Harmonizome 3.0

From ESCAPE

Sets of target genes of transcription factors from published ChIP-chip, ChIP-seq, and other transcription factor binding site profiling studies;sets of differentially expressed genes following perturbation of a protein from gene expression data in GEO; sets of interacting proteins from high- and low-throughput protein-protein interaction studies; sets of targets of microRNAs from public databases, computationally predicted or experimentally verified

From Hub Proteins

Sets of proteins interacting with hub proteins aggregated from data

From SILAC Phosphoproteomics

Phosphorylation levels of proteins in cell lines following drug treatment

From SILAC Phosphoproteomics

Phosphorylation levels of proteins in cell lines following genetic perturbation (knockdown, knockout, over-expression, mutation)

From SILAC Phosphoproteomics

Phosphorylation levels of proteins in cell lines following ligand treatment

From GlyGen

Proteins glycosylated by saccharide ligands from glycosylation site citations

From ChIP-X Enrichment Analysis

Target genes of transcription factors from published ChIP-chip, ChIP-seq, and other transcription factor binding site profiling studies

From DrugBank

Sets of proteins targeted by drugs by manual literature curation

From Encyclopedia of DNA Elements

Target genes of transcription factors from transcription factor binding site profiles

From Jaspar PWMs

Target genes of transcription factors predicted using known transcription factor binding site motifs

From LINCS KinomeScan

Kinase inhibitor targets from percent inhibition of kinases by small molecules measured using purified kinases

From MiRTarBase

Target genes of microRNAs from published experiments

From MotifMap

Target genes of transcription factors predicted using known transcription factor binding site motifs

From TargetScan

Target genes of microRNAs predicted by searching genes for sites matching conserved miRNA seed regions

From TargetScan

Target genes of microRNAs predicted by searching genes for sites matching nonconserved miRNA seed regions

From ChIP-X Enrichment Analysis

Target genes of transcription factors from published ChIP-chip, ChIP-seq, and other transcription factor binding site profiling studies

From Jaspar PWMs

Target genes of human transcription factors predicted using known transcription factor binding site motifs

From Jaspar PWMs

Target genes of mouse transcription factors predicted using known transcription factor binding site motifs

From Drug-Gene Interaction Database

Sets of proteins targeted by drugs by data aggregation

seryl-tRNA synthetase

This gene belongs to the class II amino-acyl tRNA family. The encoded enzyme catalyzes the transfer of L-serine to tRNA (Ser) and is related to bacterial and yeast counterparts. Multiple alternatively spliced transcript variants have been described but the biological validity of all variants is unknown. [provided by RefSeq, Jul 2010]

post-GPI attachment to proteins 2 pseudogene

post-GPI attachment to proteins 1

The protein encoded by this gene functions early in the glycosylphosphatidylinositol (GPI) biosynthetic pathway, catalyzing the inositol deacylation of GPI. The encoded protein is required for the production of GPI that can attach to proteins, and this may be an important factor in the transport of GPI-anchored proteins from the endoplasmic reticulum to the Golgi. Defects in this gene are a cause an autosomal recessive form of cognitive impairment. [provided by RefSeq, Jul 2017]

post-GPI attachment to proteins 3

This gene encodes a glycosylphosphatidylinositol (GPI)-specific phospholipase that primarily localizes to the Golgi apparatus. This ubiquitously expressed gene is predicted to encode a seven-transmembrane protein that removes unsaturated fatty acids from the sn-2 position of GPI. The remodeling of the constituent fatty acids on GPI is thought to be important for the proper association between GPI-anchored proteins and lipid rafts. The tethering of proteins to plasma membranes via posttranslational GPI-anchoring is thought to play a role in protein sorting and trafficking. Mutations in this gene cause an autosomal recessive form of neurologic hyperphosphatasia with cognitive disability (HPMRS4). Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2017]

post-GPI attachment to proteins 2

The protein encoded by this gene plays a role in the maturation of glycosylphosphatidylinositol (GPI) anchors on GPI-anchored proteins. Mutations in this gene are associated with an autosomal recessive syndrome characterized by hyperphosphatasia and intellectual disability. [provided by RefSeq, Jul 2017]

negative regulator of ubiquitin-like proteins 1

This gene encodes a protein that functions as a negative regulator of NEDD8, a ubiquitin-like protein that conjugates with cullin family members in order to regulate vital biological events. The protein encoded by this gene regulates the NEDD8 conjugation system post-transcriptionally by recruiting NEDD8 and its conjugates to the proteasome for degradation. This protein interacts with the product of the AIPL1 gene, which is associated with Leber congenital amaurosis, an inherited retinopathy, and mutations in that gene can abolish interaction with this protein, which may contribute to the pathogenesis. This protein is also known to accumulate in Lewy bodies in Parkinson's disease and dementia with Lewy bodies, and in glial cytoplasmic inclusions in multiple system atrophy, with this abnormal accumulation being specific to alpha-synucleinopathy lesions. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Aug 2011]

