 10, Y-linked |
ZNF688 Genezinc finger protein 688 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF689 Genezinc finger protein 689 Enables histone binding activity. Involved in regulation of transcription by RNA polymerase II. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF682 Genezinc finger protein 682 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF683 Genezinc finger protein 683 Enables RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in T cell receptor signaling pathway; cellular response to ionomycin; and regulation of gene expression. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF680 Genezinc finger protein 680 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF681 Genezinc finger protein 681 This gene encodes a protein containing the krueppel associated box (KRAB) and zinc-finger domains, which may be involved in transcriptional regulation. Non-functional alleles of this gene are present in alternate genome assemblies including T2T-CHM13v1.1, resulting from a 'TG' deletion (rs61397759) which causes a frameshift and a premature stop codon. [provided by RefSeq, Sep 2022] |
ZNF687 Genezinc finger protein 687 This gene encodes C2H2 zinc finger protein. The encoded protein may play a role in bone differentiation and development. Mutations in this gene are the cause of Paget disease of bone-6. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016] |
ZNF684 Genezinc finger protein 684 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within innate immune response and negative regulation of single stranded viral RNA replication via double stranded DNA intermediate. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419707 Genezinc finger protein 41 pseudogene |
LOC100419704 Genezinc finger protein 57 pseudogene |
ZNF350 Genezinc finger protein 350 Enables DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II intronic transcription regulatory region sequence-specific DNA binding activity. Involved in negative regulation of transcription by RNA polymerase II. Located in nuclear body. Part of transcription repressor complex. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF358 Genezinc finger protein 358 Predicted to enable DNA-binding transcription factor activity and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in several processes, including embryonic forelimb morphogenesis; neural tube development; and regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419515 Genezinc finger protein 41 pseudogene |
LOC100419512 Genezinc finger protein 19 pseudogene |
LOC100419511 Genezinc finger protein 79 pseudogene |
ZNF75BP Genezinc finger protein 75B, pseudogene |
ZNF705G Genezinc finger protein 705G Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF705F Genezinc finger protein 705F |
ZNF705E Genezinc finger protein 705E Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF705D Genezinc finger protein 705D Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF705C Genezinc finger protein 705C, pseudogene |
ZNF705B Genezinc finger protein 705B Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF705A Genezinc finger protein 705A Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419451 Genezinc finger protein 3 pseudogene |
ZNF601P Genezinc finger protein 601, pseudogene |
ZNF267 Genezinc finger protein 267 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF444 Genezinc finger protein 444 This gene encodes a zinc finger protein which activates transcription of a scavenger receptor gene involved in the degradation of acetylated low density lipoprotein (Ac-LDL) (PMID: 11978792). This gene is located in a cluster of zinc finger genes on chromosome 19 at q13.4. A pseudogene of this gene is located on chromosome 15. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011] |
ZNF445 Genezinc finger protein 445 Enables double-stranded methylated DNA binding activity. Involved in epigenetic programing of female pronucleus and negative regulation of gene expression via chromosomal CpG island methylation. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF446 Genezinc finger protein 446 Enables identical protein binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF440 Genezinc finger protein 440 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF441 Genezinc finger protein 441 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF442 Genezinc finger protein 442 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF443 Genezinc finger protein 443 Zinc finger proteins (ZNFs) bind DNA and, through this binding, regulate gene transcription. Most ZNFs contain conserved C2H2 motifs and are classified as Kruppel-type zinc fingers. For a general description of these proteins, see ZNF91 (MIM 603971).[supplied by OMIM, Jul 2002] |
ZNF449 Genezinc finger protein 449 This gene encodes a nuclear protein that likely functions as a transcription factor. The protein includes an N-terminal SCAN domain, and seven C2H2-type zinc finger motifs. [provided by RefSeq, May 2010] |
LOC100418548 Genezinc finger protein 70 pseudogene |
LOC100418547 Genezinc finger protein 93 pseudogene |
LOC100418546 Genezinc finger protein 70 pseudogene |
LOC100288844 Genezinc finger protein 133-like |
ZNF385D Genezinc finger protein 385D Enables sequence-specific double-stranded DNA binding activity. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF322P1 Genezinc finger protein 322 pseudogene 1 |
ZNF724P Genezinc finger protein 724, pseudogene Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF600 Genezinc finger protein 600 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF606 Genezinc finger protein 606 This gene encodes a zinc finger protein containing a Kruppel-associated box (KRAB) domain at its N-terminus, followed by contiguous C2H2 zinc finger motifs. The encoded protein is a nuclear protein that can act as a transcriptional repressor of growth factor-mediated signaling pathways in a reporter gene assay. This protein has been shown to interact with the SRY-box 9 gene product, and suppresses its transcriptional activity by inhibiting its DNA binding activity. Reduced expression of this gene promotes chondrocyte differentiation. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2016] |
ZNF607 Genezinc finger protein 607 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in mitochondrial inner membrane. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF608 Genezinc finger protein 608 Predicted to enable metal ion binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF609 Genezinc finger protein 609 Predicted to enable promoter-specific chromatin binding activity. Involved in regulation of myoblast proliferation. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419786 Genezinc finger protein 670 pseudogene |
LOC100419784 Genezinc finger protein 484 pseudogene |
LOC100419782 Genezinc finger protein 717 pseudogene |
LOC100419783 Genezinc finger protein 831 pseudogene |
LOC100419780 Genezinc finger protein 479 pseudogene Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419781 Genezinc finger protein 267 pseudogene |
ZPR1 GeneZPR1 zinc finger The protein encoded by this gene is found in the cytoplasm of quiescent cells but translocates to the nucleolus in proliferating cells. The encoded protein interacts with survival motor neuron protein (SMN1) to enhance pre-mRNA splicing and to induce neuronal differentiation and axonal growth. Defects in this gene or the SMN1 gene can cause spinal muscular atrophy. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015] |
ZNF285B Genezinc finger protein 285B, pseudogene |
ZNF729 Genezinc finger protein 729 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF585A Genezinc finger protein 585A Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF585B Genezinc finger protein 585B Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419848 Genezinc finger protein 250 pseudogene |
LOC645481 Genezinc finger protein 248 pseudogene |
ZMYM2 Genezinc finger, MYM-type 2 The protein encoded by this gene is a zinc finger protein that may act as a transcription factor. The encoded protein may be part of a BHC histone deacetylase complex. Translocation of this gene with the fibroblast growth factor receptor-1 gene (FGFR1) results in a fusion gene, which may be a cause of stem cell leukemia lymphoma syndrome (SCLL). Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2010] |
ZMYM3 Genezinc finger, MYM-type 3 This gene is located on the X chromosome and is subject to X inactivation. It is highly conserved in vertebrates and most abundantly expressed in the brain. The encoded protein is a component of histone deacetylase-containing multiprotein complexes that function through modifying chromatin structure to keep genes silent. A chromosomal translocation (X;13) involving this gene is associated with X-linked cognitive disability. Several alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2010] |
ZMYM1 Genezinc finger, MYM-type 1 Predicted to enable protein dimerization activity and zinc ion binding activity. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZMYM6 Genezinc finger, MYM-type 6 Predicted to enable DNA binding activity. Involved in cytoskeleton organization and regulation of cell morphogenesis. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZMYM4 Genezinc finger, MYM-type 4 Predicted to enable DNA binding activity. Involved in cytoskeleton organization and regulation of cell morphogenesis. [provided by Alliance of Genome Resources, Mar 2025] |
ZMYM5 Genezinc finger, MYM-type 5 Predicted to enable zinc ion binding activity. Involved in negative regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC392264 Genezinc finger protein 532 pseudogene |
LOC100129265 Genezinc finger protein 66-like |
CASZ1 Genecastor zinc finger 1 The protein encoded by this gene is a zinc finger transcription factor. The encoded protein may function as a tumor suppressor, and single nucleotide polymorphisms in this gene are associated with blood pressure variation. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012] |
LOC645135 Genezinc finger protein 532 pseudogene |
ZNF300P1 Genezinc finger protein 300 pseudogene 1 (functional) |
ZNF197 Genezinc finger protein 197 This gene product belongs to the zinc finger protein superfamily, members of which are regulatory proteins characterized by nucleic acid-binding zinc finger domains. The encoded protein contains 20 tandemly arrayed C2H2-type zinc fingers, a Kruppel-associated box (KRAB) domain, and a SCAN box. This transcript turns over rapidly and contains 3' UTR AUUUA motifs, which are often a hallmark of rapid turnover. It is overexpressed in some thyroid papillary carcinomas. This gene is located in a cluster of zinc finger genes at 3p21. Naturally-occurring readthrough transcription is observed between this gene and the upstream zinc finger protein 660 gene and is represented by GeneID:110354863. [provided by RefSeq, May 2017] |
ZNF195 Genezinc finger protein 195 This gene encodes a protein belonging to the Krueppel C2H2-type zinc-finger protein family. These family members are transcription factors that are implicated in a variety of cellular processes. This gene is located near the centromeric border of chromosome 11p15.5, next to an imprinted domain that is associated with maternal-specific loss of heterozygosity in Wilms' tumors. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012] |
ZNF221 Genezinc finger protein 221 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF222 Genezinc finger protein 222 Predicted to enable DNA-binding transcription factor activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF223 Genezinc finger protein 223 This gene encodes a protein containing a Kruppel-associated box domain and multiple zinc finger domains. The function of this protein has yet to be determined. [provided by RefSeq, Mar 2014] |
ZNF224 Genezinc finger protein 224 This gene encodes a member of the Krueppel C2H2-type zinc-finger family of proteins. The encoded protein represses transcription of the aldolase A gene, which encodes a key enzyme in glycolysis. The encoded zinc-finger protein may also function as a transcriptional co-activator with Wilms' tumor protein 1 to regulate apoptotic genes in leukemia. [provided by RefSeq, Jul 2016] |
ZNF225 Genezinc finger protein 225 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF226 Genezinc finger protein 226 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF227 Genezinc finger protein 227 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within negative regulation of DNA-templated transcription. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF229 Genezinc finger protein 229 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC105377200 Genezinc finger protein Rlf-like |
ZNF965P Genezinc finger protein 965, pseudogene |
ZC3HAV1 Genezinc finger CCCH-type, antiviral 1 This gene encodes a CCCH-type zinc finger protein. This antiviral protein inhibits viral replication by recruiting cellular RNA degradation machineries to degrade viral mRNAs. The encoded protein plays an important role in the innate immune response against multiple DNA and RNA viruses, including Ebola virus, HIV and SARS-CoV-2 (which causes COVID-19). [provided by RefSeq, Sep 2021] |
LOC100131556 Genezinc finger CCHC-type and RNA binding motif 1 pseudogene |
LOC100419792 Genezinc finger protein 622 pseudogene |
ZNF521 Genezinc finger protein 521 Enables protein domain specific binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within neuron fate commitment. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZCRB1 Genezinc finger CCHC-type and RNA binding motif 1 Pre-mRNA splicing is catalyzed by the spliceosome. U12-type spliceosome binds U12-type pre-mRNAs and recognizes the 5' splice site and branch-point sequence. U11 and U12 snRNPs are components of U12-type spliceosome and function as a molecular bridge connecting both ends of the intron. The protein encoded by this gene contains a RNA recognition motif. It was identified as one of the protein components of U11/U12 snRNPs. This protein and many other U11/U12 snRNP proteins are highly conserved in organisms known to contain U12-type introns. These proteins have been shown to be essential for cell viability, suggesting the key roles in U12-type splicing. [provided by RefSeq, Jul 2008] |
ZNF527 Genezinc finger protein 527 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF526 Genezinc finger protein 526 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF525 Genezinc finger protein 525 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF524 Genezinc finger protein 524 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF529 Genezinc finger protein 529 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF528 Genezinc finger protein 528 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
BCL11A GeneB-cell CLL/lymphoma 11A (zinc finger protein) This gene encodes a C2H2 type zinc-finger protein by its similarity to the mouse Bcl11a/Evi9 protein. The corresponding mouse gene is a common site of retroviral integration in myeloid leukemia, and may function as a leukemia disease gene, in part, through its interaction with BCL6. During hematopoietic cell differentiation, this gene is down-regulated. It is possibly involved in lymphoma pathogenesis since translocations associated with B-cell malignancies also deregulates its expression. Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
BCL11B GeneB-cell CLL/lymphoma 11B (zinc finger protein) This gene encodes a C2H2-type zinc finger protein and is closely related to BCL11A, a gene whose translocation may be associated with B-cell malignancies. Although the specific function of this gene has not been determined, the encoded protein is known to be a transcriptional repressor, and is regulated by the NURD nucleosome remodeling and histone deacetylase complex. Four alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Aug 2013] |
LOC102724436 Geneputative zinc finger protein 66 |
ZNF721 Genezinc finger protein 721 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF720 Genezinc finger protein 720 Predicted to enable metal ion binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF727 Genezinc finger protein 727 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF726 Genezinc finger protein 726 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF728 Genezinc finger protein 728 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF72P Genezinc finger protein 72, pseudogene |
LOC100533707 GeneZFP37 zinc finger protein pseudogene |
ZNF79 Genezinc finger protein 79 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF73 Genezinc finger protein 73 |
ZNF70 Genezinc finger protein 70 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytoplasm and megasporocyte nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF71 Genezinc finger protein 71 Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF76 Genezinc finger protein 76 Enables DNA-binding transcription activator activity, RNA polymerase II-specific and sequence-specific double-stranded DNA binding activity. Involved in positive regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF77 Genezinc finger protein 77 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF74 Genezinc finger protein 74 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in actin cytoskeleton and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF767P Genezinc finger family member 767, pseudogene |
ZNRF2P1 Genezinc and ring finger 2 pseudogene 1 |
ZNRF2P3 Genezinc and ring finger 2 pseudogene 3 |
ZNRF2P2 Genezinc and ring finger 2 pseudogene 2 |
ZNF724 Genezinc finger protein 724 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC122539214 GeneZinc finger protein LOC122539214 |
ZFTA Genezinc finger translocation associated Predicted to be involved in negative regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF723 Genezinc finger protein 723 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF875 Genezinc finger protein 875 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II transcription regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF788P Genezinc finger family member 788, pseudogene Predicted to be involved in regulation of DNA-templated transcription. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF812P Genezinc finger protein 812, pseudogene |
ZNF807P Genezinc finger protein 807, pseudogene |
LOC124904660 Geneputative zinc finger protein 826 |
ZNF475 Genezinc finger protein 475 Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ZNF892 Genezinc finger protein 892 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
NOAZFP Genenucleolar atypical zinc finger Predicted to enable metal ion binding activity. Located in chromosome, centromeric region; midbody; and nuclear lumen. [provided by Alliance of Genome Resources, Mar 2025] |
SEMA5B Genesema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5B This gene encodes a member of the semaphorin protein family which regulates axon growth during development of the nervous system. The encoded protein has a characteristic Sema domain near the N-terminus, through which semaphorins bind to plexin, and five thrombospondin type 1 repeats in the C-terminal region of the protein. The protein product may be cleaved and exist as a secreted molecule (PMID: 19463192). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012] |
SEMA5A Genesema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A This gene belongs to the semaphorin gene family that encodes membrane proteins containing a semaphorin domain and several thrombospondin type-1 repeats. Members of this family are involved in axonal guidance during neural development. This gene has been implicated as an autism susceptibility gene.[provided by RefSeq, Jan 2010] |
SEMA6D Genesema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6D Semaphorins are a large family, including both secreted and membrane associated proteins, many of which have been implicated as inhibitors or chemorepellents in axon pathfinding, fasciculation and branching, and target selection. All semaphorins possess a semaphorin (Sema) domain and a PSI domain (found in plexins, semaphorins and integrins) in the N-terminal extracellular portion. Additional sequence motifs C-terminal to the semaphorin domain allow classification into distinct subfamilies. Results demonstrate that transmembrane semaphorins, like the secreted ones, can act as repulsive axon guidance cues. This gene encodes a class 6 vertebrate transmembrane semaphorin that demonstrates alternative splicing. Several transcript variants have been identified and expression of the distinct encoded isoforms is thought to be regulated in a tissue- and development-dependent manner. [provided by RefSeq, Nov 2010] |
SEMA6B Genesema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6B This gene encodes a member of the semaphorin family, a group of proteins characterized by the presence of a conserved semaphorin (sema) domain. Whereas some semaphorins are transmembrane proteins, others are secreted. Semaphorins play a major role in axon guidance. The protein encoded by this gene may be involved in both peripheral and central nervous system development. [provided by RefSeq, Jul 2008] |
SEMA6C Genesema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6C This gene encodes a member of the semaphorin family. Semaphorins represent important molecular signals controlling multiple aspects of the cellular response that follows CNS injury, and thus may play an important role in neural regeneration. [provided by RefSeq, May 2010] |
SEMA6A Genesema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6A Predicted to enable identical protein binding activity; signaling receptor binding activity; and transmembrane signaling receptor activity. Involved in cellular response to vascular endothelial growth factor stimulus; negative regulation of cell adhesion involved in sprouting angiogenesis; and negative regulation of signal transduction. Predicted to be located in axon and membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SEMA3A Genesema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A This gene is a member of the semaphorin family and encodes a protein with an Ig-like C2-type (immunoglobulin-like) domain, a PSI domain and a Sema domain. This secreted protein can function as either a chemorepulsive agent, inhibiting axonal outgrowth, or as a chemoattractive agent, stimulating the growth of apical dendrites. In both cases, the protein is vital for normal neuronal pattern development. Increased expression of this protein is associated with schizophrenia and is seen in a variety of human tumor cell lines. Also, aberrant release of this protein is associated with the progression of Alzheimer's disease. [provided by RefSeq, Jul 2008] |
SEMA3C Genesema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C This gene encodes a secreted glycoprotein that belongs to the semaphorin class 3 family of neuronal guidance cues. The encoded protein contains an N-terminal sema domain, integrin and immunoglobulin-like domains, and a C-terminal basic domain. Homodimerization and proteolytic cleavage of the C-terminal propeptide are necessary for the function of the encoded protein. It binds a neuropilin co-receptor before forming a heterotrimeric complex with an associated plexin. An increase in the expression of this gene correlates with an increase in cancer cell invasion and adhesion. Naturally occurring mutations in this gene are associated with Hirschsprung disease. [provided by RefSeq, May 2017] |
SEMA3B Genesema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3B The protein encoded by this gene belongs to the class-3 semaphorin/collapsin family, whose members function in growth cone guidance during neuronal development. This family member inhibits axonal extension and has been shown to act as a tumor suppressor by inducing apoptosis. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Feb 2014] |
SEMA3E Genesema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E Semaphorins are a large family of conserved secreted and membrane associated proteins which possess a semaphorin (Sema) domain and a PSI domain (found in plexins, semaphorins and integrins) in the N-terminal extracellular portion. Based on sequence and structural similarities, semaphorins are put into eight classes: invertebrates contain classes 1 and 2, viruses have class V, and vertebrates contain classes 3-7. Semaphorins serve as axon guidance ligands via multimeric receptor complexes, some (if not all) containing plexin proteins. This gene encodes a class 4 semaphorin. This gene encodes a class 3 semaphorin. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2010] |
SEMA3D Genesema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D This gene encodes a member of the semaphorin III family of secreted signaling proteins that are involved in axon guidance during neuronal development. The encoded protein contains an N-terminal Sema domain, an immunoglobulin like domain and a C-terminal basic domain. The protein encoded by this gene binds neuropilin and plays an important role in cardiovascular development. [provided by RefSeq, Aug 2016] |
SEMA3G Genesema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3G The transcription of this gene is activated by PPAR-gamma, and the resulting protein product plays a role in endothelial cell migration. Expression of this gene also inhibits tumor cell migration and invasion. [provided by RefSeq, Jul 2016] |
SEMA3F Genesema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F This gene encodes a member of the semaphorin III family of secreted signaling proteins that are involved in axon guidance during neuronal development. The encoded protein contains an N-terminal Sema domain, an immunoglobulin loop and a C-terminal basic domain. This gene is expressed by the endothelial cells where it was found to act in an autocrine fashion to induce apoptosis, inhibit cell proliferation and survival, and function as an anti-tumorigenic agent. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jan 2016] |
LOC100422730 Genesema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A pseudogene |
RFWD2P1 Genering finger and WD repeat domain 2, E3 ubiquitin protein ligase pseudogene 1 |
LOC100288437 Genering finger and WD repeat domain 2, E3 ubiquitin protein ligase pseudogene |
CGRRF1 Genecell growth regulator with ring finger domain 1 Predicted to enable metal ion binding activity. Predicted to be involved in negative regulation of cell growth. Located in endoplasmic reticulum and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100421809 GeneLON peptidase N-terminal domain and ring finger 2 pseudogene |
LONRF2P2 GeneLON peptidase N-terminal domain and ring finger 2 pseudogene 2 |
LONRF2P1 GeneLON peptidase N-terminal domain and ring finger 2 pseudogene 1 |
LONRF3 GeneLON peptidase N-terminal domain and ring finger 3 The protein encoded by this gene contains a RING finger domain, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. Multiple alternatively spliced transcript variants have been suggested, but their full length natures are not clear. [provided by RefSeq, Jul 2008] |
LONRF2 GeneLON peptidase N-terminal domain and ring finger 2 Predicted to enable ubiquitin protein ligase activity. Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LONRF1 GeneLON peptidase N-terminal domain and ring finger 1 Predicted to enable ubiquitin protein ligase activity. Predicted to be located in cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100421810 GeneLON peptidase N-terminal domain and ring finger 2 pseudogene |
RLIMP2 Genering finger protein, LIM domain interacting pseudogene 2 |
RLIMP3 Genering finger protein, LIM domain interacting pseudogene 3 |
RLIMP1 Genering finger protein, LIM domain interacting pseudogene 1 |
RFWD2 Genering finger and WD repeat domain 2, E3 ubiquitin protein ligase Enables ubiquitin protein ligase activity. Involved in positive regulation of proteasomal ubiquitin-dependent protein catabolic process; proteasome-mediated ubiquitin-dependent protein catabolic process; and response to ionizing radiation. Part of Cul4A-RING E3 ubiquitin ligase complex. [provided by Alliance of Genome Resources, Mar 2025] |
RFWD3 Genering finger and WD repeat domain 3 Enables MDM2/MDM4 family protein binding activity; p53 binding activity; and ubiquitin protein ligase activity. Involved in several processes, including DNA metabolic process; regulation of cell cycle phase transition; and response to ionizing radiation. Located in nucleoplasm and site of double-strand break. Implicated in Fanconi anemia complementation group W. [provided by Alliance of Genome Resources, Mar 2025] |
RLIM Genering finger protein, LIM domain interacting The protein encoded by this gene is a RING-H2 zinc finger protein. It has been shown to be an E3 ubiquitin protein ligase that targets LIM domain binding 1 (LDB1/CLIM), and causes proteasome-dependent degradation of LDB1. This protein and LDB1 are co-repressors of LHX1/LIM-1, a homeodomain transcription factor. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Feb 2009] |
SAMSN1 GeneSAM domain, SH3 domain and nuclear localization signals 1 SAMSN1 is a member of a novel gene family of putative adaptors and scaffold proteins containing SH3 and SAM (sterile alpha motif) domains (Claudio et al., 2001 [PubMed 11536050]).[supplied by OMIM, Mar 2008] |
AGAP1 GeneArfGAP with GTPase domain, ankyrin repeat and PH domain 1 This gene encodes a member of an ADP-ribosylation factor GTPase-activating protein family involved in membrane trafficking and cytoskeleton dynamics. This gene functions as a direct regulator of the adaptor-related protein complex 3 on endosomes. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011] |
AGAP2 GeneArfGAP with GTPase domain, ankyrin repeat and PH domain 2 The protein encoded by this gene belongs to the centaurin gamma-like family. It mediates anti-apoptotic effects of nerve growth factor by activating nuclear phosphoinositide 3-kinase. It is overexpressed in cancer cells, and promotes cancer cell invasion. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011] |
AGAP3 GeneArfGAP with GTPase domain, ankyrin repeat and PH domain 3 This gene encodes an essential component of the N-methyl-D-aspartate (NMDA) receptor signaling complex which mediates long-term potentiation in synapses by linking activation of NMDA receptor to alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor trafficking. The encoded protein contains an N-terminal GTPase-like domain, a pleckstrin homology domain, an ArfGAP domain and several C-terminal ankryn repeat domains. [provided by RefSeq, Apr 2017] |
AGAP4 GeneArfGAP with GTPase domain, ankyrin repeat and PH domain 4 Predicted to enable GTPase activator activity and GTPase activity. [provided by Alliance of Genome Resources, Mar 2025] |
AGAP5 GeneArfGAP with GTPase domain, ankyrin repeat and PH domain 5 Predicted to enable GTPase activator activity and GTPase activity. [provided by Alliance of Genome Resources, Mar 2025] |
AGAP6 GeneArfGAP with GTPase domain, ankyrin repeat and PH domain 6 Predicted to enable GTPase activator activity and GTPase activity. [provided by Alliance of Genome Resources, Mar 2025] |
AGAP9 GeneArfGAP with GTPase domain, ankyrin repeat and PH domain 9 Predicted to enable GTPase activator activity and GTPase activity. [provided by Alliance of Genome Resources, Mar 2025] |
LOC126860 GeneArfGAP with GTPase domain, ankyrin repeat and PH domain 1 pseudogene |
TBC1D9B GeneTBC1 domain family, member 9B (with GRAM domain) Predicted to enable GTPase activator activity. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ASAP1 GeneArfGAP with SH3 domain, ankyrin repeat and PH domain 1 This gene encodes an ADP-ribosylation factor (ARF) GTPase-activating protein. The GTPase-activating activity is stimulated by phosphatidylinositol 4,5-biphosphate (PIP2), and is greater towards ARF1 and ARF5, and lesser for ARF6. This gene maybe involved in regulation of membrane trafficking and cytoskeleton remodeling. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011] |
ASAP2 GeneArfGAP with SH3 domain, ankyrin repeat and PH domain 2 This gene encodes a multidomain protein containing an N-terminal alpha-helical region with a coiled-coil motif, followed by a pleckstrin homology (PH) domain, an Arf-GAP domain, an ankyrin homology region, a proline-rich region, and a C-terminal Src homology 3 (SH3) domain. The protein localizes in the Golgi apparatus and at the plasma membrane, where it colocalizes with protein tyrosine kinase 2-beta (PYK2). The encoded protein forms a stable complex with PYK2 in vivo. This interaction appears to be mediated by binding of its SH3 domain to the C-terminal proline-rich domain of PYK2. The encoded protein is tyrosine phosphorylated by activated PYK2. It has catalytic activity for class I and II ArfGAPs in vitro, and can bind the class III Arf ARF6 without immediate GAP activity. The encoded protein is believed to function as an ARF GAP that controls ARF-mediated vesicle budding when recruited to Golgi membranes. In addition, it functions as a substrate and downstream target for PYK2 and SRC, a pathway that may be involved in the regulation of vesicular transport. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2008] |
ASAP3 GeneArfGAP with SH3 domain, ankyrin repeat and PH domain 3 This gene encodes a member of a subfamily of ADP-ribosylation factor(Arf) GTPase-activating proteins that contain additional ankyrin repeat and pleckstrin homology domains. The Arf GAP domain of this protein catalyzes the hydrolysis of GTP bound to Arf proteins. The encoded protein promotes cell differentiation and migration and has been implicated in cancer cell invasion. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2009] |
SAMHD1 GeneSAM domain and HD domain 1 This gene may play a role in regulation of the innate immune response. The encoded protein is upregulated in response to viral infection and may be involved in mediation of tumor necrosis factor-alpha proinflammatory responses. Mutations in this gene have been associated with Aicardi-Goutieres syndrome. [provided by RefSeq, Mar 2010] |
AGAP7P GeneArfGAP with GTPase domain, ankyrin repeat and PH domain 7, pseudogene Predicted to enable GTPase activator activity and GTPase activity. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100422376 GeneArfGAP with GTPase domain, ankyrin repeat and PH domain 1 pseudogene |
TBC1D8B GeneTBC1 domain family, member 8B (with GRAM domain) This gene encodes a protein with a TBC (Tre-2/Bub2/CDC16) domain. Some mammalian proteins with this domain have been shown to function as Rab-GAPs by binding to specific Rab proteins and affecting their GTPase activity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2011] |
ANKRD27 Geneankyrin repeat domain 27 (VPS9 domain) Enables guanyl-nucleotide exchange factor activity and small GTPase binding activity. Involved in endocytic recycling and negative regulation of SNARE complex assembly. Acts upstream of or within early endosome to late endosome transport. Located in several cellular components, including cytosol; endosome; and lysosome. Implicated in eosinophilic esophagitis. [provided by Alliance of Genome Resources, Mar 2025] |
ARAP3 GeneArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 This gene encodes a phosphoinositide binding protein containing ARF-GAP, RHO-GAP, RAS-associating, and pleckstrin homology domains. The ARF-GAP and RHO-GAP domains cooperate in mediating rearrangements in the cell cytoskeleton and cell shape. It is a specific PtdIns(3,4,5)P3/PtdIns(3,4)P2-stimulated Arf6-GAP protein. An alternatively spliced transcript has been found for this gene, but its biological validity has not been determined. [provided by RefSeq, Sep 2015] |
ARAP2 GeneArfGAP with RhoGAP domain, ankyrin repeat and PH domain 2 The protein encoded by this gene contains ARF-GAP, RHO-GAP, ankyrin repeat, RAS-associating, and pleckstrin homology domains. The protein is a phosphatidylinositol (3,4,5)-trisphosphate-dependent Arf6 GAP that binds RhoA-GTP, but it lacks the predicted catalytic arginine in the RHO-GAP domain and does not have RHO-GAP activity. The protein associates with focal adhesions and functions downstream of RhoA to regulate focal adhesion dynamics. [provided by RefSeq, Sep 2008] |
AGAP10P GeneArfGAP with GTPase domain, ankyrin repeat and PH domain 10 pseudogene |
ARAP1 GeneArfGAP with RhoGAP domain, ankyrin repeat and PH domain 1 The protein encoded by this gene contains SAM, ARF-GAP, RHO-GAP, ankyrin repeat, RAS-associating, and pleckstrin homology (PH) domains. In vitro, this protein displays RHO-GAP and phosphatidylinositol (3,4,5) trisphosphate (PIP3)-dependent ARF-GAP activity. The encoded protein associates with the Golgi, and the ARF-GAP activity mediates changes in the Golgi and the formation of filopodia. It is thought to regulate the cell-specific trafficking of a receptor protein involved in apoptosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2008] |
TBC1D8 GeneTBC1 domain family, member 8 (with GRAM domain) Predicted to enable GTPase activator activity. Predicted to be involved in blood circulation and positive regulation of cell population proliferation. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
TBC1D9 GeneTBC1 domain family, member 9 (with GRAM domain) Predicted to enable GTPase activator activity. [provided by Alliance of Genome Resources, Mar 2025] |
AGAP12P GeneArfGAP with GTPase domain, ankyrin repeat and PH domain 12, pseudogene |
LOC101929026 Genezinc-activated ligand-gated ion channel-like |
LOC100422091 Genesolute carrier family 30 (zinc transporter), member 6 pseudogene |
LOC101060052 Genezinc transporter ZIP1-like |
AZGP1P1 Genealpha-2-glycoprotein 1, zinc-binding pseudogene 1 |
ZHX2 Genezinc fingers and homeoboxes 2 The members of the zinc fingers and homeoboxes gene family are nuclear homodimeric transcriptional repressors that interact with the A subunit of nuclear factor-Y (NF-YA) and contain two C2H2-type zinc fingers and five homeobox DNA-binding domains. This gene encodes member 2 of this gene family. In addition to forming homodimers, this protein heterodimerizes with member 1 of the zinc fingers and homeoboxes family. [provided by RefSeq, Jul 2008] |
ZHX3 Genezinc fingers and homeoboxes 3 This gene encodes a member of the zinc fingers and homeoboxes (ZHX) gene family. The encoded protein contains two C2H2-type zinc fingers and five homeodomains and forms a dimer with itself or with zinc fingers and homeoboxes family member 1. In the nucleus, the dimerized protein interacts with the A subunit of the ubiquitous transcription factor nuclear factor-Y and may function as a transcriptional repressor. [provided by RefSeq, Jul 2008] |
ZHX1 Genezinc fingers and homeoboxes 1 The members of the zinc fingers and homeoboxes gene family are nuclear homodimeric transcriptional repressors that interact with the A subunit of nuclear factor-Y (NF-YA) and contain two C2H2-type zinc fingers and five homeobox DNA-binding domains. This gene encodes member 1 of this gene family. In addition to forming homodimers, this protein heterodimerizes with members 2 and 3 of the zinc fingers and homeoboxes family. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream chromosome 8 open reading frame 76 (C8orf76) gene. [provided by RefSeq, Feb 2011] |
OMA1 GeneOMA1 zinc metallopeptidase Enables metalloendopeptidase activity. Involved in several processes, including HRI-mediated signaling; proteolysis; and regulation of mitochondrion organization. Located in mitochondrial inner membrane. Is active in mitochondrial intermembrane space. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100421246 GeneD4, zinc and double PHD fingers family 2 pseudogene |
AZGP1P2 Genealpha-2-glycoprotein 1, zinc-binding pseudogene 2 |
SLC39A12 Genesolute carrier family 39 (zinc transporter), member 12 Zinc is an essential cofactor for hundreds of enzymes. It is involved in protein, nucleic acid, carbohydrate, and lipid metabolism, as well as in the control of gene transcription, growth, development, and differentiation. SLC39A12 belongs to a subfamily of proteins that show structural characteristics of zinc transporters (Taylor and Nicholson, 2003 [PubMed 12659941]).[supplied by OMIM, Aug 2008] |
SLC39A13 Genesolute carrier family 39 (zinc transporter), member 13 This gene encodes a member of the LIV-1 subfamily of the ZIP transporter family. The encoded transmembrane protein functions as a zinc transporter. Mutations in this gene have been associated with the spondylocheiro dysplastic form of Ehlers-Danlos syndrome. Alternate transcript variants have been found for this gene. [provided by RefSeq, Jan 2016] |
SLC39A10 Genesolute carrier family 39 (zinc transporter), member 10 Zinc is an essential cofactor for hundreds of enzymes. It is involved in protein, nucleic acid, carbohydrate, and lipid metabolism, as well as in the control of gene transcription, growth, development, and differentiation. SLC39A10 belongs to a subfamily of proteins that show structural characteristics of zinc transporters (Taylor and Nicholson, 2003 [PubMed 12659941]).[supplied by OMIM, Mar 2008] |
SLC39A14 Genesolute carrier family 39 (zinc transporter), member 14 This gene encodes a member of the the SLC39A family of divalent metal transporters that mediates the cellular uptake of manganese, zinc, iron, and cadmium. The encoded protein contains eight transmembrane domains, a histidine-rich motif, and a metalloprotease motif, and is expressed on the plasma membrane and the endocytic vesicle membrane. It is an important transporter of nontransferrin-bound iron and a critical regulator of manganese homeostasis. Naturally occurring mutations in this gene are associated with neurodegeneration with brain iron accumulation and early-onset parkinsonism-dystonia with hypermanganesemia. [provided by RefSeq, May 2017] |
SLC39A8 Genesolute carrier family 39 (zinc transporter), member 8 This gene encodes a member of the SLC39 family of solute-carrier genes, which show structural characteristics of zinc transporters. The encoded protein is glycosylated and found in the plasma membrane and mitochondria, and functions in the cellular import of zinc at the onset of inflammation. It is also thought to be the primary transporter of the toxic cation cadmium, which is found in cigarette smoke. Multiple transcript variants encoding different isoforms have been found for this gene. Additional alternatively spliced transcript variants of this gene have been described, but their full-length nature is not known. [provided by RefSeq, Oct 2008] |
SLC39A1 Genesolute carrier family 39 (zinc transporter), member 1 This gene encodes a member of the zinc-iron permease family. The encoded protein is localized to the cell membrane and acts as a zinc uptake transporter. This gene has been linked to prostate cancer, breast cancer, and Alzheimer's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012] |
SLC39A2 Genesolute carrier family 39 (zinc transporter), member 2 This gene encodes a member of the ZIP family of metal ion transporters. The encoded protein functions as a zinc transporter. Mutations in this gene may be associated with susceptibility to carotid artery disease. Multiple transcript variants have been described. [provided by RefSeq, Mar 2010] |
SLC39A3 Genesolute carrier family 39 (zinc transporter), member 3 Predicted to enable zinc ion transmembrane transporter activity. Predicted to be involved in zinc ion transmembrane transport. Predicted to act upstream of or within several processes, including T cell homeostasis; chordate embryonic development; and zinc ion transport. Predicted to be located in hippocampal mossy fiber to CA3 synapse. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SLC39A4 Genesolute carrier family 39 (zinc transporter), member 4 This gene encodes a member of the zinc/iron-regulated transporter-like protein (ZIP) family. The encoded protein localizes to cell membranes and is required for zinc uptake in the intestine. Mutations in this gene result in acrodermatitis enteropathica. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2013] |
SLC39A5 Genesolute carrier family 39 (zinc transporter), member 5 The protein encoded by this gene belongs to the ZIP family of zinc transporters that transport zinc into cells from outside, and play a crucial role in controlling intracellular zinc levels. Zinc is an essential cofactor for many enzymes and proteins involved in gene transcription, growth, development and differentiation. Mutations in this gene have been associated with autosomal dominant high myopia (MYP24). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2014] |
SLC39A6 Genesolute carrier family 39 (zinc transporter), member 6 Zinc is an essential cofactor for hundreds of enzymes. It is involved in protein, nucleic acid, carbohydrate, and lipid metabolism, as well as in the control of gene transcription, growth, development, and differentiation. SLC39A6 belongs to a subfamily of proteins that show structural characteristics of zinc transporters (Taylor and Nicholson, 2003 [PubMed 12659941]).[supplied by OMIM, Mar 2008] |
SLC39A7 Genesolute carrier family 39 (zinc transporter), member 7 The protein encoded by this gene transports zinc from the Golgi and endoplasmic reticulum to the cytoplasm. This transport may be important for activation of tyrosine kinases, some of which could be involved in cancer progression. Therefore, modulation of the encoded protein could be useful as a therapeutic agent against cancer. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014] |
PAPL Geneiron/zinc purple acid phosphatase-like protein Purple acid phosphatases (PAPs), including PAPL, are a family of binuclear metallohydrolases that have been identified in plants, animals, and fungi (Flanagan et al., 2006 [PubMed 16793224]).[supplied by OMIM, Mar 2008] |
SLC30A9 Genesolute carrier family 30 (zinc transporter), member 9 Enables zinc ion transmembrane transporter activity. Involved in intracellular zinc ion homeostasis; regulation of mitochondrion organization; and zinc ion transport. Located in several cellular components, including cytoplasmic vesicle; endoplasmic reticulum; and mitochondrial membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SLC30A8 Genesolute carrier family 30 (zinc transporter), member 8 The protein encoded by this gene is a zinc efflux transporter involved in the accumulation of zinc in intracellular vesicles. This gene is expressed at a high level only in the pancreas, particularly in islets of Langerhans. The encoded protein colocalizes with insulin in the secretory pathway granules of the insulin-secreting INS-1 cells. Allelic variants of this gene exist that confer susceptibility to diabetes mellitus, noninsulin-dependent (NIDDM). Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2010] |
SLC30A5 Genesolute carrier family 30 (zinc transporter), member 5 This gene encodes a member of the SLC30A/ZnT family of zinc transporter proteins. ZnT proteins mediate both cellular zinc efflux and zinc sequestration into membrane-bound organelles. The encoded protein plays a role in the early secretory pathway as a heterodimer with zinc transporter 6, and may also regulate zinc sequestration into secretory granules of pancreatic beta cells. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 19. [provided by RefSeq, Oct 2011] |
SLC30A4 Genesolute carrier family 30 (zinc transporter), member 4 Zinc is the second most abundant trace metal in the human body. It is an essential element, serving both a structural role, as in the formation of zinc fingers in DNA-binding proteins, and a catalytic role in metalloenzymes, such as pancreatic carboxypeptidases (e.g., MIM 114852), alkaline phosphatases (e.g., MIM 171760), various dehydrogenases, and superoxide dismutases (e.g., MIM 147450). SLC30A4, or ZNT4, belongs to the ZNT family of zinc transporters. ZNTs are involved in transporting zinc out of the cytoplasm and have similar structures, consisting of 6 transmembrane domains and a histidine-rich cytoplasmic loop (Huang and Gitschier, 1997 [PubMed 9354792]).[supplied by OMIM, Mar 2008] |
SLC30A7 Genesolute carrier family 30 (zinc transporter), member 7 Zinc functions as a cofactor for numerous enzymes, nuclear factors, and hormones and as an intra- and intercellular signal ion. Members of the zinc transporter (ZNT)/SLC30 subfamily of the cation diffusion facilitator family, such as SLC30A7, permit cellular efflux of zinc (Seve et al., 2004 [PubMed 15154973]).[supplied by OMIM, Mar 2008] |
SLC30A6 Genesolute carrier family 30 (zinc transporter), member 6 This gene encodes a member of a family of proteins that function as zinc transporters. This protein can regulate subcellular levels of zinc in the Golgi and vesicles. Expression of this gene is altered in the Alzheimer's disease brain plaques. [provided by RefSeq, Aug 2016] |
SLC30A1 Genesolute carrier family 30 (zinc transporter), member 1 Predicted to enable calcium channel inhibitor activity and zinc:proton antiporter activity. Involved in defense response to bacterium; intracellular zinc ion homeostasis; and zinc ion import into organelle. Located in several cellular components, including Golgi apparatus; basolateral plasma membrane; and nuclear membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SLC30A3 Genesolute carrier family 30 (zinc transporter), member 3 Enables zinc ion transmembrane transporter activity. Involved in zinc ion import into lysosome. Located in late endosome and synaptic vesicle. [provided by Alliance of Genome Resources, Mar 2025] |
SLC30A2 Genesolute carrier family 30 (zinc transporter), member 2 The protein encoded by this gene is a zinc transporter that acts as a homodimer. The encoded protein plays a role in secreting zinc into breast milk. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2015] |
AZGP1 Genealpha-2-glycoprotein 1, zinc-binding Predicted to enable RNA nuclease activity and protein transmembrane transporter activity. Involved in cell adhesion and detection of chemical stimulus involved in sensory perception of bitter taste. Located in extracellular space. Implicated in prostate carcinoma. Biomarker of several diseases, including gastrointestinal system cancer (multiple); kidney failure (multiple); liver cirrhosis; lung adenocarcinoma; and obesity. [provided by Alliance of Genome Resources, Mar 2025] |
ZACN Genezinc activated ligand-gated ion channel LGICZ1 is a zinc-activated ligand-gated ion channel that defines a new subgroup of the cysteine-loop superfamily of ligand-gated ion channels (Davies et al., 2003 [PubMed 12381728]).[supplied by OMIM, Mar 2008] |
DZANK1 Genedouble zinc ribbon and ankyrin repeat domains 1 This gene contains two ankyrin repeat-encoding regions. Ankyrin repeats are tandemly repeated modules of about 33 amino acids described as L-shaped structures consisting of a beta-hairpin and two alpha-helices. Ankyrin repeats occur in a large number of functionally diverse proteins, mainly from eukaryotes, and are known to function as protein-protein interaction domains. [provided by RefSeq, Dec 2018] |
DPF2 GeneD4, zinc and double PHD fingers family 2 The protein encoded by this gene is a member of the d4 domain family, characterized by a zinc finger-like structural motif. This protein functions as a transcription factor which is necessary for the apoptotic response following deprivation of survival factors. It likely serves a regulatory role in rapid hematopoietic cell growth and turnover. This gene is considered a candidate gene for multiple endocrine neoplasia type I, an inherited cancer syndrome involving multiple parathyroid, enteropancreatic, and pituitary tumors. [provided by RefSeq, Jul 2008] |
DPF3 GeneD4, zinc and double PHD fingers, family 3 This gene encodes a member of the D4 protein family. The encoded protein is a transcription regulator that binds acetylated histones and is a component of the BAF chromatin remodeling complex. Alternate splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013] |
DPF1 GeneD4, zinc and double PHD fingers family 1 Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in nervous system development. Predicted to be located in nucleoplasm. Predicted to be part of nBAF complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100131725 Genesolute carrier family 39 (zinc transporter), member 14 pseudogene |
LOC100533846 Genesolute carrier family 30 (zinc transporter), member 5 pseudogene |
ZMPSTE24 Genezinc metallopeptidase STE24 This gene encodes a member of the peptidase M48A family. The encoded protein is a zinc metalloproteinase involved in the two step post-translational proteolytic cleavage of carboxy terminal residues of farnesylated prelamin A to form mature lamin A. Mutations in this gene have been associated with mandibuloacral dysplasia and restrictive dermopathy. [provided by RefSeq, Jul 2008] |
RFPL4AL1 Generet finger protein-like 4A-like 1 Predicted to enable protein homodimerization activity; protein kinase binding activity; and ubiquitin protein ligase activity. Predicted to be involved in several processes, including positive regulation of autophagy; positive regulation of canonical NF-kappaB signal transduction; and regulation of viral entry into host cell. Predicted to be active in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
RNF175 Genering finger protein 175 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in ERAD pathway. Predicted to be located in membrane. Predicted to be active in Golgi membrane and endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNF170 Genering finger protein 170 This gene encodes a RING domain-containing protein that resides in the endoplasmic reticulum (ER) membrane. This protein functions as an E3 ubiquitin ligase and mediates ubiquitination and processing of inositol 1,4,5-trisphosphate (IP3) receptors via the ER-associated protein degradation pathway. It is recruited to the activated IP3 receptors by the ERLIN1/ERLIN2 complex to which it is constitutively bound. Mutations in this gene are associated with autosomal dominant sensory ataxia. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2012] |
MKRN6P Genemakorin ring finger protein 6, pseudogene |
PHF5EP GenePHD finger protein 5E pseudogene |
RFPL4B Generet finger protein-like 4B Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in several processes, including defense response to symbiont; negative regulation of viral entry into host cell; and negative regulation of viral transcription. Predicted to be active in cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
RFPL4A Generet finger protein-like 4A Predicted to enable protein homodimerization activity; protein kinase binding activity; and ubiquitin protein ligase activity. Predicted to be involved in several processes, including positive regulation of autophagy; positive regulation of canonical NF-kappaB signal transduction; and regulation of viral entry into host cell. Predicted to be located in female germ cell nucleus. Predicted to be active in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
MARCH11 Genemembrane-associated ring finger (C3HC4) 11 MARCH11 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). These enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their intracellular transport. March11 appears to have a role in ubiquitin-mediated protein sorting in the trans-Golgi network (TGN)-multivesicular body (MVB) transport pathway (Morokuma et al., 2007 [PubMed 17604280]).[supplied by OMIM, Apr 2010] |
MARCH10 Genemembrane-associated ring finger (C3HC4) 10, E3 ubiquitin protein ligase MARCH10 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments (Morokuma et al., 2007 [PubMed 17604280]).[supplied by OMIM, Apr 2010] |
LOC105376669 Generet finger protein-like 4A |
PHF20 GenePHD finger protein 20 Predicted to enable DNA binding activity and metal ion binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in cytosol; nuclear membrane; and nucleoplasm. Part of MLL1 complex and NSL complex. [provided by Alliance of Genome Resources, Mar 2025] |
PHF23 GenePHD finger protein 23 Predicted to enable metal ion binding activity. Involved in negative regulation of autophagosome assembly; negative regulation of autophagosome maturation; and positive regulation of protein ubiquitination. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
PYGO1 Genepygopus family PHD finger 1 Enables methylated histone binding activity. Predicted to be involved in kidney development and spermatid nucleus differentiation. Predicted to act upstream of or within several processes, including hematopoietic progenitor cell differentiation; positive regulation of transcription by RNA polymerase II; and spermatid development. Predicted to be located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
PYGO2 Genepygopus family PHD finger 2 Predicted to enable several functions, including chromatin binding activity; histone acetyltransferase regulator activity; and histone binding activity. Predicted to be involved in kidney development and spermatid nucleus differentiation. Predicted to act upstream of or within several processes, including canonical Wnt signaling pathway; lens development in camera-type eye; and regulation of mammary gland epithelial cell proliferation. Part of beta-catenin-TCF complex. [provided by Alliance of Genome Resources, Mar 2025] |
RNF208 Genering finger protein 208 Enables ubiquitin-protein transferase activity. Involved in protein autoubiquitination. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
RNF207 Genering finger protein 207 Enables Hsp70 protein binding activity and transmembrane transporter binding activity. Involved in positive regulation of gene expression. Located in perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
RNF11P2 Genering finger protein 11 pseudogene 2 |
RNF11P1 Genering finger protein 11 pseudogene 1 |
LOC100289442 GenePHD finger protein 5A pseudogene |
LOC647253 Genering finger protein 13 pseudogene |
RNF19BPX Genering finger protein 19B pseudogene, X-linked |
RNF19BPY Genering finger protein 19B pseudogene, Y-linked |
LOC644006 Genering finger protein 4 pseudogene |
RNF128 Genering finger protein 128, E3 ubiquitin protein ligase The protein encoded by this gene is a type I transmembrane protein that localizes to the endocytic pathway. This protein contains a RING zinc-finger motif and has been shown to possess E3 ubiquitin ligase activity. Expression of this gene in retrovirally transduced T cell hybridoma significantly inhibits activation-induced IL2 and IL4 cytokine production. Induced expression of this gene was observed in anergic CD4(+) T cells, which suggested a role in the induction of anergic phenotype. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008] |
RNF126 Genering finger protein 126 The protein encoded by this gene contains a RING finger domain, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. [provided by RefSeq, Jul 2008] |
RNF125 Genering finger protein 125, E3 ubiquitin protein ligase This gene encodes a novel E3 ubiquitin ligase that contains a RING finger domain in the N-terminus and three zinc-binding and one ubiquitin-interacting motif in the C-terminus. As a result of myristoylation, this protein associates with membranes and is primarily localized to intracellular membrane systems. The encoded protein may function as a positive regulator in the T-cell receptor signaling pathway. [provided by RefSeq, Mar 2012] |
RNF123 Genering finger protein 123 The protein encoded by this gene contains a C-terminal RING finger domain, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions, and an N-terminal SPRY domain. This protein displays E3 ubiquitin ligase activity toward the cyclin-dependent kinase inhibitor 1B which is also known as p27 or KIP1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016] |
RNF122 Genering finger protein 122 The encoded protein contains a RING finger, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. The encoded protein is localized to the endoplasmic reticulum and golgi apparatus, and may be associated with cell viability. [provided by RefSeq, Jul 2013] |
RNF121 Genering finger protein 121 The protein encoded by this gene contains a RING finger, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. Several alternatively spliced transcript variants have been noted for this gene, however, not all are likely to encode viable protein products. [provided by RefSeq, Sep 2008] |
PHF3 GenePHD finger protein 3 This gene encodes a member of a PHD finger-containing gene family. This gene may function as a transcription factor and may be involved in glioblastomas development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014] |
RNF225 Genering finger protein 225 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in protein ubiquitination. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
MKRN8P Genemakorin ring finger protein 8, pseudogene |
PHF8 GenePHD finger protein 8 The protein encoded by this gene is a histone lysine demethylase that preferentially acts on histones in the monomethyl or dimethyl states. The encoded protein requires Fe(2+) ion, 2-oxoglutarate, and oxygen for its catalytic activity. The protein has an N-terminal PHD finger and a central Jumonji C domain. This gene is thought to function as a transcription activator. Defects in this gene are a cause of syndromic X-linked Siderius type intellectual disability (MRXSSD) and over-expression of this gene is associated with several forms of cancer. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017] |
PHF6 GenePHD finger protein 6 This gene is a member of the plant homeodomain (PHD)-like finger (PHF) family. It encodes a protein with two PHD-type zinc finger domains, indicating a potential role in transcriptional regulation, that localizes to the nucleolus. Mutations affecting the coding region of this gene or the splicing of the transcript have been associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a disorder characterized by cognitive disability, epilepsy, hypogonadism, hypometabolism, obesity, swelling of subcutaneous tissue of the face, narrow palpebral fissures, and large ears. Alternate splicing results in multiple transcript variants, encoding different isoforms. [provided by RefSeq, Jun 2010] |
PHF7 GenePHD finger protein 7 Spermatogenesis is a complex process regulated by extracellular and intracellular factors as well as cellular interactions among interstitial cells of the testis, Sertoli cells, and germ cells. This gene is expressed in the testis in Sertoli cells but not germ cells. The protein encoded by this gene contains plant homeodomain (PHD) finger domains, also known as leukemia associated protein (LAP) domains, believed to be involved in transcriptional regulation. The protein, which localizes to the nucleus of transfected cells, has been implicated in the transcriptional regulation of spermatogenesis. Alternate splicing results in multiple transcript variants of this gene. [provided by RefSeq, May 2013] |
PHF2 GenePHD finger protein 2 This gene encodes a protein which contains a zinc finger-like PHD (plant homeodomain) finger, distinct from other classes of zinc finger motifs, and a hydrophobic and highly conserved domain. The PHD finger shows the typical Cys4-His-Cys3 arrangement. PHD finger genes are thought to belong to a diverse group of transcriptional regulators possibly affecting eukaryotic gene expression by influencing chromatin structure. [provided by RefSeq, Jul 2008] |
PHF1 GenePHD finger protein 1 This gene encodes a Polycomb group protein. The protein is a component of a histone H3 lysine-27 (H3K27)-specific methyltransferase complex, and functions in transcriptional repression of homeotic genes. The protein is also recruited to double-strand breaks, and reduced protein levels results in X-ray sensitivity and increased homologous recombination. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009] |
LOC100419673 GenePHD finger protein 10 pseudogene |
PHF5HP GenePHD finger protein 5H pseudogene |
LOC441455 Genemakorin ring finger protein 1 pseudogene |
MKRN1 Genemakorin ring finger protein 1 This gene encodes a protein that belongs to a novel class of zinc finger proteins. The encoded protein functions as a transcriptional co-regulator, and as an E3 ubiquitin ligase that promotes the ubiquitination and proteasomal degradation of target proteins. The protein encoded by this gene is thought to regulate RNA polymerase II-catalyzed transcription. Substrates for this protein's E3 ubiquitin ligase activity include the capsid protein of the West Nile virus and the catalytic subunit of the telomerase ribonucleoprotein. This protein controls cell cycle arrest and apoptosis by regulating p21, a cell cycle regulator, and the tumor suppressor protein p53. Pseudogenes of this gene are present on chromosomes 1, 3, 9, 12 and 20, and on the X chromosome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2014] |
MKRN3 Genemakorin ring finger protein 3 The protein encoded by this gene contains a RING (C3HC4) zinc finger motif and several C3H zinc finger motifs. This gene is intronless and imprinted, with expression only from the paternal allele. Disruption of the imprinting at this locus may contribute to Prader-Willi syndrome. An antisense RNA of unknown function has been found overlapping this gene. [provided by RefSeq, Jul 2008] |
MKRN2 Genemakorin ring finger protein 2 This gene encodes a probable E3 ubiquitin ligase containing several zinc finger domains, that is a member of the makorin RING zinc-finger protein family. This gene overlaps the v-raf-1 murine leukemia viral oncogene homolog 1 (RAF1) gene in an antisense orientation and may have a co-regulatory function with RAF1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012] |
PHF21A GenePHD finger protein 21A The PHF21A gene encodes BHC80, a component of a BRAF35 (MIM 605535)/histone deacetylase (HDAC; see MIM 601241) complex (BHC) that mediates repression of neuron-specific genes through the cis-regulatory element known as repressor element-1 (RE1) or neural restrictive silencer (NRS) (Hakimi et al., 2002 [PubMed 12032298]).[supplied by OMIM, Nov 2010] |
LOC390358 Generet finger protein-like 2 pseudogene |
RNFT1 Genering finger protein, transmembrane 1 Enables ubiquitin binding activity and ubiquitin protein ligase activity. Involved in positive regulation of ERAD pathway and protein autoubiquitination. Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
UHRF1 Geneubiquitin-like with PHD and ring finger domains 1 This gene encodes a member of a subfamily of RING-finger type E3 ubiquitin ligases. The protein binds to specific DNA sequences, and recruits a histone deacetylase to regulate gene expression. Its expression peaks at late G1 phase and continues during G2 and M phases of the cell cycle. It plays a major role in the G1/S transition by regulating topoisomerase IIalpha and retinoblastoma gene expression, and functions in the p53-dependent DNA damage checkpoint. It is regarded as a hub protein for the integration of epigenetic information. This gene is up-regulated in various cancers, and it is therefore considered to be a therapeutic target. Multiple transcript variants encoding different isoforms have been found for this gene. A related pseudogene exists on chromosome 12. [provided by RefSeq, Feb 2014] |
UHRF2 Geneubiquitin-like with PHD and ring finger domains 2, E3 ubiquitin protein ligase This gene encodes a nuclear protein which is involved in cell-cycle regulation. The encoded protein is a ubiquitin-ligase capable of ubiquinating PCNP (PEST-containing nuclear protein), and together they may play a role in tumorigenesis. The encoded protein contains an NIRF_N domain, a PHD finger, a set- and ring-associated (SRA) domain, and a RING finger domain and several of these domains have been shown to be essential for the regulation of cell proliferation. This protein may also have a role in intranuclear degradation of polyglutamine aggregates. Alternative splicing results in multiple transcript variants some of which are non-protein coding. [provided by RefSeq, Feb 2012] |
LOC441711 GeneRING finger protein 145-like |
RNF138P1 Genering finger protein 138, E3 ubiquitin protein ligase pseudogene 1 |
LOC100631330 Genepolycomb group ring finger 6 pseudogene |
RNF115 Genering finger protein 115 Enables ubiquitin protein ligase activity. Involved in negative regulation of signal transduction; protein ubiquitination; and ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway. Is active in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
RNF112 Genering finger protein 112 This gene encodes a member of the RING finger protein family of transcription factors. The protein is primarily expressed in brain. The gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008] |
RNF111 Genering finger protein 111 The protein encoded by this gene is a nuclear RING-domain containing E3 ubiquitin ligase. This protein interacts with the transforming growth factor (TGF) -beta/NODAL signaling pathway by promoting the ubiquitination and proteosomal degradation of negative regulators, like SMAD proteins, and thereby enhances TGF-beta target-gene transcription. As a modulator of the nodal signaling cascade, this gene plays a critical role in the induction of mesoderm during embryonic development. Alternative splicing of this gene results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2012] |
MGRN1 Genemahogunin ring finger 1, E3 ubiquitin protein ligase Enables ubiquitin-protein transferase activity. Involved in endosome to lysosome transport; negative regulation of adenylate cyclase-activating G protein-coupled receptor signaling pathway; and protein monoubiquitination. Located in several cellular components, including early endosome; endoplasmic reticulum; and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
CHFR Genecheckpoint with forkhead and ring finger domains, E3 ubiquitin protein ligase This gene encodes an E3 ubiquitin-protein ligase required for the maintenance of the antephase checkpoint that regulates cell cycle entry into mitosis and, therefore, may play a key role in cell cycle progression and tumorigenesis. The encoded protein has an N-terminal forkhead-associated domain, a central RING-finger domain, and a cysteine-rich C-terminal region. Alternatively spliced transcript variants that encode different protein isoforms have been described. [provided by RefSeq, Mar 2014] |
RFPL1 Generet finger protein-like 1 Predicted to enable protein homodimerization activity; protein kinase binding activity; and ubiquitin protein ligase activity. Involved in several processes, including negative regulation of G2/M transition of mitotic cell cycle; negative regulation of cell division; and positive regulation of proteolysis. Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
RNF216P1 Genering finger protein 216 pseudogene 1 |
RNF19B Genering finger protein 19B This gene encodes a multi-pass membrane protein containing two RING-type and one IBR-type zinc finger motifs. The encoded protin is an E3 ubiquitin-protein ligase that plays a role in the cytotoxic effects of natural killer (NK) cells. Alternative splicing results in multiple transcript variants. There are pseudogenes for this gene on chromosomes X and Y in a possible pseudoautosomal region. [provided by RefSeq, Jul 2014] |
RNF19A Genering finger protein 19A, RBR E3 ubiquitin protein ligase This gene encodes a member of the ring between ring fingers (RBR) protein family, and the encoded protein contains two RING-finger motifs and an in between RING fingers motif. This protein is an E3 ubiquitin ligase that is localized to Lewy bodies, and ubiquitylates synphilin-1, which is an interacting protein of alpha synuclein in neurons. The encoded protein may be involved in amyotrophic lateral sclerosis and Parkinson's disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013] |
RFPL4AP1 Generet finger protein-like 4A pseudogene 1 |
RFPL4AP5 Generet finger protein-like 4A pseudogene 5 |
RNFT2 Genering finger protein, transmembrane 2 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in positive regulation of ERAD pathway. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNFT1P1 Genering finger protein, transmembrane 1 pseudogene 1 |
RNFT1P2 Genering finger protein, transmembrane 1 pseudogene 2 |
LOC100419583 Genering finger protein 4 pseudogene |
PHF5GP GenePHD finger protein 5G pseudogene |
PHF21B GenePHD finger protein 21B Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
RNF220 Genering finger protein 220 Enables beta-catenin binding activity. Involved in positive regulation of canonical Wnt signaling pathway. Acts upstream of or within positive regulation of DNA-binding transcription factor activity and protein monoubiquitination. Located in nuclear lamina. Part of protein-containing complex. Implicated in hypomyelinating leukodystrophy 23. [provided by Alliance of Genome Resources, Mar 2025] |
RNF222 Genering finger protein 222 Predicted to enable metal ion binding activity. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNF223 Genering finger protein 223 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in protein ubiquitination. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNF224 Genering finger protein 224 Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
RFPL4AP4 Generet finger protein-like 4A pseudogene 4 |
RFPL4AP6 Generet finger protein-like 4A pseudogene 6 |
RNF148 Genering finger protein 148 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in ubiquitin-dependent protein catabolic process. Predicted to be located in membrane. Predicted to be active in Golgi apparatus; endoplasmic reticulum; and late endosome. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100420347 Genepolycomb group ring finger 3 pseudogene |
RNF149 Genering finger protein 149 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in ubiquitin-dependent protein catabolic process. Predicted to act upstream of or within cellular response to xenobiotic stimulus; negative regulation of MAPK cascade; and regulation of protein stability. Located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNF141 Genering finger protein 141 The protein encoded by this gene contains a RING finger, a motif known to be involved in protein-DNA and protein-protein interactions. Abundant expression of this gene was found in the testicular tissue of fertile men, but was not detected in azoospermic patients. Studies of the mouse counterpart suggest that this gene may function as a testis specific transcription factor during spermatogenesis. [provided by RefSeq, Jul 2008] |
RNF145 Genering finger protein 145 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in proteasome-mediated ubiquitin-dependent protein catabolic process. Predicted to be located in endoplasmic reticulum membrane. Predicted to be active in endomembrane system. [provided by Alliance of Genome Resources, Mar 2025] |
RNF146 Genering finger protein 146 Enables poly-ADP-D-ribose binding activity and ubiquitin-protein transferase activity. Involved in positive regulation of canonical Wnt signaling pathway; protein ubiquitination; and ubiquitin-dependent protein catabolic process. Located in cytosol; nucleoplasm; and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNF6P1 Genering finger protein (C3H2C3 type) 6 pseudogene 1 |
BPTF Genebromodomain PHD finger transcription factor This gene was identified by the reactivity of its encoded protein to a monoclonal antibody prepared against brain homogenates from patients with Alzheimer's disease. Analysis of the original protein (fetal Alz-50 reactive clone 1, or FAC1), identified as an 810 aa protein containing a DNA-binding domain and a zinc finger motif, suggested it might play a role in the regulation of transcription. High levels of FAC1 were detected in fetal brain and in patients with neurodegenerative diseases. The protein encoded by this gene is actually much larger than originally thought, and it also contains a C-terminal bromodomain characteristic of proteins that regulate transcription during proliferation. The encoded protein is highly similar to the largest subunit of the Drosophila NURF (nucleosome remodeling factor) complex. In Drosophila, the NURF complex, which catalyzes nucleosome sliding on DNA and interacts with sequence-specific transcription factors, is necessary for the chromatin remodeling required for transcription. Two alternative transcripts encoding different isoforms have been described completely. [provided by RefSeq, Jul 2008] |
RNF126P1 Genering finger protein 126 pseudogene 1 |
BMI1P1 GeneBMI1 proto-oncogene, polycomb ring finger pseudogene 1 |
ZFP36 GeneZFP36 ring finger protein Enables several functions, including 14-3-3 protein binding activity; heat shock protein binding activity; and mRNA 3'-UTR AU-rich region binding activity. Involved in several processes, including cellular response to cytokine stimulus; cellular response to epidermal growth factor stimulus; and regulation of gene expression. Acts upstream of or within mRNA catabolic process. Located in cytoplasmic ribonucleoprotein granule; cytosol; and nucleus. Part of ribonucleoprotein complex. Biomarker of breast cancer. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100129375 Genering finger protein 14 pseudogene |
RNF138P2 Genering finger protein 138, E3 ubiquitin protein ligase pseudogene 2 |
RNF38 Genering finger protein 38 This gene encodes a protein with a coiled-coil motif and a RING-H2 motif (C3H2C2) at its carboxy-terminus. The RING motif is a zinc-binding domain found in a large set of proteins playing roles in diverse cellular processes including oncogenesis, development, signal transduction, and apoptosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008] |
RNF39 Genering finger protein 39 This gene lies within the major histocompatibility complex class I region on chromosome 6. Studies of a similar rat protein suggest that this gene encodes a protein that plays a role in an early phase of synaptic plasticity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
RNF34 Genering finger protein 34, E3 ubiquitin protein ligase The protein encoded by this gene contains a RINF finger, a motif known to be involved in protein-protein and protein-DNA interactions. This protein interacts with DNAJA3/hTid-1, which is a DnaJ protein reported to function as a modulator of apoptosis. Overexpression of this gene in Hela cells was shown to confer the resistance to TNF-alpha induced apoptosis, suggesting an anti-apoptotic function of this protein. This protein can be cleaved by caspase-3 during the induction of apoptosis. This protein also targets p53 and phospho-p53 for degradation. Alternatively splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Feb 2012] |
RNF32 Genering finger protein 32 The protein encoded by this gene contains two RING ring finger motifs. RING finger motifs are present in a variety of functionally distinct proteins and are known to be involved in protein-DNA or protein-protein interactions. This gene was found to be expressed during spermatogenesis, most likely in spermatocytes and/or in spermatids. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2015] |
RNF31 Genering finger protein 31 The protein encoded by this gene contains a RING finger, a motif present in a variety of functionally distinct proteins and known to be involved in protein-DNA and protein-protein interactions. The encoded protein is the E3 ubiquitin-protein ligase component of the linear ubiquitin chain assembly complex. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2015] |
PHF5A GenePHD finger protein 5A This gene encodes a subunit of the splicing factor 3b protein complex. Splicing factor 3b, together with splicing factor 3a and a 12S RNA unit, forms the U2 small nuclear ribonucleoproteins complex (U2 snRNP). The splicing factor 3b/3a complex binds pre-mRNA upstream of the intron's branch site in a sequence-independent manner and may anchor the U2 snRNP to the pre-mRNA. The protein encoded by this gene contains a PHD-finger-like domain that is flanked by highly basic N- and C-termini. This protein belongs to the PHD-finger superfamily and may act as a chromatin-associated protein. This gene has several pseudogenes on different chromosomes. [provided by RefSeq, Jul 2008] |
PHF10P1 GenePHD finger protein 10 pseudogene 1 |
RNF114 Genering finger protein 114 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in protein polyubiquitination and ubiquitin-dependent protein catabolic process. Located in cytosol and plasma membrane. Biomarker of male infertility. [provided by Alliance of Genome Resources, Mar 2025] |
RNF130 Genering finger protein 130 The protein encoded by this gene contains a RING finger motif and is similar to g1, a Drosophila zinc-finger protein that is expressed in mesoderm and involved in embryonic development. The expression of the mouse counterpart was found to be upregulated in myeloblastic cells following IL3 deprivation, suggesting that this gene may regulate growth factor withdrawal-induced apoptosis of myeloid precursor cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013] |
RNF133 Genering finger protein 133 The protein encoded by this gene contains a RING finger domain, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. This gene has no intron. [provided by RefSeq, Jul 2008] |
RNF135 Genering finger protein 135 The protein encoded by this gene contains a RING finger domain, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. This gene is located in a chromosomal region known to be frequently deleted in patients with neurofibromatosis. Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008] |
RNF138 Genering finger protein 138, E3 ubiquitin protein ligase The protein encoded by this gene contains a RING finger, a motif present in a variety of functionally distinct proteins and known to be involved in protein-DNA and protein-protein interactions. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008] |
RNF139 Genering finger protein 139 The protein encoded by this gene is a multi-membrane spanning protein containing a RING-H2 finger. This protein is located in the endoplasmic reticulum, and has been shown to possess ubiquitin ligase activity. This gene was found to be interrupted by a t(3:8) translocation in a family with hereditary renal and non-medulary thyroid cancer. Studies of the Drosophila counterpart suggested that this protein may interact with tumor suppressor protein VHL, as well as with COPS5/JAB1, a protein responsible for the degradation of tumor suppressor CDKN1B/P27KIP. [provided by RefSeq, Jul 2008] |
RNF7P1 Genering finger protein 7 pseudogene 1 |
ZFP36L1 GeneZFP36 ring finger protein-like 1 This gene is a member of the TIS11 family of early response genes, which are induced by various agonists such as the phorbol ester TPA and the polypeptide mitogen EGF. This gene is well conserved across species and has a promoter that contains motifs seen in other early-response genes. The encoded protein contains a distinguishing putative zinc finger domain with a repeating cys-his motif. This putative nuclear transcription factor most likely functions in regulating the response to growth factors. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011] |
ZFP36L2 GeneZFP36 ring finger protein-like 2 This gene is a member of the TIS11 family of early response genes. Family members are induced by various agonists such as the phorbol ester TPA and the polypeptide mitogen EGF. The encoded protein contains a distinguishing putative zinc finger domain with a repeating cys-his motif. This putative nuclear transcription factor most likely functions in regulating the response to growth factors. [provided by RefSeq, Jul 2008] |
RNF8 Genering finger protein 8, E3 ubiquitin protein ligase The protein encoded by this gene contains a RING finger motif and an FHA domain. This protein has been shown to interact with several class II ubiquitin-conjugating enzymes (E2), including UBE2E1/UBCH6, UBE2E2, and UBE2E3, and may act as an ubiquitin ligase (E3) in the ubiquitination of certain nuclear proteins. This protein is also known to play a role in the DNA damage response and depletion of this protein causes cell growth inhibition and cell cycle arrest. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012] |
RNF6 Genering finger protein (C3H2C3 type) 6 The protein encoded by this gene contains a RING-H2 finger motif. Deletions and mutations in this gene were detected in esophageal squamous cell carcinoma (ESCC), suggesting that this protein may be a potential tumor suppressor. Studies of the mouse counterpart suggested a role of this protein in the transcription regulation that controls germinal differentiation. Multiple alternatively spliced transcript variants encoding the same protein are observed. [provided by RefSeq, Jul 2008] |
RNF7 Genering finger protein 7 The protein encoded by this gene is a highly conserved ring finger protein. It is an essential subunit of SKP1-cullin/CDC53-F box protein ubiquitin ligases, which are a part of the protein degradation machinery important for cell cycle progression and signal transduction. This protein interacts with, and is a substrate of, casein kinase II (CSNK2A1/CKII). The phosphorylation of this protein by CSNK2A1 has been shown to promote the degradation of IkappaBalpha (CHUK/IKK-alpha/IKBKA) and p27Kip1(CDKN1B). Alternatively spliced transcript variants encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008] |
RNF4 Genering finger protein 4 The protein encoded by this gene contains a RING finger motif and acts as a transcription regulator. This protein has been shown to interact with, and inhibit the activity of, TRPS1, a transcription suppressor of GATA-mediated transcription. Transcription repressor ZNF278/PATZ is found to interact with this protein, and thus reduce the enhancement of androgen receptor-dependent transcription mediated by this protein. Studies of the mouse and rat counterparts suggested a role of this protein in spermatogenesis. A pseudogene of this gene is found on chromosome 1.[provided by RefSeq, Jul 2010] |
RNF5 Genering finger protein 5, E3 ubiquitin protein ligase The protein encoded by this gene contains a RING finger, which is a motif known to be involved in protein-protein interactions. This protein is a membrane-bound ubiquitin ligase. It can regulate cell motility by targeting paxillin ubiquitination and altering the distribution and localization of paxillin in cytoplasm and cell focal adhesions. [provided by RefSeq, Jul 2008] |
RNF2 Genering finger protein 2 Polycomb group (PcG) of proteins form the multiprotein complexes that are important for the transcription repression of various genes involved in development and cell proliferation. The protein encoded by this gene is one of the PcG proteins. It has been shown to interact with, and suppress the activity of, transcription factor CP2 (TFCP2/CP2). Studies of the mouse counterpart suggested the involvement of this gene in the specification of anterior-posterior axis, as well as in cell proliferation in early development. This protein was also found to interact with huntingtin interacting protein 2 (HIP2), an ubiquitin-conjugating enzyme, and possess ubiquitin ligase activity. [provided by RefSeq, Jul 2008] |
RNF5P1 Genering finger protein 5, E3 ubiquitin protein ligase pseudogene 1 |
PCGF1 Genepolycomb group ring finger 1 PCGF1 is a mammalian homolog of the Drosophila polycomb group genes, which act as transcriptional repressors to regulate anterior-posterior patterning in early embryonic development (Nunes et al., 2001 [PubMed 11287196]). See also PCGF2 (MIM 600346).[supplied by OMIM, Aug 2008] |
PCGF3 Genepolycomb group ring finger 3 The protein encoded by this gene contains a C3HC4 type RING finger, which is a motif known to be involved in protein-protein interactions. The specific function of this protein has not yet been determined. [provided by RefSeq, Jul 2008] |
PCGF2 Genepolycomb group ring finger 2 The protein encoded by this gene contains a RING finger motif and is similar to the polycomb group (PcG) gene products. PcG gene products form complexes via protein-protein interaction and maintain the transcription repression of genes involved in embryogenesis, cell cycles, and tumorigenesis. This protein was shown to act as a negative regulator of transcription and has tumor suppressor activity. The expression of this gene was detected in various tumor cells, but is limited in neural organs in normal tissues. Knockout studies in mice suggested that this protein may negatively regulate the expression of different cytokines, chemokines, and chemokine receptors, and thus plays an important role in lymphocyte differentiation and migration, as well as in immune responses. [provided by RefSeq, Jul 2008] |
PCGF5 Genepolycomb group ring finger 5 Predicted to enable histone H2AK119 ubiquitin ligase activity. Acts upstream of or within positive regulation of transcription by RNA polymerase II. Located in Golgi apparatus; centrosome; and nucleoplasm. Part of PcG protein complex. [provided by Alliance of Genome Resources, Mar 2025] |
PCGF6 Genepolycomb group ring finger 6 The protein encoded by this gene contains a RING finger motif, which is most closely related to those of polycomb group (PcG) proteins RNF110/MEL-18 and BMI1. PcG proteins are known to form protein complexes and function as transcription repressors. This protein has been shown to interact with some PcG proteins and act as a transcription repressor. The activity of this protein is found to be regulated by cell cycle dependent phosphorylation. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008] |
LOC100420298 Genemakorin ring finger protein 1 pseudogene |
PHF2P2 GenePHD finger protein 2 pseudogene 2 |
PHF2P1 GenePHD finger protein 2 pseudogene 1 |
LOC346671 Genering finger protein 14 pseudogene |
RFPL3 Generet finger protein-like 3 Predicted to enable protein homodimerization activity; protein kinase binding activity; and ubiquitin protein ligase activity. Predicted to be involved in several processes, including positive regulation of autophagy; positive regulation of canonical NF-kappaB signal transduction; and regulation of viral entry into host cell. Predicted to be located in nucleus. Predicted to be active in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
RFPL2 Generet finger protein-like 2 Predicted to enable protein homodimerization activity; protein kinase binding activity; and ubiquitin protein ligase activity. Predicted to be involved in several processes, including positive regulation of autophagy; positive regulation of canonical NF-kappaB signal transduction; and regulation of viral entry into host cell. Predicted to be active in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100131785 Genering finger protein 181 pseudogene |
LOC644746 Generet finger protein-like 3 pseudogene |
PJA1 Genepraja ring finger 1, E3 ubiquitin protein ligase This gene encodes an enzyme that has E2-dependent E3 ubiquitin-protein ligase activity. This enzyme belongs to a class of ubiquitin ligases that include a RING finger motif, and it can interact with the E2 ubiquitin-conjugating enzyme UbcH5B. This gene is located in an area of chromosome X where several X-linked cognitive disability disorders have been associated, and it has also been found as part of a contiguous gene deletion associated with craniofrontonasal syndrome, though a direct link to any disorder has yet to be demonstrated. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2010] |
PJA2 Genepraja ring finger 2, E3 ubiquitin protein ligase Enables protein kinase A catalytic subunit binding activity; protein kinase A regulatory subunit binding activity; and ubiquitin protein ligase activity. Involved in several processes, including proteasome-mediated ubiquitin-dependent protein catabolic process; regulation of macrophage activation; and regulation of signal transduction. Located in cytoplasm; cytoskeleton; and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNF44 Genering finger protein 44 The protein encoded by this gene contains a RING finger, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions. [provided by RefSeq, Jul 2008] |
RNF43 Genering finger protein 43 The protein encoded by this gene is a RING-type E3 ubiquitin ligase and is predicted to contain a transmembrane domain, a protease-associated domain, an ectodomain, and a cytoplasmic RING domain. This protein is thought to negatively regulate Wnt signaling, and expression of this gene results in an increase in ubiquitination of frizzled receptors, an alteration in their subcellular distribution, resulting in reduced surface levels of these receptors. Mutations in this gene have been reported in multiple tumor cells, including colorectal and endometrial cancers. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2015] |
RNF41 Genering finger protein 41, E3 ubiquitin protein ligase This gene encodes an E3 ubiquitin ligase. The encoded protein plays a role in type 1 cytokine receptor signaling by controlling the balance between JAK2-associated cytokine receptor degradation and ectodomain shedding. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2011] |
MARCH5 Genemembrane-associated ring finger (C3HC4) 5 MARCH5 is a ubiquitin ligase of the mitochondrial outer membrane that plays a role in the control of mitochondrial morphology by regulating mitofusin-2 (MFN2; MIM 608507) and DRP1 (DNM1L; MIM 603850) (Nakamura et al., 2006 [PubMed 16936636]).[supplied by OMIM, Mar 2008] |
MARCH4 Genemembrane-associated ring finger (C3HC4) 4, E3 ubiquitin protein ligase MARCH4 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH4 reduces surface accumulation of several membrane glycoproteins by directing them to the endosomal compartment (Bartee et al., 2004 [PubMed 14722266]).[supplied by OMIM, Apr 2010] |
MARCH7 Genemembrane-associated ring finger (C3HC4) 7, E3 ubiquitin protein ligase MARCH7 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH proteins add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments (Bartee et al., 2004 [PubMed 14722266]).[supplied by OMIM, Mar 2010] |
MARCH6 Genemembrane-associated ring finger (C3HC4) 6, E3 ubiquitin protein ligase This gene encodes a member of a family of membrane-associated E3 ubiquitin ligases containing RING-CH-type zinc finger motifs. Ubiquitination of type II deiodinase by the encoded protein is an important regulatory step in thyroid hormone signalling. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012] |
MARCH1 Genemembrane-associated ring finger (C3HC4) 1, E3 ubiquitin protein ligase MARCH1 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH proteins add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH1 downregulates the surface expression of major histocompatibility complex (MHC) class II molecules (see MIM 142880) and other glycoproteins by directing them to the late endosomal/lysosomal compartment (Bartee et al., 2004 [PubMed 14722266]; Thibodeau et al., 2008 [PubMed 18389477]; De Gassart et al., 2008 [PubMed 18305173]).[supplied by OMIM, Mar 2010] |
MARCH3 Genemembrane-associated ring finger (C3HC4) 3, E3 ubiquitin protein ligase This gene encodes a member of the membrane-associated RING-CH (MARCH) family. The encoded protein is an E3 ubiquitin-protein ligase that may be involved in regulation of the endosomal transport pathway. [provided by RefSeq, Mar 2013] |
MARCH2 Genemembrane-associated ring finger (C3HC4) 2, E3 ubiquitin protein ligase MARCH2 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH2 reduces surface accumulation of several glycoproteins and appears to regulate early endosome-to-trans-Golgi network (TGN) trafficking (Bartee et al., 2004 [PubMed 14722266]; Nakamura et al., 2005 [PubMed 15689499]).[supplied by OMIM, Mar 2010] |
MARCH9 Genemembrane-associated ring finger (C3HC4) 9 MARCH9 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH9 induces internalization of several membrane glycoproteins and directs them to the endosomal compartment (Bartee et al., 2004 [PubMed 14722266]; Hoer et al., 2007 [PubMed 17174307]).[supplied by OMIM, Apr 2010] |
MARCH8 Genemembrane-associated ring finger (C3HC4) 8, E3 ubiquitin protein ligase MARCH8 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH8 induces the internalization of several membrane glycoproteins (Goto et al., 2003 [PubMed 12582153]; Bartee et al., 2004 [PubMed 14722266]).[supplied by OMIM, Apr 2010] |
RNF167 Genering finger protein 167 RNF167 is an E3 ubiquitin ligase that interacts with TSSC5 (SLC22A18; MIM 602631) and, together with UBCH6 (UBE2E1; MIM 602916), facilitates TSSC5 polyubiquitylation (Yamada and Gorbsky, 2006 [PubMed 16314844]).[supplied by OMIM, Mar 2008] |
RNF166 Genering finger protein 166 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in protein polyubiquitination and ubiquitin-dependent protein catabolic process. Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
RNF165 Genering finger protein 165 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in motor neuron axon guidance and positive regulation of BMP signaling pathway. Predicted to act upstream of or within several processes, including forelimb morphogenesis; nervous system development; and protein polyubiquitination. Predicted to be part of protein-containing complex. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNF169 Genering finger protein 169 Enables K63-linked polyubiquitin modification-dependent protein binding activity; nucleosome binding activity; and ubiquitin-modified histone reader activity. Involved in double-strand break repair via homologous recombination and negative regulation of double-strand break repair. Located in cytosol; nuclear lumen; and site of double-strand break. [provided by Alliance of Genome Resources, Mar 2025] |
RNF168 Genering finger protein 168, E3 ubiquitin protein ligase This gene encodes an E3 ubiquitin ligase protein that contains a RING finger, a motif present in a variety of functionally distinct proteins and known to be involved in protein-DNA and protein-protein interactions. The protein is involved in DNA double-strand break (DSB) repair. Mutations in this gene result in Riddle syndrome. [provided by RefSeq, Sep 2011] |
CXXC1 GeneCXXC finger protein 1 This gene encodes a protein that functions as a transcriptional activator that binds specifically to non-methylated CpG motifs through its CXXC domain. The protein is a component of the SETD1 complex, regulates gene expression and is essential for vertebrate development. [provided by RefSeq, Sep 2015] |
CXXC5 GeneCXXC finger protein 5 The protein encoded by this gene is a retinoid-inducible nuclear protein containing a CXXC-type zinc finger motif. The encoded protein is involved in myelopoiesis, is required for DNA damage-induced p53 activation, regulates the differentiation of C2C12 myoblasts into myocytes, and negatively regulates cutaneous wound healing. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Nov 2015] |
CXXC4 GeneCXXC finger protein 4 This gene encodes a CXXC-type zinc finger domain-containing protein that functions as an antagonist of the canonical wingless/integrated signaling pathway. The encoded protein negatively regulates wingless/integrated signaling through interaction with the post synaptic density protein/ Drosophila disc large tumor suppressor/ zonula occludens-1 protein domain of Dishevelled, a scaffolding protein required for the stabilization of the transcriptional co-activator beta-catenin. In addition, the CXXC domain of this protein has been shown to bind unmethylated CpG dinucleotides, localize to promoters and CpG islands, and interact with the catalytic domain of methylcytosine dioxygenase ten-eleven-translocation 2, an iron and alpha-ketoglutarate-dependent dioxygenase that modifies the methylation status of DNA. In humans, a mutation in this gene has been associated with development of malignant renal cell carcinoma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2015] |
PCGF7P Genepolycomb group ring finger 7 pseudogene |
MKRN7P Genemakorin ring finger protein 7, pseudogene |
PHF5DP GenePHD finger protein 5D pseudogene |
RNF219 Genering finger protein 219 Enables chromatin binding activity and ubiquitin-protein transferase activity. Involved in protein autoubiquitination; protein monoubiquitination; and regulation of DNA replication. Located in chromatin. [provided by Alliance of Genome Resources, Mar 2025] |
RNF215 Genering finger protein 215 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in ubiquitin-dependent protein catabolic process. Predicted to be located in membrane. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
RNF214 Genering finger protein 214 Predicted to enable ubiquitin-protein transferase activity. [provided by Alliance of Genome Resources, Mar 2025] |
RNF217 Genering finger protein 217 This protein encoded by this gene is a member of the RING1-IBR-RING24 (RBR) ubiquitin protein ligase family, and it belongs to a subfamily of these proteins that contain a transmembrane domain. This protein can interact with the HAX1 anti-apoptotic protein via its C-terminal RING finger motif, which suggests a role in apoptosis signaling. It is thought that deregulation of this gene can be a mechanism in leukemogenesis. Mutations in the region encoding the protein GXXXG motif, which appears to be necessary for protein self-association, have been found in human cancers. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Apr 2016] |
RNF216 Genering finger protein 216 This gene encodes a cytoplasmic protein which specifically colocalizes and interacts with the serine/threonine protein kinase, receptor-interacting protein (RIP). Zinc finger domains of the encoded protein are required for its interaction with RIP and for inhibition of TNF- and IL1-induced NF-kappa B activation pathways. The encoded protein may also function as an E3 ubiquitin-protein ligase which accepts ubiquitin from E2 ubiquitin-conjugating enzymes and transfers it to substrates. Several alternatively spliced transcript variants have been described for this locus but the full-length natures of only some are known. [provided by RefSeq, Jul 2008] |
RNF213 Genering finger protein 213 This gene encodes a protein containing a C3HC4-type RING finger domain, which is a specialized type of Zn-finger that binds two atoms of zinc and is thought to be involved in mediating protein-protein interactions. The protein also contains an AAA domain, which is associated with ATPase activity. This gene is a susceptibility gene for Moyamoya disease, a vascular disorder of intracranial arteries. This gene is also a translocation partner in anaplastic large cell lymphoma and inflammatory myofibroblastic tumor cases, where a t(2;17)(p23;q25) translocation has been identified with the anaplastic lymphoma kinase (ALK) gene on chromosome 2, and a t(8;17)(q24;q25) translocation has been identified with the MYC gene on chromosome 8. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2011] |
RNF212 Genering finger protein 212 This gene encodes a RING finger protein that may function as a ubiquitin ligase. The encoded protein may be involved in meiotic recombination. This gene is located within a linkage disequilibrium block and polymorphisms in this gene may influence recombination rates. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Oct 2010] |
LOC100419643 Genering finger protein 14 pseudogene |
LOC100419645 Genering finger protein 14 pseudogene |
RNF14 Genering finger protein 14 The protein encoded by this gene contains a RING zinc finger, a motif known to be involved in protein-protein interactions. This protein interacts with androgen receptor (AR) and may function as a coactivator that induces AR target gene expression in prostate. A dominant negative mutant of this gene has been demonstrated to inhibit the AR-mediated growth of prostate cancer. This protein also interacts with class III ubiquitin-conjugating enzymes (E2s) and may act as a ubiquitin-ligase (E3) in the ubiquitination of certain nuclear proteins. Six alternatively spliced transcript variants encoding two distinct isoforms have been reported. [provided by RefSeq, Jan 2011] |
RNF17 Genering finger protein 17 This gene is similar to a mouse gene that encodes a testis-specific protein containing a RING finger domain. Alternatively spliced transcript variants encoding different isoforms have been found. [provided by RefSeq, May 2010] |
RNF10 Genering finger protein 10 The protein encoded by this gene contains a ring finger motif, which is known to be involved in protein-protein interactions. The specific function of this protein has not yet been determined. EST data suggests the existence of multiple alternatively spliced transcript variants, however, their full length nature is not known. [provided by RefSeq, Jul 2008] |
RNF11 Genering finger protein 11 The protein encoded by this gene contains a RING-H2 finger motif, which is known to be important for protein-protein interactions. The expression of this gene has been shown to be induced by mutant RET proteins (MEN2A/MEN2B). The germline mutations in RET gene are known to be responsible for the development of multiple endocrine neoplasia (MEN). [provided by RefSeq, Jul 2008] |
RNF13 Genering finger protein 13 The protein encoded by this gene contains a RING zinc finger, a motif known to be involved in protein-protein interactions. The specific function of this gene has not yet been determined. Alternatively spliced transcript variants that encode the same protein have been reported. A pseudogene, which is also located on chromosome 3, has been defined for this gene. [provided by RefSeq, Jul 2008] |
PHRF1 GenePHD and ring finger domains 1 Predicted to enable RNA polymerase binding activity. Predicted to be involved in protein ubiquitination. Located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNF152 Genering finger protein 152 Enables small GTPase binding activity and ubiquitin protein ligase activity. Involved in several processes, including cellular response to amino acid starvation; negative regulation of TORC1 signaling; and protein ubiquitination. Located in lysosomal membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNF150 Genering finger protein 150 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in ubiquitin-dependent protein catabolic process. Predicted to be located in membrane. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
RNF151 Genering finger protein 151 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in protein ubiquitination. Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNF157 Genering finger protein 157 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in negative regulation of apoptotic process; positive regulation of dendrite extension; and protein ubiquitination. Predicted to be located in cell body. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
RC3H1 Genering finger and CCCH-type domains 1 This gene encodes a protein containing RING-type and C3H1-type zinc finger motifs. The encoded protein recognizes and binds to a constitutive decay element (CDE) in the 3' UTR of mRNAs, leading to mRNA deadenylation and degradation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014] |
RC3H2 Genering finger and CCCH-type domains 2 Enables nucleic acid binding activity and ubiquitin protein ligase activity. Involved in protein polyubiquitination. Located in cell surface; intracellular membrane-bounded organelle; and membrane. [provided by Alliance of Genome Resources, Mar 2025] |
MKRN4P Genemakorin ring finger protein 4, pseudogene Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in protein ubiquitination. [provided by Alliance of Genome Resources, Mar 2025] |
RFPL4AP2 Generet finger protein-like 4A pseudogene 2 |
RNF40 Genering finger protein 40, E3 ubiquitin protein ligase The protein encoded by this gene contains a RING finger, a motif known to be involved in protein-protein and protein-DNA interactions. This protein was reported to interact with the tumor suppressor protein RB1. Studies of the rat counterpart suggested that this protein may function as an E3 ubiquitin-protein ligase, and facilitate the ubiquitination and degradation of syntaxin 1, which is an essential component of the neurotransmitter release machinery. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2011] |
MKRN5P Genemakorin ring finger protein 5, pseudogene |
RNF212B Genering finger protein 212B Predicted to enable SUMO transferase activity and ubiquitin protein ligase activity. Predicted to be involved in chiasma assembly and protein ubiquitination. Predicted to be located in chromosome. Predicted to be active in synaptonemal complex. [provided by Alliance of Genome Resources, Mar 2025] |
RNF10P1 Genering finger protein 10 pseudogene 1 |
BMI1 GeneBMI1 proto-oncogene, polycomb ring finger This gene encodes a ring finger protein that is major component of the polycomb group complex 1 (PRC1). This complex functions through chromatin remodeling as an essential epigenetic repressor of multiple regulatory genes involved in embryonic development and self-renewal in somatic stem cells. This protein also plays a central role in DNA damage repair. This gene is an oncogene and aberrant expression is associated with numerous cancers and is associated with resistance to certain chemotherapies. A pseudogene of this gene is found on chromosome X. Read-through transcription also exists between this gene and the upstream COMM domain containing 3 (COMMD3) gene. [provided by RefSeq, Sep 2015] |
PHF5CP GenePHD finger protein 5C pseudogene |
RNF113B Genering finger protein 113B Predicted to enable metal ion binding activity. Predicted to be involved in snoRNA splicing. Predicted to be part of U2-type spliceosomal complex. [provided by Alliance of Genome Resources, Mar 2025] |
RNF113A Genering finger protein 113A This intronless gene encodes a protein which contains a C3H1-type zinc finger domain and a C3HC4 Ring-type (Really Interesting New Gene-type) zinc finger domain. The Ring-type zinc finger domain is identified in various tumor suppressors, DNA repair genes and cytokine receptor-associated molecules, and is probably involved in mediating protein-protein interactions. [provided by RefSeq, May 2010] |
RNF25 Genering finger protein 25 The protein encoded by this gene contains a RING finger motif. The mouse counterpart of this protein has been shown to interact with Rela, the p65 subunit of NF-kappaB (NFKB), and modulate NFKB-mediated transcription activity. The mouse protein also binds ubiquitin-conjugating enzymes (E2s) and is a substrate for E2-dependent ubiquitination. [provided by RefSeq, Jul 2008] |
RNF24 Genering finger protein 24 This gene encodes an integral membrane protein that contains a RING-type zinc finger. The encoded protein may interact with multiple transient receptor potential cation channel subfamily C (TRPC) proteins and regulate the trafficking and insertion of these proteins into the plasma membrane. [provided by RefSeq, Mar 2016] |
RNF26 Genering finger protein 26 The protein encoded by this intronless gene contains a C3HC5 type of RING finger, a motif known to be involved in protein-DNA and protein-protein interactions. The expression of this gene was found to be upregulated in cancer cell lines derived from different types of cancer. [provided by RefSeq, Jul 2008] |
RNF20 Genering finger protein 20, E3 ubiquitin protein ligase The protein encoded by this gene shares similarity with BRE1 of S. cerevisiae. The protein encoded by this human gene is an E3 ubiquitin ligase that regulates chromosome structure by monoubiquitinating histone H2B. This protein acts as a putative tumor suppressor and positively regulates the p53 tumor suppressor as well as numerous histone H2A and H2B genes. In contrast, this protein also suppresses the expression of several protooncogenes and growth-related genes, including many genes that are induced by epidermal growth factor. This gene selectively suppresses the expression of some genes by interfering with chromatin recruitment of transcription elongation factor SII (TFIIS). [provided by RefSeq, Feb 2012] |
RNF103 Genering finger protein 103 The protein encoded by this gene contains a RING-H2 finger, a motif known to be involved in protein-protein and protein-DNA interactions. This gene is highly expressed in normal cerebellum, but not in the cerebral cortex. The expression of the rat counterpart in the frontal cortex and hippocampus was shown to be induced by elctroconvulsive treatment (ECT) as well as chronic antidepressant treatment, suggesting that this gene may be a molecular target for ECT and antidepressants. The protein is a ubiquitin ligase that functions in the endoplasmic reticulum-associated degradation pathway. Alternative splicing of this gene results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream CHMP3 (charged multivesicular body protein 3) gene. [provided by RefSeq, Oct 2011] |
RING1 Genering finger protein 1 This gene belongs to the RING finger family, members of which encode proteins characterized by a RING domain, a zinc-binding motif related to the zinc finger domain. The gene product can bind DNA and can act as a transcriptional repressor. It is associated with the multimeric polycomb group protein complex. The gene product interacts with the polycomb group proteins BMI1, EDR1, and CBX4, and colocalizes with these proteins in large nuclear domains. It interacts with the CBX4 protein via its glycine-rich C-terminal domain. The gene maps to the HLA class II region, where it is contiguous with the RING finger genes FABGL and HKE4. [provided by RefSeq, Jul 2008] |
RNF144A Genering finger protein 144A This gene encodes a member of a family of RING finger domain-containing E3 ubiquitin ligases that also includes parkin and parc. The expression of this gene is induced by DNA damage. The encoded protein interacts with the cytoplasmic DNA-dependent protein kinase, catalytic subunit (DNA-PKcs) and promotes its degradation through ubiquitination. The orthologous mouse protein has been shown to interact with a ubiquitin-conjugating enzyme involved in embryonic development. [provided by RefSeq, Mar 2017] |
LOC401805 Genering finger protein 145 pseudogene |
RNF185 Genering finger protein 185 Enables ubiquitin binding activity; ubiquitin protein ligase activity; and ubiquitin-like protein conjugating enzyme binding activity. Involved in several processes, including positive regulation of ERAD pathway; protein ubiquitination; and proteolysis involved in protein catabolic process. Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
RNF187 Genering finger protein 187 Enables ubiquitin-protein transferase activity. Involved in positive regulation of DNA-templated transcription; proteasome-mediated ubiquitin-dependent protein catabolic process; and protein ubiquitination. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
RNF186 Genering finger protein 186 Enables ubiquitin protein ligase activity and ubiquitin protein ligase binding activity. Involved in several processes, including intrinsic apoptotic signaling pathway in response to endoplasmic reticulum stress; proteasome-mediated ubiquitin-dependent protein catabolic process; and protein ubiquitination. Acts upstream of with a positive effect on regulation of autophagosome assembly. Located in endoplasmic reticulum membrane. Is active in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
RNF181 Genering finger protein 181 RNF181 binds the integrin alpha-IIb (ITGA2B; MIM 607759)/beta-3 (ITGB3; MIM 173470) complex and has E3 ubiquitin ligase activity (Brophy et al., 2008 [PubMed 18331836]).[supplied by OMIM, Dec 2008] |
RNF180 Genering finger protein 180 Predicted to enable ubiquitin conjugating enzyme binding activity and ubiquitin protein ligase activity. Predicted to be involved in norepinephrine metabolic process; positive regulation of proteasomal ubiquitin-dependent protein catabolic process; and serotonin metabolic process. Predicted to act upstream of or within several processes, including adult behavior; positive regulation of protein ubiquitination; and protein polyubiquitination. Predicted to be located in endoplasmic reticulum; membrane; and nuclear envelope. Predicted to be active in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNF183 Genering finger protein 183 Enables ubiquitin protein ligase activity. Involved in positive regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway; protein ubiquitination; and response to endoplasmic reticulum stress. Located in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNF182 Genering finger protein 182 Enables ubiquitin-protein transferase activity. Involved in protein ubiquitination. Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
UHRF2P1 Geneubiquitin-like with PHD and ring finger domains 2 pseudogene 1 |
CXXC1P1 GeneCXXC finger protein 1 pseudogene 1 |
RNF152P1 Genering finger protein 152 pseudogene 1 |
RFPL4AP7 Generet finger protein-like 4A pseudogene 7 |
RNF2P1 Genering finger protein 2 pseudogene 1 |
PHF5FP GenePHD finger protein 5F pseudogene |
JADE3 Genejade family PHD finger 3 This gene encodes a member of a family of large proteins containing PHD (plant homeo domain)-type zinc fingers. The encoded protein may be associated in a nuclear complex that functions in histone H4 acetylation. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Aug 2013] |
JADE2 Genejade family PHD finger 2 Enables histone H4K12 acetyltransferase activity; histone H4K5 acetyltransferase activity; and histone H4K8 acetyltransferase activity. Contributes to histone H3K14 acetyltransferase activity. Involved in regulation of DNA biosynthetic process; regulation of DNA replication; and regulation of cell cycle. Located in nucleoplasm. Part of histone acetyltransferase complex. [provided by Alliance of Genome Resources, Mar 2025] |
JADE1 Genejade family PHD finger 1 Enables transcription coactivator activity. Contributes to histone acetyltransferase activity. Involved in several processes, including negative regulation of canonical Wnt signaling pathway; regulation of cell growth; and regulation of nucleobase-containing compound metabolic process. Acts upstream of or within negative regulation of G1/S transition of mitotic cell cycle. Located in several cellular components, including cytosol; microtubule organizing center; and nuclear speck. Part of histone acetyltransferase complex. [provided by Alliance of Genome Resources, Mar 2025] |
PHF14 GenePHD finger protein 14 Enables histone binding activity. Predicted to be involved in several processes, including germinal center B cell differentiation; lung development; and negative regulation of mesenchymal cell proliferation involved in lung development. Located in chromatin; cytoplasm; and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
PHF10 GenePHD finger protein 10 This gene contains a predicted ORF that encodes a protein with two zinc finger domains. The function of the encoded protein is not known. Sequence analysis suggests that multiple alternatively spliced transcript variants are derived from this gene but the full-length nature of only two of them is known. These two splice variants encode different isoforms. A pseudogene for this gene is located on Xq28. [provided by RefSeq, Jul 2008] |
PHF11 GenePHD finger protein 11 This gene encodes a protein containing a PHD (plant homeodomain) type zinc finger. This gene has been identified in some studies as a candidate gene for asthma. Naturally-occurring readthrough transcription may occur from the upstream SETDB2 (SET domain bifurcated 2) gene to this locus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016] |
PHF12 GenePHD finger protein 12 Enables phosphatidylinositol binding activity and transcription corepressor activity. Involved in negative regulation of DNA-templated transcription. Acts upstream of or within negative regulation of transcription by RNA polymerase II. Located in nucleoplasm. Part of Sin3-type complex and transcription repressor complex. [provided by Alliance of Genome Resources, Mar 2025] |
PHF13 GenePHD finger protein 13 Enables chromatin binding activity; chromatin-protein adaptor activity; and methylated histone binding activity. Involved in mitotic chromosome condensation and regulation of DNA repair. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
PHF19 GenePHD finger protein 19 Enables methylated histone binding activity. Involved in negative regulation of gene expression, epigenetic. Located in ESC/E(Z) complex. [provided by Alliance of Genome Resources, Mar 2025] |
RNF144B Genering finger protein 144B Enables ubiquitin-protein transferase activity. Involved in negative regulation of apoptotic process and ubiquitin-dependent protein catabolic process. Located in mitochondrial membrane. [provided by Alliance of Genome Resources, Mar 2025] |
MKRN9P Genemakorin ring finger protein 9, pseudogene |
PHF20L1 GenePHD finger protein 20-like 1 Enables methylation-dependent protein binding activity. Involved in negative regulation of proteasomal ubiquitin-dependent protein catabolic process. Predicted to be located in nucleoplasm. Predicted to be part of NSL complex. [provided by Alliance of Genome Resources, Mar 2025] |
PHF24 GenePHD finger protein 24 Predicted to enable transcription corepressor activity. Predicted to be involved in negative regulation of DNA-templated transcription. Predicted to act upstream of or within several processes, including detection of mechanical stimulus involved in sensory perception of pain; gamma-aminobutyric acid signaling pathway; and regulation of GABAergic synaptic transmission. Predicted to be active in glutamatergic synapse; nucleus; and synaptic vesicle membrane. [provided by Alliance of Genome Resources, Mar 2025] |
MARCHF1 Genemembrane associated ring-CH-type finger 1 MARCH1 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH proteins add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH1 downregulates the surface expression of major histocompatibility complex (MHC) class II molecules (see MIM 142880) and other glycoproteins by directing them to the late endosomal/lysosomal compartment (Bartee et al., 2004 [PubMed 14722266]; Thibodeau et al., 2008 [PubMed 18389477]; De Gassart et al., 2008 [PubMed 18305173]).[supplied by OMIM, Mar 2010] |
MARCHF7 Genemembrane associated ring-CH-type finger 7 MARCH7 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH proteins add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments (Bartee et al., 2004 [PubMed 14722266]).[supplied by OMIM, Mar 2010] |
MARCHF6 Genemembrane associated ring-CH-type finger 6 This gene encodes a member of a family of membrane-associated E3 ubiquitin ligases containing RING-CH-type zinc finger motifs. Ubiquitination of type II deiodinase by the encoded protein is an important regulatory step in thyroid hormone signalling. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jul 2012] |
MARCHF5 Genemembrane associated ring-CH-type finger 5 MARCH5 is a ubiquitin ligase of the mitochondrial outer membrane that plays a role in the control of mitochondrial morphology by regulating mitofusin-2 (MFN2; MIM 608507) and DRP1 (DNM1L; MIM 603850) (Nakamura et al., 2006 [PubMed 16936636]).[supplied by OMIM, Mar 2008] |
LOC122513141 Genering finger protein-like |
MARCHF3 Genemembrane associated ring-CH-type finger 3 This gene encodes a member of the membrane-associated RING-CH (MARCH) family. The encoded protein is an E3 ubiquitin-protein ligase that may be involved in regulation of the endosomal transport pathway. [provided by RefSeq, Mar 2013] |
MARCHF8 Genemembrane associated ring-CH-type finger 8 MARCH8 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH8 induces the internalization of several membrane glycoproteins (Goto et al., 2003 [PubMed 12582153]; Bartee et al., 2004 [PubMed 14722266]).[supplied by OMIM, Apr 2010] |
MARCHF2 Genemembrane associated ring-CH-type finger 2 MARCH2 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH2 reduces surface accumulation of several glycoproteins and appears to regulate early endosome-to-trans-Golgi network (TGN) trafficking (Bartee et al., 2004 [PubMed 14722266]; Nakamura et al., 2005 [PubMed 15689499]).[supplied by OMIM, Mar 2010] |
MARCHF10 Genemembrane associated ring-CH-type finger 10 MARCH10 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments (Morokuma et al., 2007 [PubMed 17604280]).[supplied by OMIM, Apr 2010] |
RNF227 Genering finger protein 227 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in protein ubiquitination. [provided by Alliance of Genome Resources, Mar 2025] |
MARCHF9 Genemembrane associated ring-CH-type finger 9 MARCH9 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH9 induces internalization of several membrane glycoproteins and directs them to the endosomal compartment (Bartee et al., 2004 [PubMed 14722266]; Hoer et al., 2007 [PubMed 17174307]).[supplied by OMIM, Apr 2010] |
MARCHF11 Genemembrane associated ring-CH-type finger 11 MARCH11 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). These enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their intracellular transport. March11 appears to have a role in ubiquitin-mediated protein sorting in the trans-Golgi network (TGN)-multivesicular body (MVB) transport pathway (Morokuma et al., 2007 [PubMed 17604280]).[supplied by OMIM, Apr 2010] |
MARCHF4 Genemembrane associated ring-CH-type finger 4 MARCH4 is a member of the MARCH family of membrane-bound E3 ubiquitin ligases (EC 6.3.2.19). MARCH enzymes add ubiquitin (see MIM 191339) to target lysines in substrate proteins, thereby signaling their vesicular transport between membrane compartments. MARCH4 reduces surface accumulation of several membrane glycoproteins by directing them to the endosomal compartment (Bartee et al., 2004 [PubMed 14722266]).[supplied by OMIM, Apr 2010] |
BPTFP1 Genebromodomain PHD finger transcription factor pseudogene 1 |
RNF228 Genering finger protein 228 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in protein ubiquitination. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ARK2C Genearkadia (RNF111) C-terminal like ring finger ubiquitin ligase 2C Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in motor neuron axon guidance and positive regulation of BMP signaling pathway. Predicted to act upstream of or within several processes, including forelimb morphogenesis; nervous system development; and protein polyubiquitination. Predicted to be part of protein-containing complex. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SRBD1 GeneS1 RNA binding domain 1 Predicted to enable mRNA binding activity. Predicted to be a structural constituent of ribosome. Predicted to be involved in translation. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100420186 GeneWW domain binding protein 2 pseudogene |
HMGN2P31 Genehigh mobility group nucleosomal binding domain 2 pseudogene 31 |
HMGN2P19 Genehigh mobility group nucleosomal binding domain 2 pseudogene 19 |
HMGN2P18 Genehigh mobility group nucleosomal binding domain 2 pseudogene 18 |
HMGN2P12 Genehigh mobility group nucleosomal binding domain 2 pseudogene 12 |
HMGN2P11 Genehigh mobility group nucleosomal binding domain 2 pseudogene 11 |
HMGN2P10 Genehigh mobility group nucleosomal binding domain 2 pseudogene10 |
HMGN2P17 Genehigh mobility group nucleosomal binding domain 2 pseudogene 17 |
HMGN2P16 Genehigh mobility group nucleosomal binding domain 2 pseudogene 16 |
HMGN2P15 Genehigh mobility group nucleosomal binding domain 2 pseudogene 15 |
HMGN2P14 Genehigh mobility group nucleosomal binding domain 2 pseudogene14 |
SH3KBP1 GeneSH3-domain kinase binding protein 1 This gene encodes an adapter protein that contains one or more N-terminal Src homology domains, a proline rich region and a C-terminal coiled-coil domain. The encoded protein facilitates protein-protein interactions and has been implicated in numerous cellular processes including apoptosis, cytoskeletal rearrangement, cell adhesion and in the regulation of clathrin-dependent endocytosis. Alternate splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2017] |
HMGN1P9 Genehigh mobility group nucleosome binding domain 1 pseudogene |
HMGN1P4 Genehigh mobility group nucleosome binding domain 1 pseudogene 4 |
HMGN1P5 Genehigh mobility group nucleosome binding domain 1 pseudogene 5 |
HMGN1P6 Genehigh mobility group nucleosome binding domain 1 pseudogene 6 |
HMGN1P7 Genehigh mobility group nucleosome binding domain 1 pseudogene 7 |
HMGN1P1 Genehigh mobility group nucleosome binding domain 1 pseudogene 1 |
HMGN1P2 Genehigh mobility group nucleosome binding domain 1 pseudogene 2 |
WBP2P1 GeneWW domain binding protein 2 pseudogene 1 |
TTC28 Genetetratricopeptide repeat domain 28 Enables kinase binding activity. Involved in regulation of mitotic cell cycle. Located in midbody. [provided by Alliance of Genome Resources, Mar 2025] |
TTC29 Genetetratricopeptide repeat domain 29 Involved in cilium movement and cilium organization. Located in sperm flagellum. Implicated in spermatogenic failure 42. [provided by Alliance of Genome Resources, Mar 2025] |
TTC24 Genetetratricopeptide repeat domain 24 |
TTC25 Genetetratricopeptide repeat domain 25 This gene encodes a tetratricopeptide repeat domain-containing protein that localizes to ciliary axonmenes and plays a role in the docking of the outer dynein arm to cilia. Mutations in this gene cause severely reduced ciliary motility and the disorder CILD35 (ciliary dyskinesia,primary, 35). Primary ciliary dyskinesia is often associated with recurrent respiratory infections, immotile spermatozoa, and situs inversus; an inversion in left-right body symmetry. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Apr 2017] |
TTC26 Genetetratricopeptide repeat domain 26 Predicted to enable intraciliary transport particle B binding activity. Involved in cilium assembly. Located in cilium. Part of intraciliary transport particle B. [provided by Alliance of Genome Resources, Mar 2025] |
TTC27 Genetetratricopeptide repeat domain 27 |
TTC22 Genetetratricopeptide repeat domain 22 This gene encodes a protein with seven tetratricopeptide (TPR) repeats. Tetratricopeptide repeat containing motifs are found in a variety of proteins and may mediate protein-protein interactions and chaperone activity. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2011] |
TTC23 Genetetratricopeptide repeat domain 23 Predicted to be involved in positive regulation of smoothened signaling pathway. Predicted to be located in cilium. [provided by Alliance of Genome Resources, Mar 2025] |
RCN1P1 Genereticulocalbin 1, EF-hand calcium binding domain pseudogene 1 |
LOC100129956 Genehigh mobility group nucleosomal binding domain 2 pseudogene |
ANKRD19P Geneankyrin repeat domain 19, pseudogene |
CLEC18A GeneC-type lectin domain family 18, member A This is one of three closely related paralogous genes on chromosome 16 encoding secreted proteins containing C-type lectin domains. These domains bind to carbohydrates in the presence of calcium, and may be involved in cell adhesion, immune response and apoptosis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2012] |
CLEC18B GeneC-type lectin domain family 18, member B Predicted to enable polysaccharide binding activity. Predicted to be located in Golgi apparatus; endosome; and sarcoplasmic reticulum. Predicted to be active in extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
ADAM10 GeneADAM metallopeptidase domain 10 Members of the ADAM family are cell surface proteins with a unique structure possessing both potential adhesion and protease domains. This gene encodes and ADAM family member that cleaves many proteins including TNF-alpha and E-cadherin. Alternate splicing results in multiple transcript variants encoding different proteins that may undergo similar processing. [provided by RefSeq, Feb 2016] |
ADAM11 GeneADAM metallopeptidase domain 11 This gene encodes a member of the ADAM (a disintegrin and metalloprotease) protein family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The encoded preproprotein is proteolytically processed to generate the mature protease. This gene represents a candidate tumor suppressor gene for human breast cancer based on its location within a minimal region of chromosome 17q21 previously defined by tumor deletion mapping. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Jan 2016] |
ADAM12 GeneADAM metallopeptidase domain 12 This gene encodes a member of a family of proteins that are structurally related to snake venom disintegrins and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. Expression of this gene has been used as a maternal serum marker for pre-natal development. Alternative splicing results in multiple transcript variants encoding different isoforms. Shorter isoforms are secreted, while longer isoforms are membrane-bound form. [provided by RefSeq, Jan 2014] |
ADAM15 GeneADAM metallopeptidase domain 15 The protein encoded by this gene is a member of the ADAM (a disintegrin and metalloproteinase) protein family. ADAM family members are type I transmembrane glycoproteins known to be involved in cell adhesion and proteolytic ectodomain processing of cytokines and adhesion molecules. This protein contains multiple functional domains including a zinc-binding metalloprotease domain, a disintegrin-like domain, as well as a EGF-like domain. Through its disintegrin-like domain, this protein specifically interacts with the integrin beta chain, beta 3. It also interacts with Src family protein-tyrosine kinases in a phosphorylation-dependent manner, suggesting that this protein may function in cell-cell adhesion as well as in cellular signaling. Multiple alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008] |
ADAM17 GeneADAM metallopeptidase domain 17 This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biologic processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The encoded preproprotein is proteolytically processed to generate the mature protease. The encoded protease functions in the ectodomain shedding of tumor necrosis factor-alpha, in which soluble tumor necrosis factor-alpha is released from the membrane-bound precursor. This protease also functions in the processing of numerous other substrates, including cell adhesion proteins, cytokine and growth factor receptors and epidermal growth factor (EGF) receptor ligands, and plays a prominent role in the activation of the Notch signaling pathway. Elevated expression of this gene has been observed in specific cell types derived from psoriasis, rheumatoid arthritis, multiple sclerosis and Crohn's disease patients, suggesting that the encoded protein may play a role in autoimmune disease. Additionally, this protease may play a role in viral infection through its cleavage of ACE2, the cellular receptor for SARS-CoV and SARS-CoV-2. [provided by RefSeq, Aug 2020] |