guided entry of tail-anchored proteins factor 3, ATPase

This gene represents the human homolog of the bacterial arsA gene, encoding the arsenite-stimulated ATPase component of the arsenite transporter responsible for resistance to arsenicals. This protein is also a central component of a transmembrane domain (TMD) recognition complex (TRC) that is involved in the post-translational delivery of tail-anchored (TA) proteins from the cytosol to the endoplasmic reticulum (ER). It recognizes and selectively binds the TMD of TA proteins in the cytosol, and delivers them to the ER for insertion. [provided by RefSeq, Oct 2011]

guided entry of tail-anchored proteins factor 1

This gene is located in the candidate region for congenital heart disease (CHD) in Down syndrome (DS). It encodes a basic protein that functions as a receptor that promotes insertion of tail-anchored proteins in the endoplasmic reticulum membrane. This gene is located at a maternally-methylated differentially methylated region (DMR); however, its transcription may be biallelic, not imprinted. Alternative splicing results in different transcript variants. A pseudogene has been defined on chromosome 4. [provided by RefSeq, Apr 2017]

post-GPI attachment to proteins GalNAc transferase 4

Enables glycosyltransferase activity. Involved in GPI anchor biosynthetic process. Located in Golgi membrane. [provided by Alliance of Genome Resources, Mar 2025]

post-GPI attachment to proteins 6

Predicted to enable calcium-dependent phospholipase A2 activity and calcium-independent phospholipase A2 activity. Predicted to be involved in lipid metabolic process. Located in extracellular exosome and lysosomal membrane. [provided by Alliance of Genome Resources, Mar 2025]

PDZ domain containing ring finger 4

Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Mar 2025]

PDZ domain containing ring finger 3

This gene encodes a member of the LNX (Ligand of Numb Protein-X) family of RING-type ubiquitin E3 ligases. This protein may function in vascular morphogenesis and the differentiation of adipocytes, osteoblasts and myoblasts. This protein may be targeted for degradation by the human papilloma virus E6 protein. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]

FERM and PDZ domain-containing protein 2-like

PDZ domain containing 1 pseudogene 1

Predicted to enable protein-membrane adaptor activity and signaling receptor binding activity. Predicted to be involved in protein localization to plasma membrane. Predicted to be active in apical plasma membrane. [provided by Alliance of Genome Resources, Mar 2025]

PDZ binding kinase

This gene encodes a serine/threonine protein kinase related to the dual specific mitogen-activated protein kinase kinase (MAPKK) family. Evidence suggests that mitotic phosphorylation is required for its catalytic activity. The encoded protein may be involved in the activation of lymphoid cells and support testicular functions, with a suggested role in the process of spermatogenesis. Overexpression of this gene has been implicated in tumorigenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]

PDZ domain containing 11 pseudogene

FERM and PDZ domain containing 4

This gene encodes a multi-domain (WW, PDZ, FERM) containing protein. Through its interaction with other proteins (such as PSD-95), it functions as a positive regulator of dendritic spine morphogenesis and density, and is required for the maintenance of excitatory synaptic transmission. [provided by RefSeq, Jan 2010]

FERM and PDZ domain containing 1

Involved in establishment of protein localization to membrane and regulation of G protein-coupled receptor signaling pathway. Located in cell cortex and plasma membrane. Part of protein-containing complex. [provided by Alliance of Genome Resources, Mar 2025]

FERM and PDZ domain containing 3

This gene encodes a protein that contains a PDZ (post synaptic density protein (PSD95), Drosophila disc large tumor suppressor (Dlg1), and zonula occludens-1 protein (zo-1) domain at the N-terminus followed by a FERM domain. The encoded protein is involved in signal transduction. The PDZ domain is thought to function in protein-protein interactions, mainly by binding to specific C-terminal peptides of other proteins. The FERM domain is found in proteins that are localized to the plasma membrane and are associated with the cytoskeleton. [provided by RefSeq, May 2017]

FERM and PDZ domain containing 2

This gene encodes a peripheral membrane protein and is located in a region of chromosome 10q that contains a segmental duplication. This copy of the gene is full-length and is in the telomeric duplicated region. Two other more centromerically proximal copies of the gene are partial and may represent pseudogenes. This full-length gene appears to function in the establishment and maintenance of cell polarization. The protein is recruited to cell-cell junctions in an E-cadherin-dependent manner, and is selectively localized at the basolateral membrane in polarized epithelial cells. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2009]

PDZ and LIM domain 1 pseudogene 4

PDZ and LIM domain 1 pseudogene 3

PDZ and LIM domain 1 pseudogene 2

PDZ and LIM domain 1 pseudogene 1

FERM and PDZ domain-containing protein 2

golgi-associated PDZ and coiled-coil motif containing

This gene encodes a Golgi protein with a PDZ domain. The PDZ domain is globular and proteins which contain them bind other proteins through short motifs near the C-termini. Mice which are deficient in the orthologous protein have globozoospermia and are infertile. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]

PDZ domain containing 1

This gene encodes a PDZ domain-containing scaffolding protein. PDZ domain-containing molecules bind to and mediate the subcellular localization of target proteins. The encoded protein mediates the localization of cell surface proteins and plays a critical role in cholesterol metabolism by regulating the HDL receptor, scavenger receptor class B type 1. Single nucleotide polymorphisms in this gene may be associated with metabolic syndrome, and overexpression of this gene may play a role in drug resistance of multiple myeloma. Pseudogenes of this gene are located on the long arm of chromosome 1. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jan 2011]

cysteine-rich PDZ-binding protein

This gene encodes a protein that binds to the PDZ3 peptide recognition domain. The encoded protein may modulates protein interactions with the cytoskeleton. A mutation in this gene resulted in short stature with microcephaly and distinctive facies. [provided by RefSeq, Jun 2014]

PDZ domain containing 7

This gene encodes a ciliary protein homologous to proteins which are mutated in Usher syndrome patients, and mutations and translocations involving this gene have been associated with two types of Usher syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2010]

PDZ domain containing 4

Predicted to be located in cell cortex. [provided by Alliance of Genome Resources, Mar 2025]

PDZ domain containing 3

Guanylyl cyclase C (GCC, or GUCY2C; MIM 601330) produces cGMP following the binding of either endogenous ligands or heat-stable enterotoxins secreted by E. coli and other enteric bacteria. Activation of GCC initiates a signaling cascade that leads to phosphorylation of the cystic fibrosis transmembrane conductance regulator (CFTR; MIM 602421), followed by a net efflux of ions and water into the intestinal lumen. IKEPP is a regulatory protein that associates with GCC and regulates the amount of cGMP produced following receptor stimulation (Scott et al., 2002 [PubMed 11950846]).[supplied by OMIM, Mar 2008]

PDZ domain containing 2

The protein encoded by this gene contains six PDZ domains and shares sequence similarity with pro-interleukin-16 (pro-IL-16). Like pro-IL-16, the encoded protein localizes to the endoplasmic reticulum and is thought to be cleaved by a caspase to produce a secreted peptide containing two PDZ domains. In addition, this gene is upregulated in primary prostate tumors and may be involved in the early stages of prostate tumorigenesis. [provided by RefSeq, Dec 2015]

PDZ domain containing 9

PDZ domain containing 8

Predicted to enable lipid binding activity and metal ion binding activity. Involved in several processes, including mitochondrial calcium ion homeostasis; mitochondrion-endoplasmic reticulum membrane tethering; and regulation of cell morphogenesis. Located in endoplasmic reticulum membrane and mitochondria-associated endoplasmic reticulum membrane contact site. [provided by Alliance of Genome Resources, Mar 2025]

PDZ domain containing 11

Predicted to enable protein-macromolecule adaptor activity. Involved in pore complex assembly. Located in basolateral plasma membrane and cytosol. Part of pore complex. [provided by Alliance of Genome Resources, Mar 2025]

PDZ 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]

PDZ 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]

PDZ 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]

PDZ 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]

PDZ 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]

PDZ 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]

FERM and PDZ domain containing 2 pseudogene

PDZ and LIM domain 7 (enigma) pseudogene

FERM and PDZ domain containing 2B, pseudogene

This gene represents a pseudogene of the FERM and PDZ domain containing 2 gene (FRMPD2, GeneID 143162). Along with the functional gene, this gene is located in a region of segmental duplication on chromosome 10q. [provided by RefSeq, Dec 2014]

multiple 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]

membrane associated guanylate kinase, WW and PDZ domain containing 3

Predicted to enable frizzled binding activity. Predicted to be involved in signal transduction. Predicted to act upstream of or within positive regulation of JUN kinase activity. Located in cell junction. [provided by Alliance of Genome Resources, Mar 2025]

membrane associated guanylate kinase, WW and PDZ domain containing 2

The protein encoded by this gene interacts with atrophin-1. Atrophin-1 contains a polyglutamine repeat, expansion of which is responsible for dentatorubral and pallidoluysian atrophy. This encoded protein is characterized by two WW domains, a guanylate kinase-like domain, and multiple PDZ domains. It has structural similarity to the membrane-associated guanylate kinase homologue (MAGUK) family. [provided by RefSeq, Jul 2008]

membrane associated guanylate kinase, WW and PDZ domain containing 1

The protein encoded by this gene is a member of the membrane-associated guanylate kinase homologue (MAGUK) family. MAGUK proteins participate in the assembly of multiprotein complexes on the inner surface of the plasma membrane at regions of cell-cell contact. The product of this gene may play a role as scaffolding protein at cell-cell junctions. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