ADAM18 GeneADAM metallopeptidase domain 18 This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biologic processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The encoded preproprotein is proteolytically processed to generate the mature sperm surface protein. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Feb 2016] |
ADAM19 GeneADAM metallopeptidase domain 19 This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. This member is a type I transmembrane protein and serves as a marker for dendritic cell differentiation. It has been demonstrated to be an active metalloproteinase, which may be involved in normal physiological processes such as cell migration, cell adhesion, cell-cell and cell-matrix interactions, and signal transduction. It is proposed to play a role in pathological processes, such as cancer, inflammatory diseases, renal diseases, and Alzheimer's disease. [provided by RefSeq, May 2013] |
G3BP1 GeneGTPase activating protein (SH3 domain) binding protein 1 This gene encodes one of the DNA-unwinding enzymes which prefers partially unwound 3'-tailed substrates and can also unwind partial RNA/DNA and RNA/RNA duplexes in an ATP-dependent fashion. This enzyme is a member of the heterogeneous nuclear RNA-binding proteins and is also an element of the Ras signal transduction pathway. It binds specifically to the Ras-GTPase-activating protein by associating with its SH3 domain. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jul 2008] |
ADAM1A GeneADAM metallopeptidase domain 1A (pseudogene) Predicted to act upstream of or within binding activity of sperm to zona pellucida. Predicted to be located in membrane raft. [provided by Alliance of Genome Resources, Mar 2025] |
ADAM1B GeneADAM metallopeptidase domain 1B (pseudogene) |
PAXIP1 GenePAX interacting (with transcription-activation domain) protein 1 This gene is a member of the paired box (PAX) gene family and encodes a nuclear protein with six BRCT (breast cancer carboxy-terminal) domains. This protein plays a critical role in maintaining genome stability, condensation of chromatin and progression through mitosis. [provided by RefSeq, Jul 2008] |
CITED1 GeneCbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 1 This gene encodes a member of the CREB-binding protein/p300-interacting transactivator with Asp/Glu-rich C-terminal domain (CITED) family of proteins. The encoded protein, also known as melanocyte-specific gene 1, may function as a transcriptional coactivator and may play a role in pigmentation of melanocytes. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jan 2009] |
CITED4 GeneCbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 4 The protein encoded by this intronless gene belongs to the CITED family of transcriptional coactivators that bind to several proteins, including CREB-binding protein (CBP) and p300, via a conserved 32 aa C-terminal motif, and regulate gene transcription. This protein also interacts with transcription factor AP2 (TFAP2), and thus may function as a co-activator for TFAP2. Hypermethylation and transcriptional downregulation of this gene has been observed in oligodendroglial tumors with deletions of chromosomal arms 1p and 19q, and associated with longer recurrence-free and overall survival of patients with oligodendroglial tumors. [provided by RefSeq, Aug 2011] |
TTC30A Genetetratricopeptide repeat domain 30A Predicted to enable intraciliary transport particle B binding activity. Predicted to be involved in intraciliary transport. Predicted to be located in centrosome. Predicted to be part of intraciliary transport particle B. Predicted to be active in axonemal microtubule. [provided by Alliance of Genome Resources, Mar 2025] |
TTC30B Genetetratricopeptide repeat domain 30B Predicted to enable intraciliary transport particle B binding activity. Predicted to be involved in intraciliary transport. Part of intraciliary transport particle B. [provided by Alliance of Genome Resources, Mar 2025] |
PTCD2P2 Genepentatricopeptide repeat domain 2 pseudogene 2 |
LOC101929101 Genecarboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 2 pseudogene |
ANKRD20A10P Geneankyrin repeat domain 20 family, member A10, pseudogene |
EFCAB11 GeneEF-hand calcium binding domain 11 Predicted to enable calcium ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
EFCAB10 GeneEF-hand calcium binding domain 10 Predicted to enable calcium ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
EFCAB13 GeneEF-hand calcium binding domain 13 |
EFCAB12 GeneEF-hand calcium binding domain 12 Predicted to enable calcium ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
EFCAB14 GeneEF-hand calcium binding domain 14 Predicted to enable calcium ion binding activity. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
WDR13 GeneWD repeat domain 13 This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by Gly-His and Trp-Asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. A similar protein in mouse is thought to be a negative regulator of the pancreatic beta cell proliferation. Mice lacking this gene exhibit increased pancreatic islet mass and higher serum insulin levels, and are mildly obese. [provided by RefSeq, Nov 2016] |
WDR12 GeneWD repeat domain 12 This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This protein is highly similar to the mouse WD repeat domain 12 protein at the amino acid level. The protein encoded by this gene is a component of a nucleolar protein complex that affects maturation of the large ribosomal subunit.[provided by RefSeq, Dec 2008] |
WDR11 GeneWD repeat domain 11 This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This gene is located in the chromosome 10q25-26 region, which is frequently deleted in gliomas and tumors of other tissues, and is disrupted by the t(10;19) translocation rearrangement in glioblastoma cells. The gene location suggests that it is a candidate gene for the tumor suppressor locus. [provided by RefSeq, Jul 2008] |
WDR17 GeneWD repeat domain 17 This gene encodes a WD repeat-containing protein. It is abundantly expressed in retina and testis, and is thought to be a candidate gene for retinal disease. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Nov 2009] |
WDR19 GeneWD repeat domain 19 The protein encoded by this gene is a member of the WD (tryptophan-aspartic acid) repeat family, which is a large family of structurally-related proteins known to participate in a wide range of cellular processes. Each WD repeat typically contains about 40 amino acids that are usually bracketed by glycine-histidine and tryptophan-aspartic acid (WD) dipeptides. This protein contains six WD repeats, three transmembrane domains, and a clathrin heavy-chain repeat. Mutations in this gene have been described in individuals with a wide range of disorders affecting function of the cilium. These disorders are known as ciliopathies, and include Jeune syndrome, Sensenbrenner syndromes, Senior-Loken syndrome, combined or isolated nephronophthisis (NPHP), and retinitis pigmentosa (RP). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015] |
WDR18 GeneWD repeat domain 18 This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. [provided by RefSeq, Jul 2008] |
RIBC2 GeneRIB43A domain with coiled-coils 2 Predicted to be involved in flagellated sperm motility. Located in axonemal microtubule. [provided by Alliance of Genome Resources, Mar 2025] |
RIBC1 GeneRIB43A domain with coiled-coils 1 Predicted to be involved in flagellated sperm motility. Predicted to be located in cytoplasm; cytoskeleton; and motile cilium. Predicted to be active in axonemal A tubule inner sheath and sperm flagellum. [provided by Alliance of Genome Resources, Mar 2025] |
CLEC1A GeneC-type lectin domain family 1, member A This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signaling, glycoprotein turnover, and roles in inflammation and immune response. The encoded protein may play a role in regulating dendritic cell function. This gene is closely linked to other CTL/CTLD superfamily members on chromosome 12p13 in the natural killer gene complex region. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014] |
CLEC1B GeneC-type lectin domain family 1, member B Natural killer (NK) cells express multiple calcium-dependent (C-type) lectin-like receptors, such as CD94 (KLRD1; MIM 602894) and NKG2D (KLRC4; MIM 602893), that interact with major histocompatibility complex class I molecules and either inhibit or activate cytotoxicity and cytokine secretion. CLEC2 is a C-type lectin-like receptor expressed in myeloid cells and NK cells (Colonna et al., 2000 [PubMed 10671229]).[supplied by OMIM, Jan 2011] |
TTC39CP1 Genetetratricopeptide repeat domain 39C pseudogene 1 |
TMPPE Genetransmembrane protein with metallophosphoesterase domain Predicted to enable hydrolase activity and metal ion binding activity. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
HMGN2P13 Genehigh mobility group nucleosomal binding domain 2 pseudogene 13 |
TTC4P1 Genetetratricopeptide repeat domain 4 pseudogene 1 |
CALCOCO1 Genecalcium binding and coiled-coil domain 1 Enables RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; beta-catenin binding activity; and nuclear receptor coactivator activity. Involved in positive regulation of DNA-templated transcription and positive regulation of gene expression. Located in cytosol and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
CALCOCO2 Genecalcium binding and coiled-coil domain 2 This gene encodes a coiled-coil domain-containing protein. The encoded protein functions as a receptor for ubiquitin-coated bacteria and plays an important role in innate immunity by mediating macroautophagy. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2012] |
ANKRD20A8P Geneankyrin repeat domain 20 family, member A8, pseudogene |
CLEC4A GeneC-type lectin domain family 4, member A This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signalling, glycoprotein turnover, and roles in inflammation and immune response. The encoded type 2 transmembrane protein may play a role in inflammatory and immune response. Multiple transcript variants encoding distinct isoforms have been identified for this gene. This gene is closely linked to other CTL/CTLD superfamily members on chromosome 12p13 in the natural killer gene complex region. [provided by RefSeq, Jul 2008] |
CHIC2 Genecysteine-rich hydrophobic domain 2 This gene encodes a member of the CHIC family of proteins. The encoded protein contains a cysteine-rich hydrophobic (CHIC) motif, and is localized to vesicular structures and the plasma membrane. This gene is associated with some cases of acute myeloid leukemia. [provided by RefSeq, Jul 2008] |
CHIC1 Genecysteine-rich hydrophobic domain 1 This gene encodes a cysteine-rich hydrophobic (CHIC) domain-containing protein, and is one of the few protein-coding genes found near the X-inactivation center. Studies in mouse indicate that the mouse ortholog of this gene is subject to X-inactivation in mouse. Experiments with other CHIC domain-containing family members show that the cysteine residues are palmitoylated post-translationally, resulting in membrane association. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2017] |
UBXN10 GeneUBX domain protein 10 Predicted to enable ubiquitin binding activity. Involved in cilium assembly. Located in cilium and intraciliary transport particle B. [provided by Alliance of Genome Resources, Mar 2025] |
UBXN11 GeneUBX domain protein 11 This gene encodes a protein with a divergent C-terminal UBX domain. The homologous protein in the rat interacts with members of the Rnd subfamily of Rho GTPases at the cell periphery through its C-terminal region. It also interacts with several heterotrimeric G proteins through their G-alpha subunits and promotes Rho GTPase activation. It is proposed to serve a bidirectional role in the promotion and inhibition of Rho activity through upstream signaling pathways. The 3' coding sequence of this gene contains a polymoprhic region of 24 nt tandem repeats. Several transcripts containing between 1.5 and five repeat units have been reported. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
POTEM GenePOTE ankyrin domain family, member M Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
HIGD2A GeneHIG1 hypoxia inducible domain family, member 2A The protein encoded by this gene is a subunit of the cytochrome c oxidase complex (complex IV), which is the terminal enzyme in the mitochondrial respiratory chain. The encoded protein is an inner mitochondrial membrane protein and is a functional ortholog of the yeast respiratory supercomplex factor 1 (Rcf1). In mouse, the orthologous protein enhances cell survival under conditions of hypoxia. [provided by RefSeq, Sep 2016] |
HIGD2B GeneHIG1 hypoxia inducible domain family, member 2B Predicted to be involved in mitochondrial respirasome assembly. Predicted to be located in membrane. Predicted to be active in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100420024 Geneankyrin repeat domain 33B pseudogene |
B9D2 GeneB9 protein domain 2 This gene encodes a B9 domain protein, which are exclusively found in ciliated organisms. The gene is upregulated during mucociliary differentiation, and the encoded protein localizes to basal bodies and cilia. Disrupting expression of this gene results in ciliogenesis defects. [provided by RefSeq, Oct 2009] |
LOC653071 Geneankyrin repeat domain 57 pseudogene |
LOC644669 Geneankyrin repeat domain 30B pseudogene |
LOC101060321 GeneTBC1 domain family member-like Predicted to enable GTPase activator activity. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
JARID2 Genejumonji, AT rich interactive domain 2 This gene encodes a Jumonji- and AT-rich interaction domain (ARID)-domain-containing protein. The encoded protein is a DNA-binding protein that functions as a transcriptional repressor. This protein interacts with the Polycomb repressive complex 2 (PRC2) which plays an essential role in regulating gene expression during embryonic development. This protein facilitates the recruitment of the PRC2 complex to target genes. Alternate splicing results in multiple transcript variants. Mutations in this gene are associated with chronic myeloid malignancies. [provided by RefSeq, May 2012] |
POGK Genepogo transposable element with KRAB domain The exact function of the protein encoded by this gene is not known. However, this gene product contains a KRAB domain (which is involved in protein-protein interactions) at the N-terminus, and a transposase domain at the C-terminus, suggesting that it may belong to the family of DNA-mediated transposons in human. [provided by RefSeq, Jul 2008] |
POGZ Genepogo transposable element with ZNF domain The protein encoded by this gene appears to be a zinc finger protein containing a transposase domain at the C-terminus. This protein was found to interact with the transcription factor SP1 in a yeast two-hybrid system. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Aug 2010] |
WDR92 GeneWD repeat domain 92 This gene encodes a protein with two WD40 repeat domains thought to be involved in an apoptosis via activation of caspase-3. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2012] |
WDR91 GeneWD repeat domain 91 Enables phosphatidylinositol 3-kinase inhibitor activity. Involved in early endosome to late endosome transport and regulation of protein catabolic process. Located in cytosol; early endosome membrane; and late endosome membrane. [provided by Alliance of Genome Resources, Mar 2025] |
TMCC1P1 Genetransmembrane and coiled-coil domain family 1 pseudogene 1 |
HMGN1P8 Genehigh mobility group nucleosome binding domain 1 pseudogene 8 |
HMGN1P3 Genehigh mobility group nucleosome binding domain 1 pseudogene 3 |
CLEC9A GeneC-type lectin domain family 9, member A CLEC9A is a group V C-type lectin-like receptor (CTLR) that functions as an activation receptor and is expressed on myeloid lineage cells (Huysamen et al., 2008 [PubMed 18408006]).[supplied by OMIM, Aug 2008] |
LOC286059 Genetumor necrosis factor receptor superfamily, member 10d, decoy with truncated death domain pseudogene |
SCUBE2 Genesignal peptide, CUB domain, EGF-like 2 Predicted to enable calcium ion binding activity; hedgehog family protein binding activity; and lipid binding activity. Predicted to be involved in signal transduction. Predicted to act upstream of or within several processes, including chondrocyte differentiation involved in endochondral bone morphogenesis; positive regulation of chondrocyte proliferation; and positive regulation of osteoblast differentiation. Predicted to be located in extracellular region. Predicted to be active in cell surface and extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
SCUBE3 Genesignal peptide, CUB domain, EGF-like 3 This gene encodes a member of the signal peptide, complement subcomponents C1r/C1s, Uegf, bone morphogenetic protein-1 and epidermal growth factor-like domain containing protein family. Overexpression of this gene in human embryonic kidney cells results in secretion of a glycosylated form of the protein that forms oligomers and tethers to the cell surface. This gene is upregulated in lung cancer tumor tissue compared to healthy tissue and is associated with loss of the epithelial marker E-cadherin and with increased expression of vimentin, a mesenchymal marker. In addition, the protein encoded by this gene is a transforming growth factor beta receptor ligand, and when secreted by cancer cells, it can be cleaved in vitro to release the N-terminal epidermal growth factor-like repeat domain and the C-terminal complement subcomponents C1r/C1s domain. Both the full length protein and C-terminal fragment can bind to the transforming growth factor beta type II receptor to promote the epithelial-mesenchymal transition and tumor angiogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014] |
SCUBE1 Genesignal peptide, CUB domain, EGF-like 1 This gene encodes a cell surface glycoprotein that is a member of the SCUBE (signal peptide, CUB domain, EGF (epidermal growth factor)-like protein) family. Family members have an amino-terminal signal peptide, nine copies of EGF-like repeats and a CUB domain at the carboxyl terminus. This protein is expressed in platelets and endothelial cells and may play an important role in vascular biology. [provided by RefSeq, Oct 2011] |
NRADDP Geneneurotrophin receptor associated death domain, pseudogene The neurotrophin receptor alike death domain proteins belong to the death domain superfamily and are involved in mediating apoptosis. This gene has been inactivated by mutation and is nonfunctional in humans. [provided by RefSeq, Oct 2008] |
ANKRD52 Geneankyrin repeat domain 52 |
ANKRD53 Geneankyrin repeat domain 53 Involved in mitotic metaphase chromosome alignment; regulation of microtubule cytoskeleton organization; and regulation of mitotic cytokinesis. Located in spindle pole. [provided by Alliance of Genome Resources, Mar 2025] |
ANKRD50 Geneankyrin repeat domain 50 Involved in endocytic recycling. Predicted to be located in endosome. [provided by Alliance of Genome Resources, Mar 2025] |
ANKRD54 Geneankyrin repeat domain 54 Predicted to enable protein kinase regulator activity. Predicted to be involved in positive regulation of erythrocyte differentiation and regulation of intracellular signal transduction. Predicted to act upstream of or within nucleocytoplasmic transport and regulation of protein kinase activity. Predicted to be located in midbody. Predicted to be active in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ANKRD55 Geneankyrin repeat domain 55 |
PIDD1 Genep53-induced death domain protein 1 The protein encoded by this gene contains a leucine-rich repeat and a death domain. This protein has been shown to interact with other death domain proteins, such as Fas (TNFRSF6)-associated via death domain (FADD) and MAP-kinase activating death domain-containing protein (MADD), and thus may function as an adaptor protein in cell death-related signaling processes. The expression of the mouse counterpart of this gene has been found to be positively regulated by the tumor suppressor p53 and to induce cell apoptosis in response to DNA damage, which suggests a role for this gene as an effector of p53-dependent apoptosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010] |
WDR82P2 GeneWD repeat domain 82 pseudogene 2 |
HMGN1P16 Genehigh mobility group nucleosome binding domain 1 pseudogene 16 |
HMGN1P17 Genehigh mobility group nucleosome binding domain 1 pseudogene 17 |
HMGN1P13 Genehigh mobility group nucleosome binding domain 1 pseudogene 13 |
HMGN1P10 Genehigh mobility group nucleosome binding domain 1 pseudogene 10 |
HMGN1P11 Genehigh mobility group nucleosome binding domain 1 pseudogene 11 |
TEAD3 GeneTEA domain family member 3 This gene product is a member of the transcriptional enhancer factor (TEF) family of transcription factors, which contain the TEA/ATTS DNA-binding domain. It is predominantly expressed in the placenta and is involved in the transactivation of the chorionic somatomammotropin-B gene enhancer. Translation of this protein is initiated at a non-AUG (AUA) start codon. [provided by RefSeq, Jul 2008] |
TEAD2 GeneTEA domain family member 2 Enables several functions, including DNA-binding transcription factor activity; disordered domain specific binding activity; and transcription coactivator binding activity. Involved in hippo signaling; positive regulation of DNA-templated transcription; and protein-containing complex assembly. Located in cytosol and nucleoplasm. Part of TEAD-YAP complex. [provided by Alliance of Genome Resources, Mar 2025] |
TEAD1 GeneTEA domain family member 1 (SV40 transcriptional enhancer factor) This gene encodes a ubiquitous transcriptional enhancer factor that is a member of the TEA/ATTS domain family. This protein directs the transactivation of a wide variety of genes and, in placental cells, also acts as a transcriptional repressor. Mutations in this gene cause Sveinsson's chorioretinal atrophy. Additional transcript variants have been described but their full-length natures have not been experimentally verified. [provided by RefSeq, May 2010] |
TEAD4 GeneTEA domain family member 4 This gene product is a member of the transcriptional enhancer factor (TEF) family of transcription factors, which contain the TEA/ATTS DNA-binding domain. It is preferentially expressed in the skeletal muscle, and binds to the M-CAT regulatory element found in promoters of muscle-specific genes to direct their gene expression. Alternatively spliced transcripts encoding distinct isoforms, some of which are translated through the use of a non-AUG (UUG) initiation codon, have been described for this gene. [provided by RefSeq, Jul 2008] |
LOC727874 GeneWW domain binding protein 11 pseudogene |
TTC21B Genetetratricopeptide repeat domain 21B This gene encodes a member of TTC21 family, containing several tetratricopeptide repeat (TPR) domains. This protein is localized to the cilium axoneme, and may play a role in retrograde intraflagellar transport in cilia. Mutations in this gene are associated with various ciliopathies, nephronophthisis 12, and asphyxiating thoracic dystrophy 4. [provided by RefSeq, Oct 2011] |
LOC646548 GeneADAM metallopeptidase domain 20 pseudogene |
TBC1D3P5 GeneTBC1 domain family, member 3 pseudogene 5 |
TTC14 Genetetratricopeptide repeat domain 14 Predicted to enable nucleic acid binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
TTC17 Genetetratricopeptide repeat domain 17 Involved in actin filament polymerization and cilium organization. Located in actin cytoskeleton; cytosol; and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
TTC16 Genetetratricopeptide repeat domain 16 |
TTC13 Genetetratricopeptide repeat domain 13 |
TTC12 Genetetratricopeptide repeat domain 12 Involved in axonemal dynein complex assembly and sperm axoneme assembly. Located in centrosome and cytoplasm. Implicated in acute lymphoblastic leukemia; alcohol dependence; drug dependence (multiple); nicotine dependence; and primary ciliary dyskinesia 45. [provided by Alliance of Genome Resources, Mar 2025] |
TTC19 Genetetratricopeptide repeat domain 19 This gene encodes a protein with a tetratricopeptide repeat (TPR) domain containing several TPRs of about 34 aa each. These repeats are found in a variety of organisms including bacteria, fungi and plants, and are involved in a variety of functions including protein-protein interactions. This protein is embedded in the inner mitochondrial membrane and is involved in the formation of the mitochondrial respiratory chain III. It has also been suggested that this protein plays a role in cytokinesis. Mutations in this gene cause mitochondrial complex III deficiency. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2012] |
RCN1P2 Genereticulocalbin 1, EF-hand calcium binding domain pseudogene 2 |
WBP2 GeneWW domain binding protein 2 The globular WW domain is composed of 38 to 40 semiconserved amino acids shared by proteins of diverse functions including structural, regulatory, and signaling proteins. The domain is involved in mediating protein-protein interactions through the binding of polyproline ligands. This gene encodes a WW domain binding protein that is a transcriptional coactivator of estrogen receptor alpha and progesterone receptor. Defects in this gene have been associated with hearing impairment. [provided by RefSeq, Jan 2017] |
WBP1 GeneWW domain binding protein 1 The globular WW domain, named for the conserved tryptophan residues in the protein motif present in various structural and regulatory proteins, is known to play a role in the mediation of protein-protein interactions. This gene encodes a ligand of the WW domain of the Yes kinase-associated protein. Readthrough transcription of the neighboring upstream gene, which encodes INO80 complex subunit B, into this gene generates a non-coding transcript. [provided by RefSeq, Feb 2011] |
WBP5 GeneWW domain binding protein 5 The globular WW domain is composed of 38 to 40 semiconserved amino acids shared by proteins of diverse functions including structural, regulatory, and signaling proteins. The domain is involved in mediating protein-protein interactions through the binding of polyproline ligands. This gene encodes a WW domain binding protein. This gene also encodes a domain with similarity to the transcription elongation factor A, SII-related family. Alternative splicing results in multiple transcript variants encoding a single isoform. [provided by RefSeq, Jul 2008] |
WBP4 GeneWW domain binding protein 4 This gene encodes WW domain-containing binding protein 4. The WW domain represents a small and compact globular structure that interacts with proline-rich ligands. This encoded protein is a general spliceosomal protein that may play a role in cross-intron bridging of U1 and U2 snRNPs in the spliceosomal complex A. [provided by RefSeq, Jul 2008] |
ANKRD20A2 Geneankyrin repeat domain 20 family, member A2 |
ANKRD20A3 Geneankyrin repeat domain 20 family, member A3 |
ANKRD20A1 Geneankyrin repeat domain 20 family, member A1 Located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ANKRD20A4 Geneankyrin repeat domain 20 family, member A4 |
PHLPP1 GenePH domain and leucine rich repeat protein phosphatase 1 This gene encodes a member of the serine/threonine phosphatase family. The encoded protein promotes apoptosis by dephosphorylating and inactivating the serine/threonine kinase Akt, and functions as a tumor suppressor in multiple types of cancer. Increased expression of this gene may also play a role in obesity and type 2 diabetes by interfering with Akt-mediated insulin signaling. [provided by RefSeq, Dec 2011] |
SHARPIN GeneSHANK-associated RH domain interactor Enables polyubiquitin modification-dependent protein binding activity. Involved in defense response to bacterium; protein linear polyubiquitination; and regulation of signal transduction. Located in cytosol. Part of LUBAC complex. [provided by Alliance of Genome Resources, Mar 2025] |
FADD GeneFas (TNFRSF6)-associated via death domain The protein encoded by this gene is an adaptor molecule that interacts with various cell surface receptors and mediates cell apoptotic signals. Through its C-terminal death domain, this protein can be recruited by TNFRSF6/Fas-receptor, tumor necrosis factor receptor, TNFRSF25, and TNFSF10/TRAIL-receptor, and thus it participates in the death signaling initiated by these receptors. Interaction of this protein with the receptors unmasks the N-terminal effector domain of this protein, which allows it to recruit caspase-8, and thereby activate the cysteine protease cascade. Knockout studies in mice also suggest the importance of this protein in early T cell development. [provided by RefSeq, Jul 2008] |
SH3GLB1 GeneSH3-domain GRB2-like endophilin B1 This gene encodes a SRC homology 3 domain-containing protein. The encoded protein interacts with the proapoptotic member of the Bcl-2 family, Bcl-2-associated X protein (Bax) and may be involved in regulating apoptotic signaling pathways. This protein may also be involved in maintaining mitochondrial morphology. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2011] |
SH3GLB2 GeneSH3-domain GRB2-like endophilin B2 Enables identical protein binding activity. Predicted to be involved in membrane organization and postsynaptic neurotransmitter receptor internalization. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC646938 GeneTBC1 domain family, member 2B pseudogene |
EFHD2 GeneEF-hand domain family, member D2 Enables cadherin binding activity. Predicted to be located in membrane raft. [provided by Alliance of Genome Resources, Mar 2025] |
EFHD1 GeneEF-hand domain family, member D1 This gene encodes a member of the EF-hand super family of calcium binding proteins, which are involved in a variety of cellular processes including mitosis, synaptic transmission, and cytoskeletal rearrangement. The protein encoded by this gene is composed of an N-terminal disordered region, proline-rich elements, two EF-hands, and a C-terminal coiled-coil domain. This protein has been shown to associate with the mitochondrial inner membrane, and in HeLa cells, acts as a novel mitochondrial calcium ion sensor for mitochondrial flash activation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2016] |
CLEC18C GeneC-type lectin domain family 18, member C Enables polysaccharide binding activity. Predicted to be located in Golgi apparatus; endoplasmic reticulum; and endosome. Predicted to be active in extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
GPKOW GeneG patch domain and KOW motifs This gene encodes a putative RNA-binding protein containing G-patch and KOW (Kyprides, Ouzounis, Woese) domains. The encoded protein interacts directly with protein kinase A and protein kinase X and is also found associated with the spliceosome. [provided by RefSeq, Aug 2013] |
LOC728853 GeneWD repeat domain 87 pseudogene |
HMGN1P33 Genehigh mobility group nucleosome binding domain 1 pseudogene 33 |
HMGN1P34 Genehigh mobility group nucleosome binding domain 1 pseudogene 34 |
GARNL3 GeneGTPase activating Rap/RanGAP domain-like 3 Predicted to enable GTPase activator activity. Predicted to be involved in regulation of small GTPase mediated signal transduction. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
YTHDF1P1 GeneYTH domain family, member 1 pseudogene 1 |
MCCD1 Genemitochondrial coiled-coil domain 1 Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
LOC390251 GeneSH3-domain GRB2-like 1 pseudogene |
FCHO2 GeneFCH domain only 2 Enables identical protein binding activity. Involved in clathrin coat assembly and clathrin-dependent endocytosis. Located in clathrin-coated pit and clathrin-coated vesicle. [provided by Alliance of Genome Resources, Mar 2025] |
FCHO1 GeneFCH domain only 1 Enables AP-2 adaptor complex binding activity. Involved in several processes, including T cell receptor signaling pathway; clathrin coat assembly; and clathrin-dependent endocytosis. Located in cytosol; nucleoplasm; and plasma membrane. Is active in clathrin-coated pit. Implicated in primary immunodeficiency disease. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419096 GeneWD repeat domain 12 pseudogene |
TTC9C Genetetratricopeptide repeat domain 9C |
TTC9B Genetetratricopeptide repeat domain 9B |
LOC642204 Geneankyrin repeat domain 20 family, member A1 pseudogene |
WDR7 GeneWD repeat domain 7 This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD) that may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. The encoded protein forms the beta subunit of rabconnectin-3 and binds directly with Rab3A GDP/GTP exchange protein and indirectly with Rab3A GDP/GTP activating protein; these proteins are regulators of Rab3 small G protein family members involved in control of the calcium-dependant exocytosis of neurotransmitters. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008] |
WDR6 GeneWD repeat domain 6 This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. The encoded protein interacts with serine/threonine kinase 11, and is implicated in cell growth arrest. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Feb 2016] |
WDR5 GeneWD repeat domain 5 This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This protein contains 7 WD repeats. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008] |
WDR4 GeneWD repeat domain 4 This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This gene is excluded as a candidate for a form of nonsyndromic deafness (DFNB10), but is still a candidate for other disorders mapped to 21q22.3 as well as for the development of Down syndrome phenotypes. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, May 2012] |
WDR3 GeneWD repeat domain 3 This gene encodes a nuclear protein containing 10 WD repeats. WD repeats are approximately 30- to 40-amino acid domains containing several conserved residues, which usually include a trp-asp at the C-terminal end. Proteins belonging to the WD repeat family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. [provided by RefSeq, Jul 2008] |
WDR1 GeneWD repeat domain 1 This gene encodes a protein containing 9 WD repeats. WD repeats are approximately 30- to 40-amino acid domains containing several conserved residues, mostly including a trp-asp at the C-terminal end. WD domains are involved in protein-protein interactions. The encoded protein may help induce the disassembly of actin filaments. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
CLEC4M GeneC-type lectin domain family 4, member M This gene encodes a C-type lectin that functions in cell adhesion and pathogen recognition. This receptor recognizes a wide range of evolutionarily divergent pathogens with a large impact on public health, including tuberculosis mycobacteria, and viruses including Ebola, hepatitis C, HIV-1, influenza A, West Nile virus and the SARS-CoV acute respiratory syndrome coronavirus. The protein is organized into four distinct domains: a C-terminal carbohydrate recognition domain, a flexible tandem-repeat neck domain of variable length, a transmembrane region and an N-terminal cytoplasmic domain involved in internalization. This gene is closely related in terms of both sequence and function to a neighboring gene, CD209 (Gene ID: 30835), also known as DC-SIGN. The two genes differ in viral recognition and expression patterns, with this gene showing high expression in endothelial cells of the liver, lymph node and placenta. Polymorphisms in the tandem repeat neck domain are associated with resistance to SARS infection. [provided by RefSeq, May 2020] |
CLEC4G GeneC-type lectin domain family 4, member G This gene encodes a glycan-binding receptor and member of the C-type lectin family which plays a role in the immune response. C-type lectin receptors are pattern recognition receptors located on immune cells that play a role in the recognition and uptake of both self and non-self glycoproteins as well as mediating cell adhesion, glycoprotein clearance, and cell signaling functions. This gene's protein binds complex-type N-glycans of the viral envelope proteins of Ebola virus, West Nile filovirus, and SARS coronavirus, but not HIV or hepatitis C virus. In mouse, this protein has been shown to recognize activated T-cells and to negatively regulate T-cell receptor-mediated signalling. It also acts as a novel, liver-specific regulator of NK cell-mediated immunity in mouse. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2020] |
CLEC4F GeneC-type lectin domain family 4, member F Predicted to enable galactose binding activity; glycolipid binding activity; and pattern recognition receptor activity. Predicted to be involved in immune response. Predicted to act upstream of or within NK T cell activation. Predicted to be located in plasma membrane. Predicted to be active in external side of plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
CLEC4E GeneC-type lectin domain family 4, member E This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signalling, glycoprotein turnover, and roles in inflammation and immune response. The encoded type II transmembrane protein is a downstream target of CCAAT/enhancer binding protein (C/EBP), beta (CEBPB) and may play a role in inflammation. Alternative splice variants have been described but their full-length sequence has not been determined. This gene is closely linked to other CTL/CTLD superfamily members on chromosome 12p13 in the natural killer gene complex region. [provided by RefSeq, Jul 2008] |
CLEC4D GeneC-type lectin domain family 4, member D This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signalling, glycoprotein turnover, and roles in inflammation and immune response. This gene is closely linked to other CTL/CTLD superfamily members on chromosome 12p13 in the natural killer gene complex region. [provided by RefSeq, Jul 2008] |
CLEC4C GeneC-type lectin domain family 4, member C This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signalling, glycoprotein turnover, and roles in inflammation and immune response. The encoded type 2 transmembrane protein may play a role in dendritic cell function. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008] |
B9D1 GeneB9 protein domain 1 This gene encodes a B9 domain-containing protein, one of several that are involved in ciliogenesis. Alterations in expression of this gene have been found in a family with Meckel syndrome. Meckel syndrome has been associated with at least six different genes. This gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Mar 2016] |
LOC102724525 Genecarboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 2 pseudogene |
ITSN1 Geneintersectin 1 (SH3 domain protein) The protein encoded by this gene is a cytoplasmic membrane-associated protein that indirectly coordinates endocytic membrane traffic with the actin assembly machinery. In addition, the encoded protein may regulate the formation of clathrin-coated vesicles and could be involved in synaptic vesicle recycling. This protein has been shown to interact with dynamin, CDC42, SNAP23, SNAP25, SPIN90, EPS15, EPN1, EPN2, and STN2. Multiple transcript variants encoding different isoforms have been found for this gene, but the full-length nature of only two of them have been characterized so far. [provided by RefSeq, Jul 2008] |
PRAF2 GenePRA1 domain family, member 2 Predicted to be involved in L-glutamate transmembrane transport. Predicted to be located in endosome membrane. Predicted to be active in several cellular components, including GABA-ergic synapse; glutamatergic synapse; and postsynapse. [provided by Alliance of Genome Resources, Mar 2025] |
LOC401127 GeneWD repeat domain 5 pseudogene |
TMED2 Genetransmembrane emp24 domain trafficking protein 2 Predicted to enable frizzled binding activity and smoothened binding activity. Involved in several processes, including Golgi organization; negative regulation of GTPase activity; and protein localization to plasma membrane. Located in Golgi apparatus; endoplasmic reticulum; and endoplasmic reticulum-Golgi intermediate compartment. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100420289 GeneTBC1 domain family, member 3H pseudogene |
ANKRD33B Geneankyrin repeat domain 33B |
SIGIRR Genesingle immunoglobulin and toll-interleukin 1 receptor (TIR) domain Involved in negative regulation of Toll signaling pathway. Located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SH3BGRL GeneSH3 domain binding glutamate-rich protein like Enables protein-RNA adaptor activity and ubiquitin-like ligase-substrate adaptor activity. Involved in positive regulation of cytoplasmic translational initiation and proteasome-mediated ubiquitin-dependent protein catabolic process. Located in cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
TRADD GeneTNFRSF1A-associated via death domain The protein encoded by this gene is a death domain containing adaptor molecule that interacts with TNFRSF1A/TNFR1 and mediates programmed cell death signaling and NF-kappaB activation. This protein binds adaptor protein TRAF2, reduces the recruitment of inhibitor-of-apoptosis proteins (IAPs) by TRAF2, and thus suppresses TRAF2 mediated apoptosis. This protein can also interact with receptor TNFRSF6/FAS and adaptor protein FADD/MORT1, and is involved in the Fas-induced cell death pathway. [provided by RefSeq, Jul 2008] |
LOC650226 Geneankyrin repeat domain 26 pseudogene |
ADAM6 GeneADAM metallopeptidase domain 6 (pseudogene) Predicted to be located in external side of plasma membrane and sperm head plasma membrane. Predicted to be part of protein-containing complex. [provided by Alliance of Genome Resources, Mar 2025] |
ADAM7 GeneADAM metallopeptidase domain 7 This gene encodes a member of the ADAMs family of zinc proteases. These transmembrane proteins play roles in multiple processes including cell signaling, adhesion and migration. The encoded protein lacks protease activity and may play roles in protein-protein interactions and cell adhesion processes including sperm-egg fusion. Mutations in this gene may be involved in the progression of melanoma. [provided by RefSeq, Oct 2011] |
ADAM5 GeneADAM metallopeptidase domain 5 (pseudogene) Predicted to be active in cell surface. [provided by Alliance of Genome Resources, Mar 2025] |
ADAM2 GeneADAM metallopeptidase domain 2 This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The encoded protein is a subunit of an integral sperm membrane glycoprotein called fertilin, which plays an important role in sperm-egg interactions. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2013] |
ADAM8 GeneADAM metallopeptidase domain 8 This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The protein encoded by this gene may be involved in cell adhesion during neurodegeneration, and it is thought to be a target for allergic respiratory diseases, including asthma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2009] |
ADAM9 GeneADAM metallopeptidase domain 9 This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The protein encoded by this gene interacts with SH3 domain-containing proteins, binds mitotic arrest deficient 2 beta protein, and is also involved in TPA-induced ectodomain shedding of membrane-anchored heparin-binding EGF-like growth factor. Several alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Jul 2010] |
WFDC9 GeneWAP four-disulfide core domain 9 The WAP-type four-disulfide core (WFDC) domain, or WAP signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor in many members of the WFDC domain family. This gene encodes a protein which contains a WFDC domain, and is thus a member of the WFDC domain family. This gene and several other gene family members are clustered at 20q13.12. [provided by RefSeq, Jul 2008] |
WFDC8 GeneWAP four-disulfide core domain 8 This gene encodes a member of the WAP-type four-disulfide core (WFDC) domain family. The WFDC domain, or WAP signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor. The encoded protein contains a Kunitz-inhibitor domain, in addition to three WFDC domains. Most WFDC genes are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene belongs to the telomeric cluster. Two alternatively spliced transcript variants have been found for this gene, and they encode the same protein. [provided by RefSeq, Jul 2008] |
WFDC1 GeneWAP four-disulfide core domain 1 This gene encodes a member of the WAP-type four disulfide core domain family. The WAP-type four-disulfide core domain contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor in many family members. This gene is mapped to chromosome 16q24, an area of frequent loss of heterozygosity in cancers, including prostate, breast and hepatocellular cancers and Wilms' tumor. This gene is downregulated in many cancer types and may be involved in the inhibition of cell proliferation. The encoded protein may also play a role in the susceptibility of certain CD4 memory T cells to human immunodeficiency virus infection. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013] |
WFDC3 GeneWAP four-disulfide core domain 3 This gene encodes a member of the WAP-type four-disulfide core (WFDC) domain family. The WFDC domain, or WAP signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor. The encoded protein contains four WFDC domains. Most WFDC genes are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene belongs to the telomeric cluster. Alternatively spliced transcript variants have been observed but their full-length nature has not been determined. [provided by RefSeq, Jul 2008] |
WFDC5 GeneWAP four-disulfide core domain 5 This gene encodes a member of the WAP-type four-disulfide core (WFDC) domain family. Most WFDC proteins contain only one WFDC domain, and this encoded protein contains two WFDC domains. The WFDC domain, or WAP signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor. Most WFDC gene members are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene belongs to the centromeric cluster. [provided by RefSeq, Jul 2008] |
WFDC6 GeneWAP four-disulfide core domain 6 This gene encodes a member of the WAP-type four-disulfide core (WFDC) domain family. The WFDC domain, or WAP signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor. Most WFDC gene members are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene belongs to the telomeric cluster. Read-through transcription exists between this gene and the upstream SPINLW1 (serine peptidase inhibitor-like, with Kunitz and WAP domains 1) gene. [provided by RefSeq, Nov 2010] |
TBC1D10C GeneTBC1 domain family, member 10C The protein encoded by this gene has an N-terminal Rab-GTPase domain and a binding site at the C-terminus for calcineurin, and is an inhibitor of both the Ras signaling pathway and calcineurin, a phosphatase regulated by calcium and calmodulin. Genes encoding similar proteins are located on chromosomes 16 and 22. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2013] |
TBC1D10A GeneTBC1 domain family, member 10A Enables PDZ domain binding activity. Involved in activation of cysteine-type endopeptidase activity and retrograde transport, endosome to Golgi. Located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
KAZALD1 GeneKazal-type serine peptidase inhibitor domain 1 This gene encodes a secreted member of the insulin growth factor-binding protein (IGFBP) superfamily. The protein contains an insulin growth factor-binding domain in its N-terminal region, a Kazal-type serine protease inhibitor and follistatin-like domain in its central region, and an immunoglobulin-like domain in its C-terminal region. Studies of the mouse ortholog suggest that this protein may function in bone development and bone regeneration. This gene is hypomethylated and over-expressed in high-grade glioma compared to low-grade glioma, and thus the hypomethylated gene may be associated with cell proliferation and the shorter survival of patients with high-grade glioma. It is also one of numerous genes found to be deleted in a novel 5.54 Mb interstitial deletion, which is associated with multiple congenital anomalies. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016] |
WDR41 GeneWD repeat domain 41 Enables GTPase activator activity. Contributes to guanyl-nucleotide exchange factor activity. Involved in regulation of autophagy. Located in cytoplasm. Part of guanyl-nucleotide exchange factor complex. [provided by Alliance of Genome Resources, Mar 2025] |
WDR43 GeneWD repeat domain 43 Enables RNA binding activity. Involved in positive regulation of rRNA processing; positive regulation of transcription by RNA polymerase I; and ribosomal small subunit biogenesis. Located in fibrillar center. Part of small-subunit processome. [provided by Alliance of Genome Resources, Mar 2025] |
WDR44 GeneWD repeat domain 44 This gene encodes a protein that interacts with the small GTPase rab11. A similar protein in rat binds the GTP-containing active form of rab11. This protein may play a role in endosome recycling. Alternate splicing results in multiple transcript variants.[provided by RefSeq, May 2010] |
WDR45 GeneWD repeat domain 45 This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This gene has a pseudogene at chromosome 4q31.3. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene, but the biological validity and full-length nature of some variants have not been determined. [provided by RefSeq, Jul 2008] |
WDR46 GeneWD repeat domain 46 Enables RNA binding activity. Involved in ribosomal small subunit biogenesis. Located in nucleolus. Part of small-subunit processome. [provided by Alliance of Genome Resources, Mar 2025] |
WDR47 GeneWD repeat domain 47 Predicted to act upstream of or within several processes, including detection of hot stimulus involved in thermoception; neuronal stem cell population maintenance; and telencephalon development. Predicted to be located in several cellular components, including growth cone; microtubule; and neuronal cell body. [provided by Alliance of Genome Resources, Mar 2025] |
WDR48 GeneWD repeat domain 48 The protein encoded by this gene has been shown to interact with ubiquitin specific peptidase 1 (USP1), activating the deubiquitinating activity of USP1 and allowing it to remove the ubiquitin moiety from monoubiquitinated FANCD2. FANCD2 is ubiquitinated in response to DNA damage. [provided by RefSeq, Sep 2016] |
WDR49 GeneWD repeat domain 49 This gene encodes a member of the WD repeat protein family with nine WD repeats. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017] |
WFDC2 GeneWAP four-disulfide core domain 2 This gene encodes a protein that is a member of the WFDC domain family. The WFDC domain, or WAP Signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor in many family members. This gene is expressed in pulmonary epithelial cells, and was also found to be expressed in some ovarian cancers. The encoded protein is a small secretory protein, which may be involved in sperm maturation. [provided by RefSeq, Jul 2008] |
WDR45BP1 GeneWD repeat domain 45B pseudogene 1 |
NOX5 GeneNADPH oxidase, EF-hand calcium binding domain 5 Enables proton channel activity and superoxide-generating NAD(P)H oxidase activity. Involved in several processes, including endothelial cell proliferation; proton transmembrane transport; and superoxide anion generation. Located in endoplasmic reticulum and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
TBC1D19 GeneTBC1 domain family, member 19 Predicted to enable GTPase activator activity. [provided by Alliance of Genome Resources, Mar 2025] |
TBC1D12 GeneTBC1 domain family, member 12 Predicted to enable GTPase activator activity. Predicted to be involved in regulation of autophagosome assembly. Predicted to be located in endosome. Predicted to be active in autophagosome and recycling endosome. [provided by Alliance of Genome Resources, Mar 2025] |
TBC1D13 GeneTBC1 domain family, member 13 Predicted to enable GTPase activator activity. Predicted to be involved in intracellular protein transport. Predicted to be located in cytosol and membrane. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
TBC1D16 GeneTBC1 domain family, member 16 Enables GTPase activator activity. Involved in regulation of receptor recycling. Located in cytosol and early endosome. [provided by Alliance of Genome Resources, Mar 2025] |
TBC1D17 GeneTBC1 domain family, member 17 Predicted to enable GTPase activator activity. Involved in retrograde transport, endosome to Golgi. Located in cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
TBC1D14 GeneTBC1 domain family, member 14 Enables protein kinase binding activity. Involved in negative regulation of autophagy; recycling endosome to Golgi transport; and regulation of autophagosome assembly. Located in several cellular components, including Golgi apparatus; autophagosome; and recycling endosome. [provided by Alliance of Genome Resources, Mar 2025] |
TBC1D15 GeneTBC1 domain family, member 15 This gene encodes a member of the Ras-like proteins in brain-GTPase activating protein superfamily that share a conserved Tre-2/Bub2/Cdc16 domain. The encoded protein interacts with Ras-like protein in brain 5A and may function as a regulator of intracellular trafficking. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Apr 2009] |
ANKRD63 Geneankyrin repeat domain 63 |
ANKRD61 Geneankyrin repeat domain 61 Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ANKRD60 Geneankyrin repeat domain 60 |
ANKRD66 Geneankyrin repeat domain 66 |
ANKRD65 Geneankyrin repeat domain 65 |
TBC1D10B GeneTBC1 domain family, member 10B Small G proteins of the RAB family (see MIM 179508) function in intracellular vesicle trafficking by switching from the GTP-bound state to the GDP-bound state with the assistance of guanine nucleotide exchange factors (GEFs; see MIM 609700) and GTPase-activating proteins (GAPs). TBC1D10B functions as a GAP for several proteins of the Rab family (Ishibashi et al., 2009 [PubMed 19077034]).[supplied by OMIM, Nov 2010] |
ADAM21P1 GeneADAM metallopeptidase domain 21 pseudogene 1 |
ANKRD20A18P Geneankyrin repeat domain 20 family, member A18, pseudogene |
EFCAB9 GeneEF-hand calcium binding domain 9 This gene encodes a protein with a C-terminal EF-hand calcium-binding domain similar to that found in penta-EF-hand (PEF) protein family members. The EF-hand is a helix-loop-helix structure with a canonical twelve-residue sequence that coordinates a calcium molecule with pentagonal bipyramidal symmetry. [provided by RefSeq, Jul 2017] |
EFCAB8 GeneEF-hand calcium binding domain 8 Predicted to enable calcium ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
EFCAB5 GeneEF-hand calcium binding domain 5 Predicted to enable calcium ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
EFCAB7 GeneEF-hand calcium binding domain 7 Predicted to enable calcium ion binding activity. Predicted to be involved in positive regulation of protein import into nucleus; positive regulation of protein localization to ciliary membrane; and positive regulation of transcription by RNA polymerase II. Predicted to be located in cytoplasmic side of plasma membrane. Predicted to be part of plasma membrane protein complex. Predicted to be active in ciliary membrane. [provided by Alliance of Genome Resources, Mar 2025] |
EFCAB6 GeneEF-hand calcium binding domain 6 This gene encodes a protein which directly binds the oncogene DJ-1 and androgen receptor to form a ternary complex in cells. This binding protein recruits histone-deacetylase complexes in order to repress transcription activity of androgen receptor. This protein may also play a role in spermatogenesis and fertilization. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011] |
EFCAB1 GeneEF-hand calcium binding domain 1 Predicted to enable calcium ion binding activity. Predicted to be involved in several processes, including cilium movement; outer dynein arm assembly; and regulation of flagellated sperm motility. Predicted to be located in cilium. Implicated in primary ciliary dyskinesia. [provided by Alliance of Genome Resources, Mar 2025] |
EFCAB3 GeneEF-hand calcium binding domain 3 Predicted to enable calcium ion binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
EFCAB2 GeneEF-hand calcium binding domain 2 The gene encodes a protein that contains two EF-hand calcium-binding domains although its function has yet to be determined. Alternatively spliced transcripts have been observed. [provided by RefSeq, Mar 2014] |
LOC101929749 Genecarboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 2 pseudogene |
AMIGO1 Geneadhesion molecule with Ig-like domain 1 Predicted to enable potassium channel regulator activity. Predicted to be involved in several processes, including heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules; nervous system development; and positive regulation of nervous system development. Predicted to be located in dendrite; neuronal cell body membrane; and voltage-gated potassium channel complex. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
AMIGO2 Geneadhesion molecule with Ig-like domain 2 Predicted to be involved in several processes, including heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules; homophilic cell adhesion via plasma membrane adhesion molecules; and positive regulation of synapse assembly. Predicted to be located in nucleus and plasma membrane. Predicted to be active in membrane. Biomarker of gastric adenocarcinoma. [provided by Alliance of Genome Resources, Mar 2025] |
ANKRD6 Geneankyrin repeat domain 6 Predicted to be involved in negative regulation of canonical Wnt signaling pathway and positive regulation of JNK cascade. Predicted to act upstream of or within positive regulation of Wnt signaling pathway, planar cell polarity pathway. Located in intracellular membrane-bounded organelle. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100421730 Genetransmembrane emp24 domain trafficking protein 2 pseudogene |
PHLDA1 Genepleckstrin homology-like domain, family A, member 1 This gene encodes an evolutionarily conserved proline-histidine rich nuclear protein. The encoded protein may play an important role in the anti-apoptotic effects of insulin-like growth factor-1. [provided by RefSeq, Jul 2008] |
PHLDA3 Genepleckstrin homology-like domain, family A, member 3 Enables phosphatidylinositol phosphate binding activity and phosphatidylinositol-3,4-bisphosphate binding activity. Involved in intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator; negative regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction; and positive regulation of apoptotic process. Located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
PHLDA2 Genepleckstrin homology-like domain, family A, member 2 This gene is located in a cluster of imprinted genes on chromosome 11p15.5, which is considered to be an important tumor suppressor gene region. Alterations in this region may be associated with the Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian, and breast cancer. This gene has been shown to be imprinted, with preferential expression from the maternal allele in placenta and liver. [provided by RefSeq, Oct 2010] |
HERC2P1 Genehect domain and RLD 2 pseudogene 1 |
HERC2P3 Genehect domain and RLD 2 pseudogene 3 Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in protein ubiquitination. [provided by Alliance of Genome Resources, Mar 2025] |
HERC2P2 Genehect domain and RLD 2 pseudogene 2 |
HERC2P5 Genehect domain and RLD 2 pseudogene 5 |
HERC2P4 Genehect domain and RLD 2 pseudogene 4 |
HERC2P7 Genehect domain and RLD 2 pseudogene 7 |
HERC2P6 Genehect domain and RLD 2 pseudogene 6 |
HERC2P9 Genehect domain and RLD 2 pseudogene 9 |
HERC2P8 Genehect domain and RLD 2 pseudogene 8 |
ANKRD30BL Geneankyrin repeat domain 30B-like |
RFX8 GeneRFX family member 8, lacking RFX DNA binding domain Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. [provided by Alliance of Genome Resources, Mar 2025] |
SOWAHA Genesosondowah ankyrin repeat domain family member A |
SOWAHC Genesosondowah ankyrin repeat domain family member C |
SOWAHD Genesosondowah ankyrin repeat domain family member D |
NSUN3 GeneNOP2/Sun domain family, member 3 Enables tRNA (cytidine-5-)-methyltransferase activity. Involved in regulation of mitochondrial translation and tRNA wobble base cytosine methylation. Located in mitochondrial matrix. Implicated in combined oxidative phosphorylation deficiency 48. [provided by Alliance of Genome Resources, Mar 2025] |
NSUN5 GeneNOP2/Sun domain family, member 5 This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2013] |
NSUN4 GeneNOP2/Sun domain family, member 4 Enables mRNA (cytidine-5-)-methyltransferase activity and rRNA (cytosine-C5-)-methyltransferase activity. Involved in mitochondrial RNA catabolic process; mitochondrial RNA modification; and rRNA methylation. Located in mitochondrial matrix. Part of mitochondrial large ribosomal subunit. [provided by Alliance of Genome Resources, Mar 2025] |
NSUN7 GeneNOP2/Sun domain family, member 7 Predicted to enable RNA binding activity and methyltransferase activity. Predicted to be involved in RNA methylation and RNA processing. Predicted to act upstream of or within flagellated sperm motility and sperm mitochondrion organization. [provided by Alliance of Genome Resources, Mar 2025] |
NSUN6 GeneNOP2/Sun domain family, member 6 Enables tRNA (cytidine-5-)-methyltransferase activity and tRNA binding activity. Involved in tRNA C5-cytosine methylation. Located in cytoplasm. Implicated in autosomal recessive intellectual developmental disorder 82. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100422604 Geneleukocyte immunoglobulin-like receptor, subfamily A (with TM domain), member 2 pseudogene |
ANKRD18EP Geneankyrin repeat domain 18E, pseudogene |
LOC100421385 Genetestin LIM domain protein pseudogene |
HIGD1AP2 GeneHIG1 hypoxia inducible domain family, member 1A pseudogene 2 |
HIGD1AP3 GeneHIG1 hypoxia inducible domain family, member 1A pseudogene 3 |
HIGD1AP1 GeneHIG1 hypoxia inducible domain family, member 1A pseudogene 1 |
HIGD1AP6 GeneHIG1 hypoxia inducible domain family, member 1A pseudogene 6 |
HIGD1AP7 GeneHIG1 hypoxia inducible domain family, member 1A pseudogene 7 |
HIGD1AP4 GeneHIG1 hypoxia inducible domain family, member 1A pseudogene 4 |
HIGD1AP5 GeneHIG1 hypoxia inducible domain family, member 1A pseudogene 5 |
HIGD1AP8 GeneHIG1 hypoxia inducible domain family, member 1A pseudogene 8 |
HIGD1AP9 GeneHIG1 hypoxia inducible domain family, member 1A pseudogene 9 |
KCNK9 Genepotassium channel, two pore domain subfamily K, member 9 This gene encodes a protein that contains multiple transmembrane regions and two pore-forming P domains and functions as a pH-dependent potassium channel. Amplification and overexpression of this gene have been observed in several types of human carcinomas. This gene is imprinted in the brain, with preferential expression from the maternal allele. A mutation in this gene was associated with Birk-Barel dysmorphism syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2017] |
KCNK4 Genepotassium channel, two pore domain subfamily K, member 4 This gene encodes a member of the TWIK-related arachidonic acid-stimulated two pore potassium channel subfamily. The encoded protein homodimerizes and functions as an outwardly rectifying channel. This channel is regulated by polyunsaturated fatty acids, temperature and mechanical deformation of the lipid membrane. This protein is expressed primarily in neural tissues and may be involved in regulating the noxious input threshold in dorsal root ganglia neurons. Alternate splicing results in multiple transcript variants. Naturally occurring read-through transcripts also exist between this gene and the downstream testis expressed 40 (TEX40) gene, as represented in GeneID: 106780802. [provided by RefSeq, Nov 2015] |
KCNK5 Genepotassium channel, two pore domain subfamily K, member 5 This gene encodes one of the members of the superfamily of potassium channel proteins containing two pore-forming P domains. The message for this gene is mainly expressed in the cortical distal tubules and collecting ducts of the kidney. The protein is highly sensitive to external pH and this, in combination with its expression pattern, suggests it may play an important role in renal potassium transport. [provided by RefSeq, Jul 2008] |
KCNK6 Genepotassium channel, two pore domain subfamily K, member 6 This gene encodes one of the members of the superfamily of potassium channel proteins containing two pore-forming P domains. This channel protein, considered an open rectifier, is widely expressed. It is stimulated by arachidonic acid, and inhibited by internal acidification and volatile anaesthetics. [provided by RefSeq, Jul 2008] |
KCNK7 Genepotassium channel, two pore domain subfamily K, member 7 This gene encodes a member of the superfamily of potassium channel proteins containing two pore-forming P domains. The product of this gene has not been shown to be a functional channel; however, it may require other non-pore-forming proteins for activity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
KCNK1 Genepotassium channel, two pore domain subfamily K, member 1 This gene encodes one of the members of the superfamily of potassium channel proteins containing two pore-forming P domains. The product of this gene has not been shown to be a functional channel, however, it may require other non-pore-forming proteins for activity. [provided by RefSeq, Jul 2008] |
KCNK2 Genepotassium channel, two pore domain subfamily K, member 2 This gene encodes one of the members of the two-pore-domain background potassium channel protein family. This type of potassium channel is formed by two homodimers that create a channel that leaks potassium out of the cell to control resting membrane potential. The channel can be opened, however, by certain anesthetics, membrane stretching, intracellular acidosis, and heat. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
KCNK3 Genepotassium channel, two pore domain subfamily K, member 3 This gene encodes a member of the superfamily of potassium channel proteins that contain two pore-forming P domains. The encoded protein is an outwardly rectifying channel that is sensitive to changes in extracellular pH and is inhibited by extracellular acidification. Also referred to as an acid-sensitive potassium channel, it is activated by the anesthetics halothane and isoflurane. Although three transcripts are detected in northern blots, there is currently no sequence available to confirm transcript variants for this gene. [provided by RefSeq, Aug 2008] |
SH3BGR GeneSH3 domain binding glutamate-rich protein Predicted to enable SH3 domain binding activity. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100287912 Geneankyrin repeat domain 11 pseudogene |
HMGN2P33 Genehigh mobility group nucleosomal binding domain 2 pseudogene 33 |
HMGN2P32 Genehigh mobility group nucleosomal binding domain 2 pseudogene 32 |
HMGN2P35 Genehigh mobility group nucleosomal binding domain 2 pseudogene 35 |
HMGN2P34 Genehigh mobility group nucleosomal binding domain 2 pseudogene 34 |
HMGN2P37 Genehigh mobility group nucleosomal binding domain 2 pseudogene 37 |
HMGN2P36 Genehigh mobility group nucleosomal binding domain 2 pseudogene 36 |
HMGN2P39 Genehigh mobility group nucleosomal binding domain 2 pseudogene 39 |
HMGN2P38 Genehigh mobility group nucleosomal binding domain 2 pseudogene 38 |
LOC100132524 GeneUBX domain protein 2A pseudogene |
CITED2 GeneCbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2 The protein encoded by this gene inhibits transactivation of HIF1A-induced genes by competing with binding of hypoxia-inducible factor 1-alpha to p300-CH1. Mutations in this gene are a cause of cardiac septal defects. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2012] |
TMCC1 Genetransmembrane and coiled-coil domain family 1 Enables identical protein binding activity. Involved in several processes, including endosome fission; endosome membrane tubulation; and membrane fission. Located in cytosol; endoplasmic reticulum-endosome membrane contact site; and rough endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
TMCC2 Genetransmembrane and coiled-coil domain family 2 Involved in amyloid precursor protein metabolic process. Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
TMCC3 Genetransmembrane and coiled-coil domain family 3 Enables 14-3-3 protein binding activity and identical protein binding activity. Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100130964 GeneADAM metallopeptidase domain 3A-like |
WBP11P1 GeneWW domain binding protein 11 pseudogene 1 |
FHAD1 Geneforkhead-associated (FHA) phosphopeptide binding domain 1 Predicted to act upstream of or within apoptotic process and spermatogenesis. [provided by Alliance of Genome Resources, Mar 2025] |
NSD1 Genenuclear receptor binding SET domain protein 1 This gene encodes a protein containing a SET domain, 2 LXXLL motifs, 3 nuclear translocation signals (NLSs), 4 plant homeodomain (PHD) finger regions, and a proline-rich region. The encoded protein enhances androgen receptor (AR) transactivation, and this enhancement can be increased further in the presence of other androgen receptor associated coregulators. This protein may act as a nucleus-localized, basic transcriptional factor and also as a bifunctional transcriptional regulator. Mutations of this gene have been associated with Sotos syndrome and Weaver syndrome. One version of childhood acute myeloid leukemia is the result of a cryptic translocation with the breakpoints occurring within nuclear receptor-binding Su-var, enhancer of zeste, and trithorax domain protein 1 on chromosome 5 and nucleoporin, 98-kd on chromosome 11. Multiple transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Sep 2018] |
STBD1 Genestarch binding domain 1 Enables enzyme binding activity and glycogen binding activity. Involved in glycophagy and intracellular transport. Located in T-tubule; endoplasmic reticulum; and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
PYHIN1 Genepyrin and HIN domain family, member 1 The protein encoded by this gene belongs to the HIN-200 family of interferon-inducible proteins that share a 200-amino acid signature motif at their C-termini. HIN200 proteins are primarily nuclear and are involved in transcriptional regulation of genes important for cell cycle control, differentiation, and apoptosis. Downregulation of this gene is associated with breast cancer. This protein acts as a tumor suppressor by promoting ubiquitination and subsequent degradation of MDM2, which leads to stabilization of p53/TP53. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011] |
IMPACT Geneimpact RWD domain protein Predicted to enable protein sequestering activity. Predicted to be involved in several processes, including GCN2-mediated signaling; cellular response to amino acid starvation; and regulation of gene expression. Predicted to act upstream of or within negative regulation of protein phosphorylation. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
CLEC7A GeneC-type lectin domain family 7, member A This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. The encoded glycoprotein is a small type II membrane receptor with an extracellular C-type lectin-like domain fold and a cytoplasmic domain with an immunoreceptor tyrosine-based activation motif. It functions as a pattern-recognition receptor that recognizes a variety of beta-1,3-linked and beta-1,6-linked glucans from fungi and plants, and in this way plays a role in innate immune response. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. This gene is closely linked to other CTL/CTLD superfamily members on chromosome 12p13 in the natural killer gene complex region. [provided by RefSeq, Jul 2008] |
PTCD2P1 Genepentatricopeptide repeat domain 2 pseudogene 1 |
ANKRD20A17P Geneankyrin repeat domain 20 family, member A17, pseudogene |
ANKRD20A6P Geneankyrin repeat domain 20 family, member A6, pseudogene |
LOC100420109 GeneWW domain binding protein 1 pseudogene |
WFDC21P GeneWAP four-disulfide core domain 21, pseudogene Predicted to enable enzyme activator activity. Predicted to act upstream of or within response to lipopolysaccharide; response to tumor necrosis factor; and white fat cell differentiation. Predicted to be located in extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100131448 GeneCTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2 pseudogene |
RASGEF1C GeneRasGEF domain family, member 1C Predicted to enable guanyl-nucleotide exchange factor activity. Predicted to be involved in Ras protein signal transduction. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RASGEF1B GeneRasGEF domain family, member 1B Enables guanyl-nucleotide exchange factor activity. Predicted to be involved in Ras protein signal transduction. Predicted to be located in early endosome; late endosome; and midbody. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RASGEF1A GeneRasGEF domain family, member 1A Enables guanyl-nucleotide exchange factor activity. Involved in cell migration and positive regulation of Ras protein signal transduction. Predicted to be located in cytosol. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
TTC41P Genetetratricopeptide repeat domain 41, pseudogene Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
SETMAR GeneSET domain and mariner transposase fusion gene This gene encodes a fusion protein that contains an N-terminal histone-lysine N-methyltransferase domain and a C-terminal mariner transposase domain. The encoded protein binds DNA and functions in DNA repair activities including non-homologous end joining and double strand break repair. The SET domain portion of this protein specifically methylates histone H3 lysines 4 and 36. This gene exists as a fusion gene only in anthropoid primates, other organisms lack mariner transposase domain. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013] |
RNPS1P1 GeneRNA binding protein S1, serine-rich domain pseudogene 1 |
TRRAP Genetransformation/transcription domain-associated protein This gene encodes a large multidomain protein of the phosphoinositide 3-kinase-related kinases (PIKK) family. The encoded protein is a common component of many histone acetyltransferase (HAT) complexes and plays a role in transcription and DNA repair by recruiting HAT complexes to chromatin. Deregulation of this gene may play a role in several types of cancer including glioblastoma multiforme. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2011] |
ANKRD20A15P Geneankyrin repeat domain 20 family, member A15, pseudogene |
ANKRD62 Geneankyrin repeat domain 62 |
LOC100130618 Genetetratricopeptide repeat domain 14 pseudogene |
IFIH1 Geneinterferon induced with helicase C domain 1 IFIH1 encodes MDA5 which is an intracellular sensor of viral RNA that triggers the innate immune response. Sensing RNA length and secondary structure, MDA5 binds dsRNA oligonucleotides with a modified DExD/H-box helicase core and a C-terminal domain, thus leading to a proinflammatory response that includes interferons. It has been shown that Coronaviruses (CoVs) as well as various other virus families, are capable of evading the MDA5-dependent interferon response, thus impeding the activation of the innate immune response to infection. MDA5 has also been shown to play an important role in enhancing natural killer cell function in malaria infection. In addition to its protective role in antiviral responses, MDA5 has been implicated in autoimmune and autoinflammatory diseases such as type 1 diabetes, systemic lupus erythematosus, and Aicardi-Goutieres syndrome[provided by RefSeq, Jul 2020] |
WDR45B GeneWD repeat domain 45B This gene encodes a member of the WIPI or SVP1 family of WD40 repeat-containing proteins. The protein contains seven WD40 repeats that are thought to fold into a beta-propeller structure that mediates protein-protein interactions, and a conserved motif for interaction with phospholipids. The human genome contains several pseudogenes of this gene. [provided by RefSeq, Jul 2008] |
WDR45P GeneWD repeat domain 45 pseudogene |
WDR78 GeneWD repeat domain 78 Predicted to enable dynein heavy chain binding activity and dynein light chain binding activity. Predicted to be involved in axonemal dynein complex assembly and cilium movement. Predicted to act upstream of or within hematopoietic progenitor cell differentiation. Predicted to be located in axoneme; dynein axonemal particle; and motile cilium. Predicted to be part of axonemal dynein complex. [provided by Alliance of Genome Resources, Mar 2025] |
WDR70 GeneWD repeat domain 70 Enables enzyme binding activity. Predicted to be located in nucleoplasm. Predicted to be active in nucleus and site of double-strand break. [provided by Alliance of Genome Resources, Mar 2025] |
WDR73 GeneWD repeat domain 73 The protein encoded by this gene is thought to contain multiple WD40 repeats. WD40 repeats are motifs that contain 40-60 amino acids, and usually end with Trp-Asp (WD). This protein is found in the cytoplasm during interphase, but accumulates at the spindle poles and astral microtubules during mitosis. Reduced expression of this gene results in abnormalities in the size and morphology of the nucleus. Mutations in this gene have been associated with Galloway-Mowat syndrome PMID: 25466283), which is a rare autosomal recessive disorder that affects both the central nervous system and kidneys. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2015] |
WDR72 GeneWD repeat domain 72 This gene encodes a protein with eight WD-40 repeats. Mutations in this gene have been associated with amelogenesis imperfecta hypomaturation type 2A3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2013] |
WDR75 GeneWD repeat domain 75 Enables RNA binding activity. Involved in positive regulation of rRNA processing; positive regulation of transcription by RNA polymerase I; and ribosomal small subunit biogenesis. Located in nucleolus. Part of small-subunit processome. [provided by Alliance of Genome Resources, Mar 2025] |
WDR74 GeneWD repeat domain 74 Involved in rRNA processing and ribosomal large subunit biogenesis. Located in nuclear exosome (RNase complex); nucleolus; and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
WDR77 GeneWD repeat domain 77 The protein encoded by this gene is an androgen receptor coactivator that forms a complex with protein arginine methyltransferase 5, which modifies specific arginines to dimethylarginines in several spliceosomal Sm proteins. The encoded protein may be involved in the early stages of prostate cancer, with most of the protein being nuclear-localized in benign cells but cytoplasmic in cancer cells. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015] |
WDR76 GeneWD repeat domain 76 Enables enzyme binding activity. Involved in DNA damage response. Located in heterochromatin; nucleus; and site of DNA damage. [provided by Alliance of Genome Resources, Mar 2025] |
ANKRD13B Geneankyrin repeat domain 13B Enables ubiquitin-modified protein reader activity. Involved in negative regulation of receptor internalization. Located in endosome; perinuclear region of cytoplasm; and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ANKRD13C Geneankyrin repeat domain 13C Enables signaling receptor binding activity. Involved in protein retention in ER lumen; regulation of anoikis; and regulation of signaling receptor activity. Located in endoplasmic reticulum and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100130102 GeneWW domain binding protein 11 pseudogene |
LARP1BP3 GeneLa ribonucleoprotein domain family, member 1B pseudogene 3 |
TBC1D23 GeneTBC1 domain family, member 23 Involved in brain development; retrograde transport, endosome to Golgi; and vesicle tethering to Golgi. Located in WASH complex; cytoplasmic vesicle; and trans-Golgi network. Implicated in pontocerebellar hypoplasia type 11. [provided by Alliance of Genome Resources, Mar 2025] |
TBC1D21 GeneTBC1 domain family, member 21 Enables GTPase activator activity and small GTPase binding activity. Predicted to be involved in sperm axoneme assembly and sperm mitochondrial sheath assembly. Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
TBC1D20 GeneTBC1 domain family, member 20 This gene encodes a protein that belongs to a family of GTPase activator proteins of Rab-like small GTPases. The encoded protein and its cognate GTPase, Rab1, bind the nonstructural protein 5A (NS5A) of the hepatitis C virus (HCV) to mediate viral replication. Depletion of this protein inhibits replication of the virus and HCV infection. Mutations in this gene are associated with Warburg micro syndrome 4. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014] |
TBC1D27 GeneTBC1 domain family, member 27 |
TBC1D26 GeneTBC1 domain family, member 26 Predicted to enable GTPase activator activity. [provided by Alliance of Genome Resources, Mar 2025] |
TBC1D25 GeneTBC1 domain family, member 25 This gene encodes a protein with a TBC domain and functions as a Rab GTPase activating protein. The encoded protein is involved in the fusion of autophagosomes with endosomes and lysosomes. This gene was previously known as ornithine aminotransferase-like 1, but has no similarity to ornithine aminotransferase. [provided by RefSeq, Jan 2017] |
TBC1D29 GeneTBC1 domain family, member 29 |
TBC1D28 GeneTBC1 domain family, member 28 |
TBC1D2B GeneTBC1 domain family, member 2B Predicted to enable GTPase activator activity. Involved in endocytosis. Located in cytosol and early endosome. [provided by Alliance of Genome Resources, Mar 2025] |
ANKRD35 Geneankyrin repeat domain 35 Predicted to enable actin binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
ANKRD36 Geneankyrin repeat domain 36 Predicted to enable ion channel inhibitor activity. [provided by Alliance of Genome Resources, Mar 2025] |
ANKRD37 Geneankyrin repeat domain 37 Located in cytosol; mitochondrion; and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ANKRD31 Geneankyrin repeat domain 31 This gene encodes a protein containing multiple ankyrin repeats. Ankyrin domains function in protein-protein interactions in a variety of cellular processes. Mutations in this gene are associated with a Rett syndrome (RTT)-like phenotype. [provided by RefSeq, Apr 2017] |
ANKRD32 Geneankyrin repeat domain 32 Enables ubiquitin protein ligase binding activity. Involved in several processes, including positive regulation of cellular component organization; positive regulation of double-strand break repair; and protein localization to site of double-strand break. Located in nucleoplasm and site of double-strand break. [provided by Alliance of Genome Resources, Mar 2025] |
ANKRD33 Geneankyrin repeat domain 33 Predicted to act upstream of or within skeletal muscle cell differentiation. Predicted to be located in cytosol and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ANKRD39 Geneankyrin repeat domain 39 |
ANKRD36C Geneankyrin repeat domain 36C Predicted to enable ion channel inhibitor activity. [provided by Alliance of Genome Resources, Mar 2025] |
CARD9 Genecaspase recruitment domain family, member 9 The protein encoded by this gene is a member of the CARD protein family, which is defined by the presence of a characteristic caspase-associated recruitment domain (CARD). CARD is a protein interaction domain known to participate in activation or suppression of CARD containing members of the caspase family, and thus plays an important regulatory role in cell apoptosis. This protein was identified by its selective association with the CARD domain of BCL10, a postive regulator of apoptosis and NF-kappaB activation, and is thought to function as a molecular scaffold for the assembly of a BCL10 signaling complex that activates NF-kappaB. Several alternatively spliced transcript variants have been observed, but their full-length nature is not clearly defined. [provided by RefSeq, Jul 2008] |
CARD8 Genecaspase recruitment domain family, member 8 The protein encoded by this gene belongs to the caspase recruitment domain (CARD)-containing family of proteins, which are involved in pathways leading to activation of caspases or nuclear factor kappa-B (NFKB). This protein may be a component of the inflammasome, a protein complex that plays a role in the activation of proinflammatory caspases. It is thought that this protein acts as an adaptor molecule that negatively regulates NFKB activation, CASP1-dependent IL1B secretion, and apoptosis. Polymorphisms in this gene may be associated with a susceptibility to rheumatoid arthritis. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, May 2010] |
CARD6 Genecaspase recruitment domain family, member 6 This gene encodes a protein that contains a caspase recruitment domain (CARD), an antiparallel six-helical bundle that mediates homotypic protein-protein interactions. The encoded protein is a microtubule-associated protein that has been shown to interact with receptor-interacting protein kinases and positively modulate signal transduction pathways converging on activation of the inducible transcription factor NF-kB. [provided by RefSeq, Jul 2008] |
LOC390308 GeneCDGSH iron sulfur domain 1 pseudogene |
YTHDF2P1 GeneYTH domain family, member 2 pseudogene 1 |
NIFK Genenucleolar protein interacting with the FHA domain of MKI67 This gene encodes a protein that interacts with the forkhead-associated domain of the Ki-67 antigen. The encoded protein may bind RNA and may play a role in mitosis and cell cycle progression. Multiple pseudogenes exist on chromosomes 5, 10, 12, 15, and 19.[provided by RefSeq, Jan 2009] |
DAND5 GeneDAN domain family member 5, BMP antagonist This gene encodes a member of the BMP (bone morphogenic protein) antagonist family. Like BMPs, BMP antagonists contain cystine knots and typically form homo- and heterodimers. The CAN (cerberus and dan) subfamily of BMP antagonists, to which this gene belongs, is characterized by a C-terminal cystine knot with an eight-membered ring. The antagonistic effect of the secreted protein encoded by this gene is likely due to its direct binding to BMP proteins. As an antagonist of BMP, this gene may play a role in regulating organogenesis, body patterning, and tissue differentiation. In mouse, this protein has been shown to bind Nodal and to inhibit the Nodal signaling pathway which patterns left/right body asymmetry. [provided by RefSeq, Jul 2008] |
PPEF2 Geneprotein phosphatase, EF-hand calcium binding domain 2 This gene encodes a member of the serine/threonine protein phosphatase with EF-hand motif family. The protein contains a protein phosphatase catalytic domain, and at least two EF-hand calcium-binding motifs in its C terminus. Although its substrate(s) is unknown, the encoded protein, which is expressed specifically in photoreceptors and the pineal, has been suggested to play a role in the visual system. This gene shares high sequence similarity with the Drosophila retinal degeneration C (rdgC) gene. [provided by RefSeq, Jul 2008] |
PPEF1 Geneprotein phosphatase, EF-hand calcium binding domain 1 This gene encodes a member of the serine/threonine protein phosphatase with EF-hand motif family. The protein contains a protein phosphatase catalytic domain, and at least two EF-hand calcium-binding motifs in its C terminus. Although its substrate(s) is unknown, the encoded protein has been suggested to play a role in specific sensory neuron function and/or development. This gene shares high sequence similarity with the Drosophila retinal degeneration C (rdgC) gene. Several alternatively spliced transcript variants, each encoding a distinct isoform, have been described. [provided by RefSeq, Jul 2008] |
POTEJ GenePOTE ankyrin domain family, member J Predicted to enable protein kinase binding activity. Predicted to be a structural constituent of postsynaptic actin cytoskeleton. Predicted to be involved in axonogenesis and cell motility. Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
POTEI GenePOTE ankyrin domain family, member I Predicted to enable protein kinase binding activity. Predicted to be a structural constituent of postsynaptic actin cytoskeleton. Predicted to be involved in axonogenesis and cell motility. Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
POTEH GenePOTE ankyrin domain family, member H Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
POTEG GenePOTE ankyrin domain family, member G |
POTEF GenePOTE ankyrin domain family, member F Predicted to enable protein kinase binding activity. Predicted to be a structural constituent of postsynaptic actin cytoskeleton. Predicted to be involved in axonogenesis and cell motility. Located in blood microparticle and extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
POTEE GenePOTE ankyrin domain family, member E Predicted to enable protein kinase binding activity. Predicted to be a structural constituent of postsynaptic actin cytoskeleton. Involved in substantia nigra development. Located in blood microparticle and extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
POTED GenePOTE ankyrin domain family, member D Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
POTEC GenePOTE ankyrin domain family, member C |
POTEB GenePOTE ankyrin domain family, member B |
POTEA GenePOTE ankyrin domain family, member A |
LOC100420025 Geneankyrin repeat domain 33B pseudogene |
LOC100420022 Geneankyrin repeat domain 33B pseudogene |
LOC100420021 Geneankyrin repeat domain 33B pseudogene |
CBFA2T3 Genecore-binding factor, runt domain, alpha subunit 2; translocated to, 3 This gene encodes a member of the myeloid translocation gene family which interact with DNA-bound transcription factors and recruit a range of corepressors to facilitate transcriptional repression. The t(16;21)(q24;q22) translocation is one of the less common karyotypic abnormalities in acute myeloid leukemia. The translocation produces a chimeric gene made up of the 5'-region of the runt-related transcription factor 1 gene fused to the 3'-region of this gene. This gene is also a putative breast tumor suppressor. Alternative splicing results in transcript variants. [provided by RefSeq, Nov 2010] |
CBFA2T2 Genecore-binding factor, runt domain, alpha subunit 2; translocated to, 2 In acute myeloid leukemia, especially in the M2 subtype, the t(8;21)(q22;q22) translocation is one of the most frequent karyotypic abnormalities. The translocation produces a chimeric gene made up of the 5'-region of the RUNX1 (AML1) gene fused to the 3'-region of the CBFA2T1 (MTG8) gene. The chimeric protein is thought to associate with the nuclear corepressor/histone deacetylase complex to block hematopoietic differentiation. The protein encoded by this gene binds to the AML1-MTG8 complex and may be important in promoting leukemogenesis. Several transcript variants are thought to exist for this gene, but the full-length natures of only three have been described. [provided by RefSeq, Jul 2008] |
NPAS4 Geneneuronal PAS domain protein 4 NXF is a member of the basic helix-loop-helix-PER (MIM 602260)-ARNT (MIM 126110)-SIM (see SIM2; MIM 600892) (bHLH-PAS) class of transcriptional regulators, which are involved in a wide range of physiologic and developmental events (Ooe et al., 2004 [PubMed 14701734]).[supplied by OMIM, Mar 2008] |
NPAS3 Geneneuronal PAS domain protein 3 This gene encodes a member of the basic helix-loop-helix and PAS domain-containing family of transcription factors. The encoded protein is localized to the nucleus and may regulate genes involved in neurogenesis. Chromosomal abnormalities that affect the coding potential of this gene are associated with schizophrenia and cognitive disability. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009] |
NPAS2 Geneneuronal PAS domain protein 2 The protein encoded by this gene is a member of the basic helix-loop-helix (bHLH)-PAS family of transcription factors. A similar mouse protein may play a regulatory role in the acquisition of specific types of memory. It also may function as a part of a molecular clock operative in the mammalian forebrain. [provided by RefSeq, Jul 2008] |
NPAS1 Geneneuronal PAS domain protein 1 The protein encoded by this gene is a member of the basic helix-loop-helix (bHLH)-PAS family of transcription factors. Studies of a related mouse gene suggest that it functions in neurons. The exact function of this gene is unclear, but it may play protective or modulatory roles during late embryogenesis and postnatal development. [provided by RefSeq, Jul 2008] |
CARD11 Genecaspase recruitment domain family, member 11 The protein encoded by this gene belongs to the membrane-associated guanylate kinase (MAGUK) family, a class of proteins that functions as molecular scaffolds for the assembly of multiprotein complexes at specialized regions of the plasma membrane. This protein is also a member of the CARD protein family, which is defined by carrying a characteristic caspase-associated recruitment domain (CARD). This protein has a domain structure similar to that of CARD14 protein. The CARD domains of both proteins have been shown to specifically interact with BCL10, a protein known to function as a positive regulator of cell apoptosis and NF-kappaB activation. When expressed in cells, this protein activated NF-kappaB and induced the phosphorylation of BCL10. [provided by RefSeq, Jul 2008] |
TNFRSF10C Genetumor necrosis factor receptor superfamily, member 10c, decoy without an intracellular domain The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor contains an extracellular TRAIL-binding domain and a transmembrane domain, but no cytoplasmic death domain. This receptor is not capable of inducing apoptosis, and is thought to function as an antagonistic receptor that protects cells from TRAIL-induced apoptosis. This gene was found to be a p53-regulated DNA damage-inducible gene. The expression of this gene was detected in many normal tissues but not in most cancer cell lines, which may explain the specific sensitivity of cancer cells to the apoptosis-inducing activity of TRAIL. [provided by RefSeq, Jul 2008] |
TNFRSF10D Genetumor necrosis factor receptor superfamily, member 10d, decoy with truncated death domain The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor contains an extracellular TRAIL-binding domain, a transmembrane domain, and a truncated cytoplamic death domain. This receptor does not induce apoptosis, and has been shown to play an inhibitory role in TRAIL-induced cell apoptosis. [provided by RefSeq, Jul 2008] |
WFDC10B GeneWAP four-disulfide core domain 10B This gene encodes a member of the WAP-type four-disulfide core (WFDC) domain family. The WFDC domain, or WAP signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor. Most WFDC gene members are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene belongs to the telomeric cluster. Two alternatively spliced transcript variants have been found for this gene, and they encode distinct isoforms. [provided by RefSeq, Jul 2008] |
WFDC10A GeneWAP four-disulfide core domain 10A This gene encodes a member of the WAP-type four-disulfide core (WFDC) domain family. The WFDC domain, or WAP signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor. Most WFDC gene members are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene belongs to the telomeric cluster. [provided by RefSeq, Jul 2008] |
LOC100127978 Genestarch binding domain 1 pseudogene |
LIMK2 GeneLIM domain kinase 2 There are approximately 40 known eukaryotic LIM proteins, so named for the LIM domains they contain. LIM domains are highly conserved cysteine-rich structures containing 2 zinc fingers. Although zinc fingers usually function by binding to DNA or RNA, the LIM motif probably mediates protein-protein interactions. LIM kinase-1 and LIM kinase-2 belong to a small subfamily with a unique combination of 2 N-terminal LIM motifs and a C-terminal protein kinase domain. The protein encoded by this gene is phosphorylated and activated by ROCK, a downstream effector of Rho, and the encoded protein, in turn, phosphorylates cofilin, inhibiting its actin-depolymerizing activity. It is thought that this pathway contributes to Rho-induced reorganization of the actin cytoskeleton. At least three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
LIMK1 GeneLIM domain kinase 1 There are approximately 40 known eukaryotic LIM proteins, so named for the LIM domains they contain. LIM domains are highly conserved cysteine-rich structures containing 2 zinc fingers. Although zinc fingers usually function by binding to DNA or RNA, the LIM motif probably mediates protein-protein interactions. LIM kinase-1 and LIM kinase-2 belong to a small subfamily with a unique combination of 2 N-terminal LIM motifs and a C-terminal protein kinase domain. LIMK1 is a serine/threonine kinase that regulates actin polymerization via phosphorylation and inactivation of the actin binding factor cofilin. This protein is ubiquitously expressed during development and plays a role in many cellular processes associated with cytoskeletal structure. This protein also stimulates axon growth and may play a role in brain development. LIMK1 hemizygosity is implicated in the impaired visuospatial constructive cognition of Williams syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Feb 2011] |
LOC643605 GeneCTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2 pseudogene |
LARP1P1 GeneLa ribonucleoprotein domain family, member 1 pseudogene 1 |
ANKRD7 Geneankyrin repeat domain 7 Predicted to act upstream of or within blastocyst hatching. Located in centrosome and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ANKRD1 Geneankyrin repeat domain 1 (cardiac muscle) The protein encoded by this gene is localized to the nucleus of endothelial cells and is induced by IL-1 and TNF-alpha stimulation. Studies in rat cardiomyocytes suggest that this gene functions as a transcription factor. Interactions between this protein and the sarcomeric proteins myopalladin and titin suggest that it may also be involved in the myofibrillar stretch-sensor system. [provided by RefSeq, Jul 2008] |
ANKRD2 Geneankyrin repeat domain 2 (stretch responsive muscle) This gene encodes a protein that belongs to the muscle ankyrin repeat protein (MARP) family. A similar gene in rodents is a component of a muscle stress response pathway and plays a role in the stretch-response associated with slow muscle function. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014] |
ANKRD9 Geneankyrin repeat domain 9 Enables ubiquitin-like ligase-substrate adaptor activity. Involved in intracellular copper ion homeostasis; proteasome-mediated ubiquitin-dependent protein catabolic process; and protein ubiquitination. Located in cytoplasmic vesicle and cytosol. Part of Cul5-RING ubiquitin ligase complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100420211 GeneSH3-domain binding protein 4 pseudogene |
LOC100419814 Geneankyrin repeat domain 49 pseudogene |
LOC100419815 Geneankyrin repeat domain 57 pseudogene |
CISD1P1 GeneCDGSH iron sulfur domain 1 pseudogene 1 |
LOC100270647 Genenucleolar protein interacting with the FHA domain of MKI67 pseudogene |
TTC33 Genetetratricopeptide repeat domain 33 |
TTC32 Genetetratricopeptide repeat domain 32 |
TTC31 Genetetratricopeptide repeat domain 31 |
TTC37 Genetetratricopeptide repeat domain 37 This gene encodes a protein with twenty tetratricopeptide (TPR) repeats. Tetratricopeptide repeat containing motifs are found in a variety of proteins and may mediate protein-protein interactions and chaperone activity. Mutations in this gene are associated with trichohepatoenteric syndrome. [provided by RefSeq, Jul 2010] |
TTC36 Genetetratricopeptide repeat domain 36 The protein encoded by this gene has three tetratricopeptide repeats and is a chaperone for heat shock protein 70. The encoded protein may function as a tumor suppressor in hepatocellular carcinoma (HCC) since it promotes apoptosis but is downregulated in HCC. [provided by RefSeq, Sep 2016] |
TTC34 Genetetratricopeptide repeat domain 34 |
TTC38 Genetetratricopeptide repeat domain 38 Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
LARP1B GeneLa ribonucleoprotein domain family, member 1B This gene encodes a protein containing domains found in the La related protein of Drosophila melanogaster. La motif-containing proteins are thought to be RNA-binding proteins, where the La motif and adjacent amino acids fold into an RNA recognition motif. The La motif is also found in proteins unrelated to the La protein. Alternative splicing has been observed at this locus and multiple variants, encoding distinct isoforms, are described. Additional splice variation has been identified but the full-length nature of these transcripts has not been determined. [provided by RefSeq, Jun 2013] |
MLKL Genemixed lineage kinase domain-like This gene belongs to the protein kinase superfamily. The encoded protein contains a protein kinase-like domain; however, is thought to be inactive because it lacks several residues required for activity. This protein plays a critical role in tumor necrosis factor (TNF)-induced necroptosis, a programmed cell death process, via interaction with receptor-interacting protein 3 (RIP3), which is a key signaling molecule in necroptosis pathway. Inhibitor studies and knockdown of this gene inhibited TNF-induced necrosis. High levels of this protein and RIP3 are associated with inflammatory bowel disease in children. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Sep 2015] |
BARD1 GeneBRCA1 associated RING domain 1 This gene encodes a protein which interacts with the N-terminal region of BRCA1. In addition to its ability to bind BRCA1 in vivo and in vitro, it shares homology with the 2 most conserved regions of BRCA1: the N-terminal RING motif and the C-terminal BRCT domain. The RING motif is a cysteine-rich sequence found in a variety of proteins that regulate cell growth, including the products of tumor suppressor genes and dominant protooncogenes. This protein also contains 3 tandem ankyrin repeats. The BARD1/BRCA1 interaction is disrupted by tumorigenic amino acid substitutions in BRCA1, implying that the formation of a stable complex between these proteins may be an essential aspect of BRCA1 tumor suppression. This protein may be the target of oncogenic mutations in breast or ovarian cancer. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013] |
PDLIM1P4 GenePDZ and LIM domain 1 pseudogene 4 |
PDLIM1P3 GenePDZ and LIM domain 1 pseudogene 3 |
PDLIM1P2 GenePDZ and LIM domain 1 pseudogene 2 |
PDLIM1P1 GenePDZ and LIM domain 1 pseudogene 1 |
ANKRD20A13P Geneankyrin repeat domain 20 family, member A13, pseudogene |
HMGN3P1 Genehigh mobility group nucleosomal binding domain 3 pseudogene 1 |
ADAM21 GeneADAM metallopeptidase domain 21 This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The expression of this gene expression is testis-specific. [provided by RefSeq, May 2011] |
ADAM20 GeneADAM metallopeptidase domain 20 This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The expression of this gene is testis-specific. [provided by RefSeq, Jul 2008] |
ADAM23 GeneADAM metallopeptidase domain 23 This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. It is reported that inactivation of this gene is associated with tumorigenesis in human cancers. [provided by RefSeq, May 2013] |
ADAM22 GeneADAM metallopeptidase domain 22 This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. Unlike other members of the ADAM protein family, the protein encoded by this gene lacks metalloprotease activity since it has no zinc-binding motif. This gene is highly expressed in the brain and may function as an integrin ligand in the brain. In mice, it has been shown to be essential for correct myelination in the peripheral nervous system. Alternative splicing results in several transcript variants.[provided by RefSeq, Dec 2010] |
ADAM29 GeneADAM metallopeptidase domain 29 This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The protein encoded by this gene is highly expressed in testis and may be involved in human spermatogenesis. Alternative splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Jul 2008] |
ADAM28 GeneADAM metallopeptidase domain 28 This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. The protein encoded by this gene is a lymphocyte-expressed ADAM protein. This gene is present in a gene cluster with other members of the ADAM family on chromosome 8. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015] |
POU5F2 GenePOU domain class 5, transcription factor 2 Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. [provided by Alliance of Genome Resources, Mar 2025] |
SBK1 GeneSH3 domain binding kinase 1 Predicted to enable protein serine/threonine kinase activity. Predicted to be involved in chromatin remodeling. Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC374443 GeneC-type lectin domain family 2, member D pseudogene |
LOC102724677 Genecarboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 2 pseudogene |
KCNK18 Genepotassium channel, two pore domain subfamily K, member 18 Potassium channels play a role in many cellular processes including maintenance of the action potential, muscle contraction, hormone secretion, osmotic regulation, and ion flow. This gene encodes a member of the superfamily of potassium channel proteins containing two pore-forming P domains and the encoded protein functions as an outward rectifying potassium channel. A mutation in this gene has been found to be associated with migraine with aura.[provided by RefSeq, Jan 2011] |
KCNK16 Genepotassium channel, two pore domain subfamily K, member 16 The protein encoded by this gene belongs to the family of potassium channel proteins containing two pore-forming P domains. This channel is an open rectifier which primarily passes outward current under physiological K+ concentrations. This gene is expressed predominantly in the pancreas and is activated at alkaline pH. Several alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Sep 2008] |
KCNK17 Genepotassium channel, two pore domain subfamily K, member 17 The protein encoded by this gene belongs to the family of potassium channel proteins containing two pore-forming P domains. This channel is an open rectifier which primarily passes outward current under physiological K+ concentrations. This gene is activated at alkaline pH. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2008] |
KCNK15 Genepotassium channel, two pore domain subfamily K, member 15 This gene encodes one of the members of the superfamily of potassium channel proteins containing two pore-forming P domains. The product of this gene has not been shown to be a functional channel, however, it may require other non-pore-forming proteins for activity. [provided by RefSeq, Jul 2008] |
KCNK12 Genepotassium channel, two pore domain subfamily K, member 12 This gene encodes one of the members of the superfamily of potassium channel proteins containing two pore-forming P domains. The product of this gene has not been shown to be a functional channel, however, it may require other non-pore-forming proteins for activity. [provided by RefSeq, Jul 2008] |
KCNK13 Genepotassium channel, two pore domain subfamily K, member 13 Potassium channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a potassium channel containing two pore-forming domains. This protein is an open channel that can be stimulated by arachidonic acid and inhibited by the anesthetic halothane. [provided by RefSeq, Jul 2013] |
KCNK10 Genepotassium channel, two pore domain subfamily K, member 10 The protein encoded by this gene belongs to the family of potassium channel proteins containing two pore-forming P domains. This channel is an open rectifier which primarily passes outward current under physiological K+ concentrations, and is stimulated strongly by arachidonic acid and to a lesser degree by membrane stretching, intracellular acidification, and general anaesthetics. Several alternatively spliced transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Sep 2008] |
LOC389834 Geneankyrin repeat domain 57 pseudogene |
ANKRD20A16P Geneankyrin repeat domain 20 family, member A16, pseudogene |
LOC102723859 GeneTBC1 domain family member-like Predicted to enable GTPase activator activity. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SGIP1 GeneSH3-domain GRB2-like (endophilin) interacting protein 1 SGIP1 functions as an endocytic protein that affects signaling by receptors in neuronal systems involved in energy homeostasis via its interaction with endophilins (see SH3GL3; MIM 603362) (Trevaskis et al., 2005 [PubMed 15919751] and Uezu et al., 2007 [PubMed 17626015]).[supplied by OMIM, Mar 2008] |
WDR26 GeneWD repeat domain 26 This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Two transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
WDR27 GeneWD repeat domain 27 This gene encodes a protein with multiple WD repeats. Proteins with these repeats may form scaffolds for protein-protein interaction and play key roles in cell signalling. Alternative splicing results in multiple transcript variants, but the full-length structure of some of these variants cannot be determined. [provided by RefSeq, Nov 2015] |
WDR24 GeneWD repeat domain 24 Enables ubiquitin protein ligase activity. Involved in several processes, including cellular response to amino acid starvation; positive regulation of TORC1 signaling; and protein K6-linked ubiquitination. Located in cytosol and lysosomal membrane. Part of GATOR2 complex. [provided by Alliance of Genome Resources, Mar 2025] |
WDR25 GeneWD repeat domain 25 This gene encodes a protein containing 7 WD repeats. WD repeats are approximately 30 to 40-amino acid domains containing several conserved residues, typically having a Tryptophan-Aspartic acid dipeptide (WD) at the C-terminal end. WD domains are involved in protein-protein interactions in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2017] |
WDR20 GeneWD repeat domain 20 This gene encodes a WD repeat-containing protein that functions to preserve and regulate the activity of the USP12-UAF1 deubiquitinating enzyme complex. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2011] |
MCCD1P1 Genemitochondrial coiled-coil domain 1 pseudogene 1 |
CTDSP1 GeneCTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase 1 This gene encodes a member of the small C-terminal domain phosphatase (SCP) family of nuclear phosphatases. These proteins play a role in transcriptional regulation through specific dephosphorylation of phosphoserine 5 within tandem heptapeptide repeats of the C-terminal domain of RNA polymerase II. The encoded protein plays a role in neuronal gene silencing in non-neuronal cells, and may also inhibit osteoblast differentiation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2011] |
CTDSP2 GeneCTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase 2 Enables RNA polymerase II CTD heptapeptide repeat phosphatase activity. Involved in protein dephosphorylation. Predicted to be located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
CTDSPL GeneCTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase-like Predicted to enable RNA polymerase II CTD heptapeptide repeat phosphatase activity. Predicted to be involved in chromatin remodeling and regulation of transcription by RNA polymerase II. Predicted to act upstream of or within negative regulation of G1/S transition of mitotic cell cycle and negative regulation of protein phosphorylation. Located in extracellular exosome. Biomarker of lung non-small cell carcinoma. [provided by Alliance of Genome Resources, Mar 2025] |
CLEC2L GeneC-type lectin domain family 2, member L Predicted to enable carbohydrate binding activity. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
CLEC2A GeneC-type lectin domain family 2, member A Enables protein homodimerization activity. Predicted to be involved in natural killer cell mediated cytotoxicity. Predicted to act upstream of or within several processes, including T cell receptor signaling pathway; regulation of actin filament polymerization; and regulation of interleukin-2 production. Located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
CLEC2B GeneC-type lectin domain family 2, member B This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signalling, glycoprotein turnover, and roles in inflammation and immune response. The encoded type 2 transmembrane protein may function as a cell activation antigen. An alternative splice variant has been described but its full-length sequence has not been determined. This gene is closely linked to other CTL/CTLD superfamily members on chromosome 12p13 in the natural killer gene complex region. [provided by RefSeq, Jul 2008] |
CLEC2D GeneC-type lectin domain family 2, member D This gene encodes a member of the natural killer cell receptor C-type lectin family. The encoded protein inhibits osteoclast formation and contains a transmembrane domain near the N-terminus as well as the C-type lectin-like extracellular domain. Several alternatively spliced transcript variants have been identified for this gene. [provided by RefSeq, Oct 2010] |
IQSEC1 GeneIQ motif and Sec7 domain 1 Predicted to enable protein kinase binding activity. Predicted to be involved in several processes, including positive regulation of focal adhesion disassembly; positive regulation of keratinocyte migration; and regulation of postsynaptic neurotransmitter receptor internalization. Located in nucleolus. Implicated in intellectual developmental disorder with short stature and behavioral abnormalities and lung adenocarcinoma. Biomarker of lung non-small cell carcinoma. [provided by Alliance of Genome Resources, Mar 2025] |
IQSEC3 GeneIQ motif and Sec7 domain 3 Predicted to enable guanyl-nucleotide exchange factor activity. Predicted to be involved in several processes, including activation of GTPase activity; postsynapse organization; and regulation of small GTPase mediated signal transduction. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
IQSEC2 GeneIQ motif and Sec7 domain 2 This gene encodes a guanine nucleotide exchange factor for the ARF family of small GTP-binding proteins. The encoded protein is a component of the postsynaptic density at excitatory synapses, and may play a critical role in cytoskeletal and synaptic organization through the activation of selected ARF substrates including ARF1 and ARF6. Mutations in this gene have been implicated in nonsyndromic X-linked cognitive disability. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2011] |
ANKRD30A Geneankyrin repeat domain 30A This gene encodes a DNA-binding transcription factor that is uniquely expressed in mammary epithelium and the testis. Altered expression levels have been associated with breast cancer progression. [provided by RefSeq, Nov 2016] |
ANKRD30B Geneankyrin repeat domain 30B |
ANKRD20A9P Geneankyrin repeat domain 20 family, member A9, pseudogene |
AMIGO3 Geneadhesion molecule with Ig-like domain 3 Predicted to be involved in brain development; heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules; and positive regulation of synapse assembly. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
WFDC11 GeneWAP four-disulfide core domain 11 This gene encodes a member of the WAP-type four-disulfide core (WFDC) domain family. The WFDC domain, or WAP signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor. Most WFDC gene members are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene belongs to the telomeric cluster. [provided by RefSeq, Jul 2008] |
WFDC13 GeneWAP four-disulfide core domain 13 This gene encodes a member of the WAP-type four-disulfide core (WFDC) domain family. The WFDC domain, or WAP signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor. Most WFDC gene members are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene belongs to the telomeric cluster. [provided by RefSeq, Jul 2008] |
WFDC12 GeneWAP four-disulfide core domain 12 This gene encodes a member of the WAP-type four-disulfide core (WFDC) domain family. The WFDC domain, or WAP signature motif, contains eight cysteines forming four disulfide bonds at the core of the protein, and functions as a protease inhibitor. Most WFDC gene members are localized to chromosome 20q12-q13 in two clusters: centromeric and telomeric. This gene belongs to the centromeric cluster. [provided by RefSeq, Jul 2008] |
WDR53 GeneWD repeat domain 53 This gene encodes a protein containing WD domains. The function of this gene is unknown. [provided by RefSeq, Jul 2008] |
RCN3 Genereticulocalbin 3, EF-hand calcium binding domain Enables calcium ion binding activity. Involved in several processes, including collagen biosynthetic process; positive regulation of peptidase activity; and regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction. Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
RCN2 Genereticulocalbin 2, EF-hand calcium binding domain The protein encoded by this gene is a calcium-binding protein located in the lumen of the ER. The protein contains six conserved regions with similarity to a high affinity Ca(+2)-binding motif, the EF-hand. This gene maps to the same region as type 4 Bardet-Biedl syndrome, suggesting a possible causative role for this gene in the disorder. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2012] |
RCN1 Genereticulocalbin 1, EF-hand calcium binding domain Reticulocalbin 1 is a calcium-binding protein located in the lumen of the ER. The protein contains six conserved regions with similarity to a high affinity Ca(+2)-binding motif, the EF-hand. High conservation of amino acid residues outside of these motifs, in comparison to mouse reticulocalbin, is consistent with a possible biochemical function besides that of calcium binding. In human endothelial and prostate cancer cell lines this protein localizes to the plasma membrane.[provided by RefSeq, Jan 2009] |
LOC100130487 GeneWD repeat domain 89 pseudogene |
HIGD1A GeneHIG1 hypoxia inducible domain family, member 1A Acts upstream of or within negative regulation of apoptotic process. Located in mitochondrion and nucleoplasm. Part of protein-containing complex. [provided by Alliance of Genome Resources, Mar 2025] |
HIGD1C GeneHIG1 hypoxia inducible domain family, member 1C Predicted to be involved in mitochondrial respirasome assembly. Predicted to be located in mitochondrial membrane. Predicted to be active in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
HIGD1B GeneHIG1 hypoxia inducible domain family, member 1B This gene encodes a member of the hypoxia inducible gene 1 (HIG1) domain family. The encoded protein is localized to the cell membrane and has been linked to tumorigenesis and the progression of pituitary adenomas. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012] |
CACUL1 GeneCDK2-associated, cullin domain 1 Enables protein kinase binding activity. Involved in G1/S transition of mitotic cell cycle; positive regulation of cell population proliferation; and positive regulation of protein kinase activity. [provided by Alliance of Genome Resources, Mar 2025] |
ENC1 Geneectodermal-neural cortex 1 (with BTB domain) This gene encodes a member of the kelch-related family of actin-binding proteins. The encoded protein plays a role in the oxidative stress response as a regulator of the transcription factor Nrf2, and expression of this gene may play a role in malignant transformation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2012] |
ARID5B GeneAT rich interactive domain 5B (MRF1-like) This gene encodes a member of the AT-rich interaction domain (ARID) family of DNA binding proteins. The encoded protein forms a histone H3K9Me2 demethylase complex with PHD finger protein 2 and regulates the transcription of target genes involved in adipogenesis and liver development. This gene also plays a role in cell growth and differentiation of B-lymphocyte progenitors, and single nucleotide polymorphisms in this gene are associated with acute lymphoblastic leukemia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2011] |
ARID5A GeneAT rich interactive domain 5A (MRF1-like) Members of the ARID protein family, including ARID5A, have diverse functions but all appear to play important roles in development, tissue-specific gene expression, and regulation of cell growth (Patsialou et al., 2005 [PubMed 15640446]).[supplied by OMIM, Mar 2008] |
TSPEAR Genethrombospondin-type laminin G domain and EAR repeats This gene encodes a protein that contains a N-terminal thrombospondin-type laminin G domain and several tandem arranged epilepsy-associated repeats (EARs). A mutation in this gene is the cause of autosomal recessive deafness-98. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012] |
ANKRD36BP2 Geneankyrin repeat domain 36B pseudogene 2 |
ANKRD45 Geneankyrin repeat domain 45 Involved in cell population proliferation. Located in cleavage furrow; cytoplasm; and midbody. [provided by Alliance of Genome Resources, Mar 2025] |
ANKRD44 Geneankyrin repeat domain 44 |
ANKRD46 Geneankyrin repeat domain 46 This gene encodes a protein containing multiple ankyrin repeats. Ankyrin domains function in protein-protein interactions in a variety of cellular processes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2012] |
ANKRD40 Geneankyrin repeat domain 40 |
ANKRD42 Geneankyrin repeat domain 42 Predicted to enable NF-kappaB binding activity. Predicted to act upstream of or within positive regulation of NF-kappaB transcription factor activity and positive regulation of cytokine production involved in inflammatory response. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ANKRD49 Geneankyrin repeat domain 49 Involved in positive regulation of DNA-templated transcription. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SH3GL1 GeneSH3-domain GRB2-like 1 This gene encodes a member of the endophilin family of Src homology 3 domain-containing proteins. The encoded protein is involved in endocytosis and may also play a role in the cell cycle. Overexpression of this gene may play a role in leukemogenesis, and the encoded protein has been implicated in acute myeloid leukemia as a fusion partner of the myeloid-lymphoid leukemia protein. Pseudogenes of this gene are located on the long arm of chromosomes 11 and 17. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011] |
SH3GL3 GeneSH3-domain GRB2-like 3 Enables identical protein binding activity. Predicted to be involved in synaptic vesicle uncoating. Predicted to be located in acrosomal vesicle and early endosome membrane. Predicted to be part of early endosome. Predicted to be active in several cellular components, including glutamatergic synapse; postsynaptic density, intracellular component; and postsynaptic endosome. [provided by Alliance of Genome Resources, Mar 2025] |
SH3GL2 GeneSH3-domain GRB2-like 2 Enables identical protein binding activity. Involved in negative regulation of blood-brain barrier permeability; negative regulation of gene expression; and negative regulation of protein phosphorylation. Located in perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100505995 Geneapoptosis-inducing, TAF9-like domain 1 pseudogene |
DNHD1 Genedynein heavy chain domain 1 Predicted to enable dynein intermediate chain binding activity; dynein light intermediate chain binding activity; and minus-end-directed microtubule motor activity. Involved in sperm flagellum assembly. Located in sperm flagellum. Implicated in spermatogenic failure 65. [provided by Alliance of Genome Resources, Mar 2025] |
ANKRD18CP Geneankyrin repeat domain 18C, pseudogene |
HMGN1P23 Genehigh mobility group nucleosome binding domain 1 pseudogene 23 |
HMGN1P22 Genehigh mobility group nucleosome binding domain 1 pseudogene 22 |
HMGN1P21 Genehigh mobility group nucleosome binding domain 1 pseudogene 21 |
HMGN1P27 Genehigh mobility group nucleosome binding domain 1 pseudogene 27 |
HMGN1P26 Genehigh mobility group nucleosome binding domain 1 pseudogene 26 |
HMGN1P25 Genehigh mobility group nucleosome binding domain 1 pseudogene 25 |
HMGN1P24 Genehigh mobility group nucleosome binding domain 1 pseudogene 24 |
HMGN1P29 Genehigh mobility group nucleosome binding domain 1 pseudogene 29 |
HMGN1P28 Genehigh mobility group nucleosome binding domain 1 pseudogene 28 |
WDR86 GeneWD repeat domain 86 |
LOC100132009 Genepentatricopeptide repeat domain 3 pseudogene |
LOC102724822 Genecarboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 2 pseudogene |
LOC100420587 GeneSHC SH2-domain binding protein 1 pseudogene |
CLEC16A GeneC-type lectin domain family 16, member A This gene encodes a member of the C-type lectin domain containing family. Single nucleotide polymorphisms in introns of this gene have been associated with diabetes mellitus, multiple sclerosis and rheumatoid arthritis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011] |
LOC646555 GeneAT rich interactive domain 3B pseudogene |
LARP4B GeneLa ribonucleoprotein domain family, member 4B This gene encodes a member of an evolutionarily conserved protein family implicated in RNA metabolism and translation. Members of this family are characterized by the presence of an La motif, which is often located adjacent to one or more RNA recognition motifs (RRM). Together, the two motifs constitute the functional region of the protein and enable its interaction with the RNA substrate. This protein family is divided into five sub-families: the genuine La proteins and four La-related protein (LARP) sub-families. The protein encoded by this gene belongs to LARP sub-family 4. It is a cytoplasmic protein that may play a stimulatory role in translation. [provided by RefSeq, Oct 2012] |
LARP4P GeneLa ribonucleoprotein domain family, member 4 pseudogene |
CLEC14A GeneC-type lectin domain family 14, member A This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signalling, glycoprotein turnover, and roles in inflammation and immune response. This family member plays a role in cell-cell adhesion and angiogenesis. It functions in filopodia formation, cell migration and tube formation. Due to its presence at higher levels in tumor endothelium than in normal tissue endothelium, it is considered to be a candidate for tumor vascular targeting. [provided by RefSeq, Jan 2012] |
NIFKP1 Genenucleolar protein interacting with the FHA domain of MKI67 pseudogene 1 |
NIFKP2 Genenucleolar protein interacting with the FHA domain of MKI67 pseudogene 2 |
NIFKP3 Genenucleolar protein interacting with the FHA domain of MKI67 pseudogene 3 |
NIFKP4 Genenucleolar protein interacting with the FHA domain of MKI67 pseudogene 4 |
NIFKP5 Genenucleolar protein interacting with the FHA domain of MKI67 pseudogene 5 |
NIFKP6 Genenucleolar protein interacting with the FHA domain of MKI67 pseudogene 6 |
NIFKP8 Genenucleolar protein interacting with the FHA domain of MKI67 pseudogene 8 |
TBC1D3 GeneTBC1 domain family, member 3 Predicted to enable GTPase activator activity. Predicted to be located in early endosome membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RASSF9 GeneRas association (RalGDS/AF-6) domain family (N-terminal) member 9 The protein encoded by this gene localizes to perinuclear endosomes. This protein associates with peptidylglycine alpha-amidating monooxygenase, and may be involved with the trafficking of this enzyme through secretory or endosomal pathways. [provided by RefSeq, Jul 2008] |
RASSF8 GeneRas association (RalGDS/AF-6) domain family (N-terminal) member 8 This gene encodes a member of the Ras-assocation domain family (RASSF) of tumor suppressor proteins. This gene is essential for maintaining adherens junction function in epithelial cells and has a role in epithelial cell migration. It is a lung tumor suppressor gene candidate. A chromosomal translocation t(12;22)(p11.2;q13.3) leading to the fusion of this gene and the FBLN1 gene is found in a complex type of synpolydactyly. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2011] |
RASSF1 GeneRas association (RalGDS/AF-6) domain family member 1 This gene encodes a protein similar to the RAS effector proteins. Loss or altered expression of this gene has been associated with the pathogenesis of a variety of cancers, which suggests the tumor suppressor function of this gene. The inactivation of this gene was found to be correlated with the hypermethylation of its CpG-island promoter region. The encoded protein was found to interact with DNA repair protein XPA. The protein was also shown to inhibit the accumulation of cyclin D1, and thus induce cell cycle arrest. Several alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported. [provided by RefSeq, May 2011] |
RASSF3 GeneRas association (RalGDS/AF-6) domain family member 3 The RAS oncogene (MIM 190020) is mutated in nearly one-third of all human cancers. Members of the RAS superfamily are plasma membrane GTP-binding proteins that modulate intracellular signal transduction pathways. A subfamily of RAS effectors, including RASSF3, share a RAS association (RA) domain.[supplied by OMIM, Jul 2003] |
RASSF2 GeneRas association (RalGDS/AF-6) domain family member 2 This gene encodes a protein that contains a Ras association domain. Similar to its cattle and sheep counterparts, this gene is located near the prion gene. Two alternatively spliced transcripts encoding the same isoform have been reported. [provided by RefSeq, Jul 2008] |
RASSF5 GeneRas association (RalGDS/AF-6) domain family member 5 This gene is a member of the Ras association domain family. It functions as a tumor suppressor, and is inactivated in a variety of cancers. The encoded protein localizes to centrosomes and microtubules, and associates with the GTP-activated forms of Ras, Rap1, and several other Ras-like small GTPases. The protein regulates lymphocyte adhesion and suppresses cell growth in response to activated Rap1 or Ras. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
RASSF4 GeneRas association (RalGDS/AF-6) domain family member 4 The function of this gene has not yet been determined but may involve a role in tumor suppression. Alternative splicing of this gene results in several transcript variants; however, most of the variants have not been fully described. [provided by RefSeq, Jul 2008] |
RASSF7 GeneRas association (RalGDS/AF-6) domain family (N-terminal) member 7 Predicted to be involved in apoptotic process and signal transduction. Located in centriolar satellite. [provided by Alliance of Genome Resources, Mar 2025] |
RASSF6 GeneRas association (RalGDS/AF-6) domain family member 6 This gene encodes a member of the Ras-association domain family (RASSF). Members of this family form the core of a highly conserved tumor suppressor network, the Salvador-Warts-Hippo (SWH) pathway. The protein encoded by this gene is a Ras effector protein that induces apoptosis. A genomic region containing this gene has been linked to susceptibility to viral bronchiolitis. Alternative splicing results in multiple transcript variants and protein isoforms. [provided by RefSeq, Jul 2012] |
TTC5 Genetetratricopeptide repeat domain 5 Enables ribosome binding activity. Involved in positive regulation of mRNA catabolic process. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
TTC4 Genetetratricopeptide repeat domain 4 This gene encodes a protein that contains tetratricopeptide (TPR) repeats, which often mediate protein-protein interactions and chaperone activity. The encoded protein interacts with heat shock proteins 70 and 90. Alternative splicing results in multiple transcript variants. Naturally-occuring readthrough transcription occurs from upstream gene MROH (maestro heat-like repeat family member 7) to this gene. [provided by RefSeq, Apr 2014] |
TTC6 Genetetratricopeptide repeat domain 6 |
TTC1 Genetetratricopeptide repeat domain 1 This gene encodes a protein that belongs to the tetratrico peptide repeat superfamily of proteins. The encoded protein plays a role in protein-protein interactions, and binds to the Galpha subunit of G protein-coupled receptors to activate the Ras signaling pathway. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013] |
TTC3 Genetetratricopeptide repeat domain 3 Enables ubiquitin-protein transferase activity. Involved in protein K48-linked ubiquitination and ubiquitin-dependent protein catabolic process. Located in cytosol; nucleolus; and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
TTC9 Genetetratricopeptide repeat domain 9 This gene encodes a protein that contains three tetratricopeptide repeats. The gene has been shown to be hormonally regulated in breast cancer cells and may play a role in cancer cell invasion and metastasis. [provided by RefSeq, Mar 2009] |
TTC8 Genetetratricopeptide repeat domain 8 This gene encodes a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities. Experimentation in non-human eukaryotes suggests that this gene is expressed in ciliated cells and that it is involved in the formation of cilia. A mutation in this gene has also been implicated in nonsyndromic retinitis pigmentosa. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014] |
LOC777650 GeneUBX domain protein 2B pseudogene |
LOC100420742 Genetetratricopeptide repeat domain 22 pseudogene |
TBC1D4 GeneTBC1 domain family, member 4 This gene is a member of the Tre-2/BUB2/CDC16 domain family. The protein encoded by this gene is a Rab-GTPase-activating protein, and contains two phopshotyrosine-binding domains (PTB1 and PTB2), a calmodulin-binding domain (CBD), a Rab-GTPase domain, and multiple AKT phosphomotifs. This protein is thought to play an important role in glucose homeostasis by regulating the insulin-dependent trafficking of the glucose transporter 4 (GLUT4), important for removing glucose from the bloodstream into skeletal muscle and fat tissues. Reduced expression of this gene results in an increase in GLUT4 levels at the plasma membrane, suggesting that this protein is important in intracellular retention of GLUT4 under basal conditions. When exposed to insulin, this protein is phosphorylated, dissociates from GLUT4 vesicles, resulting in increased GLUT4 at the cell surface, and enhanced glucose transport. Phosphorylation of this protein by AKT is required for proper translocation of GLUT4 to the cell surface. Individuals homozygous for a mutation in this gene are at higher risk for type 2 diabetes and have higher levels of circulating glucose and insulin levels after glucose ingestion. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2015] |