GIPC PDZ domain containing family, member 1

GIPC1 is a scaffolding protein that regulates cell surface receptor expression and trafficking (Lee et al., 2008 [PubMed 18775991]).[supplied by OMIM, Apr 2009]

GIPC PDZ domain containing family, member 2

Enables identical protein binding activity. Located in extracellular exosome. [provided by Alliance of Genome Resources, Mar 2025]

GIPC PDZ domain containing family, member 3

The protein encoded by this gene belongs to the GIPC family. Studies in mice suggest that this gene is required for postnatal maturation of the hair bundle and long-term survival of hair cells and spiral ganglion in the ear. Mutations in this gene are associated with autosomal recessive deafness. [provided by RefSeq, Dec 2011]

NHERF family PDZ scaffold protein 4

Guanylyl cyclase C (GCC, or GUCY2C; MIM 601330) produces cGMP following the binding of either endogenous ligands or heat-stable enterotoxins secreted by E. coli and other enteric bacteria. Activation of GCC initiates a signaling cascade that leads to phosphorylation of the cystic fibrosis transmembrane conductance regulator (CFTR; MIM 602421), followed by a net efflux of ions and water into the intestinal lumen. IKEPP is a regulatory protein that associates with GCC and regulates the amount of cGMP produced following receptor stimulation (Scott et al., 2002 [PubMed 11950846]).[supplied by OMIM, Mar 2008]

From Reactome Pathways 2024

proteins participating in the SARS-CoV-1 targets PDZ proteins in cell-cell junction pathway from the Reactome Pathways 2024 dataset.

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term pdz in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

From GO Molecular Function Annotations 2015

genes performing the pdz domain binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the PDZ-associated domain of NMDA receptors protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the FERM and PDZ domain-containing protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Uncharacterised conserved protein UCP038083, PDZ protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From 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.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the PDZ domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the PDZ domain-containing protein MAGIX protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the GRASP55/65 PDZ-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From 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.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the PDZ-binding protein, CRIPT protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term pdz in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From GO Molecular Function Annotations 2023

genes performing the PDZ domain binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.

From GO Molecular Function Annotations 2025

genes performing the PDZ domain binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.

From Biocarta Pathways

proteins participating in the phosphoinositides and their downstream targets pathway from the Biocarta Pathways dataset.

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term targets in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

From PID Pathways

proteins participating in the Validated transcriptional targets of AP1 family members Fra1 and Fra2 pathway from the PID Pathways dataset.

From PID Pathways

proteins participating in the Validated transcriptional targets of TAp63 isoforms pathway from the PID Pathways dataset.

From PID Pathways

proteins participating in the Validated targets of C-MYC transcriptional repression pathway from the PID Pathways dataset.

From PID Pathways

proteins participating in the Validated targets of C-MYC transcriptional activation pathway from the PID Pathways dataset.

From PID Pathways

proteins participating in the Validated transcriptional targets of deltaNp63 isoforms pathway from the PID Pathways dataset.

From Reactome Pathways 2014

proteins participating in the ERK/MAPK targets pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the AKT phosphorylates targets in the cytosol pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the MAPK targets/ Nuclear events mediated by MAP kinases pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the AKT phosphorylates targets in the nucleus pathway from the Reactome Pathways dataset.

From WikiPathways Pathways 2024

proteins participating in the miRNA targets in ECM and membrane receptors pathway from the WikiPathways Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the AKT phosphorylates targets in the cytosol pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the AKT phosphorylates targets in the nucleus pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the ERK/MAPK targets pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the MAPK targets/ Nuclear events mediated by MAP kinases pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Transcription of E2F targets under negative control by DREAM complex pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 pathway from the Reactome Pathways 2024 dataset.

From Rummagene Transcription Factor Associations 2026

target genes of the PMC9235320-mmc2.xlsx-ST10_MR-353-targets-Supplementary_Table_10A_The_effects_of_353_targets_on_COVID-19_severity_with_suggestive_Mendelian_randomization_evidence_P_0_05_using_HGI_data_NR3C2 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.

From Rummagene Transcription Factor Associations 2026

target genes of the PMC9235320-mmc2.xlsx-ST10_MR-353-targets-Unnamed_1_NR3C2 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.