TBC1D5 GeneTBC1 domain family, member 5 Enables AP-2 adaptor complex binding activity and retromer complex binding activity. Involved in several processes, including macroautophagy; positive regulation of receptor internalization; and retrograde transport, endosome to Golgi. Located in several cellular components, including Atg1/ULK1 kinase complex; autophagosome; and cytoplasmic vesicle membrane. Part of retromer complex. [provided by Alliance of Genome Resources, Mar 2025] |
DAXX Genedeath-domain associated protein This gene encodes a multifunctional protein that resides in multiple locations in the nucleus and in the cytoplasm. It interacts with a wide variety of proteins, such as apoptosis antigen Fas, centromere protein C, and transcription factor erythroblastosis virus E26 oncogene homolog 1. In the nucleus, the encoded protein functions as a potent transcription repressor that binds to sumoylated transcription factors. Its repression can be relieved by the sequestration of this protein into promyelocytic leukemia nuclear bodies or nucleoli. This protein also associates with centromeres in G2 phase. In the cytoplasm, the encoded protein may function to regulate apoptosis. The subcellular localization and function of this protein are modulated by post-translational modifications, including sumoylation, phosphorylation and polyubiquitination. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2008] |
PTCD2 Genepentatricopeptide repeat domain 2 Enables RNA binding activity. Predicted to be involved in mitochondrion organization and regulation of mRNA processing. Predicted to act upstream of or within several processes, including liver development; muscle cell development; and ventricular cardiac muscle tissue morphogenesis. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
PTCD3 Genepentatricopeptide repeat domain 3 Enables rRNA binding activity and ribosomal small subunit binding activity. Involved in mitochondrial translation. Located in several cellular components, including cytosol; mitochondrial matrix; and nucleoplasm. Implicated in combined oxidative phosphorylation deficiency 51. [provided by Alliance of Genome Resources, Mar 2025] |
PTCD1 Genepentatricopeptide repeat domain 1 This gene encodes a mitochondrial protein that binds leucine tRNAs and other mitochondrial RNAs and plays a role in the regulation of translation. Increased expression of this gene results in decreased mitochondrial leucine tRNA levels. Naturally occurring read-through transcription exists between upstream ATP5J2 (ATP synthase, H+ transporting, mitochondrial Fo complex, subunit F2) and this gene. [provided by RefSeq, Aug 2015] |
LOC105371371 GeneSH3 domain-binding protein 1-like |
LOC724104 GeneSH3 domain binding glutamate-rich protein like 3 pseudogene |
GPANK1 GeneG patch domain and ankyrin repeats 1 This gene is located in a cluster of HLA-B-associated transcripts, which is included in the human major histocompatability complex III region. This gene encodes a protein which is thought to play a role in immunity. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Nov 2010] |
HMGN1P35 Genehigh mobility group nucleosome binding domain 1 pseudogene 35 |
LARP1 GeneLa ribonucleoprotein domain family, member 1 Enables eukaryotic initiation factor 4E binding activity; nucleic acid binding activity; and ribosomal small subunit binding activity. Involved in several processes, including TORC1 signaling; cellular response to rapamycin; and post-transcriptional regulation of gene expression. Located in TORC1 complex and cytoplasmic stress granule. [provided by Alliance of Genome Resources, Mar 2025] |
LARP4 GeneLa ribonucleoprotein domain family, member 4 Enables mRNA 3'-UTR binding activity and poly(A) binding activity. Involved in cytoskeleton organization; positive regulation of translation; and regulation of cell morphogenesis. Located in cytoplasmic stress granule and cytosolic small ribosomal subunit. [provided by Alliance of Genome Resources, Mar 2025] |
LARP6 GeneLa ribonucleoprotein domain family, member 6 Enables RNA binding activity and myosin binding activity. Involved in positive regulation of collagen biosynthetic process. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LARP7 GeneLa ribonucleoprotein domain family, member 7 This gene encodes a protein which is found in the 7SK snRNP (small nuclear ribonucleoprotein). This snRNP complex inhibits a cyclin-dependent kinase, positive transcription elongation factor b, which is required for paused RNA polymerase II at a promoter to begin transcription elongation. A pseudogene of this gene is located on chromosome 3. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2012] |
LOC653380 GeneTBC1 domain family member 3C-like protein ENSP00000341742 |
ANKRD11 Geneankyrin repeat domain 11 This locus encodes an ankryin repeat domain-containing protein. The encoded protein inhibits ligand-dependent activation of transcription. Mutations in this gene have been associated with KBG syndrome, which is characterized by macrodontia, distinctive craniofacial features, short stature, skeletal anomalies, global developmental delay, seizures and intellectual disability. Alternatively spliced transcript variants have been described. Related pseudogenes exist on chromosomes 2 and X. [provided by RefSeq, Jan 2012] |
TBC1D22B GeneTBC1 domain family, member 22B Enables 14-3-3 protein binding activity. Predicted to be active in Golgi apparatus. [provided by Alliance of Genome Resources, Mar 2025] |
TBC1D22A GeneTBC1 domain family, member 22A Enables 14-3-3 protein binding activity and protein homodimerization activity. Predicted to be active in Golgi apparatus. [provided by Alliance of Genome Resources, Mar 2025] |
SOWAHB Genesosondowah ankyrin repeat domain family member B |
LOC100420311 GeneTBC1 domain family, member 3 pseudogene |
AGAP11 Geneankyrin repeat and GTPase domain Arf GTPase activating protein 11 Predicted to enable GTPase activator activity and GTPase activity. [provided by Alliance of Genome Resources, Mar 2025] |
HILS1 Genehistone linker H1 domain, spermatid-specific 1, pseudogene This locus is the ortholog of a mouse protein-coding gene that displays characteristics of a linker histone and is expressed in nuclei of late maturing spermatids. The human locus is expressed; however, the open reading frame has been disrupted by a frameshift so it is unlikely to encode a functional protein. [provided by RefSeq, Oct 2008] |
LOC100288656 Geneankyrin repeat domain 20 family, member A2 pseudogene |
HMGN5 Genehigh mobility group nucleosome binding domain 5 This gene encodes a nuclear protein with similarities to the high mobility group proteins, HMG14 and HMG17, which suggests that this protein may function as a nucleosomal binding and transcriptional activating protein. [provided by RefSeq, Sep 2009] |
HMGN4 Genehigh mobility group nucleosomal binding domain 4 The protein encoded by this gene, a member of the HMGN protein family, is thought to reduce the compactness of the chromatin fiber in nucleosomes, thereby enhancing transcription from chromatin templates. [provided by RefSeq, Mar 2013] |
HMGN3 Genehigh mobility group nucleosomal binding domain 3 The protein encoded by this gene binds thyroid hormone receptor beta in the presence of thyroid hormone. The encoded protein, a member of the HMGN protein family, is thought to reduce the compactness of the chromatin fiber in nucleosomes, thereby enhancing transcription from chromatin templates. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. There is a related pseudogene on chromosome 1. [provided by RefSeq, Jan 2016] |
HMGN2 Genehigh mobility group nucleosomal binding domain 2 The protein encoded by this gene binds nucleosomal DNA and is associated with transcriptionally active chromatin. Along with a similar protein, HMGN1, the encoded protein may help maintain an open chromatin configuration around transcribable genes. The protein has also been found to have antimicrobial activity against bacteria, viruses and fungi. [provided by RefSeq, Oct 2014] |
HMGN1 Genehigh mobility group nucleosome binding domain 1 The protein encoded by this gene binds nucleosomal DNA and is associated with transcriptionally active chromatin. Along with a similar protein, HMG17, the encoded protein may help maintain an open chromatin configuration around transcribable genes. [provided by RefSeq, Aug 2011] |
CLEC5A GeneC-type lectin domain family 5, member A This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signalling, glycoprotein turnover, and roles in inflammation and immune response. The encoded type II transmembrane protein interacts with dnax-activation protein 12 and may play a role in cell activation. Alternative splice variants have been described but their full-length sequence has not been determined. [provided by RefSeq, Jul 2008] |
LOC391834 Geneankyrin repeat domain 49 pseudogene |
WDR90 GeneWD repeat domain 90 Involved in cilium assembly. Located in centriole and centrosome. [provided by Alliance of Genome Resources, Mar 2025] |
SHCBP1 GeneSHC SH2-domain binding protein 1 Predicted to enable SH2 domain binding activity. Predicted to be involved in fibroblast growth factor receptor signaling pathway and regulation of neural precursor cell proliferation. Predicted to be located in cytoplasm; midbody; and spindle. [provided by Alliance of Genome Resources, Mar 2025] |
EHBP1L1 GeneEH domain binding protein 1-like 1 Predicted to act upstream of or within several processes, including enucleation; erythrocyte differentiation; and mitochondrion localization. Located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100128335 GeneWD repeat domain 12 pseudogene |
ELK3 GeneELK3, ETS-domain protein (SRF accessory protein 2) This gene encodes a member of the ETS-domain transcription factor family and the ternary complex factor (TCF) subfamily. Proteins in this subfamily regulate transcription when recruited by serum response factor to bind to serum response elements. This protein is activated by signal-induced phosphorylation; studies in rodents suggest that it is a transcriptional inhibitor in the absence of Ras, but activates transcription when Ras is present. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015] |
ELK4 GeneELK4, ETS-domain protein (SRF accessory protein 1) This gene is a member of the Ets family of transcription factors and of the ternary complex factor (TCF) subfamily. Proteins of the TCF subfamily form a ternary complex by binding to the the serum response factor and the serum reponse element in the promoter of the c-fos proto-oncogene. The protein encoded by this gene is phosphorylated by the kinases, MAPK1 and MAPK8. Several transcript variants have been described for this gene. [provided by RefSeq, Jul 2008] |
POTEKP GenePOTE ankyrin domain family, member K, pseudogene Predicted to enable protein kinase binding activity. Predicted to be a structural constituent of postsynaptic actin cytoskeleton. Predicted to be involved in axonogenesis and cell motility. Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
HERC2P11 Genehect domain and RLD 2 pseudogene 11 |
HERC2P10 Genehect domain and RLD 2 pseudogene 10 |
CTDP1 GeneCTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) phosphatase, subunit 1 This gene encodes a protein which interacts with the carboxy-terminus of the RAP74 subunit of transcription initiation factor TFIIF, and functions as a phosphatase that processively dephosphorylates the C-terminus of POLR2A (a subunit of RNA polymerase II), making it available for initiation of gene expression. Mutations in this gene are associated with congenital cataracts, facial dysmorphism and neuropathy syndrome (CCFDN). Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Feb 2011] |
LOC391383 GeneWD repeat domain 4 pseudogene |
WDR5B GeneWD repeat domain 5B This intronless gene encodes a protein containing several WD40 repeats. WD repeats are approximately 30- to 40-amino acid domains containing several conserved residues, including a trp-asp at the C-terminal end. The encoded protein may mediate protein-protein interactions. [provided by RefSeq, Jul 2008] |
WDR55 GeneWD repeat domain 55 Predicted to be involved in rRNA processing. Located in nucleolus and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
WDR54 GeneWD repeat domain 54 Enables protein homodimerization activity. Involved in negative regulation of receptor internalization; regulation of MAPK cascade; and regulation of epidermal growth factor receptor signaling pathway. Located in intracellular membrane-bounded organelle and vesicle. [provided by Alliance of Genome Resources, Mar 2025] |
WDR59 GeneWD repeat domain 59 Predicted to enable signaling adaptor activity. Involved in cellular response to amino acid starvation and positive regulation of TORC1 signaling. Located in cytosol and lysosomal membrane. Part of GATOR2 complex. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100420563 GeneADAM metallopeptidase domain 20 pseudogene |
HERPUD1 Genehomocysteine-inducible, endoplasmic reticulum stress-inducible, ubiquitin-like domain member 1 The accumulation of unfolded proteins in the endoplasmic reticulum (ER) triggers the ER stress response. This response includes the inhibition of translation to prevent further accumulation of unfolded proteins, the increased expression of proteins involved in polypeptide folding, known as the unfolded protein response (UPR), and the destruction of misfolded proteins by the ER-associated protein degradation (ERAD) system. This gene may play a role in both UPR and ERAD. Its expression is induced by UPR and it has an ER stress response element in its promoter region while the encoded protein has an N-terminal ubiquitin-like domain which may interact with the ERAD system. This protein has been shown to interact with presenilin proteins and to increase the level of amyloid-beta protein following its overexpression. Alternative splicing of this gene produces multiple transcript variants encoding different isoforms. The full-length nature of all transcript variants has not been determined. [provided by RefSeq, Jan 2013] |
LOC100887081 Geneleukocyte immunoglobulin-like receptor, subfamily A (with TM domain), member 6 pseudogene |
TSC22D1 GeneTSC22 domain family, member 1 This gene encodes a member of the TSC22 domain family of leucine zipper transcription factors. The encoded protein is stimulated by transforming growth factor beta, and regulates the transcription of multiple genes including C-type natriuretic peptide. The encoded protein may play a critical role in tumor suppression through the induction of cancer cell apoptosis, and a single nucleotide polymorphism in the promoter of this gene has been associated with diabetic nephropathy. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2011] |
TSC22D3 GeneTSC22 domain family, member 3 This gene encodes the anti-inflammatory protein glucocorticoid (GC)-induced leucine zipper. Expression of this gene stimulated by glucocorticoids and interleukin 10 and it appears to play a key role in the anti-inflammatory and immunosuppressive effects of this steroid. This protein has also been shown to inhibit pro-inflammatory molecules including nuclear factor κB. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016] |
TSC22D2 GeneTSC22 domain family, member 2 Involved in negative regulation of cell cycle. [provided by Alliance of Genome Resources, Mar 2025] |
TSC22D4 GeneTSC22 domain family, member 4 TSC22D4 is a member of the TSC22 domain family of leucine zipper transcriptional regulators (see TSC22D3; MIM 300506) (Kester et al., 1999 [PubMed 10488076]; Fiorenza et al., 2001 [PubMed 11707329]).[supplied by OMIM, Mar 2008] |
IQSEC3P1 GeneIQ motif and Sec7 domain 3 pseudogene 1 |
IQSEC3P2 GeneIQ motif and Sec7 domain 3 pseudogene 2 |
IQSEC3P3 GeneIQ motif and Sec7 domain 3 pseudogene 3 |
ANKRD30BP1 Geneankyrin repeat domain 30B pseudogene 1 |
ANKRD30BP3 Geneankyrin repeat domain 30B pseudogene 3 |
ANKRD30BP2 Geneankyrin repeat domain 30B pseudogene 2 |
TTC3P1 Genetetratricopeptide repeat domain 3 pseudogene 1 |
ADAM24P GeneADAM metallopeptidase domain 24, pseudogene |
LOC100419616 Geneimpact RWD domain protein pseudogene |
LOC100302591 GeneTBC1 domain family member |
LOC574080 GeneCDGSH iron sulfur domain 1 pseudogene |
ANKRD16 Geneankyrin repeat domain 16 Predicted to be involved in tRNA modification. Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
ANKRD17 Geneankyrin repeat domain 17 The protein encoded by this gene belongs to the family of ankyrin repeat-containing proteins, and contains two distinct arrays of ankyrin repeats in its amino-terminal region, one with 15 ankyrin repeats, and the other with 10 ankyrin repeats. It also contains a nuclear export signal, nuclear localization signal, and a cyclin-binding RXL motif. Localization of this protein to the nucleus has been shown experimentally, and interactions between this protein and cyclin-dependent kinase 2 have been observed. It has been suggested that this protein plays a role in both DNA replication and in both anti-viral and anti-bacterial innate immune pathways. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015] |
ANKRD12 Geneankyrin repeat domain 12 This gene encodes a member of the ankyrin repeats-containing cofactor family. These proteins may inhibit the transcriptional activity of nuclear receptors through the recruitment of histone deacetylases. The encoded protein interacts with p160 coactivators and also represses transcription mediated by the coactivator alteration/deficiency in activation 3 (ADA3). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2011] |
ANKRD10 Geneankyrin repeat domain 10 Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ANKRD34A Geneankyrin repeat domain 34A Predicted to be active in pi-body. [provided by Alliance of Genome Resources, Mar 2025] |
ANKRD34C Geneankyrin repeat domain 34C Predicted to be active in pi-body. [provided by Alliance of Genome Resources, Mar 2025] |
ANKRD34B Geneankyrin repeat domain 34B Predicted to be located in cytoplasm and nucleus. Predicted to be active in pi-body. [provided by Alliance of Genome Resources, Mar 2025] |
MCCD1P2 Genemitochondrial coiled-coil domain 1 pseudogene 2 |
LOC100132651 GeneUBX domain protein 2A pseudogene |
SHCBP1L GeneSHC SH2-domain binding protein 1-like This gene encodes a Src homology 2 domain-binding protein 1-like protein. The encoded protein interacts with heat shock 70 kDa protein 2 and may be involved in maintaining spindle integrity during meiosis. This gene is located in region of chromoso0me 1 encompassing a prostate cancer susceptibility locus. [provided by RefSeq, Sep 2016] |
LOC100130331 GenePOTE ankyrin domain family, member F pseudogene |
ADAM20P3 GeneADAM metallopeptidase domain 20 pseudogene 3 |
ADAM20P2 GeneADAM metallopeptidase domain 20 pseudogene 2 |
ADAM20P1 GeneADAM metallopeptidase domain 20 pseudogene 1 |
SH3BGRL3 GeneSH3 domain binding glutamate-rich protein like 3 Involved in cytoskeleton organization. Located in cytosol; nuclear body; and ruffle membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SH3BGRL2 GeneSH3 domain binding glutamate-rich protein like 2 Predicted to enable SH3 domain binding activity. Located in nuclear membrane and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
CLEC11A GeneC-type lectin domain family 11, member A This gene encodes a member of the C-type lectin superfamily. The encoded protein is a secreted sulfated glycoprotein and functions as a growth factor for primitive hematopoietic progenitor cells. An alternative splice variant has been described but its biological nature has not been determined. [provided by RefSeq, Jul 2008] |
TROVE2 GeneTROVE domain family, member 2 Enables RNA binding activity. Involved in cellular response to interferon-alpha and regulation of gene expression. Located in cytosol and nuclear body. Part of ribonucleoprotein complex. [provided by Alliance of Genome Resources, Mar 2025] |
HMGN2P30 Genehigh mobility group nucleosomal binding domain 2 pseudogene 30 |
LOC100419319 GeneUBX domain protein 2A pseudogene |
NOL3 Genenucleolar protein 3 (apoptosis repressor with CARD domain) This gene encodes an anti-apoptotic protein that has been shown to down-regulate the enzyme activities of caspase 2, caspase 8 and tumor protein p53. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010] |
ADAM33 GeneADAM metallopeptidase domain 33 This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. This protein is a type I transmembrane protein implicated in asthma and bronchial hyperresponsiveness. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2013] |
DDR2 Genediscoidin domain receptor tyrosine kinase 2 This gene encodes a member of the discoidin domain receptor subclass of the receptor tyrosine kinase (RTKs) protein family. RTKs play a key role in the communication of cells with their microenvironment. The encoded protein is a collagen-induced receptor that activates signal transduction pathways involved in cell adhesion, proliferation, and extracellular matrix remodeling. This protein is expressed in numerous cell types and may alos be involved in wound repair and regulate tumor growth and invasiveness. Mutations in this gene are the cause of short limb-hand type spondylometaepiphyseal dysplasia. [provided by RefSeq, Aug 2017] |
DDR1 Genediscoidin domain receptor tyrosine kinase 1 Receptor tyrosine kinases play a key role in the communication of cells with their microenvironment. These kinases are involved in the regulation of cell growth, differentiation and metabolism. The protein encoded by this gene belongs to a subfamily of tyrosine kinase receptors with homology to Dictyostelium discoideum protein discoidin I in their extracellular domain, and that are activated by various types of collagen. Expression of this protein is restricted to epithelial cells, particularly in the kidney, lung, gastrointestinal tract, and brain. In addition, it has been shown to be significantly overexpressed in several human tumors. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Feb 2011] |
MBD3L1 Genemethyl-CpG binding domain protein 3-like 1 This gene encodes a protein that is related to methyl-CpG-binding proteins but lacks the methyl-CpG binding domain. The protein is localized to discrete areas in the nucleus, and expression appears to be restricted to round spermatids, suggesting that the protein plays a role in the postmeiotic stages of male germ cell development. [provided by RefSeq, Jul 2008] |
MBD3L2 Genemethyl-CpG binding domain protein 3-like 2 This gene encodes a protein that is related to methyl-CpG-binding proteins but lacks the methyl-CpG binding domain. The protein has been found in germ cell tumors and some somatic tissues. [provided by RefSeq, Jul 2008] |
MBD3L3 Genemethyl-CpG binding domain protein 3-like 3 Predicted to enable methyl-CpG binding activity. Predicted to be involved in DNA methylation-dependent constitutive heterochromatin formation and negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
MBD3L4 Genemethyl-CpG binding domain protein 3-like 4 This gene encodes a member of a family of proteins that are related to methyl-CpG-binding proteins but lack the methyl-CpG binding domain. There is no definitive support for transcription of this locus, and the transcript structure is inferred from other family members. [provided by RefSeq, Aug 2009] |
MBD3L5 Genemethyl-CpG binding domain protein 3-like 5 Predicted to enable methyl-CpG binding activity. Predicted to be involved in DNA methylation-dependent constitutive heterochromatin formation and negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SH3BP5L GeneSH3-binding domain protein 5-like Enables guanyl-nucleotide exchange factor activity. Predicted to be involved in intracellular signal transduction. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
TES Genetestin LIM domain protein Cancer-associated chromosomal changes often involve regions containing fragile sites. This gene maps to a common fragile site on chromosome 7q31.2 designated FRA7G. This gene is similar to mouse Testin, a testosterone-responsive gene encoding a Sertoli cell secretory protein containing three LIM domains. LIM domains are double zinc-finger motifs that mediate protein-protein interactions between transcription factors, cytoskeletal proteins and signaling proteins. This protein is a negative regulator of cell growth and may act as a tumor suppressor. This scaffold protein may also play a role in cell adhesion, cell spreading and in the reorganization of the actin cytoskeleton. Multiple protein isoforms are encoded by transcript variants of this gene.[provided by RefSeq, Aug 2023] |
LOC441784 GeneTBC1 domain family, member 25 pseudogene |
HMGN2P26 Genehigh mobility group nucleosomal binding domain 2 pseudogene 26 |
HMGN2P27 Genehigh mobility group nucleosomal binding domain 2 pseudogene 27 |
HMGN2P22 Genehigh mobility group nucleosomal binding domain 2 pseudogene 22 |
HMGN2P23 Genehigh mobility group nucleosomal binding domain 2 pseudogene 23 |
HMGN2P20 Genehigh mobility group nucleosomal binding domain 2 pseudogene 20 |
HMGN2P21 Genehigh mobility group nucleosomal binding domain 2 pseudogene 21 |
LMO1 GeneLIM domain only 1 (rhombotin 1) This locus encodes a transcriptional regulator that contains two cysteine-rich LIM domains but lacks a DNA-binding domain. LIM domains may play a role in protein interactions; thus the encoded protein may regulate transcription by competitively binding to specific DNA-binding transcription factors. Alterations at this locus have been associated with acute lymphoblastic T-cell leukemia. Chromosomal rearrangements have been observed between this locus and at least two loci, the delta subunit of the T-cell antigen receptor gene and the LIM domain binding 1 gene. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jul 2012] |
LMO2 GeneLIM domain only 2 (rhombotin-like 1) LMO2 encodes a cysteine-rich, two LIM-domain protein that is required for yolk sac erythropoiesis. The LMO2 protein has a central and crucial role in hematopoietic development and is highly conserved. The LMO2 transcription start site is located approximately 25 kb downstream from the 11p13 T-cell translocation cluster (11p13 ttc), where a number T-cell acute lymphoblastic leukemia-specific translocations occur. Alternative splicing results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Nov 2008] |
LMO3 GeneLIM domain only 3 (rhombotin-like 2) The protein encoded by this gene belongs to the rhombotin family of cysteine-rich LIM domain oncogenes. This gene is predominantly expressed in the brain. Related family members, LMO1 and LMO2 on chromosome 11, have been reported to be involved in chromosomal translocations in T-cell leukemia. Many alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2011] |
LMO4 GeneLIM domain only 4 This gene encodes a cysteine-rich protein that contains two LIM domains but lacks a DNA-binding homeodomain. The encoded protein may play a role as a transcriptional regulator or as an oncogene. [provided by RefSeq, Aug 2008] |
LMO7 GeneLIM domain 7 This gene encodes a protein containing a calponin homology (CH) domain, a PDZ domain, and a LIM domain, and may be involved in protein-protein interactions. Several alternatively spliced transcript variants encoding different isoforms have been found for this gene, however, the full-length nature of some variants is not known. [provided by RefSeq, Jan 2009] |
LOC100130607 GeneWD repeat domain 4 pseudogene |
ANKRD18B Geneankyrin repeat domain 18B |
ANKRD18A Geneankyrin repeat domain 18A |
CLEC19A GeneC-type lectin domain family 19, member A Predicted to enable carbohydrate binding activity. Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Mar 2025] |
HMGN2P7 Genehigh mobility group nucleosomal binding domain 2 pseudogene 7 |
HMGN2P6 Genehigh mobility group nucleosomal binding domain 2 pseudogene 6 |
HMGN2P5 Genehigh mobility group nucleosomal binding domain 2 pseudogene 5 |
HMGN2P3 Genehigh mobility group nucleosomal binding domain 2 pseudogene 3 |
HMGN2P2 Genehigh mobility group nucleosomal binding domain 2 pseudogene 2 |
HMGN2P1 Genehigh mobility group nucleosomal binding domain 2 pseudogene 1 |
HMGN2P9 Genehigh mobility group nucleosomal binding domain 2 pseudogene 9 |
RNPS1 GeneRNA binding protein S1, serine-rich domain This gene encodes a protein that is part of a post-splicing multiprotein complex involved in both mRNA nuclear export and mRNA surveillance. mRNA surveillance detects exported mRNAs with truncated open reading frames and initiates nonsense-mediated mRNA decay (NMD). When translation ends upstream from the last exon-exon junction, this triggers NMD to degrade mRNAs containing premature stop codons. This protein binds to the mRNA and remains bound after nuclear export, acting as a nucleocytoplasmic shuttling protein. This protein contains many serine residues. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2013] |
RASSF10 GeneRas association (RalGDS/AF-6) domain family (N-terminal) member 10 Predicted to be involved in positive regulation of neural precursor cell proliferation and positive regulation of neurogenesis. Predicted to be located in centrosome; cytosol; and spindle pole. [provided by Alliance of Genome Resources, Mar 2025] |
LIMA1 GeneLIM domain and actin binding 1 This gene encodes a cytoskeleton-associated protein that inhibits actin filament depolymerization and cross-links filaments in bundles. It is downregulated in some cancer cell lines. Alternatively spliced transcript variants encoding different isoforms have been described for this gene, and expression of some of the variants maybe independently regulated. [provided by RefSeq, Aug 2011] |
EHBP1 GeneEH domain binding protein 1 This gene encodes an Eps15 homology domain binding protein. The encoded protein may play a role in endocytic trafficking. A single nucleotide polymorphism in this gene is associated with an aggressive form of prostate cancer. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010] |
ANKRD20A7P Geneankyrin repeat domain 20 family, member A7, pseudogene |
LOC751837 GeneWD repeat domain 57 (U5 snRNP specific) pseudogene |
G3BP2 GeneGTPase activating protein (SH3 domain) binding protein 2 Enables molecular condensate scaffold activity. Involved in positive regulation of stress granule assembly; protein homooligomerization; and stress granule assembly. Located in cytoplasmic stress granule and cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
PDLIM4 GenePDZ and LIM domain 4 Enables alpha-actinin binding activity; protein homodimerization activity; and protein phosphatase binding activity. Involved in actin cytoskeleton organization. Located in several cellular components, including lamellipodium; perinuclear region of cytoplasm; and stress fiber. Part of filamentous actin. Implicated in osteoporosis. [provided by Alliance of Genome Resources, Mar 2025] |
PDLIM5 GenePDZ and LIM domain 5 This gene encodes a member of a family of proteins that possess a 100-amino acid PDZ domain at the N terminus and one to three LIM domains at the C-terminus. This family member functions as a scaffold protein that tethers protein kinases to the Z-disk in striated muscles. It is thought to function in cardiomyocyte expansion and in restraining postsynaptic growth of excitatory synapses. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jan 2012] |
PDLIM7 GenePDZ and LIM domain 7 (enigma) The protein encoded by this gene is representative of a family of proteins composed of conserved PDZ and LIM domains. LIM domains are proposed to function in protein-protein recognition in a variety of contexts including gene transcription and development and in cytoskeletal interaction. The LIM domains of this protein bind to protein kinases, whereas the PDZ domain binds to actin filaments. The gene product is involved in the assembly of an actin filament-associated complex essential for transmission of ret/ptc2 mitogenic signaling. The biological function is likely to be that of an adapter, with the PDZ domain localizing the LIM-binding proteins to actin filaments of both skeletal muscle and nonmuscle tissues. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Jul 2008] |
PDLIM1 GenePDZ and LIM domain 1 This gene encodes a member of the enigma protein family. The protein contains two protein interacting domains, a PDZ domain at the amino terminal end and one to three LIM domains at the carboxyl terminal. It is a cytoplasmic protein associated with the cytoskeleton. The protein may function as an adapter to bring other LIM-interacting proteins to the cytoskeleton. Pseudogenes associated with this gene are located on chromosomes 3, 14 and 17. [provided by RefSeq, Oct 2012] |
PDLIM2 GenePDZ and LIM domain 2 (mystique) This gene encodes a member of the ALP subfamily of PDZ-LIM domain proteins. The encoded protein suppresses anchorage-dependent growth and promotes cell migration and adhesion through interactions with the actin cytoskeleton via the PDZ domain. The encoded protein is also a putative tumor suppressor protein, and decreased expression of this gene is associated with several malignancies including breast cancer and adult T-cell leukemia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2011] |
PDLIM3 GenePDZ and LIM domain 3 The protein encoded by this gene contains a PDZ domain and a LIM domain, indicating that it may be involved in cytoskeletal assembly. In support of this, the encoded protein has been shown to bind the spectrin-like repeats of alpha-actinin-2 and to colocalize with alpha-actinin-2 at the Z lines of skeletal muscle. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. Aberrant alternative splicing of this gene may play a role in myotonic dystrophy. [provided by RefSeq, Apr 2012] |
TTC39C Genetetratricopeptide repeat domain 39C Predicted to be involved in cilium assembly and otolith morphogenesis. [provided by Alliance of Genome Resources, Mar 2025] |
TTC39B Genetetratricopeptide repeat domain 39B Predicted to be involved in several processes, including cholesterol homeostasis; negative regulation of cholesterol storage; and regulation of cholesterol efflux. [provided by Alliance of Genome Resources, Mar 2025] |
TTC39A Genetetratricopeptide repeat domain 39A Located in centrosome. [provided by Alliance of Genome Resources, Mar 2025] |
WDR60 GeneWD repeat domain 60 This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD) and may facilitate the formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes including cell cycle progression, signal transduction, apoptosis, and gene regulation. The encoded protein contains four WD repeats and may play a role in the formation of cilia. Mutations in this gene have been associated with short-rib polydactyly and Jeune syndromes. [provided by RefSeq, Mar 2014] |
ANKRD20A14P Geneankyrin repeat domain 20 family, member A14, pseudogene |
LOC100533628 GeneWD repeat domain 75 pseudogene |
TBC1D3P4 GeneTBC1 domain family, member 3 pseudogene 4 |
TTC21A Genetetratricopeptide repeat domain 21A Involved in flagellated sperm motility and spermatid development. Predicted to be located in cilium. Predicted to be part of intraciliary transport particle A. Implicated in spermatogenic failure 37. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100289360 GeneHIG1 hypoxia inducible domain family, member 2A pseudogene |
EGFL7 GeneEGF-like-domain, multiple 7 This gene encodes a secreted endothelial cell protein that contains two epidermal growth factor-like domains. The encoded protein may play a role in regulating vasculogenesis. This protein may be involved in the growth and proliferation of tumor cells. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012] |
EGFL6 GeneEGF-like-domain, multiple 6 This gene encodes a member of the epidermal growth factor (EGF) repeat superfamily. Members of this superfamily are characterized by the presence of EGF-like repeats and are often involved in the regulation of cell cycle, proliferation, and developmental processes. The gene product contains a signal peptide, suggesting that it is secreted; an EGF repeat region consisting of 4 complete EGF-like repeats and 1 partial EGF-like repeat, 3 of which have a calcium-binding consensus sequence; an arg-gly-asp integrin association motif; and a MAM domain, which is believed to have an adhesive function. This gene is expressed early during development, and its expression has been detected in lung and meningioma tumors. [provided by RefSeq, Jul 2008] |
EGFL8 GeneEGF-like-domain, multiple 8 Predicted to enable signaling receptor binding activity. Predicted to be involved in vasculogenesis. Predicted to be active in cell surface and extracellular region. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100124373 Geneankyrin repeat domain 39 pseudogene |
ANKRD26 Geneankyrin repeat domain 26 This gene encodes a protein containing N-terminal ankyrin repeats which function in protein-protein interactions. Mutations in this gene are associated with autosomal dominant thrombocytopenia-2. Pseudogenes of this gene are found on chromosome 7, 10, 13 and 16. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011] |
ANKRD24 Geneankyrin repeat domain 24 Predicted to enable actin binding activity. Predicted to be involved in auditory receptor cell stereocilium organization and sensory perception of sound. Predicted to be located in plasma membrane. Predicted to be part of stereocilium. [provided by Alliance of Genome Resources, Mar 2025] |
ANKRD23 Geneankyrin repeat domain 23 This gene is a member of the muscle ankyrin repeat protein (MARP) family and encodes a protein with four tandem ankyrin-like repeats. The protein is localized to the nucleus, functioning as a transcriptional regulator. Expression of this protein is induced during recovery following starvation. [provided by RefSeq, Jul 2008] |
ANKRD22 Geneankyrin repeat domain 22 |
ANKRD29 Geneankyrin repeat domain 29 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419906 Geneankyrin repeat domain 11 pseudogene |
LOC729859 GeneWW domain binding protein 1 pseudogene |
ADAM32 GeneADAM metallopeptidase domain 32 This gene encodes a member of the disintegrin family of membrane-anchored proteins that play a role in diverse biological processes such as brain development, fertilization, tumor development and inflammation. This gene is predominantly expressed in the testis. The encoded protein undergoes proteolytic processing to generate a mature polypeptide comprised of an metalloprotease, disintegrin and epidermal growth factor-like domains. This gene is located in a cluster of other disintegrin and metallopeptidase family genes on chromosome 8. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Sep 2015] |
LOC105375817 GenePOTE ankyrin domain family member A-like |
MADD GeneMAP-kinase activating death domain Tumor necrosis factor alpha (TNF-alpha) is a signaling molecule that interacts with one of two receptors on cells targeted for apoptosis. The apoptotic signal is transduced inside these cells by cytoplasmic adaptor proteins. The protein encoded by this gene is a death domain-containing adaptor protein that interacts with the death domain of TNF-alpha receptor 1 to activate mitogen-activated protein kinase (MAPK) and propagate the apoptotic signal. It is membrane-bound and expressed at a higher level in neoplastic cells than in normal cells. Several transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008] |
EPAS1 Geneendothelial PAS domain protein 1 This gene encodes a transcription factor involved in the induction of genes regulated by oxygen, which is induced as oxygen levels fall. The encoded protein contains a basic-helix-loop-helix domain protein dimerization domain as well as a domain found in proteins in signal transduction pathways which respond to oxygen levels. Mutations in this gene are associated with erythrocytosis familial type 4. [provided by RefSeq, Nov 2009] |
HMGN1P14 Genehigh mobility group nucleosome binding domain 1 pseudogene 14 |
HMGN1P15 Genehigh mobility group nucleosome binding domain 1 pseudogene 15 |
HMGN1P19 Genehigh mobility group nucleosome binding domain 1 pseudogene 19 |
WDR87 GeneWD repeat domain 87 |
WDR81 GeneWD repeat domain 81 This gene encodes a multi-domain transmembrane protein which is predominantly expressed in the brain and is thought to play a role in endolysosomal trafficking. Mutations in this gene are associated with an autosomal recessive form of a syndrome exhibiting cerebellar ataxia, cognitive disability, and disequilibrium (CAMRQ2). Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2017] |
WDR82 GeneWD repeat domain 82 TMEM113 (WDR82) is a component of the mammalian SET1A (MIM 611052)/SET1B (MIM 611055) histone H3-Lys4 methyltransferase complexes (Lee and Skalnik, 2005 [PubMed 16253997]; Lee et al., 2007 [PubMed 17355966]).[supplied by OMIM, Jul 2010] |
WDR83 GeneWD repeat domain 83 This gene encodes a member of the WD-40 protein family. The protein is proposed to function as a molecular scaffold for various multimeric protein complexes. The protein associates with several components of the extracellular signal-regulated kinase (ERK) pathway, and promotes ERK activity in response to serum or other signals. The protein also interacts with egl nine homolog 3 (EGLN3, also known as PHD3) and regulates expression of hypoxia-inducible factor 1, and has been purified as part of the spliceosome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009] |
WDR88 GeneWD repeat domain 88 |
WDR89 GeneWD repeat domain 89 Predicted to act upstream of or within corpus callosum development and ventricular system development. [provided by Alliance of Genome Resources, Mar 2025] |
CARD18 Genecaspase recruitment domain family, member 18 Enables CARD domain binding activity and caspase binding activity. Involved in inhibition of cysteine-type endopeptidase activity and negative regulation of interleukin-1 beta production. Part of protein-containing complex. [provided by Alliance of Genome Resources, Mar 2025] |
CARD10 Genecaspase recruitment domain family, member 10 The caspase recruitment domain (CARD) is a protein module that consists of 6 or 7 antiparallel alpha helices. It participates in apoptosis signaling through highly specific protein-protein homophilic interactions. Like several other CARD proteins, CARD10 belongs to the membrane-associated guanylate kinase (MAGUK) family and activates NF-kappa-B (NFKB; see MIM 164011) through BCL10 (MIM 603517) (Wang et al., 2001 [PubMed 11259443]).[supplied by OMIM, Mar 2008] |
CARD17 Genecaspase recruitment domain family, member 17 Enables caspase binding activity and identical protein binding activity. Involved in cellular response to lipopolysaccharide and negative regulation of interleukin-1 beta production. Part of protein-containing complex. [provided by Alliance of Genome Resources, Mar 2025] |
CARD16 Genecaspase recruitment domain family, member 16 Enables several functions, including CARD domain binding activity; cysteine-type endopeptidase inhibitor activity; and enzyme binding activity. Involved in cellular response to lipopolysaccharide; regulation of gene expression; and regulation of signal transduction. Part of protease inhibitor complex. [provided by Alliance of Genome Resources, Mar 2025] |
CARD14 Genecaspase recruitment domain family, member 14 This gene encodes a caspase recruitment domain-containing protein that is a member of the membrane-associated guanylate kinase (MAGUK) family of proteins. Members of this protein family are scaffold proteins that are involved in a diverse array of cellular processes including cellular adhesion, signal transduction and cell polarity control. This protein has been shown to specifically interact with BCL10, a protein known to function as a positive regulator of cell apoptosis and NF-kappaB activation. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Apr 2012] |
TIFAB GeneTRAF-interacting protein with forkhead-associated domain, family member B Predicted to enable deubiquitinase activator activity. Involved in several processes, including cochlea morphogenesis; cranial nerve development; and hard palate morphogenesis. [provided by Alliance of Genome Resources, Mar 2025] |
ERDA1 Geneexpanded repeat domain, CAG/CTG 1 |
STAM2 Genesignal transducing adaptor molecule (SH3 domain and ITAM motif) 2 The protein encoded by this gene is closely related to STAM, an adaptor protein involved in the downstream signaling of cytokine receptors, both of which contain a SH3 domain and the immunoreceptor tyrosine-based activation motif (ITAM). Similar to STAM, this protein acts downstream of JAK kinases, and is phosphorylated in response to cytokine stimulation. This protein and STAM thus are thought to exhibit compensatory effects on the signaling pathway downstream of JAK kinases upon cytokine stimulation. [provided by RefSeq, Jul 2008] |
ARID3A GeneAT rich interactive domain 3A (BRIGHT-like) This gene encodes a member of the ARID (AT-rich interaction domain) family of DNA binding proteins. It was found by homology to the Drosophila dead ringer gene, which is important for normal embryogenesis. Other ARID family members have roles in embryonic patterning, cell lineage gene regulation, cell cycle control, transcriptional regulation, and possibly in chromatin structure modification. [provided by RefSeq, Jul 2008] |
ARID3C GeneAT rich interactive domain 3C (BRIGHT-like) This gene is a member of the ARID (AT-rich interaction domain) family of proteins. The ARID domain is a helix-turn-helix motif-based DNA-binding domain. ARID family members have roles in embryonic patterning, cell lineage gene regulation, cell cycle control, transcriptional regulation and possibly in chromatin structure modification. [provided by RefSeq, Jul 2008] |
ARID3B GeneAT rich interactive domain 3B (BRIGHT-like) This gene encodes a member of the ARID (AT-rich interaction domain) family of DNA-binding proteins. The encoded protein is homologous with two proteins that bind to the retinoblastoma gene product, and also with the mouse Bright and Drosophila dead ringer proteins. A pseudogene on chromosome 1p31 exists for this gene. Members of the ARID family have roles in embryonic patterning, cell lineage gene regulation, cell cycle control, transcriptional regulation and possibly in chromatin structure modification. [provided by RefSeq, Jul 2008] |
CLEC12B GeneC-type lectin domain family 12, member B Enables protein phosphatase binding activity and signaling receptor inhibitor activity. Involved in several processes, including melanocyte proliferation; natural killer cell inhibitory signaling pathway; and regulation of signal transduction. Located in external side of plasma membrane. Part of protein-containing complex. [provided by Alliance of Genome Resources, Mar 2025] |
CLEC12A GeneC-type lectin domain family 12, member A This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signaling, glycoprotein turnover, and roles in inflammation and immune response. The protein encoded by this gene is a negative regulator of granulocyte and monocyte function. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. This gene is closely linked to other CTL/CTLD superfamily members in the natural killer gene complex region on chromosome 12p13. [provided by RefSeq, May 2011] |
LOC100130891 GenePDZ and LIM domain 7 (enigma) pseudogene |
WIPI2 GeneWD repeat domain, phosphoinositide interacting 2 WD40 repeat proteins are key components of many essential biologic functions. They regulate the assembly of multiprotein complexes by presenting a beta-propeller platform for simultaneous and reversible protein-protein interactions. Members of the WIPI subfamily of WD40 repeat proteins, such as WIPI2, have a 7-bladed propeller structure and contain a conserved motif for interaction with phospholipids (Proikas-Cezanne et al., 2004 [PubMed 15602573]).[supplied by OMIM, Mar 2008] |
WIPI1 GeneWD repeat domain, phosphoinositide interacting 1 This gene encodes a WD40 repeat protein. Members of the WD40 repeat family are key components of many essential biologic functions. They regulate the assembly of multiprotein complexes by presenting a beta-propeller platform for simultaneous and reversible protein-protein interactions. Members of the WIPI subfamily of WD40 repeat proteins have a 7-bladed propeller structure and contain a conserved motif for interaction with phospholipids. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016] |
LILRA6 Geneleukocyte immunoglobulin-like receptor, subfamily A (with TM domain), member 6 Predicted to be involved in immune response-regulating signaling pathway. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LILRA4 Geneleukocyte immunoglobulin-like receptor, subfamily A (with TM domain), member 4 This gene encodes an immunoglobulin-like cell surface protein that is expressed predominantly on plasmacytoid dendritic cells (PDCs) and modulates the function of these cells in the immune response. Expression of this gene is downregulated by interleukin 3 (IL3). This gene is one of a cluster of highly related genes located at chromosomal region 19q13.4. [provided by RefSeq, Jan 2015] |
LILRA5 Geneleukocyte immunoglobulin-like receptor, subfamily A (with TM domain), member 5 The protein encoded by this gene is a member of the leukocyte immunoglobulin-like receptor (LIR) family. LIR family members are known to have activating and inibitory functions in leukocytes. Crosslink of this receptor protein on the surface of monocytes has been shown to induce calcium flux and secretion of several proinflammatory cytokines, which suggests the roles of this protein in triggering innate immune responses. This gene is one of the leukocyte receptor genes that form a gene cluster on the chromosomal region 19q13.4. Four alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008] |
LILRA2 Geneleukocyte immunoglobulin-like receptor, subfamily A (with TM domain), member 2 This gene encodes a member of a family of immunoreceptors that are expressed predominantly on monocytes and B cells, and at lower levels on dendritic cells and natural killer cells. The encoded protein is an activating receptor that inhibits dendritic cell differentiation and antigen presentation and suppresses innate immune response. Alternatively spliced transcript variants encoding different isoforms have been found. This gene is located in a cluster of related genes on chromosome 19 and there is a pseudogene for this gene on chromosome 3. [provided by RefSeq, Mar 2014] |
LILRA3 Geneleukocyte immunoglobulin-like receptor, subfamily A (without TM domain), member 3 This gene encodes a member of a family of immunoreceptors that are expressed predominantly in monocytes and B cells, and at lower levels in dendritic cells and natural killer cells. The encoded protein lacks the transmembrane region found in other members of this family. It acts as a soluble receptor for class I major histocompatibility complex (MHC) antigens. Alternatively spliced transcript variants encoding different isoforms have been found. This gene is located in a cluster of related genes on chromosome 19 and is polymorphic in human populations, with many individuals containing a deletion of this genomic region. [provided by RefSeq, Mar 2014] |
LILRA1 Geneleukocyte immunoglobulin-like receptor, subfamily A (with TM domain), member 1 This gene encodes an activating member of the leukocyte immunoglobulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein is predominantly expressed in B cells, interacts with major histocompatibility complex class I ligands, and contributes to the regulation of immune responses. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2013] |
TTC39DP Genetetratricopeptide repeat domain 39D, pseudogene |
WDR82P1 GeneWD repeat domain 82 pseudogene 1 |
TBC1D3K GeneTBC1 domain family, member 3K Predicted to enable GTPase activator activity. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
ELF1 GeneE74-like factor 1 (ets domain transcription factor) This gene encodes an E26 transformation-specific related transcription factor. The encoded protein is primarily expressed in lymphoid cells and acts as both an enhancer and a repressor to regulate transcription of various genes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2009] |
ELF3 GeneE74-like factor 3 (ets domain transcription factor, epithelial-specific ) Enables DNA-binding transcription activator activity, RNA polymerase II-specific and sequence-specific double-stranded DNA binding activity. Involved in inflammatory response; negative regulation of DNA-templated transcription; and positive regulation of transcription by RNA polymerase II. Located in Golgi apparatus; cytosol; and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
ELF2 GeneE74-like factor 2 (ets domain transcription factor) Enables DNA-binding transcription factor activity, RNA polymerase II-specific and sequence-specific double-stranded DNA binding activity. Involved in negative regulation of DNA-templated transcription; positive regulation of DNA-templated transcription; and regulation of transcription by RNA polymerase II. Located in cytosol and nuclear body. [provided by Alliance of Genome Resources, Mar 2025] |
ELF5 GeneE74-like factor 5 (ets domain transcription factor) This gene encodes an epithelium-specific ETS family transcription factor. In addition to its role in regulating the later stages of terminal differentiation of keratinocytes, it appears to regulate a number of epithelium-specific genes found in tissues containing glandular epithelium such as salivary gland and prostate. It has very low affinity to DNA due to its negative regulatory domain at the amino terminus. This gene has been implicated as a tumor suppressive transcription factor in breast cancer. [provided by RefSeq, May 2022] |
ELF4 GeneE74-like factor 4 (ets domain transcription factor) The protein encoded by this gene is a transcriptional activator that binds and activates the promoters of the CSF2, IL3, IL8, and PRF1 genes. The encoded protein is involved in natural killer cell development and function, innate immunity, and induction of cell cycle arrest in naive CD8+ cells. Two transcript variants encoding the same protein have been found for this gene.[provided by RefSeq, Jan 2010] |
SBK2 GeneSH3 domain binding kinase family, member 2 Predicted to enable MAP kinase kinase activity. Predicted to be involved in MAPK cascade. [provided by Alliance of Genome Resources, Mar 2025] |
SBK3 GeneSH3 domain binding kinase family, member 3 Predicted to enable protein serine/threonine kinase activity. Predicted to be involved in chromatin remodeling. [provided by Alliance of Genome Resources, Mar 2025] |
CISD2 GeneCDGSH iron sulfur domain 2 The protein encoded by this gene is a zinc finger protein that localizes to the endoplasmic reticulum. The encoded protein binds an iron/sulfur cluster and may be involved in calcium homeostasis. Defects in this gene are a cause of Wolfram syndrome 2. [provided by RefSeq, Mar 2011] |
CISD3 GeneCDGSH iron sulfur domain 3 CISD3 is a member of the CDGSH domain-containing family, which may play a role in regulating electron transport and oxidative phosphorylation (Wiley et al., 2007 [PubMed 17376863]).[supplied by OMIM, Apr 2008] |
CISD1 GeneCDGSH iron sulfur domain 1 This gene encodes a protein with a CDGSH iron-sulfur domain and has been shown to bind a redox-active [2Fe-2S] cluster. The encoded protein has been localized to the outer membrane of mitochondria and is thought to play a role in regulation of oxidation. Genes encoding similar proteins are located on chromosomes 4 and 17, and a pseudogene of this gene is located on chromosome 2. [provided by RefSeq, Feb 2012] |
LOC100420648 GeneDer1-like domain family, member 2 pseudogene |
ADAM30 GeneADAM metallopeptidase domain 30 This gene encodes a member of the ADAM (a disintegrin and metalloprotease domain) family. Members of this family are membrane-anchored proteins structurally related to snake venom disintegrins, and have been implicated in a variety of biological processes involving cell-cell and cell-matrix interactions, including fertilization, muscle development, and neurogenesis. This gene is testis-specific and contains a polymorphic region, resulting in isoforms with varying numbers of C-terminal repeats. [provided by RefSeq, Jul 2008] |
ADAM3B GeneADAM metallopeptidase domain 3B (pseudogene) |
ADAM3A GeneADAM metallopeptidase domain 3A (pseudogene) Predicted to be involved in fertilization and flagellated sperm motility. Predicted to act upstream of or within binding activity of sperm to zona pellucida; gene expression; and regulation of macromolecule metabolic process. Predicted to be located in membrane raft; plasma membrane; and sperm head. Predicted to be part of protein-containing complex. Predicted to be active in cell surface. Implicated in brain glioma and conjunctival squamous cell carcinoma. [provided by Alliance of Genome Resources, Mar 2025] |
HMGN1P18 Genehigh mobility group nucleosome binding domain 1 pseudogene 18 |
EFHB GeneEF-hand domain family, member B Enables calcium ion sensor activity. Involved in regulation of calcineurin-NFAT signaling cascade and regulation of store-operated calcium entry. Located in axonemal microtubule. [provided by Alliance of Genome Resources, Mar 2025] |
RALGPS2 GeneRal GEF with PH domain and SH3 binding motif 2 Predicted to enable guanyl-nucleotide exchange factor activity. Predicted to be involved in Ras protein signal transduction. Predicted to be located in cytoplasm. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RALGPS1 GeneRal GEF with PH domain and SH3 binding motif 1 Enables guanyl-nucleotide exchange factor activity. Involved in regulation of Ral protein signal transduction. Predicted to be located in cytoplasm. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
TMEM9B GeneTMEM9 domain family, member B Involved in positive regulation of canonical NF-kappaB signal transduction. Located in early endosome membrane and lysosomal membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100421684 Genetetratricopeptide repeat domain 34 pseudogene |
LOC100421685 Genetetratricopeptide repeat domain 34 pseudogene |
APITD1 Geneapoptosis-inducing, TAF9-like domain 1 This gene was identified in the neuroblastoma tumor suppressor candidate region on chromosome 1p36. It contains a TFIID-31 domain, similar to that found in TATA box-binding protein-associated factor, TAF(II)31, which is required for p53-mediated transcription activation. This gene was expressed at very low levels in neuroblastoma tumors, and was shown to reduce cell growth in neuroblastoma cells, suggesting that it may have a role in a cell death pathway. The protein is a component of multiple complexes, including the Fanconi anemia (FA) core complex, the APITD1/CENPS complex, and the CENPA-CAD (nucleosome distal) complex. Known functions include an involvement with chromatin associations of the FA core complex, and a role in the stable assembly of the outer kinetochore. Alternative splicing of this gene results in multiple transcript variants. Naturally occurring read-through transcripts also exist between this gene and the downstream cortistatin (CORT) gene, as represented in GeneID:100526739. An APITD1-related pseudogene has been identified on chromosome 7. [provided by RefSeq, Nov 2010] |
WDR35 GeneWD repeat domain 35 This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. Two patients with Sensenbrenner syndrome / cranioectodermal dysplasia (CED) were identified with mutations in this gene, consistent with a possible ciliary function.[provided by RefSeq, Sep 2010] |
WDR34 GeneWD repeat domain 34 This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Defects in this gene are a cause of short-rib thoracic dysplasia 11 with or without polydactyly. [provided by RefSeq, Mar 2014] |
WDR37 GeneWD repeat domain 37 This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. [provided by RefSeq, Jul 2008] |
WDR36 GeneWD repeat domain 36 This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Mutations in this gene have been associated with adult-onset primary open-angle glaucoma (POAG). [provided by RefSeq, Jul 2008] |
WDR31 GeneWD repeat domain 31 This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008] |
WDR33 GeneWD repeat domain 33 This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This gene is highly expressed in testis and the protein is localized to the nucleus. This gene may play important roles in the mechanisms of cytodifferentiation and/or DNA recombination. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
WDR38 GeneWD repeat domain 38 Predicted to act upstream of or within hematopoietic progenitor cell differentiation. [provided by Alliance of Genome Resources, Mar 2025] |
MBD5 Genemethyl-CpG binding domain protein 5 This gene encodes a member of the methyl-CpG-binding domain (MBD) family. The MBD consists of about 70 residues and is the minimal region required for a methyl-CpG-binding protein binding specifically to methylated DNA. In addition to the MBD domain, this protein contains a PWWP domain (Pro-Trp-Trp-Pro motif), which consists of 100-150 amino acids and is found in numerous proteins that are involved in cell division, growth and differentiation. Mutations in this gene cause an autosomal dominant type of cognitive disability. The encoded protein interacts with the polycomb repressive complex PR-DUB which catalyzes the deubiquitination of a lysine residue of histone 2A. Haploinsufficiency of this gene is associated with a syndrome involving microcephaly, intellectual disabilities, severe speech impairment, and seizures. Alternatively spliced transcript variants have been found, but their full-length nature is not determined. [provided by RefSeq, Jul 2017] |
MBD4 Genemethyl-CpG binding domain protein 4 The protein encoded by this gene is a member of a family of nuclear proteins related by the presence of a methyl-CpG binding domain (MBD). These proteins are capable of binding specifically to methylated DNA, and some members can also repress transcription from methylated gene promoters. This protein contains an MBD domain at the N-terminus that functions both in binding to methylated DNA and in protein interactions and a C-terminal mismatch-specific glycosylase domain that is involved in DNA repair. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2013] |
MBD6 Genemethyl-CpG binding domain protein 6 Enables chromatin binding activity. Located in chromocenter; fibrillar center; and nucleoplasm. Implicated in autism spectrum disorder. [provided by Alliance of Genome Resources, Mar 2025] |
MBD1 Genemethyl-CpG binding domain protein 1 The protein encoded by this gene is a member of a family of nuclear proteins related by the presence of a methyl-CpG binding domain (MBD). These proteins are capable of binding specifically to methylated DNA, and some members can also repress transcription from methylated gene promoters. This protein contains multiple domains: MBD at the N-terminus that functions both in binding to methylated DNA and in protein interactions; several CXXC-type zinc finger domains that mediate binding to non-methylated CpG dinucleotides; transcriptional repression domain (TRD) at the C-terminus that is involved in transcription repression and in protein interactions. Numerous alternatively spliced transcript variants encoding different isoforms have been noted for this gene.[provided by RefSeq, Feb 2011] |
MBD3 Genemethyl-CpG binding domain protein 3 DNA methylation is the major modification of eukaryotic genomes and plays an essential role in mammalian development. This gene belongs to a family of nuclear proteins which are characterized by the presence of a methyl-CpG binding domain (MBD). The encoded protein is a subunit of the NuRD, a multisubunit complex containing nucleosome remodeling and histone deacetylase activities. Unlike the other family members, the encoded protein is not capable of binding to methylated DNA. The protein mediates the association of metastasis-associated protein 2 with the core histone deacetylase complex. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013] |
MBD2 Genemethyl-CpG binding domain protein 2 DNA methylation is the major modification of eukaryotic genomes and plays an essential role in mammalian development. Human proteins MECP2, MBD1, MBD2, MBD3, and MBD4 comprise a family of nuclear proteins related by the presence in each of a methyl-CpG binding domain (MBD). Each of these proteins, with the exception of MBD3, is capable of binding specifically to methylated DNA. MECP2, MBD1 and MBD2 can also repress transcription from methylated gene promoters. The protein encoded by this gene may function as a mediator of the biological consequences of the methylation signal. It is also reported that the this protein functions as a demethylase to activate transcription, as DNA methylation causes gene silencing. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2011] |
HIGD1AP18 GeneHIG1 hypoxia inducible domain family, member 1A pseudogene 18 |
HIGD1AP10 GeneHIG1 hypoxia inducible domain family, member 1A pseudogene 10 |
HIGD1AP11 GeneHIG1 hypoxia inducible domain family, member 1A pseudogene 11 |
HIGD1AP12 GeneHIG1 hypoxia inducible domain family, member 1A pseudogene 12 |
HIGD1AP14 GeneHIG1 hypoxia inducible domain family, member 1A pseudogene 14 |
HIGD1AP15 GeneHIG1 hypoxia inducible domain family, member 1A pseudogene 15 |
HIGD1AP16 GeneHIG1 hypoxia inducible domain family, member 1A pseudogene 16 |
HIGD1AP17 GeneHIG1 hypoxia inducible domain family, member 1A pseudogene 17 |
STAC GeneSH3 and cysteine rich domain Predicted to enable transmembrane transporter binding activity. Predicted to be involved in positive regulation of protein localization to plasma membrane; positive regulation of voltage-gated calcium channel activity; and skeletal muscle contraction. Predicted to act upstream of or within cellular response to heat; muscle contraction; and regulation of voltage-gated calcium channel activity. Predicted to be located in cytoplasmic side of plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
STAM Genesignal transducing adaptor molecule (SH3 domain and ITAM motif) 1 This gene encodes a member of the signal-transducing adaptor molecule family. These proteins mediate downstream signaling of cytokine receptors and also play a role in ER to Golgi trafficking by interacting with the coat protein II complex. The encoded protein also associates with hepatocyte growth factor-regulated substrate to form the endosomal sorting complex required for transport-0 (ESCRT-0), which sorts ubiquitinated membrane proteins to the ESCRT-1 complex for lysosomal degradation. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Feb 2011] |