From GAD Gene-Disease Associations

genes associated with the disease sars (severe acute respiratory syndrome) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease sars in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease sars-coronavirus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease sars infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term sars in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Severe acute respiratory syndrome (SARS)_Peripheral blood mononuclear cell_GSE1739 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-dORF6_24Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_96Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_12Hour_20090954_GSE17400 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_0Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_60Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-dORF6_24Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-dORF6_48Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-dORF6_48Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_0Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_0Hour_23935999_GSE47961 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_84Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_84Hour_23935999_GSE47961 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_84Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_Day7_None_GSE50000 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-dORF6_12Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-dORF6_12Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_24Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_72Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_72Hour_23935999_GSE47961 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_72Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-ddORF6_60Hour_23935999_GSE47961 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_60Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_60Hour_23935999_GSE47961 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-ddORF6_48Hour_23935999_GSE47961 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-dORF6_96Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-dORF6_96Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_48Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-dORF6_60Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_96Hour_23935999_GSE47961 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_96Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_96Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-ddORF6_96Hour_23935999_GSE47961 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-ddORF6_84Hour_23935999_GSE47961 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_Day4_None_GSE50000 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-dORF6_72Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-dORF6_84Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-dORF6_72Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-dORF6_84Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_72Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_72Hour_23935999_GSE47961 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_72Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-dORF6_60Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_24Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-ddORF6_24Hour_23935999_GSE47961 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_0Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_0Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-ddORF6_72Hour_23935999_GSE47961 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_24Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_24Hour_23935999_GSE47961 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_48Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_48Hour_23935999_GSE47961 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_48Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_48Hour_23935999_GSE47961 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_48Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_0Hour_23935999_GSE47961 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_60Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_60Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_60Hour_23935999_GSE47961 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_96Hour_23935999_GSE47961 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_96Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-dORF6_0Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-dORF6_0Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_12Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_12Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_12Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_12Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-dORF6_36Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-dORF6_36Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_36Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_84Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_84Hour_23935999_GSE47961 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_84Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_24Hour_20090954_GSE17400 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_36Hour_23935999_GSE47960 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_Day1_None_GSE50000 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_36Hour_23935999_GSE47962 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-BatSRBD_Day2_None_GSE50000 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-CoV_48Hour_20090954_GSE17400 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From GEO Signatures of Differentially Expressed Genes for Viral Infections

genes differentially expressed following the SARS-ddORF6_0Hour_23935999_GSE47961 virus perturbation from the GEO Signatures of Differentially Expressed Genes for Viral Infections dataset.

From NURSA Protein-Protein Interactions

interacting proteins for SARS from the NURSA Protein-Protein Interactions dataset.

From OMIM Gene-Disease Associations

genes associated with the sars infection, protection against phenotype from the curated OMIM Gene-Disease Associations dataset.

From OMIM Gene-Disease Associations

genes associated with the {sars, progression of} phenotype from the curated OMIM Gene-Disease Associations dataset.

From Pathway Commons Protein-Protein Interactions

interacting proteins for SARS from the Pathway Commons Protein-Protein Interactions dataset.

From Virus MINT Protein-Virus Interactions

interacting proteins for the virus Human SARS coronavirus from the Virus MINT Protein-Virus Interactions dataset.

From WikiPathways Pathways 2024

proteins participating in the SARS coronavirus and innate immunity pathway from the WikiPathways Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Potential therapeutics for SARS pathway from the Reactome Pathways 2024 dataset.

From Biocarta Pathways

proteins participating in the influence of ras and rho proteins on g1 to s transition pathway from the Biocarta Pathways dataset.

From Biocarta Pathways

proteins participating in the g-protein signaling through tubby proteins pathway from the Biocarta Pathways dataset.

From CORUM Protein Complexes

proteins in the 6S methyltransferase and RG-containing Sm proteins complex protein complex from the CORUM Protein Complexes dataset.

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Amino Acids, Peptides, and Proteins from the curated CTD Gene-Chemical Interactions dataset.

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Adenovirus E1A Proteins from the curated CTD Gene-Chemical Interactions dataset.

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Proteins in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

From dbGAP Gene-Trait Associations

genes associated with the trait tau Proteins in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

From dbGAP Gene-Trait Associations

genes associated with the trait Calcium-Binding Proteins in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

From dbGAP Gene-Trait Associations

genes associated with the trait Iron-Regulatory Proteins in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

From dbGAP Gene-Trait Associations

genes associated with the trait Serotonin Plasma Membrane Transport Proteins in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease levels of antibodies to 60-kda heat-shock proteins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease two major non-ribosomal nucleolar proteins and its implication in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease iron-regulatory proteins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease tau proteins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease calcium-binding proteins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease serotonin plasma membrane transport proteins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease proteins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GAD Gene-Disease Associations

genes associated with the disease blood proteins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

From GO Biological Process Annotations 2015

genes participating in the fertilization, exchange of chromosomal proteins biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the activation of plasma proteins involved in acute inflammatory response biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the translocation of peptides or proteins into host biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the translocation of peptides or proteins into other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the spermatogenesis, exchange of chromosomal proteins biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on iron-sulfur proteins as donors molecular function from the curated GO Molecular Function Annotations 2015 dataset.

From GO Molecular Function Annotations 2015

genes performing the oxidoreductase activity, acting on iron-sulfur proteins as donors, nad or nadp as acceptor molecular function from the curated GO Molecular Function Annotations 2015 dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Rab proteins geranylgeranyltransferase component A protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal Proteins L2, RNA binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term immediate-early-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term i-kappa-b-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term nerve-tissue-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term repressor-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term microfilament-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term gtpase-activating-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term homeodomain-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term wnt-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term adaptor-proteins-signal-transducing in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term milk-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term proto-oncogene-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term ras-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term carrier-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term heat-shock-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term adaptor-proteins-vesicular-transport in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term dna-binding-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term nuclear-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term gtp-binding-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term neoplasm-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term proto-oncogene-proteins-c-abl in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term microtubule-associated-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term tumor-suppressor-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term luminescent-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term tau-proteins in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

From PID Pathways

proteins participating in the Hedgehog signaling events mediated by Gli proteins pathway from the PID Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Trafficking of myristoylated proteins to the cilium pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the ABC-family proteins mediated transport pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Recruitment of mitotic centrosome proteins and complexes pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the negative regulation of TCF-dependent signaling by DVL-interacting proteins pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Association of TriC/CCT with target proteins during biosynthesis pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Post-translational modification: synthesis of GPI-anchored proteins pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the APC/C:Cdc20 mediated degradation of mitotic proteins pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Asymmetric localization of PCP proteins pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Formation of editosomes by ADAR proteins pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Apoptotic cleavage of cellular proteins pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Mitochondrial Uncoupling Proteins pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Phosphorylation of proteins involved in the G2/M transition by Cyclin A:Cdc2 complexes pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Removal of aminoterminal propeptides from gamma-carboxylated proteins pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the GLI proteins bind promoters of Hh responsive genes to promote transcription pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Gamma-carboxylation, transport, and amino-terminal cleavage of proteins pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the O-glycosylation of TSR domain-containing proteins pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Membrane binding and targetting of GAG proteins pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Regulation of mRNA stability by proteins that bind AU-rich elements pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Caspase-mediated cleavage of cytoskeletal proteins pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Interactions of Tat with host cellular proteins pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Activation of BH3-only proteins pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Interactions of Vpr with host cellular proteins pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Phosphate bond hydrolysis by NUDT proteins pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Loss of proteins required for interphase microtubule organization from the centrosome pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Interactions of Rev with host cellular proteins pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Insulin-like Growth Factor-2 mRNA Binding Proteins (IGF2BPs/IMPs/VICKZs) bind RNA pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Diseases associated with N-glycosylation of proteins pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 complexes pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the ATM mediated phosphorylation of repair proteins pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the BH3-only proteins associate with and inactivate anti-apoptotic BCL-2 members pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Recruitment of repair and signaling proteins to double-strand breaks pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Metabolism of proteins pathway from the Reactome Pathways dataset.

From Reactome Pathways 2014

proteins participating in the Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. pathway from the Reactome Pathways dataset.

From WikiPathways Pathways 2014

proteins participating in the Cytoplasmic Ribosomal Proteins(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.

From WikiPathways Pathways 2014

proteins participating in the Splicing factor NOVA regulated synpatic proteins(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.

From WikiPathways Pathways 2014

proteins participating in the Cytoplasmic Ribosomal Proteins(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.

From WikiPathways Pathways 2014

proteins participating in the NLR Proteins(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.

From WikiPathways Pathways 2014

proteins participating in the NLR Proteins(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.

From GO Biological Process Annotations 2023

genes participating in the protein quality control for misfolded or incompletely synthesized proteins biological process from the curated GO Biological Process Annotations 2023 dataset.

From GO Biological Process Annotations 2023

genes participating in the activation of plasma proteins involved in acute inflammatory response biological process from the curated GO Biological Process Annotations 2023 dataset.

From GO Molecular Function Annotations 2023

genes performing the oxidoreductase activity, acting on iron-sulfur proteins as donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2023 dataset.

From WikiPathways Pathways 2024

proteins participating in the Sterol regulatory element binding proteins SREBP signaling pathway from the WikiPathways Pathways 2024 dataset.

From WikiPathways Pathways 2024

proteins participating in the Fas ligand pathway and stress induction of heat shock proteins pathway from the WikiPathways Pathways 2024 dataset.

From WikiPathways Pathways 2024

proteins participating in the Splicing factor NOVA regulated synaptic proteins pathway from the WikiPathways Pathways 2024 dataset.

From WikiPathways Pathways 2024

proteins participating in the Intraflagellar transport proteins binding to dynein pathway from the WikiPathways Pathways 2024 dataset.

From WikiPathways Pathways 2024

proteins participating in the Envelope proteins and their potential roles in EDMD physiopathology pathway from the WikiPathways Pathways 2024 dataset.

From WikiPathways Pathways 2024

proteins participating in the Cytoplasmic ribosomal proteins pathway from the WikiPathways Pathways 2024 dataset.

From WikiPathways Pathways 2024

proteins participating in the Intracellular trafficking proteins involved in CMT neuropathy pathway from the WikiPathways Pathways 2024 dataset.

From WikiPathways Pathways 2024

proteins participating in the Vitamin K metabolism and activation of dependent proteins pathway from the WikiPathways Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the ABC-family proteins mediated transport pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the APC/C:Cdc20 mediated degradation of mitotic proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Activation of BH3-only proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Apoptotic cleavage of cellular proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Association of TriC/CCT with target proteins during biosynthesis pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Asymmetric localization of PCP proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the BH3-only proteins associate with and inactivate anti-apoptotic BCL-2 members pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Caspase-mediated cleavage of cytoskeletal proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Diseases associated with N-glycosylation of proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Diseases associated with O-glycosylation of proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the E3 ubiquitin ligases ubiquitinate target proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the FASTK family proteins regulate processing and stability of mitochondrial RNAs pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Formation of editosomes by ADAR proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the GLI proteins bind promoters of Hh responsive genes to promote transcription pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Gamma-carboxylation, transport, and amino-terminal cleavage of proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Insertion of tail-anchored proteins into the endoplasmic reticulum membrane pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Insulin-like Growth Factor-2 mRNA Binding Proteins (IGF2BPs/IMPs/VICKZs) bind RNA pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Interactions of Rev with host cellular proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Interactions of Tat with host cellular proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Interactions of Vpr with host cellular proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Loss of proteins required for interphase microtubule organization from the centrosome pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the MET interacts with TNS proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Maturation of hRSV A proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Membrane binding and targetting of GAG proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Metabolism of proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Metal sequestration by antimicrobial proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Negative regulation of TCF-dependent signaling by DVL-interacting proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the O-glycosylation of TSR domain-containing proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the PTK6 Regulates Proteins Involved in RNA Processing pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Phosphate bond hydrolysis by NTPDase proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Phosphate bond hydrolysis by NUDT proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 complexes pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Phosphorylation of proteins involved in the G2/M transition by Cyclin A:Cdc2 complexes pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Post-translational modification: synthesis of GPI-anchored proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Recruitment of mitotic centrosome proteins and complexes pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Regulation of endogenous retroelements by KRAB-ZFP proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Regulation of mRNA stability by proteins that bind AU-rich elements pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Removal of aminoterminal propeptides from gamma-carboxylated proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the SUMO E3 ligases SUMOylate target proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the SUMOylation of DNA damage response and repair proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the SUMOylation of DNA methylation proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the SUMOylation of DNA replication proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the SUMOylation of RNA binding proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the SUMOylation of SUMOylation proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the SUMOylation of chromatin organization proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the SUMOylation of immune response proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the SUMOylation of nuclear envelope proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the SUMOylation of ubiquitinylation proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Signaling by FLT3 fusion proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Signaling by cytosolic PDGFRA and PDGFRB fusion proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the TYSND1 cleaves peroxisomal proteins pathway from the Reactome Pathways 2024 dataset.

From Reactome Pathways 2024

proteins participating in the Trafficking of myristoylated proteins to the cilium pathway from the Reactome Pathways 2024 dataset.

From GO Biological Process Annotations 2025

genes participating in the protein quality control for misfolded or incompletely synthesized proteins biological process from the curated GO Biological Process Annotations 2025 dataset.

From GO Biological Process Annotations 2025

genes participating in the activation of plasma proteins involved in acute inflammatory response biological process from the curated GO Biological Process Annotations 2025 dataset.

From GO Molecular Function Annotations 2025

genes performing the oxidoreductase activity, acting on iron-sulfur proteins as donors, NAD or NADP as acceptor molecular function from the curated GO Molecular Function Annotations 2025 dataset.

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Cerebrospinal fluid levels of Alzheimer's disease-related proteins phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

From KEGG Pathways 2026

proteins participating in the Motor proteins pathway from the KEGG Pathways 2026 dataset.

From Rummagene Transcription Factor Associations 2026

target genes of the PMC9859931-mmc5.xlsx-MSC_PP_pred-proteins-Protein_MSC transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.

From Rummagene Transcription Factor Associations 2026

target genes of the PMC9859931-mmc5.xlsx-MSC_ADP_pred-proteins-Protein_MSC transcription factor from the Rummagene Transcription Factor Associations 2026 dataset.

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the spot adherens junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the gap junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the tight junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the muscle tendon junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the apical junction complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the occluding junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the exon-exon junction complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the adherens junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the anchoring junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the paranodal junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the neuromuscular junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

From COMPARTMENTS Experimental Protein Localization Evidence Scores

proteins localized to the adherens junction cellular component in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores dataset.

From COMPARTMENTS Experimental Protein Localization Evidence Scores

proteins localized to the anchoring junction cellular component in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the spot adherens junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the gap junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the tight junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the septate junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the anchoring junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the nucleus-vacuole junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the smooth septate junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the muscle tendon junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the holliday junction resolvase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the apical junction complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the occluding junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the pleated septate junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the exon-exon junction complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial crista junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the adherens junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the paranodal junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the neuromuscular junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

From CORUM Protein Complexes

proteins in the Exon junction complex (EIF4A3-MLN51-MAGOH-Y14) protein complex from the CORUM Protein Complexes dataset.

From CORUM Protein Complexes

proteins in the Exon junction complex (EIF4A3-MLN51-MAGOH-Y14), RNA-protein complex protein complex from the CORUM Protein Complexes dataset.

From CORUM Protein Complexes

proteins in the Exon junction complex (mRNA splicing-dependent) protein complex from the CORUM Protein Complexes dataset.

From CORUM Protein Complexes

proteins in the Exon junction complex, EIF4A3-MLN51-MAGOH-Y14 (RNA-protein complex) protein complex from the CORUM Protein Complexes dataset.

From CORUM Protein Complexes

proteins in the Exon junction complex protein complex from the CORUM Protein Complexes dataset.

From CORUM Protein Complexes

proteins in the Exon junction complex (EIF4A3-MLN51-UPF3B-MAGOH-Y14) protein complex from the CORUM Protein Complexes dataset.

From CORUM Protein Complexes

proteins in the Exon junction complex (F4A3-MLN51-UPF3B-MAGOH-Y14-PYM) protein complex from the CORUM Protein Complexes dataset.

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease neuromuscular junction disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease rectosigmoid junction cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease gastroesophageal junction adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease neuromuscular junction disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term junction in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

From GO Biological Process Annotations 2015

genes participating in the positive regulation of adherens junction organization biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the establishment of synaptic specificity at neuromuscular junction biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the regulation of synaptic growth at neuromuscular junction biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the protein localization to tight junction biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the positive regulation of synaptic growth at neuromuscular junction biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the adherens junction maintenance biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the apical junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the adherens junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the paranodal junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the tight junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the protein localization to adherens junction biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the gap junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the negative regulation of gap junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the regulation of tight junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the synaptic growth at neuromuscular junction biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the neuromuscular junction development biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the atrial ventricular junction remodeling biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the positive regulation of gap junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the negative regulation of adherens junction organization biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the regulation of adherens junction organization biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the adherens junction organization biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Biological Process Annotations 2015

genes participating in the regulation of gap junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

From GO Cellular Component Annotations 2015

proteins localized to the spot adherens junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

From GO Cellular Component Annotations 2015

proteins localized to the tight junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

From GO Cellular Component Annotations 2015

proteins localized to the nucleus-vacuole junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

From GO Cellular Component Annotations 2015

proteins localized to the muscle tendon junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

From GO Cellular Component Annotations 2015

proteins localized to the holliday junction resolvase complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.

From GO Cellular Component Annotations 2015

proteins localized to the apical junction complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.

From GO Cellular Component Annotations 2015

proteins localized to the occluding junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

From GO Cellular Component Annotations 2015

proteins localized to the anchoring junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

From GO Cellular Component Annotations 2015

proteins localized to the exon-exon junction complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.

From GO Cellular Component Annotations 2015

proteins localized to the adherens junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

From GO Cellular Component Annotations 2015

proteins localized to the gap junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

From GO Cellular Component Annotations 2015

proteins localized to the paranodal junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

From GO Cellular Component Annotations 2015

proteins localized to the neuromuscular junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

From GO Molecular Function Annotations 2015

genes performing the gap junction hemi-channel activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

From GO Molecular Function Annotations 2015

genes performing the gap junction channel activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

From GO Molecular Function Annotations 2015

genes performing the double-strand/single-strand dna junction binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.

From GO Molecular Function Annotations 2015

genes performing the crossover junction endodeoxyribonuclease activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

From GO Molecular Function Annotations 2015

genes performing the four-way junction helicase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

From GO Molecular Function Annotations 2015

genes performing the four-way junction dna binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.

From GO Molecular Function Annotations 2015

genes performing the gap junction channel activity involved in cardiac conduction electrical coupling molecular function from the curated GO Molecular Function Annotations 2015 dataset.

From GWASdb SNP-Disease Associations

genes associated with the disease neuromuscular junction disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.