BID GeneBH3 interacting domain death agonist This gene encodes a death agonist that heterodimerizes with either agonist BAX or antagonist BCL2, and thus regulate apoptosis. The encoded protein is a member of the BCL-2 family of cell death regulators. It is a mediator of mitochondrial damage induced by caspase-8 (CASP8); CASP8 cleaves this encoded protein, and the COOH-terminal part translocates to mitochondria where it triggers cytochrome c release. Multiple alternatively spliced transcript variants have been found. [provided by RefSeq, Aug 2020] |
NXPE1 Geneneurexophilin and PC-esterase domain family, member 1 Predicted to be located in extracellular region and membrane. [provided by Alliance of Genome Resources, Mar 2025] |
NXPE2 Geneneurexophilin and PC-esterase domain family, member 2 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
NXPE3 Geneneurexophilin and PC-esterase domain family, member 3 This gene encodes a member of the neurexophilin family of neuropeptide-like glycoproteins. The encoded protein contains a variable N-terminal domain, a highly conserved neurexophilin and PC-esterase (NXPE) central domain, a short linker region, and a cysteine-rich C-terminal domain. This protein binds alpha neurexins, a group of presynaptic transmembrane receptors that promote adhesion between dendrites and axons. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017] |
NXPE4 Geneneurexophilin and PC-esterase domain family, member 4 Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025] |
LOC645763 Geneintersectin 1 (SH3 domain protein) pseudogene |
CLEC3B GeneC-type lectin domain family 3, member B Enables calcium ion binding activity; heparin binding activity; and kringle domain binding activity. Involved in bone mineralization. Located in cytoplasm; extracellular space; and granular component. Implicated in osteoarthritis and retinal macular dystrophy 4. [provided by Alliance of Genome Resources, Mar 2025] |
CLEC3A GeneC-type lectin domain family 3, member A Predicted to enable carbohydrate binding activity. Predicted to be involved in ossification. Predicted to be located in extracellular region. Predicted to be active in extracellular space. [provided by Alliance of Genome Resources, Mar 2025] |
HIGD1AP13 GeneHIG1 hypoxia inducible domain family, member 1A pseudogene 13 |
LOC643348 Geneankyrin repeat domain 26 pseudogene |
ANKRD57P1 Geneankyrin repeat domain 57 pseudogene 1 |
ARID2 GeneAT rich interactive domain 2 (ARID, RFX-like) This gene encodes a member of the AT-rich interactive domain (ARID)-containing family of DNA-binding proteins. Members of the ARID family have roles in embryonic patterning, cell lineage gene regulation, cell cycle control, transcriptional regulation and chromatin structure modification. This protein functions as a subunit of the polybromo- and BRG1-associated factor or PBAF (SWI/SNF-B) chromatin remodeling complex which facilitates ligand-dependent transcriptional activation by nuclear receptors. Mutations in this gene are associated with hepatocellular carcinomas. A pseudogene of this gene is found on chromosome1. [provided by RefSeq, Dec 2016] |
LOC646377 Genepyrin and HIN domain family, member 1 pseudogene |
WBP1LP2 GeneWW domain binding protein 1-like pseudogene 2 |
ANKRD20A11P Geneankyrin repeat domain 20 family, member A11, pseudogene |
ANKRD36P1 Geneankyrin repeat domain 36 pseudogene 1 |
FARP2 GeneFERM, RhoGEF and pleckstrin domain protein 2 Enables guanyl-nucleotide exchange factor activity. Acts upstream of or within Rac protein signal transduction and neuron remodeling. Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
FARP1 GeneFERM, RhoGEF (ARHGEF) and pleckstrin domain protein 1 (chondrocyte-derived) This gene encodes a protein containing a FERM (4.2, exrin, radixin, moesin) domain, a Dbl homology domain, and two pleckstrin homology domains. These domains are found in guanine nucleotide exchange factors and proteins that link the cytoskeleton to the cell membrane. The encoded protein functions in neurons to promote dendritic growth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2013] |
PHLPP2 GenePH domain and leucine rich repeat protein phosphatase 2 Predicted to enable protein serine/threonine phosphatase activity. Predicted to be involved in intracellular signal transduction. Located in several cellular components, including intercellular bridge; mitotic spindle; and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
SETDB1 GeneSET domain, bifurcated 1 This gene encodes a histone methyltransferase which regulates histone methylation, gene silencing, and transcriptional repression. This gene has been identified as a target for treatment in Huntington Disease, given that gene silencing and transcription dysfunction likely play a role in the disease pathogenesis. Alternatively spliced transcript variants of this gene have been described.[provided by RefSeq, Jun 2011] |
SETDB2 GeneSET domain, bifurcated 2 This gene encodes a member of a family of proteins that contain a methyl-CpG-binding domain (MBD) and a SET domain and function as histone methyltransferases. This protein is recruited to heterochromatin and plays a role in the regulation of chromosome segregation. This region is commonly deleted in chronic lymphocytic leukemia. Naturally-occuring readthrough transcription occurs from this gene to the downstream PHF11 (PHD finger protein 11) gene. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016] |
LOC100420408 GeneTBC1 domain family, member 29 pseudogene |
CGREF1 Genecell growth regulator with EF-hand domain 1 Predicted to enable calcium ion binding activity. Predicted to be involved in negative regulation of cell population proliferation. Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Mar 2025] |
ARID4A GeneAT rich interactive domain 4A (RBP1-like) The protein encoded by this gene is a ubiquitously expressed nuclear protein. It binds directly, with several other proteins, to retinoblastoma protein (pRB) which regulates cell proliferation. pRB represses transcription by recruiting the encoded protein. This protein, in turn, serves as a bridging molecule to recruit HDACs and, in addition, provides a second HDAC-independent repression function. The encoded protein possesses transcriptional repression activity. Multiple alternatively spliced transcripts have been observed for this gene, although not all transcript variants have been fully described. [provided by RefSeq, Jul 2008] |
ARID4B GeneAT rich interactive domain 4B (RBP1-like) This gene encodes a protein with sequence similarity to retinoblastoma-binding protein-1. The encoded protein is a subunit of the histone deacetylase-dependant SIN3A transcriptional corepressor complex, which functions in diverse cellular processes including proliferation, differentiation, apoptosis, oncogenesis, and cell fate determination. The gene product is recognized by IgG antibody isolated from a breast cancer patient and appears to be a molecular marker associated with a broad range of human malignancies. Alternate transcriptional splice variants encoding different isoforms have been characterized. [provided by RefSeq, Jul 2008] |
UBXN8 GeneUBX domain protein 8 p97 or VCP (valosin-containing protein) is a versatile ATPase complex, and many cofactors are required for the p97 functional diversity. This gene encodes one of the p97 cofactors. This cofactor is a transmembrane protein and localized in the endoplasmic reticulum (ER) membrane. It tethers p97 to the ER membrane via its UBX domain. The association of this cofactor with p97 facilitates efficient ER-associated degradation of misfolded proteins. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Aug 2013] |
UBXN4 GeneUBX domain protein 4 UBXD2 is an integral membrane protein of the endoplasmic reticulum (ER) that binds valosin-containing protein (VCP; MIM 601023) and promotes ER-associated protein degradation (ERAD) (Liang et al., 2006 [PubMed 16968747]).[supplied by OMIM, Mar 2008] |
UBXN6 GeneUBX domain protein 6 Involved in ERAD pathway; endosome to lysosome transport via multivesicular body sorting pathway; and macroautophagy. Located in bounding membrane of organelle and cytosol. Part of endosome and protein-containing complex. [provided by Alliance of Genome Resources, Mar 2025] |
UBXN7 GeneUBX domain protein 7 Enables RNA polymerase II-specific DNA-binding transcription factor binding activity; ubiquitin binding activity; and ubiquitin protein ligase binding activity. Predicted to be involved in proteasome-mediated ubiquitin-dependent protein catabolic process. Located in nucleoplasm. Part of VCP-NPL4-UFD1 AAA ATPase complex. [provided by Alliance of Genome Resources, Mar 2025] |
UBXN1 GeneUBX domain protein 1 Enables several functions, including enzyme binding activity; polyubiquitin modification-dependent protein binding activity; and proteasome regulatory particle binding activity. Involved in negative regulation of protein metabolic process. Located in cytosol; endoplasmic reticulum; and nucleoplasm. Part of VCP-NPL4-UFD1 AAA ATPase complex. [provided by Alliance of Genome Resources, Mar 2025] |
SH3GL1P2 GeneSH3-domain GRB2-like 1 pseudogene 2 |
SH3GL1P3 GeneSH3-domain GRB2-like 1 pseudogene 3 |
SH3GL1P1 GeneSH3-domain GRB2-like 1 pseudogene 1 |
SPRTN GeneSprT-like N-terminal domain The protein encoded by this gene may play a role in DNA repair during replication of damaged DNA. This protein recruits valosin containing protein (p97) to stalled DNA replication forks where it may prevent excessive translesional DNA synthesis and limit the number of DNA-damage induced mutations. It may also be involved in replication-related G2/M-checkpoint regulation. Deficiency of a similar protein in mouse causes chromosomal instability and progeroid phenotypes. Mutations in this gene have been associated with Ruijs-Aalfs syndrome (RJALS). Alternatively spliced transcript variants have been identified. [provided by RefSeq, Mar 2015] |
LOC100128428 GeneUBX domain protein 2A pseudogene |
POTEB3 GenePOTE ankyrin domain family, member B3 |
HMGN2P28 Genehigh mobility group nucleosomal binding domain 2 pseudogene 28 |
HMGN2P29 Genehigh mobility group nucleosomal binding domain 2 pseudogene 29 |
TIFA GeneTRAF-interacting protein with forkhead-associated domain This gene encodes an adapter protein involved in adaptive and innate immunity. This protein includes a forkhead-associated (FHA) domain that specifically binds to phosphorylated serine and threonine residues. In response to bacterial infection, the encoded host cell protein undergoes an intermolecular interaction between the FHA domain and a phosphorylated threonine that leads to protein oligomerization and stimulation of the NF-kappa B and other downstream signaling pathways. This protein exhibits reduced expression in hepatocellular carcinoma and may suppress hepatocellular carcinoma progression. This protein may also play a role in the DNA damage response. [provided by RefSeq, Jun 2018] |
HMGN2P25 Genehigh mobility group nucleosomal binding domain 2 pseudogene 25 |
SH3TC2 GeneSH3 domain and tetratricopeptide repeats 2 This gene encodes a protein with two N-terminal Src homology 3 (SH3) domains and 10 tetratricopeptide repeat (TPR) motifs, and is a member of a small gene family. The gene product has been proposed to be an adapter or docking molecule. Mutations in this gene result in autosomal recessive Charcot-Marie-Tooth disease type 4C, a childhood-onset neurodegenerative disease characterized by demyelination of motor and sensory neurons. [provided by RefSeq, Jul 2008] |
SH3TC1 GeneSH3 domain and tetratricopeptide repeats 1 |
LOC100287033 GeneTSC22 domain family, member 3 pseudogene |
HMGN2P24 Genehigh mobility group nucleosomal binding domain 2 pseudogene 24 |
LOC100422645 GeneCTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase 2 pseudogene |
HMGN1P30 Genehigh mobility group nucleosome binding domain 1 pseudogene 30 |
HMGN1P31 Genehigh mobility group nucleosome binding domain 1 pseudogene 31 |
HMGN1P32 Genehigh mobility group nucleosome binding domain 1 pseudogene 32 |
HMGN1P36 Genehigh mobility group nucleosome binding domain 1 pseudogene 36 |
HMGN1P37 Genehigh mobility group nucleosome binding domain 1 pseudogene 37 |
HMGN1P38 Genehigh mobility group nucleosome binding domain 1 pseudogene 38 |
ANKRD20A19P Geneankyrin repeat domain 20 family, member A19, pseudogene |
ANKRD28 Geneankyrin repeat domain 28 Predicted to be located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC101060389 GeneTBC1 domain family member-like Predicted to enable GTPase activator activity. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
CLEC4GP1 GeneC-type lectin domain family 4, member G pseudogene 1 |
LOC100422338 GeneGTPase activating protein (SH3 domain) binding protein 1 pseudogene |
LARP7P4 GeneLa ribonucleoprotein domain family, member 7 pseudogene 4 |
CLEC17A GeneC-type lectin domain family 17, member A Enables D-mannose binding activity; fucose binding activity; and identical protein binding activity. Predicted to be involved in immune response. Located in cell surface. [provided by Alliance of Genome Resources, Mar 2025] |
PHLDB1 Genepleckstrin homology-like domain, family B, member 1 Involved in regulation of embryonic development; regulation of epithelial to mesenchymal transition; and regulation of microtubule cytoskeleton organization. Located in several cellular components, including basal cortex; cytosol; and intercellular bridge. Implicated in osteogenesis imperfecta. [provided by Alliance of Genome Resources, Mar 2025] |
PHLDB2 Genepleckstrin homology-like domain, family B, member 2 Enables cadherin binding activity. Involved in several processes, including negative regulation of focal adhesion assembly; regulation of cytoskeleton organization; and regulation of embryonic development. Located in several cellular components, including basal cortex; cytoskeleton; and focal adhesion. [provided by Alliance of Genome Resources, Mar 2025] |
PHLDB3 Genepleckstrin homology-like domain, family B, member 3 Enables enzyme binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100419957 Geneankyrin repeat domain 57 pseudogene |
LOC100288966 GenePOTE ankyrin domain family member D-like |
ANKRD20A20P Geneankyrin repeat domain 20 family, member A20, pseudogene |
EOGT GeneEGF domain-specific O-linked N-acetylglucosamine (GlcNAc) transferase This gene encodes an enzyme that acts in the lumen of the endoplasmic reticulum to catalyze the transfer of N-acetylglucosamine to serine or threonine residues of extracellular-targeted proteins. This enzyme modifies proteins containing eukaryotic growth factor (EGF)-like domains, including the Notch receptor, thereby regulating developmental signalling. Mutations in this gene have been observed in individuals with Adams-Oliver syndrome 4. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2015] |
ANKRD18DP Geneankyrin repeat domain 18D, pseudogene |
NSUN5P2 GeneNOP2/Sun domain family, member 5 pseudogene 2 This locus represents a transcribed pseudogene of a nearby locus on chromosome 7, which encodes a putative methyltransferase. There is also a third closely related pseudogene locus in this region. There is extensive alternative splicing at this locus. [provided by RefSeq, Jul 2013] |
NSUN5P1 GeneNOP2/Sun domain family, member 5 pseudogene 1 This locus represents a transcribed pseudogene of a nearby locus on chromosome 7, which encodes a putative methyltransferase. There is also a third closely related pseudogene locus in this region. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013] |
LOC100419174 GeneWD repeat domain 12 pseudogene |
LOC100379290 Genetransmembrane and coiled-coil domain family 1 pseudogene |
LOC100129078 Genetetratricopeptide repeat domain 5 pseudogene |
LOC729458 Genemethyl-CpG-binding domain protein 3-like 2 Predicted to enable methyl-CpG binding activity. Predicted to be involved in DNA methylation-dependent constitutive heterochromatin formation and negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
HMGN2P44 Genehigh mobility group nucleosomal binding domain 2 pseudogene 44 |
HMGN2P45 Genehigh mobility group nucleosomal binding domain 2 pseudogene 45 |
HMGN2P46 Genehigh mobility group nucleosomal binding domain 2 pseudogene 46 Predicted to enable chromatin binding activity. Predicted to be involved in chromatin organization. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
HMGN2P40 Genehigh mobility group nucleosomal binding domain 2 pseudogene 40 |
HMGN2P41 Genehigh mobility group nucleosomal binding domain 2 pseudogene 41 |
HMGN2P42 Genehigh mobility group nucleosomal binding domain 2 pseudogene 42 |
HMGN2P43 Genehigh mobility group nucleosomal binding domain 2 pseudogene 43 |
WBP1L GeneWW domain binding protein 1-like Predicted to enable ubiquitin protein ligase binding activity. Predicted to be involved in CXCL12-activated CXCR4 signaling pathway. Predicted to act upstream of or within hemopoiesis and positive regulation of protein ubiquitination. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
WBP11 GeneWW domain binding protein 11 This gene encodes a nuclear protein, which colocalizes with mRNA splicing factors and intermediate filament-containing perinuclear networks. This protein has 95% amino acid sequence identity to the mouse Wbp11 protein. It contains two proline-rich regions that bind to the WW domain of Npw38, a nuclear protein, and thus this protein is also called Npw38-binding protein NpwBP. The Npw38-NpwBP complex may function as a component of an mRNA factory in the nucleus. [provided by RefSeq, Jul 2008] |
LGSN Genelengsin, lens protein with glutamine synthetase domain This gene encodes a protein with similarity to the GS I members of the glutamine synthetase superfamily. The encoded protein is referred to as a pseudo-glutamine synthetase because it has no glutamine synthesis activity and may function as a chaperone protein. This protein is localized to the lens and may be associated with cataract disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2009] |
ANKRD36BP1 Geneankyrin repeat domain 36B pseudogene 1 |
MPDZ Genemultiple PDZ domain protein The protein encoded by this gene has multiple PDZ domains, which are hallmarks of protein-protein interactions. The encoded protein is known to interact with the HTR2C receptor and may cause it to clump at the cell surface. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2015] |
LOC100130680 Geneankyrin repeat domain 49 pseudogene |
WDR93 GeneWD repeat domain 93 Predicted to be involved in electron transport chain. Predicted to be part of respiratory chain complex I. [provided by Alliance of Genome Resources, Mar 2025] |
PYROXD2 Genepyridine nucleotide-disulphide oxidoreductase domain 2 Predicted to enable oxidoreductase activity. Involved in mitochondrion organization. Located in mitochondrial matrix. [provided by Alliance of Genome Resources, Mar 2025] |
PYROXD1 Genepyridine nucleotide-disulphide oxidoreductase domain 1 This gene encodes a nuclear-cytoplasmic pyridine nucleotide-disulphide reductase (PNDR). PNDRs are flavoproteins that catalyze the pyridine nucleotide-dependent reduction of thiol residues in other proteins. The encoded protein belongs to the class I pyridine nucleotide-disulphide oxidoreductase family but lacks the C-terminal dimerization domain found in other family members and instead has a C-terminal nitrile reductase domain. It localizes to the nucleus and to striated sarcomeric compartments. Naturally occurring mutations in this gene cause early-onset myopathy with internalized nuclei and myofibrillar disorganization. A pseudogene of this gene has been defined on chromosome 11. [provided by RefSeq, Apr 2017] |
LOC100128050 GeneWD repeat domain 77 pseudogene |
LOC100128056 GeneCTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase 2 pseudogene |
TTC7B Genetetratricopeptide repeat domain 7B Involved in phosphatidylinositol phosphate biosynthetic process and protein localization to plasma membrane. Located in cytosol and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
TTC7A Genetetratricopeptide repeat domain 7A This gene encodes a protein containing tetratricopeptide repeats. Mutations in this gene disrupt intestinal development and can cause early onset inflammatory bowel disease and intestinal atresia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014] |
ANKRD13D Geneankyrin repeat domain 13 family, member D The protein encoded by this gene is a member of the ankyrin repeat domain (ANKRD) 13 family, which currently consists of four proteins containing ubiquitin-interacting motifs. These proteins are integral membrane proteins that bind specifically to Lys-63-linked ubiquitin chains on membrane-bound proteins, targeting those proteins for rapid internalization. [provided by RefSeq, Dec 2016] |
ANKRD13A Geneankyrin repeat domain 13A Enables ubiquitin-modified protein reader activity. Involved in negative regulation of protein localization to endosome and negative regulation of receptor internalization. Located in late endosome; perinuclear region of cytoplasm; and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
KDR Genekinase insert domain receptor Vascular endothelial growth factor (VEGF) is a major growth factor for endothelial cells. This gene encodes one of the two receptors of the VEGF. This receptor, known as kinase insert domain receptor, is a type III receptor tyrosine kinase. It functions as the main mediator of VEGF-induced endothelial proliferation, survival, migration, tubular morphogenesis and sprouting. The signalling and trafficking of this receptor are regulated by multiple factors, including Rab GTPase, P2Y purine nucleotide receptor, integrin alphaVbeta3, T-cell protein tyrosine phosphatase, etc.. Mutations of this gene are implicated in infantile capillary hemangiomas. [provided by RefSeq, May 2009] |
STAC2 GeneSH3 and cysteine rich domain 2 This gene encodes a protein containing an SH3 domain and a zinc finger domain. The encoded protein has been shown to regulate calcium channel inactivation in a human cell line. Reduced expression of this gene has been observed in human heart failure. [provided by RefSeq, May 2017] |
STAC3 GeneSH3 and cysteine rich domain 3 The protein encoded by this gene is a component of the excitation-contraction coupling machinery of muscles. This protein is a member of the Stac gene family and contains an N-terminal cysteine-rich domain and two SH3 domains. Mutations in this gene are a cause of Native American myopathy. [provided by RefSeq, Nov 2013] |
TBC1D1 GeneTBC1 (tre-2/USP6, BUB2, cdc16) domain family, member 1 TBC1D1 is the founding member of a family of proteins sharing a 180- to 200-amino acid TBC domain presumed to have a role in regulating cell growth and differentiation. These proteins share significant homology with TRE2 (USP6; MIM 604334), yeast Bub2, and CDC16 (MIM 603461) (White et al., 2000 [PubMed 10965142]).[supplied by OMIM, Mar 2008] |
TBC1D2 GeneTBC1 domain family, member 2 Enables GTPase activator activity and cadherin binding activity. Involved in positive regulation of GTPase activity. Located in several cellular components, including cytoplasmic vesicle; cytosol; and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
TBC1D7 GeneTBC1 domain family, member 7 This gene encodes a member of the TBC-domain containing protein family. The encoded protein functions as a subunit of the tuberous sclerosis TSC1-TSC2 complex which plays a role in the regulation of cellular growth and differentiation. Mutations in this gene have been associated with autosomal recessive megalencephaly. Alternative splicing results in multiple transcript variants. Naturally occurring readthrough transcription occurs between this locus and downstream LOC100130357. [provided by RefSeq, Jan 2016] |
CLEC6A GeneC-type lectin domain family 6, member A The protein encoded by this gene is a type II membrane receptor with an extracellular C-type lectin-like domain fold. The extracellular portion binds structures with a high mannose content and has been shown to recognize several pathogens, including C. elegans, S. cerevisiae, M. tuberculosis, C. neoformans, and house dust mite. When stimulated, the encoded protein initiates signalling through the CARD9-Bcl10-Malt1 pathway, leading to the induction of cytokines. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015] |
LOC100421202 GeneC-type lectin domain family 1, member B pseudogene |
LOC139952 GeneLIM domain kinase 2 pseudogene |
ANKRD20A5P Geneankyrin repeat domain 20 family, member A5, pseudogene |
SH3BP4 GeneSH3-domain binding protein 4 This gene encodes a protein with 3 Asn-Pro-Phe (NPF) motifs, an SH3 domain, a PXXP motif, a bipartite nuclear targeting signal, and a tyrosine phosphorylation site. This protein is involved in cargo-specific control of clathrin-mediated endocytosis, specifically controlling the internalization of a specific protein receptor. [provided by RefSeq, Jul 2008] |
SH3BP5 GeneSH3-domain binding protein 5 (BTK-associated) Enables guanyl-nucleotide exchange factor activity and protein kinase inhibitor activity. Acts upstream of or within intracellular signal transduction. Located in cytoplasmic vesicle membrane and nuclear body. [provided by Alliance of Genome Resources, Mar 2025] |
SH3BP1 GeneSH3-domain binding protein 1 This gene encodes a member of the Rho GTPase activating protein (RhoGAP) family. The encoded protein regulates Rac signaling and plays a role in cytoskeletal dynamics, cell motility and epithelial junction formation. This protein's association with the exocyst complex, which tethers secretory vesicles to the plasma membrane, has been demonstrated to be important in cell motility. In a distinct complex, this protein has been shown to regulate epithelial junction formation and morphogenesis. By interacting with the Plexin-D1 cell surface receptor, this protein mediates changes in the cytoskeleton in response to semaphorin binding. This protein may promote metastasis in human liver cancer cells and tissues. [provided by RefSeq, Mar 2017] |
SH3BP2 GeneSH3-domain binding protein 2 The protein encoded by this gene has an N-terminal pleckstrin homology (PH) domain, an SH3-binding proline-rich region, and a C-terminal SH2 domain. The protein binds to the SH3 domains of several proteins including the ABL1 and SYK protein tyrosine kinases , and functions as a cytoplasmic adaptor protein to positively regulate transcriptional activity in T, natural killer (NK), and basophilic cells. Mutations in this gene result in cherubism. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009] |
ANKRD54P1 Geneankyrin repeat domain 54 pseudogene 1 |
HMGN1P20 Genehigh mobility group nucleosome binding domain 1 pseudogene 20 |
LOC100419232 GeneUBX domain protein 4 pseudogene |
ANKRD20A12P Geneankyrin repeat domain 20 family, member A12, pseudogene |
WDR62 GeneWD repeat domain 62 This gene is proposed to play a role in cerebral cortical development. Mutations in this gene have been associated with microencephaly, cortical malformations, and cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2011] |
WDR63 GeneWD repeat domain 63 Enables Arp2/3 complex binding activity. Involved in negative regulation of Arp2/3 complex-mediated actin nucleation and negative regulation of cell migration. Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
WDR61 GeneWD repeat domain 61 WDR61 is a subunit of the human PAF and SKI complexes, which function in transcriptional regulation and are involved in events downstream of RNA synthesis, such as RNA surveillance (Zhu et al., 2005 [PubMed 16024656]).[supplied by OMIM, Mar 2008] |
WDR66 GeneWD repeat domain 66 This protein encoded by this gene belongs to the WD repeat-containing family of proteins, which function in the formation of protein-protein complexes in a variety of biological pathways. This family member appears to function in the determination of mean platelet volume (MPV), and polymorphisms in this gene have been associated with variance in MPV. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Sep 2011] |
WDR64 GeneWD repeat domain 64 |
TTC23L Genetetratricopeptide repeat domain 23-like Predicted to be involved in response to endoplasmic reticulum stress. Predicted to be located in cytoplasm; microtubule cytoskeleton; and midbody. [provided by Alliance of Genome Resources, Mar 2025] |
LOC342443 GeneADAM metallopeptidase domain 21 pseudogene |
LOC102723502 GenePOTE ankyrin domain family member B-like |
HMGN2P4 Genehigh mobility group nucleosomal binding domain 2 pseudogene 4 |
HMGN2P8 Genehigh mobility group nucleosomal binding domain 2 pseudogene 8 |
TBC1D3B GeneTBC1 domain family, member 3B This gene encodes a protein that is similar to TBC1 domain family, member 3. This protein contains a TBC (Tre-2, Bub2p, and Cdc16p) domain, which is found in proteins involved in RAB GTPase signaling and vesicle trafficking. There are multiple copies of this gene located within a cluster of chemokine genes on chromosome 17q. [provided by RefSeq, Apr 2009] |
TBC1D3C GeneTBC1 domain family, member 3C This gene represents one of a cluster of related genes found on chromosome 17. The proteins encoded by this gene family contain a TBC (Tre-2, Bub2p, and Cdc16p) domain and may be involved in GTPase signaling and vesicle trafficking. [provided by RefSeq, Apr 2014] |
TBC1D3F GeneTBC1 domain family, member 3F Predicted to enable GTPase activator activity. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
TBC1D3H GeneTBC1 domain family, member 3H Predicted to enable GTPase activator activity. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
TBC1D3J GeneTBC1 domain family, member 3J |
TBC1D3L GeneTBC1 domain family, member 3L Predicted to enable GTPase activator activity. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
TBC1D30 GeneTBC1 domain family, member 30 Enables GTPase activator activity and small GTPase binding activity. Involved in negative regulation of cilium assembly and positive regulation of GTPase activity. Located in ciliary basal body; cytosol; and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
TBC1D31 GeneTBC1 domain family, member 31 Enables molecular adaptor activity. Involved in cilium assembly. Located in centriolar satellite and ciliary basal body. [provided by Alliance of Genome Resources, Mar 2025] |
TBC1D32 GeneTBC1 domain family, member 32 This gene encodes a TBC-domain containing protein. Studies of a similar protein in mouse and zebrafish suggest that the encoded protein is involved in sonic hedgehog signaling, and that it interacts with and stabilizes cell cycle-related kinase. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014] |
LOC100419920 Geneankyrin repeat domain 33B pseudogene |
LARP1BP1 GeneLa ribonucleoprotein domain family, member 1B pseudogene 1 |
UBXN2B GeneUBX domain protein 2B Predicted to enable ubiquitin binding activity. Involved in establishment of mitotic spindle orientation; negative regulation of protein localization to centrosome; and positive regulation of mitotic centrosome separation. Predicted to be located in Golgi apparatus; endoplasmic reticulum; and spindle pole centrosome. Predicted to be active in cytosol and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
UBXN2A GeneUBX domain protein 2A Predicted to enable ubiquitin binding activity. Involved in negative regulation of ERAD pathway and positive regulation of protein catabolic process. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
EDARADD GeneEDAR-associated death domain This gene was identified by its association with ectodermal dysplasia, a genetic disorder characterized by defective development of hair, teeth, and eccrine sweat glands. The protein encoded by this gene is a death domain-containing protein, and is found to interact with EDAR, a death domain receptor known to be required for the development of hair, teeth and other ectodermal derivatives. This protein and EDAR are coexpressed in epithelial cells during the formation of hair follicles and teeth. Through its interaction with EDAR, this protein acts as an adaptor, and links the receptor to downstream signaling pathways. Two alternatively spliced transcript variants of this gene encoding distinct isoforms have been reported. [provided by RefSeq, Jul 2008] |
LOC102724862 GeneTBC1 domain family member-like Predicted to enable GTPase activator activity. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LDB2 GeneLIM domain binding 2 The protein encoded by this gene belongs to the LIM-domain binding family. Members of this family are characterized by a conserved nuclear localization sequence, an amino-terminal homodimerization domain and a carboxy-terminal LIM interaction domain. These proteins function as adapter molecules to allow assembly of transcriptional regulatory complexes. Genetic association studies suggest functions for this gene in rhegmatogenous retinal detachment and coronary artery disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015] |
LDB3 GeneLIM domain binding 3 This gene encodes a PDZ domain-containing protein. PDZ motifs are modular protein-protein interaction domains consisting of 80-120 amino acid residues. PDZ domain-containing proteins interact with each other in cytoskeletal assembly or with other proteins involved in targeting and clustering of membrane proteins. The protein encoded by this gene interacts with alpha-actinin-2 through its N-terminal PDZ domain and with protein kinase C via its C-terminal LIM domains. The LIM domain is a cysteine-rich motif defined by 50-60 amino acids containing two zinc-binding modules. This protein also interacts with all three members of the myozenin family. Mutations in this gene have been associated with myofibrillar myopathy and dilated cardiomyopathy. Alternatively spliced transcript variants encoding different isoforms have been identified; all isoforms have N-terminal PDZ domains while only longer isoforms (1, 2 and 5) have C-terminal LIM domains. [provided by RefSeq, Jan 2010] |
LDB1 GeneLIM domain binding 1 Enables LIM domain binding activity; RNA polymerase II-specific DNA-binding transcription factor binding activity; and enzyme binding activity. Involved in negative regulation of DNA-templated transcription and positive regulation of transcription by RNA polymerase II. Located in chromatin. Part of beta-catenin-TCF complex. [provided by Alliance of Genome Resources, Mar 2025] |
POTEB2 GenePOTE ankyrin domain family, member B2 |
CNNM1 Genecyclin and CBS domain divalent metal cation transport mediator 1 This gene encodes a member of the ancient conserved domain protein family. The encoded protein may bind copper. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016] |
CNNM3 Genecyclin and CBS domain divalent metal cation transport mediator 3 Predicted to enable transmembrane transporter activity. Predicted to be involved in magnesium ion homeostasis. Located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
CNNM2 Genecyclin and CBS domain divalent metal cation transport mediator 2 This gene encodes a member of the ancient conserved domain containing protein family. Members of this protein family contain a cyclin box motif and have structural similarity to the cyclins. The encoded protein may play an important role in magnesium homeostasis by mediating the epithelial transport and renal reabsorption of Mg2+. Mutations in this gene are associated with renal hypomagnesemia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011] |
CNNM4 Genecyclin and CBS domain divalent metal cation transport mediator 4 This gene encodes a member of the ancient conserved domain containing protein family. Members of this protein family contain a cyclin box motif and have structural similarity to the cyclins. The encoded protein may play a role in metal ion transport. Mutations in this gene are associated with Jalili syndrome which consists of cone-rod dystrophy and amelogenesis imperfecta. [provided by RefSeq, Feb 2010] |
TBC1D24 GeneTBC1 domain family, member 24 This gene encodes a protein with a conserved domain, referred to as the TBC domain, characteristic of proteins which interact with GTPases. TBC domain proteins may serve as GTPase-activating proteins for a particular group of GTPases, the Rab (Ras-related proteins in brain) small GTPases which are involved in the regulation of membrane trafficking. Mutations in this gene are associated with familial infantile myoclonic epilepsy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2011] |
CTDSPL2 GeneCTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2 Enables RNA polymerase II CTD heptapeptide repeat phosphatase activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within negative regulation of BMP signaling pathway; positive regulation of protein export from nucleus; and protein dephosphorylation. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100422300 Genepyridine nucleotide-disulphide oxidoreductase domain 1 pseudogene |
WDR83OS GeneWD repeat domain 83 opposite strand Enables protein folding chaperone. Involved in multi-pass transmembrane protein insertion into ER membrane. Located in endoplasmic reticulum membrane. Part of multi-pass translocon complex and protein folding chaperone complex. [provided by Alliance of Genome Resources, Mar 2025] |
TBC1D3P6 GeneTBC1 domain family, member 3 pseudogene 6 |
TBC1D3P3 GeneTBC1 domain family, member 3 pseudogene 3 |
TBC1D3P2 GeneTBC1 domain family, member 3 pseudogene 2 |
PHIP Genepleckstrin homology domain interacting protein This gene encodes a protein that binds to the insulin receptor substrate 1 protein and regulates glucose transporter translocation in skeletal muscle cells. The encoded protein may also regulate growth and survival of pancreatic beta cells. Elevated copy number of this gene may be associated with melanoma severity and the encoded protein may promote melanoma metastasis in human patients. [provided by RefSeq, Oct 2016] |
NCKIPSD GeneNCK interacting protein with SH3 domain The protein encoded by this gene contains a nuclear localization signal. It plays a role in signal transduction, and may function in the maintenance of sarcomeres and in the assembly of myofibrils into sarcomeres. It also plays an important role in stress fiber formation This protein is involved in the formation and maintenance of dendritic spines, and modulates synaptic activity in neurons. The gene is involved in therapy-related leukemia by a chromosomal translocation t(3;11)(p21;q23) that involves this gene and the myeloid/lymphoid leukemia gene. Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Aug 2019] |
ARID1B GeneAT rich interactive domain 1B (SWI1-like) This locus encodes an AT-rich DNA interacting domain-containing protein. The encoded protein is a component of the SWI/SNF chromatin remodeling complex and may play a role in cell-cycle activation. The protein encoded by this locus is similar to AT-rich interactive domain-containing protein 1A. These two proteins function as alternative, mutually exclusive ARID-subunits of the SWI/SNF complex. The associated complexes play opposing roles. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2016] |
ARID1A GeneAT rich interactive domain 1A (SWI-like) This gene encodes a member of the SWI/SNF family, whose members have helicase and ATPase activities and are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI, which is required for transcriptional activation of genes normally repressed by chromatin. It possesses at least two conserved domains that could be important for its function. First, it has a DNA-binding domain that can specifically bind an AT-rich DNA sequence known to be recognized by a SNF/SWI complex at the beta-globin locus. Second, the C-terminus of the protein can stimulate glucocorticoid receptor-dependent transcriptional activation. It is thought that the protein encoded by this gene confers specificity to the SNF/SWI complex and may recruit the complex to its targets through either protein-DNA or protein-protein interactions. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
YIPF1 GeneYip1 domain family, member 1 Predicted to enable small GTPase binding activity. Predicted to be involved in vesicle-mediated transport. Located in several cellular components, including Golgi apparatus subcompartment; nucleoplasm; and transport vesicle. [provided by Alliance of Genome Resources, Mar 2025] |
YIPF3 GeneYip1 domain family, member 3 Predicted to be involved in cell differentiation. Located in Golgi apparatus and transport vesicle. [provided by Alliance of Genome Resources, Mar 2025] |
YIPF2 GeneYip1 domain family, member 2 Predicted to enable small GTPase binding activity. Predicted to be involved in vesicle-mediated transport. Located in Golgi apparatus subcompartment and transport vesicle. [provided by Alliance of Genome Resources, Mar 2025] |
YIPF5 GeneYip1 domain family, member 5 Involved in insulin processing and regulation of ER to Golgi vesicle-mediated transport. Located in Golgi apparatus; endoplasmic reticulum; and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
YIPF4 GeneYip1 domain family, member 4 Predicted to be involved in endoplasmic reticulum to Golgi vesicle-mediated transport and vesicle fusion with Golgi apparatus. Located in Golgi apparatus; endoplasmic reticulum; and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
YIPF7 GeneYip1 domain family, member 7 Predicted to be involved in endoplasmic reticulum to Golgi vesicle-mediated transport and vesicle fusion with Golgi apparatus. Predicted to act upstream of or within Golgi organization. Predicted to be located in cis-Golgi network; endoplasmic reticulum membrane; and endoplasmic reticulum-Golgi intermediate compartment. Predicted to be active in trans-Golgi network. [provided by Alliance of Genome Resources, Mar 2025] |
YIPF6 GeneYip1 domain family, member 6 Predicted to enable identical protein binding activity. Predicted to be involved in endoplasmic reticulum to Golgi vesicle-mediated transport. Predicted to act upstream of or within intestinal epithelial cell development. Located in Golgi apparatus subcompartment and endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025] |
CLEC10A GeneC-type lectin domain family 10, member A This gene encodes a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. Members of this family share a common protein fold and have diverse functions, such as cell adhesion, cell-cell signalling, glycoprotein turnover, and roles in inflammation and immune response. The encoded type 2 transmembrane protein may function as a cell surface antigen. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008] |
ANKRD26P4 Geneankyrin repeat domain 26 pseudogene 4 |
ANKRD26P3 Geneankyrin repeat domain 26 pseudogene 3 |
ANKRD26P2 Geneankyrin repeat domain 26 pseudogene 2 |
ANKRD26P1 Geneankyrin repeat domain 26 pseudogene 1 |
WDR95P GeneWD repeat domain 95, pseudogene |
ANKRD36B Geneankyrin repeat domain 36B Enables identical protein binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
NOM1 Genenucleolar protein with MIF4G domain 1 Proteins that contain MIF4G (middle of eIF4G (MIM 600495)) and/or MA3 domains, such as NOM1, function in protein translation. These domains include binding sites for members of the EIF4A family of ATP-dependent DEAD box RNA helicases (see EIF4A1; MIM 602641) (Simmons et al., 2005 [PubMed 15715967]).[supplied by OMIM, Mar 2008] |
NSD3 Genenuclear receptor binding SET domain protein 3 This gene is related to the Wolf-Hirschhorn syndrome candidate-1 gene and encodes a protein with PWWP (proline-tryptophan-tryptophan-proline) domains. This protein methylates histone H3 at lysine residues 4 and 27, which represses gene transcription. Two alternatively spliced variants have been described. [provided by RefSeq, May 2015] |
NSD2 Genenuclear receptor binding SET domain protein 2 This gene encodes a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene maps to the 165 kb WHS critical region and has also been involved in the chromosomal translocation t(4;14)(p16.3;q32.3) in multiple myelomas. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms. Some transcript variants are nonsense-mediated mRNA (NMD) decay candidates, hence not represented as reference sequences. [provided by RefSeq, Jul 2008] |
MIDEAS Genemitotic deacetylase associated SANT domain protein Predicted to enable transcription corepressor activity. Predicted to be involved in negative regulation of DNA-templated transcription and regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
CARD19 Genecaspase recruitment domain family member 19 Predicted to enable CARD domain binding activity. Predicted to be involved in negative regulation of canonical NF-kappaB signal transduction. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
TBC1D3G GeneTBC1 domain family member 3G Predicted to enable GTPase activator activity. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
DIPK1B Genedivergent protein kinase domain 1B This gene encodes a member of the FAM69 family of cysteine-rich type II transmembrane proteins. These proteins localize to the endoplasmic reticulum but their specific functions are unknown. [provided by RefSeq, Nov 2011] |
DIPK1A Genedivergent protein kinase domain 1A This gene encodes a member of the FAM69 family of cysteine-rich type II transmembrane proteins. These proteins localize to the endoplasmic reticulum but their specific functions are unknown. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011] |
DIPK2A Genedivergent protein kinase domain 2A Involved in several processes, including cardiac muscle cell proliferation; negative regulation of smooth muscle cell apoptotic process; and positive regulation of protein kinase C activity. Located in Golgi membrane and extracellular space. Part of COPI vesicle coat. [provided by Alliance of Genome Resources, Mar 2025] |
EOLA2 Geneendothelium and lymphocyte associated ASCH domain 2 Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
EOLA1 Geneendothelium and lymphocyte associated ASCH domain 1 Involved in regulation of interleukin-6 production. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
DIPK2B Genedivergent protein kinase domain 2B Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Mar 2025] |
WDR97 GeneWD repeat domain 97 The function and protein-coding potential of this gene is unknown. The exon combination is based on AB058778.1 for which two possible open reading frames can be predicted (with start codons at nucleotide 26 or 2614). The position of the first ORF stop codon is consistent with a prediction of nonsense-mediated decay. Given the observation of the first ORF and its length, a predicted translation of the second ORF is inconsistent with the translation leaky scanning theory. Therefore, this gene is represented as a non-protein-coding transcript. [provided by RefSeq, Oct 2008] |
SANBR GeneSANT and BTB domain regulator of CSR Predicted to enable identical protein binding activity. Predicted to be involved in isotype switching. [provided by Alliance of Genome Resources, Mar 2025] |
DIPK1C Genedivergent protein kinase domain 1C This gene encodes a member of the FAM69 family of cysteine-rich type II transmembrane proteins. These proteins localize to the endoplasmic reticulum but their specific functions are unknown. [provided by RefSeq, Nov 2011] |
TBC1D29P GeneTBC1 domain family member 29, pseudogene |
MEIOC Genemeiosis specific with coiled-coil domain Predicted to be involved in several processes, including germ cell development; germline cell cycle switching, mitotic to meiotic cell cycle; and meiosis I. Predicted to be active in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
TBC1D3E GeneTBC1 domain family member 3E Predicted to enable GTPase activator activity. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
TBC1D27P GeneTBC1 domain family member 27, pseudogene |
ANKRD20A4P Geneankyrin repeat domain 20 family member A4, pseudogene |
CARD17P Genecaspase recruitment domain family member 17, pseudogene Enables caspase binding activity and identical protein binding activity. Involved in cellular response to lipopolysaccharide and negative regulation of interleukin-1 beta production. Part of protein-containing complex. [provided by Alliance of Genome Resources, Mar 2025] |
TMDD1 Genetransmembrane and death domain 1 Predicted to be involved in signal transduction. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
TBC1D3I GeneTBC1 domain family member 3I Predicted to enable GTPase activator activity. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
MBD3L2B Genemethyl-CpG binding domain protein 3 like 2B Predicted to enable methyl-CpG binding activity. Predicted to be involved in DNA methylation-dependent constitutive heterochromatin formation and negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
LOC128462377 Geneankyrin repeat domain 11 upstream open reading frame |
Zinc finger C2HC domain-containing protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger C2HC domain-containing protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C2HC-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C2HC-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, PHD-finger Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, PHD-finger protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
PR domain zinc finger protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the PR domain zinc finger protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
PR-domain zinc finger protein PRDM5 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the PR-domain zinc finger protein PRDM5 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
PR-domain zinc finger protein PRDM4 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the PR-domain zinc finger protein PRDM4 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Bromodomain adjacent to zinc finger domain protein 2A Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Bromodomain adjacent to zinc finger domain protein 2A protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
PR domain zinc finger protein 16 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the PR domain zinc finger protein 16 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
PR-domain zinc finger protein PRDM12 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the PR-domain zinc finger protein PRDM12 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein of unknown function DUF3669, zinc finger protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein of unknown function DUF3669, zinc finger protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Receptor-transporting protein/CXXC-type zinc finger protein 11 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Receptor-transporting protein/CXXC-type zinc finger protein 11 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
ring-like zinc finger domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the ring-like zinc finger domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
c2h2 zinc finger domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the c2h2 zinc finger domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
TRM13/UPF0224 family, U11-48K-like CHHC zinc finger domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the TRM13/UPF0224 family, U11-48K-like CHHC zinc finger domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Putative treble-clef, zinc-finger domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Putative treble-clef, zinc-finger domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Putative zinc-finger domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Putative zinc-finger domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger C2H2-type/integrase DNA-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger C2H2-type/integrase DNA-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
KRAB domain C2H2 zinc finger family Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the KRAB domain C2H2 zinc finger family protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA glycosylase/AP lyase, zinc finger domain, DNA-binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA glycosylase/AP lyase, zinc finger domain, DNA-binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc-finger domain of monoamine-oxidase A repressor R1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc-finger domain of monoamine-oxidase A repressor R1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
C2H2 zinc finger domain binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the C2H2 zinc finger domain binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
RING-like zinc finger domain binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the RING-like zinc finger domain binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
C2H2 zinc finger domain binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the C2H2 zinc finger domain binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
RING-like zinc finger domain binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the RING-like zinc finger domain binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
C2H2- zinc finger protein family Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the C2H2- zinc finger protein family protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein PLAGL1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein PLAGL1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein 446 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein 446 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein 174 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein 174 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein 131 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein 131 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cip1-interacting zinc finger protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cip1-interacting zinc finger protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger homeobox protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger homeobox protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein 496 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein 496 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger CCCH-type antiviral protein 1-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger CCCH-type antiviral protein 1-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein 18 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein 18 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein GLIS1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein GLIS1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein PLAG1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein PLAG1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Uncharacterised conserved protein UCP037948, zinc finger MYND-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Uncharacterised conserved protein UCP037948, zinc finger MYND-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein Gfi-1b Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein Gfi-1b protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Uncharacterised conserved protein UCP037956, zinc finger Ran-binding Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Uncharacterised conserved protein UCP037956, zinc finger Ran-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
CXXC-type zinc finger protein 11 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the CXXC-type zinc finger protein 11 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, V(D)J recombination-activating protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, V(D)J recombination-activating protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein 518A Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein 518A protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Interferon regulatory factor 2-binding protein 1 & 2, zinc finger Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Interferon regulatory factor 2-binding protein 1 & 2, zinc finger protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein 518B Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein 518B protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger protein NOA36 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger protein NOA36 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc Deficiency, Neonatal, Due To Low Breast Milk Zinc Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Zinc Deficiency, Neonatal, Due To Low Breast Milk Zinc in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Zinc finger, NHR/GATA-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, NHR/GATA-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, FYVE-type, endofin Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, FYVE-type, endofin protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C6HC-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C6HC-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, MYND-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, MYND-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, H2C2-type, histone UAS binding Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, H2C2-type, histone UAS binding protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, DBF-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, DBF-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C2H2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C2H2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, DNA glycosylase/AP lyase/isoleucyl tRNA synthetase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, DNA glycosylase/AP lyase/isoleucyl tRNA synthetase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, PARP-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, PARP-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, double-stranded RNA binding Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, double-stranded RNA binding protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, TFIIS-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, TFIIS-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, ZZ-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, ZZ-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, U1-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, U1-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, N-recognin Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, N-recognin protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, PMZ-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, PMZ-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, MIZ-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, MIZ-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, RING/FYVE/PHD-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, RING/FYVE/PHD-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, RING-CH-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, RING-CH-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, LIM-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, LIM-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, DNA-directed DNA polymerase, family B, alpha Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, DNA-directed DNA polymerase, family B, alpha protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, Sec23/Sec24-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, Sec23/Sec24-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, RING-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, RING-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, NF-X1-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, NF-X1-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C2CH-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C2CH-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, DPH-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, DPH-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C4H2-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C4H2-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, AN1-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, AN1-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, CXXC-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, CXXC-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C2H2, LYAR-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C2H2, LYAR-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, FLYWCH-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, FLYWCH-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, TRAF-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, TRAF-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger transcription factor Trps1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger transcription factor Trps1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, DNA glycosylase/AP lyase-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, DNA glycosylase/AP lyase-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
C4-type zinc-finger of DNA polymerase delta Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the C4-type zinc-finger of DNA polymerase delta protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C3HC-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C3HC-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, Mcm10/DnaG-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, Mcm10/DnaG-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Transcription factor IIIC, putative zinc-finger Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Transcription factor IIIC, putative zinc-finger protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, FYVE/PHD-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, FYVE/PHD-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, SWIM-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, SWIM-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, PHD-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, PHD-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
RING-type zinc-finger, LisH dimerisation motif Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the RING-type zinc-finger, LisH dimerisation motif protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, CTCHY-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, CTCHY-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, RING-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, RING-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, U1-C type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, U1-C type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, PHD-type, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, PHD-type, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Spt4/RpoE2 zinc finger Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Spt4/RpoE2 zinc finger protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C2H2, APLF-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C2H2, APLF-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, RING-type, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, RING-type, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, DHHC-type, palmitoyltransferase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, DHHC-type, palmitoyltransferase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, N-recognin, metazoa Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, N-recognin, metazoa protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, ZPR1-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, ZPR1-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, MYM-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, MYM-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, TFIIB-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, TFIIB-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, SIAH-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, SIAH-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, piccolo-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, piccolo-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, nuclear hormone receptor-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, nuclear hormone receptor-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C5HC2-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C5HC2-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, GATA-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, GATA-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, CCCH-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, CCCH-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, AD-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, AD-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C2H2-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C2H2-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, GRF-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, GRF-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, HIT-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, HIT-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C2HC5-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C2HC5-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C2H2-type matrin Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C2H2-type matrin protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, B-box, chordata Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, B-box, chordata protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, RanBP2-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, RanBP2-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, TTF-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, TTF-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, CCHC-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, CCHC-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, XPA-type, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, XPA-type, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, FYVE-related Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, FYVE-related protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, CW-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, CW-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, CHCC-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, CHCC-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, UBP-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, UBP-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, CCCH-type, TRM13 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, CCCH-type, TRM13 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
FYVE zinc finger Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the FYVE zinc finger protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tim10/DDP family zinc finger Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tim10/DDP family zinc finger protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, C3HC4 RING-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, C3HC4 RING-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, FCS-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, FCS-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, B-box Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, B-box protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, RING-H2-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, RING-H2-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, A20-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, A20-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, BED-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, BED-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, DNL-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, DNL-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, nanos-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, nanos-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, CHHC-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, CHHC-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, CHY-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, CHY-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, Btk motif Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, Btk motif protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, TAZ-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, TAZ-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger, Rad18-type putative Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc finger, Rad18-type putative protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
N-acetyltransferase ESCO, zinc-finger Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the N-acetyltransferase ESCO, zinc-finger protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Histone deacetylase complex subunit SAP30 zinc-finger Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Histone deacetylase complex subunit SAP30 zinc-finger protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc finger transcription factors Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Zinc finger transcription factors assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Drought induced 19 protein-like, zinc-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Drought induced 19 protein-like, zinc-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein S27e, zinc-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein S27e, zinc-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
RDM domain, Ret finger protein-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the RDM domain, Ret finger protein-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc-ribbon domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc-ribbon domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Iron/zinc purple acid phosphatase-like C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Iron/zinc purple acid phosphatase-like C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Superoxide dismutase, copper/zinc binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Superoxide dismutase, copper/zinc binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Hedgehog signalling/DD-peptidase zinc-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Hedgehog signalling/DD-peptidase zinc-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Integrase, N-terminal zinc-binding domain-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Integrase, N-terminal zinc-binding domain-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
c3hc4-type ring finger domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the c3hc4-type ring finger domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
DNA polymerase, Y-family, little finger domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA polymerase, Y-family, little finger domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
C3HC4-type RING finger domain binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the C3HC4-type RING finger domain binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
C3HC4-type RING finger domain binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the C3HC4-type RING finger domain binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Zinc-binding ribosomal protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc-binding ribosomal protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein kinase A anchor protein, RI-RII subunit-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein kinase A anchor protein, RI-RII subunit-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
GTP-binding protein TrmE/Glycine cleavage system T protein, domain 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the GTP-binding protein TrmE/Glycine cleavage system T protein, domain 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 13 domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 13 domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
EH domain-binding protein 1-like protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the EH domain-binding protein 1-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting protein 36, GLUE domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting protein 36, GLUE domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal RNA-processing protein 14/surfeit locus protein 6, C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal RNA-processing protein 14/surfeit locus protein 6, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Kinetochore protein Cenp-F/LEK1, Rb protein-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Kinetochore protein Cenp-F/LEK1, Rb protein-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 13A N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 13A N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Uncharacterised protein family WW domain-binding protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Uncharacterised protein family WW domain-binding protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 8, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 8, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associate protein Vta1/Callose synthase, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associate protein Vta1/Callose synthase, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Usher syndrome type-1C protein-binding protein 1, PDZ domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Usher syndrome type-1C protein-binding protein 1, PDZ domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein kinase A anchor protein, nuclear localisation signal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein kinase A anchor protein, nuclear localisation signal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Abl-interactor, homeo-domain homologous domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Abl-interactor, homeo-domain homologous domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Two pore domain potassium channel domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Two pore domain potassium channel domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Arfaptin homology (AH) domain/BAR domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Arfaptin homology (AH) domain/BAR domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
KA1 domain/Ssp2 C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the KA1 domain/Ssp2 C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; antithrombin iii deficiency; pregnancy complications, hematologic; protein c deficiency; protein s deficiency; puerperal disorders; pulmonary embolism; pulmonary embolisms; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
Reduced zinc in breast milk Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Reduced zinc in breast milk phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Zinc Oxide Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Zinc Oxide from the curated CTD Gene-Chemical Interactions dataset. |
Zinc Acetate Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Zinc Acetate from the curated CTD Gene-Chemical Interactions dataset. |
zinc deuteroporphyrin IX 2,4-bis(glycol) Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical zinc deuteroporphyrin IX 2,4-bis(glycol) from the curated CTD Gene-Chemical Interactions dataset. |
zinc bis(histidinate) Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical zinc bis(histidinate) from the curated CTD Gene-Chemical Interactions dataset. |
eugenol, zinc oxide dental cavity lining Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical eugenol, zinc oxide dental cavity lining from the curated CTD Gene-Chemical Interactions dataset. |
zinc protoporphyrin Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical zinc protoporphyrin from the curated CTD Gene-Chemical Interactions dataset. |
Zinc Sulfate Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Zinc Sulfate from the curated CTD Gene-Chemical Interactions dataset. |
zinc mesoporphyrin Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical zinc mesoporphyrin from the curated CTD Gene-Chemical Interactions dataset. |
Zinc Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Zinc from the curated CTD Gene-Chemical Interactions dataset. |
adrenocorticotropin zinc Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical adrenocorticotropin zinc from the curated CTD Gene-Chemical Interactions dataset. |
Zinc Compounds Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Zinc Compounds from the curated CTD Gene-Chemical Interactions dataset. |
dichlorido-zinc(II)-4-(2-(5-methoxybenzylideneamino)ethyl)piperazin-1-iumphenolate Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical dichlorido-zinc(II)-4-(2-(5-methoxybenzylideneamino)ethyl)piperazin-1-iumphenolate from the curated CTD Gene-Chemical Interactions dataset. |
zinc sulfide Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical zinc sulfide from the curated CTD Gene-Chemical Interactions dataset. |
zinc chromate Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical zinc chromate from the curated CTD Gene-Chemical Interactions dataset. |
zinc chloride Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical zinc chloride from the curated CTD Gene-Chemical Interactions dataset. |
zinc hematoporphyrin Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical zinc hematoporphyrin from the curated CTD Gene-Chemical Interactions dataset. |
pyrithione zinc Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical pyrithione zinc from the curated CTD Gene-Chemical Interactions dataset. |
ZINC, ELEVATED PLASMA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ZINC, ELEVATED PLASMA from the curated CTD Gene-Disease Associations dataset. |
Bis(5-Amidino-Benzimidazolyl)Methanone Zinc Gene Setinteracting proteins for the Bis(5-Amidino-Benzimidazolyl)Methanone Zinc drug from the curated DrugBank Drug Targets dataset. |
Zinc Trihydroxide Gene Setinteracting proteins for the Zinc Trihydroxide drug from the curated DrugBank Drug Targets dataset. |
Bis(5-Amidino-Benzimidazolyl)Methane Zinc Gene Setinteracting proteins for the Bis(5-Amidino-Benzimidazolyl)Methane Zinc drug from the curated DrugBank Drug Targets dataset. |
Zinc Substituted Heme C Gene Setinteracting proteins for the Zinc Substituted Heme C drug from the curated DrugBank Drug Targets dataset. |
lead blood levels; zinc Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lead blood levels; zinc in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
zinc; lead toxicity; height; weight Gene SetFrom GAD Gene-Disease Associations genes associated with the disease zinc; lead toxicity; height; weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
zinc Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term zinc in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
zinc sulfate_rattus norvegicus_gpl341_gds3369 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the zinc sulfate_rattus norvegicus_gpl341_gds3369 small molecule perturbation from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset. |
zinc acetate_homo sapiens_gds1617 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the zinc acetate_homo sapiens_gds1617 small molecule perturbation from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset. |
zinc acetate_homo sapiens_gpl570_gds1617 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the zinc acetate_homo sapiens_gpl570_gds1617 small molecule perturbation from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset. |
zinc ion transmembrane transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the zinc ion transmembrane transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of sequestering of zinc ion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of sequestering of zinc ion biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of zinc ion transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of zinc ion transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of zinc ion transmembrane import Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of zinc ion transmembrane import biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of zinc ion transmembrane import Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of zinc ion transmembrane import biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular zinc ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular zinc ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of zinc ion transmembrane transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of zinc ion transmembrane transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
zinc ion transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the zinc ion transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to zinc ion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to zinc ion biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to zinc ion starvation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to zinc ion starvation biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of zinc ion transmembrane transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of zinc ion transmembrane transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
zinc ion transmembrane import Gene SetFrom GO Biological Process Annotations 2015 genes participating in the zinc ion transmembrane import biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of zinc ion transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of zinc ion transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
zinc ion homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the zinc ion homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
sequestering of zinc ion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the sequestering of zinc ion biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of sequestering of zinc ion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of sequestering of zinc ion biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to zinc ion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to zinc ion biological process from the curated GO Biological Process Annotations 2015 dataset. |
zinc transporting atpase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the zinc transporting atpase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
alcohol dehydrogenase activity, zinc-dependent Gene SetFrom GO Molecular Function Annotations 2015 genes performing the alcohol dehydrogenase activity, zinc-dependent molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
zinc ion transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the zinc ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
zinc ion binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the zinc ion binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
zinc pyrithione Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the zinc pyrithione ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
corticotropin zinc hydroxide Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the corticotropin zinc hydroxide ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
increased serum zinc Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the increased serum zinc phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of zinc homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of zinc homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
Zinc (II) ion Gene SetFrom HMDB Metabolites of Enzymes interacting proteins for the Zinc (II) ion metabolite from the curated HMDB Metabolites of Enzymes dataset. |
abnormality of zinc homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of zinc homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
APOBEC/CMP deaminase, zinc-binding Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the APOBEC/CMP deaminase, zinc-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alcohol dehydrogenase family, zinc-type, class-V subfamily Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase family, zinc-type, class-V subfamily protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Peptidase M16, zinc-binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Peptidase M16, zinc-binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Pre-SET zinc-binding sub-group Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Pre-SET zinc-binding sub-group protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
CMP/dCMP deaminase, zinc-binding Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the CMP/dCMP deaminase, zinc-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Double zinc ribbon Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Double zinc ribbon protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
RNA polymerases, subunit N, zinc binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the RNA polymerases, subunit N, zinc binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
RAD50, zinc hook Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the RAD50, zinc hook protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Superoxide dismutase, copper/zinc, binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Superoxide dismutase, copper/zinc, binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc ribbon, NADH pyrophosphatase Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc ribbon, NADH pyrophosphatase protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alcohol dehydrogenase family, zinc-type, class-IV subfamily Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase family, zinc-type, class-IV subfamily protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc/iron permease Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc/iron permease protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alcohol dehydrogenase superfamily, zinc-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase superfamily, zinc-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
NPL4, zinc-binding putative Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the NPL4, zinc-binding putative protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Zinc knuckle CX2CX3GHX4C Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Zinc knuckle CX2CX3GHX4C protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cytochrome c oxidase, subunit Vb, zinc binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase, subunit Vb, zinc binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alcohol dehydrogenase, zinc-type, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase, zinc-type, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Aryldialkylphosphatase, zinc-binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Aryldialkylphosphatase, zinc-binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alcohol dehydrogenase family, zinc-type, class-II subfamily Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alcohol dehydrogenase family, zinc-type, class-II subfamily protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Peptidase M10A, cysteine switch, zinc binding site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Peptidase M10A, cysteine switch, zinc binding site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Translation initiation factor IF2/IF5, zinc-binding Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Translation initiation factor IF2/IF5, zinc-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal liver zinc level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal liver zinc level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain zinc level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain zinc level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased brain zinc level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased brain zinc level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal zinc homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal zinc homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
zinc deficiency, transient neonatal Gene SetFrom OMIM Gene-Disease Associations genes associated with the zinc deficiency, transient neonatal phenotype from the curated OMIM Gene-Disease Associations dataset. |
zinc Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term zinc in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
Zinc efflux and compartmentalization by the SLC30 family Gene Setproteins participating in the Zinc efflux and compartmentalization by the SLC30 family pathway from the Reactome Pathways dataset. |
Zinc transporters Gene Setproteins participating in the Zinc transporters pathway from the Reactome Pathways dataset. |
Zinc influx into cells by the SLC39 gene family Gene Setproteins participating in the Zinc influx into cells by the SLC39 gene family pathway from the Reactome Pathways dataset. |
Zinc Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Zinc Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Serum Zinc Measurement Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Serum Zinc Measurement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Dietary Zinc Deficiency Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dietary Zinc Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Serum Zinc Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Serum Zinc in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
regulation of sequestering of zinc ion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of sequestering of zinc ion biological process from the curated GO Biological Process Annotations 2023 dataset. |
zinc ion transmembrane transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the zinc ion transmembrane transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular response to zinc ion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular response to zinc ion biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular zinc ion homeostasis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular zinc ion homeostasis biological process from the curated GO Biological Process Annotations 2023 dataset. |
response to zinc ion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the response to zinc ion biological process from the curated GO Biological Process Annotations 2023 dataset. |
zinc ion transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the zinc ion transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
zinc ion import across plasma membrane Gene SetFrom GO Biological Process Annotations 2023 genes participating in the zinc ion import across plasma membrane biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of zinc ion transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of zinc ion transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
zinc ion import into Golgi lumen Gene SetFrom GO Biological Process Annotations 2023 genes participating in the zinc ion import into Golgi lumen biological process from the curated GO Biological Process Annotations 2023 dataset. |
zinc ion import into organelle Gene SetFrom GO Biological Process Annotations 2023 genes participating in the zinc ion import into organelle biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of sequestering of zinc ion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of sequestering of zinc ion biological process from the curated GO Biological Process Annotations 2023 dataset. |
zinc ion import into zymogen granule Gene SetFrom GO Biological Process Annotations 2023 genes participating in the zinc ion import into zymogen granule biological process from the curated GO Biological Process Annotations 2023 dataset. |
zinc ion import into lysosome Gene SetFrom GO Biological Process Annotations 2023 genes participating in the zinc ion import into lysosome biological process from the curated GO Biological Process Annotations 2023 dataset. |
zinc ion import into mitochondrion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the zinc ion import into mitochondrion biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of zinc ion transmembrane import Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of zinc ion transmembrane import biological process from the curated GO Biological Process Annotations 2023 dataset. |
zinc export across plasma membrane Gene SetFrom GO Biological Process Annotations 2023 genes participating in the zinc export across plasma membrane biological process from the curated GO Biological Process Annotations 2023 dataset. |
zinc ion import into secretory vesicle Gene SetFrom GO Biological Process Annotations 2023 genes participating in the zinc ion import into secretory vesicle biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of zinc ion transmembrane import Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of zinc ion transmembrane import biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of zinc ion transmembrane transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of zinc ion transmembrane transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
zinc ion binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the zinc ion binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
zinc ion transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the zinc ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
alcohol dehydrogenase activity, zinc-dependent Gene SetFrom GO Molecular Function Annotations 2023 genes performing the alcohol dehydrogenase activity, zinc-dependent molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
zinc:proton antiporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the zinc:proton antiporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
zinc efflux transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the zinc efflux transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
abnormal zinc homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal zinc homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased brain zinc level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased brain zinc level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal milk zinc level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal milk zinc level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased circulating zinc level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased circulating zinc level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal liver zinc level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal liver zinc level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal zinc level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal zinc level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
zinc ion import into synaptic vesicle Gene SetFrom SynGO Synaptic Gene Annotations genes associated with the synaptic term zinc ion import into synaptic vesicle from the SynGO Synaptic Gene Annotations dataset. |
Zinc homeostasis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Zinc homeostasis pathway from the WikiPathways Pathways 2024 dataset. |
Defective SLC39A4 causes acrodermatitis enteropathica, zinc-deficiency type (AEZ) Gene Setproteins participating in the Defective SLC39A4 causes acrodermatitis enteropathica, zinc-deficiency type (AEZ) pathway from the Reactome Pathways 2024 dataset. |
Zinc efflux and compartmentalization by the SLC30 family Gene Setproteins participating in the Zinc efflux and compartmentalization by the SLC30 family pathway from the Reactome Pathways 2024 dataset. |
Zinc influx into cells by the SLC39 gene family Gene Setproteins participating in the Zinc influx into cells by the SLC39 gene family pathway from the Reactome Pathways 2024 dataset. |
Zinc transporters Gene Setproteins participating in the Zinc transporters pathway from the Reactome Pathways 2024 dataset. |
zinc ion import into lysosome Gene SetFrom GO Biological Process Annotations 2025 genes participating in the zinc ion import into lysosome biological process from the curated GO Biological Process Annotations 2025 dataset. |
zinc ion transmembrane transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the zinc ion transmembrane transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
cellular response to zinc ion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cellular response to zinc ion biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular zinc ion homeostasis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular zinc ion homeostasis biological process from the curated GO Biological Process Annotations 2025 dataset. |
response to zinc ion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the response to zinc ion biological process from the curated GO Biological Process Annotations 2025 dataset. |
zinc ion transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the zinc ion transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
zinc ion import across plasma membrane Gene SetFrom GO Biological Process Annotations 2025 genes participating in the zinc ion import across plasma membrane biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of zinc ion transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of zinc ion transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
zinc ion import into Golgi lumen Gene SetFrom GO Biological Process Annotations 2025 genes participating in the zinc ion import into Golgi lumen biological process from the curated GO Biological Process Annotations 2025 dataset. |
zinc ion import into organelle Gene SetFrom GO Biological Process Annotations 2025 genes participating in the zinc ion import into organelle biological process from the curated GO Biological Process Annotations 2025 dataset. |
zinc export across plasma membrane Gene SetFrom GO Biological Process Annotations 2025 genes participating in the zinc export across plasma membrane biological process from the curated GO Biological Process Annotations 2025 dataset. |
zinc ion import into secretory vesicle Gene SetFrom GO Biological Process Annotations 2025 genes participating in the zinc ion import into secretory vesicle biological process from the curated GO Biological Process Annotations 2025 dataset. |
zinc ion import into zymogen granule Gene SetFrom GO Biological Process Annotations 2025 genes participating in the zinc ion import into zymogen granule biological process from the curated GO Biological Process Annotations 2025 dataset. |
zinc ion import into mitochondrion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the zinc ion import into mitochondrion biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of zinc ion transmembrane import Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of zinc ion transmembrane import biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of zinc ion transmembrane import Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of zinc ion transmembrane import biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of zinc ion transmembrane transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of zinc ion transmembrane transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
zinc ion binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the zinc ion binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
zinc ion transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the zinc ion transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
zinc:proton antiporter activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the zinc:proton antiporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
zinc ion sensor activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the zinc ion sensor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
zinc efflux transmembrane transporter activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the zinc efflux transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Zinc levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Zinc levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Immunoglobulin measurement (zinc sulfate turbidity test) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Immunoglobulin measurement (zinc sulfate turbidity test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Response to antioxidants and zinc in age-related macular degeneration (disease progression) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to antioxidants and zinc in age-related macular degeneration (disease progression) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
PYRITHIONE ZINC Gene Setinteracting proteins for the PYRITHIONE ZINC drug from theDGIdb Drug Targets 2026 dataset. |
ZINC CHLORIDE Gene Setinteracting proteins for the ZINC CHLORIDE drug from theDGIdb Drug Targets 2026 dataset. |
ZINC SULFATE ANHYDROUS Gene Setinteracting proteins for the ZINC SULFATE ANHYDROUS drug from theDGIdb Drug Targets 2026 dataset. |
INSULIN ZINC SUSP RECOMBINANT HUMAN Gene Setinteracting proteins for the INSULIN ZINC SUSP RECOMBINANT HUMAN drug from theDGIdb Drug Targets 2026 dataset. |
INSULIN HUMAN ZINC Gene Setinteracting proteins for the INSULIN HUMAN ZINC drug from theDGIdb Drug Targets 2026 dataset. |
INSULIN ZINC, EXTENDED Gene Setinteracting proteins for the INSULIN ZINC, EXTENDED drug from theDGIdb Drug Targets 2026 dataset. |
INSULIN ZINC, PROMPT Gene Setinteracting proteins for the INSULIN ZINC, PROMPT drug from theDGIdb Drug Targets 2026 dataset. |
INSULIN, PROTAMINE ZINC Gene Setinteracting proteins for the INSULIN, PROTAMINE ZINC drug from theDGIdb Drug Targets 2026 dataset. |
CEPHALOSPORIN C ZINC SALT Gene Setinteracting proteins for the CEPHALOSPORIN C ZINC SALT drug from theDGIdb Drug Targets 2026 dataset. |
CORTICOTROPIN-ZINC HYDROXIDE Gene Setinteracting proteins for the CORTICOTROPIN-ZINC HYDROXIDE drug from theDGIdb Drug Targets 2026 dataset. |
(R)-ZINC-3573 Gene Setinteracting proteins for the (R)-ZINC-3573 drug from theDGIdb Drug Targets 2026 dataset. |
ZINC PROTOPORPHYRIN IX Gene Setinteracting proteins for the ZINC PROTOPORPHYRIN IX drug from theDGIdb Drug Targets 2026 dataset. |
ANHYDROUS ZINC ACETATE Gene Setinteracting proteins for the ANHYDROUS ZINC ACETATE drug from theDGIdb Drug Targets 2026 dataset. |
finger agnosia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease finger agnosia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
finger Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term finger in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
abnormality of finger Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of phalanx of finger Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of phalanx of finger phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
sclerosis of finger phalanx Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the sclerosis of finger phalanx phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
radial deviation of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the radial deviation of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
deviation of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the deviation of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bracket epiphyses of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the bracket epiphyses of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular epiphyses of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular epiphyses of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
macrodactyly of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the macrodactyly of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tapering pointed ends of distal finger phalanges Gene SetFrom HPO Gene-Disease Associations genes associated with the tapering pointed ends of distal finger phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
camptodactyly of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the camptodactyly of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
symphalangism of middle phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the symphalangism of middle phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bracket epiphysis of the middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the bracket epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged epiphysis of the proximal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the enlarged epiphysis of the proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent middle phalanx of 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the absent middle phalanx of 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the phalanges of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the phalanges of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pseudoepiphyses of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the pseudoepiphyses of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
slender finger Gene SetFrom HPO Gene-Disease Associations genes associated with the slender finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
patchy sclerosis of finger phalanx Gene SetFrom HPO Gene-Disease Associations genes associated with the patchy sclerosis of finger phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
radial deviation of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the radial deviation of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the phalanges of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the phalanges of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
deviation of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the deviation of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular shaped middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular shaped middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the phalanges of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad finger Gene SetFrom HPO Gene-Disease Associations genes associated with the broad finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
partial duplication of the phalanges of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the partial duplication of the phalanges of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
interphalangeal joint contracture of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the interphalangeal joint contracture of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
finger clinodactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the finger clinodactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the middle phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
slender proximal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the slender proximal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
3-4 finger cutaneous syndactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the 3-4 finger cutaneous syndactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular epiphysis of the middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the phalanges of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular shaped proximal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular shaped proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of the distal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
deviation of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the deviation of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
radial deviation of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the radial deviation of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular shaped middle phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular shaped middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the proximal phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sclerosis of distal finger phalanx Gene SetFrom HPO Gene-Disease Associations genes associated with the sclerosis of distal finger phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
symphalangism of middle phalanx of 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the symphalangism of middle phalanx of 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
joint contracture of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the joint contracture of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long proximal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the long proximal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad middle phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the broad middle phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular shaped phalanges of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular shaped phalanges of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short middle phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short middle phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
partial duplication of the distal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular shaped phalanges of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular shaped phalanges of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypersegmentation of proximal phalanx of second finger Gene SetFrom HPO Gene-Disease Associations genes associated with the hypersegmentation of proximal phalanx of second finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the phalanges of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the phalanges of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the long phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
partial duplication of the phalanges of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the partial duplication of the phalanges of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
partial duplication of the distal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged epiphyses of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the enlarged epiphyses of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
radial deviation of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the radial deviation of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
ulnar deviation of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the ulnar deviation of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
slender distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the slender distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the broad distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of phalanx of 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the duplication of phalanx of 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
weakness of long finger extensor muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the weakness of long finger extensor muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanx of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short proximal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short proximal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent proximal finger flexion creases Gene SetFrom HPO Gene-Disease Associations genes associated with the absent proximal finger flexion creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bracket epiphyses of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the bracket epiphyses of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
finger syndactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the finger syndactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pseudoepiphyses of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the pseudoepiphyses of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of phalanx of 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the duplication of phalanx of 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased finger mobility Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased finger mobility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular shaped middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular shaped middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the phalanges of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal/middle symphalangism of 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal/middle symphalangism of 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cutaneous finger syndactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the cutaneous finger syndactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the phalanges of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the phalanges of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular epiphyses of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular epiphyses of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular epiphysis of the proximal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular epiphysis of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
deviation of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the deviation of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
clinodactyly of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the clinodactyly of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular epiphysis of the proximal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular epiphysis of the proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bracket epiphysis of the middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the bracket epiphysis of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the proximal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged epiphysis of the middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the enlarged epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
symphalangism of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the symphalangism of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
fifth finger distal phalanx clinodactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the fifth finger distal phalanx clinodactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
polydactyly affecting the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the polydactyly affecting the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the proximal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular shaped phalanges of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular shaped phalanges of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
2-3 finger syndactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the 2-3 finger syndactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
4-5 finger syndactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the 4-5 finger syndactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
single interphalangeal crease of fifth finger Gene SetFrom HPO Gene-Disease Associations genes associated with the single interphalangeal crease of fifth finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal/middle symphalangism of 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the distal/middle symphalangism of 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
ulnar deviation of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the ulnar deviation of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the phalanges of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the phalanges of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the long distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
finger joint hypermobility Gene SetFrom HPO Gene-Disease Associations genes associated with the finger joint hypermobility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
flexion contracture of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the flexion contracture of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
2-4 finger syndactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the 2-4 finger syndactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
deviation of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the deviation of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
congenital finger flexion contractures Gene SetFrom HPO Gene-Disease Associations genes associated with the congenital finger flexion contractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
symphalangism affecting the proximal phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the symphalangism affecting the proximal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
1-5 finger syndactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the 1-5 finger syndactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
contracture of the proximal interphalangeal joint of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the contracture of the proximal interphalangeal joint of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular shaped proximal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular shaped proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypersegmentation of proximal phalanx of third finger Gene SetFrom HPO Gene-Disease Associations genes associated with the hypersegmentation of proximal phalanx of third finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
finger joint hyperextensibility Gene SetFrom HPO Gene-Disease Associations genes associated with the finger joint hyperextensibility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of the distal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged epiphysis of the proximal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the enlarged epiphysis of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tapered distal phalanges of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the tapered distal phalanges of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
streaks of hyperkeratosis along each finger onto the palm Gene SetFrom HPO Gene-Disease Associations genes associated with the streaks of hyperkeratosis along each finger onto the palm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
1-5 finger complete cutaneous syndactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the 1-5 finger complete cutaneous syndactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged epiphyses of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the enlarged epiphyses of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hyperextensibility of the finger joints Gene SetFrom HPO Gene-Disease Associations genes associated with the hyperextensibility of the finger joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal finger flexion creases Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal finger flexion creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sclerosis of finger phalanx Gene SetFrom HPO Gene-Disease Associations genes associated with the sclerosis of finger phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the proximal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular epiphysis of the middle phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
polydactyly affecting the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the polydactyly affecting the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the middle phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
ulnar deviation of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the ulnar deviation of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the proximal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged epiphysis of the middle phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the enlarged epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tapered finger Gene SetFrom HPO Gene-Disease Associations genes associated with the tapered finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
3-4 finger syndactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the 3-4 finger syndactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent fourth finger distal interphalangeal crease Gene SetFrom HPO Gene-Disease Associations genes associated with the absent fourth finger distal interphalangeal crease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Replication termination factor 2, RING-finger Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Replication termination factor 2, RING-finger protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA topoisomerase, type IA, zn finger Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA topoisomerase, type IA, zn finger protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
finger Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term finger in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
finger Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue finger in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Joint Contracture Of The 5Th Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Joint Contracture Of The 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fifth Finger Distal Phalanx Clinodactyly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fifth Finger Distal Phalanx Clinodactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Absent Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Absent Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Finger Flexion Contractures Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Finger Flexion Contractures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cutaneous Finger Syndactyly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cutaneous Finger Syndactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Broad Middle Phalanx Of Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Broad Middle Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Tapering Pointed Ends Of Distal Finger Phalanges Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Tapering Pointed Ends Of Distal Finger Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short 5Th Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ectopic Accessory Finger-Like Appendage Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ectopic Accessory Finger-Like Appendage in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Finger Symphalangism Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Finger Symphalangism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Radial Deviation Of The 3Rd Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Radial Deviation Of The 3Rd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Partial Duplication Of The Distal Phalanx Of The 2Nd Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Partial Duplication Of The Distal Phalanx Of The 2Nd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Partial Duplication Of The Distal Phalanx Of The 3Rd Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Partial Duplication Of The Distal Phalanx Of The 3Rd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long Phalanx Of Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Deformity Of Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Deformity Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypersegmentation Of Proximal Phalanx Of Second Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypersegmentation Of Proximal Phalanx Of Second Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hypersegmentation Of Proximal Phalanx Of Third Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hypersegmentation Of Proximal Phalanx Of Third Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short 3Rd Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short 3Rd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Finger Syndactyly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Finger Syndactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Radial Deviation Of The 4Th Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Radial Deviation Of The 4Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long Distal Phalanx Of Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Distal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long Proximal Phalanx Of Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Proximal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Slender Proximal Phalanx Of Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Slender Proximal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Interphalangeal Joint Contracture Of Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Interphalangeal Joint Contracture Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acquired Trigger Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acquired Trigger Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Trigger Finger Disorder Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Trigger Finger Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Absent Fourth Finger Distal Interphalangeal Crease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Absent Fourth Finger Distal Interphalangeal Crease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia/Hypoplasia Of The 5Th Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia/Hypoplasia Of The 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Broad Phalanges Of The 5Th Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Broad Phalanges Of The 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Finger Agnosia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Finger Agnosia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Radial Deviation Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Radial Deviation Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Flexion Contracture Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Flexion Contracture Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Phalanx Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Weakness Of Long Finger Extensor Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Weakness Of Long Finger Extensor Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Broad Distal Phalanx Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Distal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Broad Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Finger Flexion Creases Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Finger Flexion Creases in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Slender Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Slender Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Finger Spasticity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Finger Spasticity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Finger Syndactyly Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Finger Syndactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal/Middle Symphalangism Of 5Th Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal/Middle Symphalangism Of 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Radial Deviation Of The 2Nd Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Radial Deviation Of The 2Nd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short 2Nd Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short 2Nd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Finger Joint Hypermobility Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Finger Joint Hypermobility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hyperextensibility Of The Finger Joints Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hyperextensibility Of The Finger Joints in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absent Proximal Finger Flexion Creases Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Proximal Finger Flexion Creases in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Deviation Of The 5Th Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Deviation Of The 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Complete Duplication Of The Middle Phalanx Of The 3Rd Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Complete Duplication Of The Middle Phalanx Of The 3Rd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Partial Duplication Of The Proximal Phalanx Of The 3Rd Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Partial Duplication Of The Proximal Phalanx Of The 3Rd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Streaks Of Hyperkeratosis Along Each Finger Onto The Palm Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Streaks Of Hyperkeratosis Along Each Finger Onto The Palm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Tapered Distal Phalanges Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tapered Distal Phalanges Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Finger Flexor Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Finger Flexor Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Finger Mobility Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Finger Mobility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absent Middle Phalanx Of 5Th Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Middle Phalanx Of 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Patchy Sclerosis Of Finger Phalanx Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Patchy Sclerosis Of Finger Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of The Middle Phalanx Of The 5Th Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Middle Phalanx Of The 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Small Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Small Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Pain In Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pain In Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Slender Distal Phalanx Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Slender Distal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Single Interphalangeal Crease Of Fifth Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Single Interphalangeal Crease Of Fifth Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Swelling Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Swelling Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Finger Contracture Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Finger Contracture in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Deviation Of The 2Nd Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Deviation Of The 2Nd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal/Middle Symphalangism Of 5Th Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal/Middle Symphalangism Of 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Symphalangism Of The 5Th Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Symphalangism Of The 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Finger agnosia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Finger agnosia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Finger Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Finger in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Congenital finger flexion contractures Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital finger flexion contractures phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Clinodactyly of the 5th finger Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Clinodactyly of the 5th finger phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Symphalangism affecting the proximal phalanx of the 4th finger Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Symphalangism affecting the proximal phalanx of the 4th finger phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Finger syndactyly Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Finger syndactyly phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Abnormal finger morphology Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal finger morphology phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Short 5th finger Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Short 5th finger phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Trigger finger Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Trigger finger phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Finger osteoarthritis severity (hand Klsum) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Finger osteoarthritis severity (hand Klsum) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
carboxy-terminal domain protein kinase complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the carboxy-terminal domain protein kinase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
carboxy-terminal domain protein kinase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the carboxy-terminal domain protein kinase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
membrane protein intracellular domain proteolysis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the membrane protein intracellular domain proteolysis biological process from the curated GO Biological Process Annotations 2015 dataset. |
carboxy-terminal domain protein kinase complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the carboxy-terminal domain protein kinase complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
protein domain specific binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the protein domain specific binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Triple functional domain protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Triple functional domain protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Axin interactor dorsalization-associated protein, C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Axin interactor dorsalization-associated protein, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Methyl-CpG binding protein 2/3, C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Methyl-CpG binding protein 2/3, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
MDM2-binding protein, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the MDM2-binding protein, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L31e domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L31e domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Nuclear fragile X mental retardation-interacting protein 1, conserved domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Nuclear fragile X mental retardation-interacting protein 1, conserved domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Storkhead-box protein, winged-helix domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Storkhead-box protein, winged-helix domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
A-kinase anchor protein 2, C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the A-kinase anchor protein 2, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein S1, RNA-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein S1, RNA-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Glycolipid transfer protein domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Glycolipid transfer protein domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L23/L15e core domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L23/L15e core domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L5 domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L5 domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cytochrome c oxidase assembly protein CtaG/Cox11, domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cytochrome c oxidase assembly protein CtaG/Cox11, domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Distal-less-like homeobox protein, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Distal-less-like homeobox protein, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Centromere protein CENP-B, dimerisation domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Centromere protein CENP-B, dimerisation domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Abscisic acid G-protein coupled receptor-like domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Abscisic acid G-protein coupled receptor-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L25/Gln-tRNA synthetase, beta-barrel domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L25/Gln-tRNA synthetase, beta-barrel domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Microtubule-associated serine/threonine-protein kinase, pre-PK domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Microtubule-associated serine/threonine-protein kinase, pre-PK domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
SKI-interacting protein SKIP, SNW domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the SKI-interacting protein SKIP, SNW domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein ASX-like, PHD domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein ASX-like, PHD domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein kinase domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein kinase domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Nuclear pore localisation protein Npl4, ubiquitin-like domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Nuclear pore localisation protein Npl4, ubiquitin-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Peptidoglycan recognition protein family domain, metazoa/bacteria Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Peptidoglycan recognition protein family domain, metazoa/bacteria protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Sorting nexin protein, WASP-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Sorting nexin protein, WASP-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Prion/Doppel protein, beta-ribbon domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Prion/Doppel protein, beta-ribbon domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Alpha-2-macroglobulin receptor-associated protein, domain 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Alpha-2-macroglobulin receptor-associated protein, domain 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein S24/S35, mitochondrial, conserved domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein S24/S35, mitochondrial, conserved domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Calmodulin-regulated spectrin-associated protein, CH domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Calmodulin-regulated spectrin-associated protein, CH domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cullin protein, neddylation domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cullin protein, neddylation domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Histone RNA hairpin-binding protein, RNA-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Histone RNA hairpin-binding protein, RNA-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
WAP four-disulfide core domain protein 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the WAP four-disulfide core domain protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Glycine cleavage T-protein, C-terminal barrel domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Glycine cleavage T-protein, C-terminal barrel domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Calcium/calmodulin-dependent protein kinase II, association-domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Calcium/calmodulin-dependent protein kinase II, association-domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Inner centromere protein, ARK-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Inner centromere protein, ARK-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA recombination and repair protein RecA-like, ATP-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA recombination and repair protein RecA-like, ATP-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
MDN2-binding protein, C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the MDN2-binding protein, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
GTP-binding protein, orthogonal bundle domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the GTP-binding protein, orthogonal bundle domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L30, ferredoxin-like fold domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L30, ferredoxin-like fold domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
LIM domain only protein 7 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the LIM domain only protein 7 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Nucleolar GTP-binding protein 1, Rossman-fold domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Nucleolar GTP-binding protein 1, Rossman-fold domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L6, alpha-beta domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L6, alpha-beta domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
T-complex protein 10, C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the T-complex protein 10, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Serine/threonine-protein kinase OSR1/WNK, CCT domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Serine/threonine-protein kinase OSR1/WNK, CCT domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
MDM2-binding protein, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the MDM2-binding protein, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
LIM domain and actin-binding protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the LIM domain and actin-binding protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
WW-domain-binding protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the WW-domain-binding protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein phosphatase 1 binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein phosphatase 1 binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small GTP-binding protein domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTP-binding protein domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Phosphorylated adapter RNA export protein, RNA-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Phosphorylated adapter RNA export protein, RNA-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Hypoxia induced protein, domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Hypoxia induced protein, domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Dishevelled protein domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Dishevelled protein domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein S10 domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein S10 domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Breast cancer type 2 susceptibility protein, helical domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Breast cancer type 2 susceptibility protein, helical domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Domain of unknown function DUF3385, target of rapamycin protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Domain of unknown function DUF3385, target of rapamycin protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tuftelin interacting protein, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tuftelin interacting protein, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tex-like protein, HTH domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tex-like protein, HTH domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
RNA-polymerase II-associated protein 3-like, C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the RNA-polymerase II-associated protein 3-like, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Hedgehog protein, Hint domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Hedgehog protein, Hint domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
AIR synthase-related protein, C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the AIR synthase-related protein, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
MAP kinase activated protein kinase, C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the MAP kinase activated protein kinase, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
WAP four-disulfide core domain protein 12 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the WAP four-disulfide core domain protein 12 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
WAP four-disulfide core domain protein 13 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the WAP four-disulfide core domain protein 13 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tyrosine-protein kinase, catalytic domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tyrosine-protein kinase, catalytic domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tyrosine-protein kinase, receptor Tie-2, Ig-like domain 1, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tyrosine-protein kinase, receptor Tie-2, Ig-like domain 1, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Gamma-secretase-activating protein, C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Gamma-secretase-activating protein, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L19/L19e domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L19/L19e domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Competence protein ComEA, helix-hairpin-helix domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Competence protein ComEA, helix-hairpin-helix domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Serine-threonine/tyrosine-protein kinase catalytic domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Serine-threonine/tyrosine-protein kinase catalytic domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein S2, flavodoxin-like domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein S2, flavodoxin-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Developmental pluripotency-associated protein 2/4, C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Developmental pluripotency-associated protein 2/4, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tyrosine-protein kinase SYK/ZAP-70, inter-SH2 domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tyrosine-protein kinase SYK/ZAP-70, inter-SH2 domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L19/L19e, domain 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L19/L19e, domain 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L19/L19e, domain 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L19/L19e, domain 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Seven-in-absentia protein, TRAF-like domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Seven-in-absentia protein, TRAF-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L15e core domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L15e core domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Rap GTPase activating protein domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Rap GTPase activating protein domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Folliculin-interacting protein, C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Folliculin-interacting protein, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tumour suppressor p53-binding protein-1 Tudor domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumour suppressor p53-binding protein-1 Tudor domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
LIM domain-binding protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the LIM domain-binding protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Growth-arrest-specific protein 2 domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Growth-arrest-specific protein 2 domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
PDZ and LIM domain protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the PDZ and LIM domain protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
FCH domain only protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the FCH domain only protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
FCH domain only protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the FCH domain only protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein kinase-like domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein kinase-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
EH domain-binding protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the EH domain-binding protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
RPA-interacting protein, C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the RPA-interacting protein, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Adaptor protein Cbl, PTB domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Adaptor protein Cbl, PTB domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
LIM domain-binding protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the LIM domain-binding protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Recombination activating protein 2, PHD domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Recombination activating protein 2, PHD domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Serine/threonine/dual specificity protein kinase, catalytic domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Serine/threonine/dual specificity protein kinase, catalytic domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Nucleolar GTP-binding protein 2, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Nucleolar GTP-binding protein 2, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein-arginine deiminase (PAD), central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein-arginine deiminase (PAD), central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Translation protein SH3-like domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Translation protein SH3-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein S5 domain 2-type fold, subgroup Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein S5 domain 2-type fold, subgroup protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar sorting protein 39/Transforming growth factor beta receptor-associated domain 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar sorting protein 39/Transforming growth factor beta receptor-associated domain 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar sorting protein 39/Transforming growth factor beta receptor-associated domain 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar sorting protein 39/Transforming growth factor beta receptor-associated domain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Nse4/EID protein, Nse3/MAGE-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Nse4/EID protein, Nse3/MAGE-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ferritin/DPS protein domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ferritin/DPS protein domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Adenomatous polyposis coli protein basic domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Adenomatous polyposis coli protein basic domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Dimerization-anchoring domain of cAMP-dependent protein kinase, regulatory subunit Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Dimerization-anchoring domain of cAMP-dependent protein kinase, regulatory subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
RPA-interacting protein, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the RPA-interacting protein, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA mismatch repair protein MutS, connector domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA mismatch repair protein MutS, connector domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
FAM69, protein-kinase domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the FAM69, protein-kinase domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Regulator of G protein signalling-like domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Regulator of G protein signalling-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
RPA-interacting protein, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the RPA-interacting protein, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein 14 C-terminal Fig4-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein 14 C-terminal Fig4-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L4 domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L4 domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L25/Gln-tRNA synthetase, anti-codon-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L25/Gln-tRNA synthetase, anti-codon-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Hydrolethalus syndrome protein 1, C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Hydrolethalus syndrome protein 1, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Methyl-CpG-binding domain protein 4 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Methyl-CpG-binding domain protein 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Developmental pluripotency-associated protein 2/4, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Developmental pluripotency-associated protein 2/4, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Periplasmic copper-binding protein NosD, beta helix domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Periplasmic copper-binding protein NosD, beta helix domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Heat shock protein 70kD, peptide-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Heat shock protein 70kD, peptide-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Translation protein, beta-barrel domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Translation protein, beta-barrel domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Regulatory factor X-associated protein, RFXANK-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Regulatory factor X-associated protein, RFXANK-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
EGF domain, merozoite surface protein 1-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the EGF domain, merozoite surface protein 1-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L2 domain 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L2 domain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
60S ribosomal protein L4, C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the 60S ribosomal protein L4, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein phosphatase 2C (PP2C)-like domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein phosphatase 2C (PP2C)-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vitamin D binding protein, domain III Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vitamin D binding protein, domain III protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Heat shock protein DnaJ, cysteine-rich domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Heat shock protein DnaJ, cysteine-rich domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA/RNA-binding protein Kin17, conserved domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA/RNA-binding protein Kin17, conserved domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
WW domain binding protein 11 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the WW domain binding protein 11 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein S16 domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein S16 domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Thrombospondin/cartilage oligomeric matrix protein, coiled-coil domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Thrombospondin/cartilage oligomeric matrix protein, coiled-coil domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Trafficking kinesin-binding protein domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Trafficking kinesin-binding protein domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
LIM-domain binding protein/SEUSS Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the LIM-domain binding protein/SEUSS protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Rho GTPase-activating protein domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Rho GTPase-activating protein domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Bactericidal permeability-increasing protein, alpha/beta domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Bactericidal permeability-increasing protein, alpha/beta domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Microspherule protein, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Microspherule protein, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Folliculin-interacting protein, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Folliculin-interacting protein, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein kinase C-like, phorbol ester/diacylglycerol-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein kinase C-like, phorbol ester/diacylglycerol-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L39e domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L39e domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Heat shock protein 70kD, C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Heat shock protein 70kD, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
ADP-ribosylation factor-like 2-binding protein, domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the ADP-ribosylation factor-like 2-binding protein, domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vesicle tethering protein Uso1/P115-like , head domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vesicle tethering protein Uso1/P115-like , head domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Membrane transport protein, MMPL domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Membrane transport protein, MMPL domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Guanine nucleotide-binding protein-like 3, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Guanine nucleotide-binding protein-like 3, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein S7 domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein S7 domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L24e domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L24e domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cwf19-like protein, C-terminal domain-2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cwf19-like protein, C-terminal domain-2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Gap junction protein, cysteine-rich domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Gap junction protein, cysteine-rich domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Microtubule-associated serine/threonine-protein kinase, domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Microtubule-associated serine/threonine-protein kinase, domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein translocase SecE domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein translocase SecE domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L14 domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L14 domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
AIR synthase related protein, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the AIR synthase related protein, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Hermansky-Pudlak syndrome 3 protein, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Hermansky-Pudlak syndrome 3 protein, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Folliculin-interacting protein, middle domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Folliculin-interacting protein, middle domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Glycine cleavage T-protein/YgfZ, C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Glycine cleavage T-protein/YgfZ, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L2, domain 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L2, domain 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Major prion protein N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Major prion protein N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar ATPase assembly integral membrane protein VMA21-like domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar ATPase assembly integral membrane protein VMA21-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein S5 domain 2-type fold Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein S5 domain 2-type fold protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Hermansky-Pudlak syndrome 3 protein, C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Hermansky-Pudlak syndrome 3 protein, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
LIM-domain binding protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the LIM-domain binding protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small acidic protein-like domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small acidic protein-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cation efflux protein transmembrane domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cation efflux protein transmembrane domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Telomere length regulation protein, conserved domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Telomere length regulation protein, conserved domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
G-protein gamma-like domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the G-protein gamma-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
WAP four-disulfide core domain protein 10A Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the WAP four-disulfide core domain protein 10A protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
WAP four-disulfide core domain protein 5 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the WAP four-disulfide core domain protein 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L13 domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L13 domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Domain of unknown function DUF3528, homeobox protein, eukaryotic Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Domain of unknown function DUF3528, homeobox protein, eukaryotic protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein/NADH dehydrogenase domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein/NADH dehydrogenase domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
membrane protein intracellular domain proteolysis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the membrane protein intracellular domain proteolysis biological process from the curated GO Biological Process Annotations 2023 dataset. |
membrane protein intracellular domain proteolysis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the membrane protein intracellular domain proteolysis biological process from the curated GO Biological Process Annotations 2025 dataset. |
carboxy-terminal domain protein kinase complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the carboxy-terminal domain protein kinase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
carboxy-terminal domain protein kinase complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the carboxy-terminal domain protein kinase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease eclampsia; pre-eclampsia; protein c deficiency; protein s deficiency; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease factor v deficiency; hypoprothrombinemias; protein c deficiency; protein s deficiency; pulmonary embolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
activated protein c resistance; protein s deficiency; thrombophilia; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease activated protein c resistance; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
protein c deficiency; protein s deficiency; venous thrombosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease protein c deficiency; protein s deficiency; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neoplasms; protein c deficiency; protein s deficiency; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
negative regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein modification by small protein conjugation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein modification by small protein conjugation biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of g-protein coupled receptor protein signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of g-protein coupled receptor protein signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein maturation by protein folding Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein maturation by protein folding biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein targeting to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein targeting to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of protein kinase activity by regulation of protein phosphorylation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of protein kinase activity by regulation of protein phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of g-protein coupled receptor protein signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of g-protein coupled receptor protein signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2015 dataset. |
activation of signaling protein activity involved in unfolded protein response Gene SetFrom GO Biological Process Annotations 2015 genes participating in the activation of signaling protein activity involved in unfolded protein response biological process from the curated GO Biological Process Annotations 2015 dataset. |
desensitization of g-protein coupled receptor protein signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the desensitization of g-protein coupled receptor protein signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein ubiquitination involved in ubiquitin-dependent protein catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein ubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein deubiquitination involved in ubiquitin-dependent protein catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein deubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of g-protein coupled receptor protein signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of g-protein coupled receptor protein signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of protein ubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein kinase c-activating g-protein coupled receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein kinase c-activating g-protein coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
desensitization of g-protein coupled receptor protein signaling pathway by arrestin Gene SetFrom GO Biological Process Annotations 2015 genes participating in the desensitization of g-protein coupled receptor protein signaling pathway by arrestin biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein modification by small protein removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein modification by small protein removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein binding involved in protein folding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the protein binding involved in protein folding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Vacuolar protein sorting-associated protein 54 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 54 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Myelin protein zero-like protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Myelin protein zero-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Myelin protein zero-like protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Myelin protein zero-like protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Myelin protein zero-like protein 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Myelin protein zero-like protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tumour protein p53-inducible nuclear protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumour protein p53-inducible nuclear protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
ADP-ribosylation factor-like protein 6-interacting protein 6 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the ADP-ribosylation factor-like protein 6-interacting protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Dyslexia-associated protein KIAA0319-like protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Dyslexia-associated protein KIAA0319-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small proline-rich protein/late cornified envelope protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small proline-rich protein/late cornified envelope protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Guanine nucleotide binding protein (G-protein), alpha subunit Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Guanine nucleotide binding protein (G-protein), alpha subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein transport protein SecG/Sec61-beta/Sbh Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein transport protein SecG/Sec61-beta/Sbh protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
50S ribosomal protein L18Ae/60S ribosomal protein L20 and L18a Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the 50S ribosomal protein L18Ae/60S ribosomal protein L20 and L18a protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cleft lip and palate transmembrane protein 1-like protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cleft lip and palate transmembrane protein 1-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Pre-rRNA-processing protein IPI1/Testis-expressed sequence 10 protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Pre-rRNA-processing protein IPI1/Testis-expressed sequence 10 protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tumor protein p53-inducible protein 11 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumor protein p53-inducible protein 11 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Actin-related protein 2/3 complex subunit 5-like protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Actin-related protein 2/3 complex subunit 5-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Insulin-like growth factor binding protein-related protein (IGFBP-rP), MAC25 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Insulin-like growth factor binding protein-related protein (IGFBP-rP), MAC25 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
SWR1-complex protein 5/Craniofacial development protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the SWR1-complex protein 5/Craniofacial development protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DMRT/protein doublesex/protein male abnormal 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DMRT/protein doublesex/protein male abnormal 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L7/L12, C-terminal/adaptor protein ClpS-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L7/L12, C-terminal/adaptor protein ClpS-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
UV radiation resistance protein/autophagy-related protein 14 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the UV radiation resistance protein/autophagy-related protein 14 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Four-jointed box protein 1/four-jointed protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Four-jointed box protein 1/four-jointed protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
G protein-coupled receptor kinase-interacting protein 1 C term Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the G protein-coupled receptor kinase-interacting protein 1 C term protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
SWR1-complex protein 4/DNA methyltransferase 1-associated protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the SWR1-complex protein 4/DNA methyltransferase 1-associated protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting protein 26 related Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting protein 26 related protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tumor protein p53-inducible nuclear protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumor protein p53-inducible nuclear protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 41 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 41 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Bone morphogenetic protein 1/tolloid-like protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Bone morphogenetic protein 1/tolloid-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Synaptonemal complex protein 2/protein 2-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Synaptonemal complex protein 2/protein 2-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Sterol regulatory element-binding protein cleavage-activating protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Sterol regulatory element-binding protein cleavage-activating protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Polyadenylate-binding protein/Hyperplastic disc protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Polyadenylate-binding protein/Hyperplastic disc protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Receptor tyrosine-protein phosphatase C-associated protein CD45-AP Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Receptor tyrosine-protein phosphatase C-associated protein CD45-AP protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Growth arrest/ DNA-damage-inducible protein-interacting protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Growth arrest/ DNA-damage-inducible protein-interacting protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 16 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 16 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Probable cytosolic iron-sulfur protein assembly protein, CIAO1/Cia1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Probable cytosolic iron-sulfur protein assembly protein, CIAO1/Cia1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Outer membrane protein Iml2/Tetratricopeptide repeat protein 39 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Outer membrane protein Iml2/Tetratricopeptide repeat protein 39 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vesicle-associated membrane protein-associated protein B Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vesicle-associated membrane protein-associated protein B protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vesicle-associated membrane protein-associated protein A Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vesicle-associated membrane protein-associated protein A protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein LIN-9/Protein ALWAYS EARLY Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein LIN-9/Protein ALWAYS EARLY protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Steroid receptor RNA activator-protein/coat protein complex II, Sec31 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Steroid receptor RNA activator-protein/coat protein complex II, Sec31 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 35, Vps35 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 35, Vps35 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tumor protein p53-inducible nuclear protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumor protein p53-inducible nuclear protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein of unknown function DUF3697, ubiquitin-associated protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein of unknown function DUF3697, ubiquitin-associated protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Retinoic acid-induced protein 2/sine oculis-binding protein homologue Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Retinoic acid-induced protein 2/sine oculis-binding protein homologue protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tetracycline resistance protein, TetA/multidrug resistance protein MdtG Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tetracycline resistance protein, TetA/multidrug resistance protein MdtG protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
TYRO protein tyrosine kinase-binding protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the TYRO protein tyrosine kinase-binding protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Proline/serine-rich coiled-coil protein 1/G2 and S phase-expressed protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Proline/serine-rich coiled-coil protein 1/G2 and S phase-expressed protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal protein L1/ribosomal biogenesis protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal protein L1/ribosomal biogenesis protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Actin-related protein 8/Plant actin-related protein 9 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Actin-related protein 8/Plant actin-related protein 9 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Regulator of G-protein signalling 9-binding protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Regulator of G-protein signalling 9-binding protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 11 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 11 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 13 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 13 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vesicle-associated membrane-protein-associated protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vesicle-associated membrane-protein-associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting protein 11, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting protein 11, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
cAMP-responsive element-binding protein 3-like protein 4 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the cAMP-responsive element-binding protein 3-like protein 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
cAMP-responsive element-binding protein 3-like protein 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the cAMP-responsive element-binding protein 3-like protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
cAMP-responsive element-binding protein 3-like protein 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the cAMP-responsive element-binding protein 3-like protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
cAMP-responsive element-binding protein 3-like protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the cAMP-responsive element-binding protein 3-like protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vacuolar protein sorting-associated protein 33 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vacuolar protein sorting-associated protein 33 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Spermatogenesis-associated protein 2-like protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Spermatogenesis-associated protein 2-like protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
A-kinase anchor protein 6/Centrosomal protein of 68kDa Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the A-kinase anchor protein 6/Centrosomal protein of 68kDa protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
PodNet: protein-protein interactions in the podocyte(Mus musculus) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the PodNet: protein-protein interactions in the podocyte(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset. |
XPodNet - protein-protein interactions in the podocyte expanded by STRING(Mus musculus) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the XPodNet - protein-protein interactions in the podocyte expanded by STRING(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset. |
protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein kinase C-activating G protein-coupled receptor signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein kinase C-activating G protein-coupled receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein modification by small protein conjugation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein modification by small protein conjugation biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of protein kinase activity by regulation of protein phosphorylation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of protein kinase activity by regulation of protein phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein initiator methionine removal involved in protein maturation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein initiator methionine removal involved in protein maturation biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein deubiquitination involved in ubiquitin-dependent protein catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein deubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2023 dataset. |
membrane protein proteolysis involved in retrograde protein transport, ER to cytosol Gene SetFrom GO Biological Process Annotations 2023 genes participating in the membrane protein proteolysis involved in retrograde protein transport, ER to cytosol biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein modification by small protein removal Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein modification by small protein removal biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2023 dataset. |
Protein-protein interactions at synapses Gene Setproteins participating in the Protein-protein interactions at synapses pathway from the Reactome Pathways 2024 dataset. |
protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein transport to vacuole involved in ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein modification by small protein conjugation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein modification by small protein conjugation biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of protein kinase activity by regulation of protein phosphorylation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of protein kinase activity by regulation of protein phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein deubiquitination involved in ubiquitin-dependent protein catabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein deubiquitination involved in ubiquitin-dependent protein catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2025 dataset. |
membrane protein proteolysis involved in retrograde protein transport, ER to cytosol Gene SetFrom GO Biological Process Annotations 2025 genes participating in the membrane protein proteolysis involved in retrograde protein transport, ER to cytosol biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein modification by small protein removal Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein modification by small protein removal biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of protein processing involved in protein targeting to mitochondrion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of protein processing involved in protein targeting to mitochondrion biological process from the curated GO Biological Process Annotations 2025 dataset. |
precommissural pretectal domain Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in precommissural pretectal domain relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
liminal alar domain of m2 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in liminal alar domain of m2 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
accumbens nucleus, shell domain Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in accumbens nucleus, shell domain relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
accumbens nucleus, core domain Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in accumbens nucleus, core domain relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
liminal alar domain of m1 Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in liminal alar domain of m1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
diagonal domain Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in diagonal domain relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
juxtacommissural pretectal domain Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in juxtacommissural pretectal domain relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
prethalamic (p3) zona limitans domain Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in prethalamic (p3) zona limitans domain relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
commissural pretectal domain Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in commissural pretectal domain relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
first (dorsal) preoptic domain Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in first (dorsal) preoptic domain relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
second (ventral) preoptic domain Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in second (ventral) preoptic domain relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
thalamic (p2) zona limitans domain Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in thalamic (p2) zona limitans domain relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
proton-transporting two-sector atpase complex, proton-transporting domain Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the proton-transporting two-sector atpase complex, proton-transporting domain cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
vacuolar proton-transporting v-type atpase, v1 domain Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the vacuolar proton-transporting v-type atpase, v1 domain cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
proton-transporting two-sector atpase complex, catalytic domain Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the proton-transporting two-sector atpase complex, catalytic domain cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
chromosome, centromeric core domain Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the chromosome, centromeric core domain cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
proton-transporting v-type atpase, v1 domain Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the proton-transporting v-type atpase, v1 domain cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
vacuolar proton-transporting v-type atpase, v0 domain Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the vacuolar proton-transporting v-type atpase, v0 domain cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
proton-transporting v-type atpase, v0 domain Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the proton-transporting v-type atpase, v0 domain cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
lysp100-associated nuclear domain Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the lysp100-associated nuclear domain cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
proton-transporting two-sector atpase complex, catalytic domain Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the proton-transporting two-sector atpase complex, catalytic domain cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
proton-transporting two-sector atpase complex, proton-transporting domain Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the proton-transporting two-sector atpase complex, proton-transporting domain cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
C-CFTR-NHERF(PDZ1 domain)-ezrin complex Gene Setproteins in the C-CFTR-NHERF(PDZ1 domain)-ezrin complex protein complex from the CORUM Protein Complexes dataset. |
C-CFTR-NHERF(PDZ2 domain)-ezrin complex Gene Setproteins in the C-CFTR-NHERF(PDZ2 domain)-ezrin complex protein complex from the CORUM Protein Complexes dataset. |
negative regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2015 dataset. |
extrinsic apoptotic signaling pathway via death domain receptors Gene SetFrom GO Biological Process Annotations 2015 genes participating in the extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of phosphorylation of rna polymerase ii c-terminal domain serine 2 residues Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of phosphorylation of rna polymerase ii c-terminal domain serine 2 residues biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of phosphorylation of rna polymerase ii c-terminal domain Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of phosphorylation of rna polymerase ii c-terminal domain biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2015 dataset. |
dephosphorylation of rna polymerase ii c-terminal domain Gene SetFrom GO Biological Process Annotations 2015 genes participating in the dephosphorylation of rna polymerase ii c-terminal domain biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of phosphorylation of rna polymerase ii c-terminal domain serine 2 residues Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of phosphorylation of rna polymerase ii c-terminal domain serine 2 residues biological process from the curated GO Biological Process Annotations 2015 dataset. |
phosphorylation of rna polymerase ii c-terminal domain Gene SetFrom GO Biological Process Annotations 2015 genes participating in the phosphorylation of rna polymerase ii c-terminal domain biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of phosphorylation of rna polymerase ii c-terminal domain Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of phosphorylation of rna polymerase ii c-terminal domain biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of extrinsic apoptotic signaling pathway via death domain receptors Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of extrinsic apoptotic signaling pathway via death domain receptors biological process from the curated GO Biological Process Annotations 2015 dataset. |
proton-transporting two-sector atpase complex, proton-transporting domain Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the proton-transporting two-sector atpase complex, proton-transporting domain cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
vacuolar proton-transporting v-type atpase, v1 domain Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the vacuolar proton-transporting v-type atpase, v1 domain cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
proton-transporting two-sector atpase complex, catalytic domain Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the proton-transporting two-sector atpase complex, catalytic domain cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
chromosome, centromeric core domain Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the chromosome, centromeric core domain cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
proton-transporting v-type atpase, v1 domain Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the proton-transporting v-type atpase, v1 domain cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
vacuolar proton-transporting v-type atpase, v0 domain Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the vacuolar proton-transporting v-type atpase, v0 domain cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
proton-transporting v-type atpase, v0 domain Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the proton-transporting v-type atpase, v0 domain cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
lbd domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the lbd domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
bh4 domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the bh4 domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
pdz domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the pdz domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
gbd domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the gbd domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
rs domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the rs domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
nacht domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the nacht domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
chromo shadow domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the chromo shadow domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
leucine zipper domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the leucine zipper domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
sh3 domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the sh3 domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
poz domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the poz domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
hmg box domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the hmg box domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
lrr domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the lrr domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
mads box domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the mads box domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
l27 domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the l27 domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
armadillo repeat domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the armadillo repeat domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
ww domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the ww domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
card domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the card domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
sam domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the sam domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
gaf domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the gaf domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
ph domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the ph domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
bh3 domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the bh3 domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
ptb domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the ptb domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
set domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the set domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
wd40-repeat domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the wd40-repeat domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
dbd domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the dbd domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
death effector domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the death effector domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
tir domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the tir domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
titin z domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the titin z domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
af-1 domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the af-1 domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
mh1 domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the mh1 domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
death domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the death domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
af-2 domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the af-2 domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
fha domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the fha domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
rna polymerase ii carboxy-terminal domain kinase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the rna polymerase ii carboxy-terminal domain kinase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
pyrin domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the pyrin domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
eh domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the eh domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
mit domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the mit domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
tpr domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the tpr domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
sh2 domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the sh2 domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
hlh domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the hlh domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
bh domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the bh domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
lim domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the lim domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
dh domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the dh domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
krueppel-associated box domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the krueppel-associated box domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
kringle domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the kringle domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
f-box domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the f-box domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
mh2 domain binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the mh2 domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Tumour necrosis factor receptor 13C, TALL-1 binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tumour necrosis factor receptor 13C, TALL-1 binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Smad anchor for receptor activation, Smad-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Smad anchor for receptor activation, Smad-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Syndecan/Neurexin domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Syndecan/Neurexin domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Helicase Helix-turn-helix domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Helicase Helix-turn-helix domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Peptidase S9A, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Peptidase S9A, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U box domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U box domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Pirin, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Pirin, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
CXC chemokine receptor 4 N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the CXC chemokine receptor 4 N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Vitamin B12-dependent methionine synthase, activation domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Vitamin B12-dependent methionine synthase, activation domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ferritin- like diiron domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ferritin- like diiron domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Potassium channel tetramerisation-type BTB domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Potassium channel tetramerisation-type BTB domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Pleiotrophin/Midkine disulphide-rich domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Pleiotrophin/Midkine disulphide-rich domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Glutaminyl-tRNA synthetase, class Ib, non-specific RNA-binding domain 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Glutaminyl-tRNA synthetase, class Ib, non-specific RNA-binding domain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
KASH domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the KASH domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Glutamate/phenylalanine/leucine/valine dehydrogenase, dimerisation domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Glutamate/phenylalanine/leucine/valine dehydrogenase, dimerisation domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Synapsin, ATP-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Synapsin, ATP-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Glycerophosphodiester phosphodiesterase domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Glycerophosphodiester phosphodiesterase domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
MoeA, N-terminal and linker domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the MoeA, N-terminal and linker domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Domain of unknown function DUF1193 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Domain of unknown function DUF1193 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Domain of unknown function DUF382 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Domain of unknown function DUF382 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
S-adenosylmethionine synthetase, central domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the S-adenosylmethionine synthetase, central domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
TM2 domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the TM2 domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Neurolysin/Thimet oligopeptidase, domain 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Neurolysin/Thimet oligopeptidase, domain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
RWD domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the RWD domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Transcription regulator GCM domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Transcription regulator GCM domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Galactose mutarotase-like domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Galactose mutarotase-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Mif2/CENP-C cupin domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Mif2/CENP-C cupin domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Target SNARE coiled-coil domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Target SNARE coiled-coil domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Death-like domain of Spt6 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Death-like domain of Spt6 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Hydroxymethylglutaryl-CoA reductase, class I/II, NAD/NADP-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Hydroxymethylglutaryl-CoA reductase, class I/II, NAD/NADP-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Cyclin, C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Cyclin, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Brf1, TBP-binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Brf1, TBP-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
SPOC like C-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the SPOC like C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |