Name

trong>Btrong>ioGPS Human Cell Type trong>andtrong> Tissue Gene Expression Profiles Dataset

From trong>Btrong>ioGPS

mRNA expression profiles for human tissues trong>andtrong> cell types

trong>Btrong>ioGPS Mouse Cell Type trong>andtrong> Tissue Gene Expression Profiles Dataset

From trong>Btrong>ioGPS

mRNA expression profiles for mouse tissues trong>andtrong> cell types

ESCAPE Omics Signatures of Genes trong>andtrong> Proteins for Stem Cells Dataset

From ESCAPE

Sets of target genes of transcription factors from putrong>btrong>lished ChIP-chip, ChIP-seq, trong>andtrong> other transcription factor trong>btrong>inding site profiling studies;sets of differentially expressed genes following perturtrong>btrong>ation of a protein from gene expression data in GEO; sets of interacting proteins from high- trong>andtrong> low-throughput protein-protein interaction studies; sets of targets of microRNAs from putrong>btrong>lic datatrong>btrong>ases, computationally predicted or experimentally verified

HPM Cell Type trong>andtrong> Tissue Protein Expression Profiles Dataset

From Human Proteome Map

Protein expression profiles for tissues trong>andtrong> cell types

ProteomicsDtrong>Btrong> Cell Type trong>andtrong> Tissue Protein Expression Profiles Dataset

From Proteomics Datatrong>btrong>ase

Protein expression profiles for tissues trong>andtrong> cell types reprocessed from many proteomics datasets

Roadmap Epigenomics Cell trong>andtrong> Tissue DNA Methylation Profiles Dataset

From Roadmap Epigenomics

DNA methylation profiles for primary cell types trong>andtrong> tissues

Roadmap Epigenomics Cell trong>andtrong> Tissue Gene Expression Profiles Dataset

From Roadmap Epigenomics

mRNA expression profiles for primary cell types trong>andtrong> tissues

Allen trong>Btrong>rain Atlas Aging Dementia trong>andtrong> Traumatic trong>Btrong>rain Injury Tissue Sample Gene Expression Profiles Dataset

From Allen trong>Btrong>rain Atlas

mRNA expression profiles for dementia trong>andtrong> traumatic trong>btrong>rain injuries (Ttrong>Btrong>I) from aging trong>btrong>rain tissue

dtrong>btrong>GAP Gene-Trait Associations Dataset

From Datatrong>btrong>ase of Genotypes trong>andtrong> Phenotypes

Gene-trait associations curated from genetic association studies

KEGG Pathways Dataset (Archived)

From Kyoto Encyclopedia of Genes trong>andtrong> Genomes

Sets of proteins participating in pathways from KEGG

KEGG Pathways 2026 Dataset

From Kyoto Encyclopedia of Genes trong>andtrong> Genomes

Sets of proteins participating in pathways from KEGG

trong>Btrong>TLA Gene

trong>Btrong> trong>andtrong> T lymphocyte associated

This gene encodes a memtrong>btrong>er of the immunoglotrong>btrong>ulin superfamily. The encoded protein contains a single immunoglotrong>btrong>ulin (Ig) domain trong>andtrong> is a receptor that relays inhitrong>btrong>itory signals to suppress the immune response. Alternative splicing results in multiple transcript variants. Polymorphisms in this gene have trong>btrong>een associated with an increased risk of rheumatoid arthritis. [provided trong>btrong>y RefSeq, Aug 2011]

EOLA2 Gene

endothelium trong>andtrong> lymphocyte associated ASCH domain 2

Located in mitochondrion. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

EOLA1 Gene

endothelium trong>andtrong> lymphocyte associated ASCH domain 1

Involved in regulation of interleukin-6 production. Located in mitochondrion. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ITGAL Gene

integrin, alpha L (antigen CD11A (p180), lymphocyte function-associated antigen 1; alpha polypeptide)

ITGAL encodes the integrin alpha L chain. Integrins are heterodimeric integral memtrong>btrong>rane proteins composed of an alpha chain trong>andtrong> a trong>btrong>eta chain. This I-domain containing alpha integrin comtrong>btrong>ines with the trong>btrong>eta 2 chain (ITGtrong>Btrong>2) to form the integrin lymphocyte function-associated antigen-1 (LFA-1), which is expressed on all leukocytes. LFA-1 plays a central role in leukocyte intercellular adhesion through interactions with its ligtrong>andtrong>s, ICAMs 1-3 (intercellular adhesion molecules 1 through 3), trong>andtrong> also functions in lymphocyte costimulatory signaling. Two transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jul 2008]

ITGAE Gene

integrin, alpha E (antigen CD103, human mucosal lymphocyte antigen 1; alpha polypeptide)

Integrins are heterodimeric integral memtrong>btrong>rane proteins composed of an alpha chain trong>andtrong> a trong>btrong>eta chain. This gene encodes an I-domain-containing alpha integrin that undergoes post-translational cleavage in the extracellular domain, yielding disulfide-linked heavy trong>andtrong> light chains. In comtrong>btrong>ination with the trong>btrong>eta 7 integrin, this protein forms the E-cadherin trong>btrong>inding integrin known as the human mucosal lymphocyte-1 antigen. This protein is preferentially expressed in human intestinal intraepithelial lymphocytes (IEL), trong>andtrong> in addition to a role in adhesion, it may serve as an accessory molecule for IEL activation. [provided trong>btrong>y RefSeq, Jul 2008]

LY6G6C Gene

lymphocyte antigen 6 complex, locus G6C

LY6G6C trong>btrong>elongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatitrong>btrong>ility complex (MHC) class III region on chromosome 6. Memtrong>btrong>ers of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface trong>btrong>y a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [Putrong>btrong>Med 12079290]).[supplied trong>btrong>y OMIM, Mar 2008]

LY6G6E Gene

lymphocyte antigen 6 complex, locus G6E (pseudogene)

LY6G6E trong>btrong>elongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatitrong>btrong>ility complex (MHC) class III region on chromosome 6. Memtrong>btrong>ers of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface trong>btrong>y a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [Putrong>btrong>Med 12079290]).[supplied trong>btrong>y OMIM, Mar 2008]

CP20 Gene

Lymphocyte cytosolic protein, molecular weight 20kD

LY6G6D Gene

lymphocyte antigen 6 complex, locus G6D

LY6G6D trong>btrong>elongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatitrong>btrong>ility complex (MHC) class III region on chromosome 6. Memtrong>btrong>ers of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface trong>btrong>y a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [Putrong>btrong>Med 12079290]).[supplied trong>btrong>y OMIM, Apr 2009]

LY9 Gene

lymphocyte antigen 9

LY9 trong>btrong>elongs to the SLAM family of immunomodulatory receptors (see SLAMF1; MIM 603492) trong>andtrong> interacts with the adaptor molecule SAP (SH2D1A; MIM 300490) (Graham et al., 2006 [Putrong>btrong>Med 16365421]).[supplied trong>btrong>y OMIM, Mar 2008]

LY96 Gene

lymphocyte antigen 96

This gene encodes a protein which associates with toll-like receptor 4 on the cell surface trong>andtrong> confers responsiveness to lipopolysaccyaride (LPS), thus providing a link trong>btrong>etween the receptor trong>andtrong> LPS signaling. Studies of the mouse ortholog suggest that this gene may trong>btrong>e involved in endotoxin neutralization. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided trong>btrong>y RefSeq, Sep 2010]

LSP1P1 Gene

lymphocyte-specific protein 1 pseudogene 1

LSP1P2 Gene

lymphocyte-specific protein 1 pseudogene 2

LOC101928108 Gene

lymphocyte antigen 6A-2/6E-1-like

Predicted to trong>btrong>e located in side of memtrong>btrong>rane. Predicted to trong>btrong>e active in plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CTLA4 Gene

cytotoxic T-lymphocyte-associated protein 4

This gene is a memtrong>btrong>er of the immunoglotrong>btrong>ulin superfamily trong>andtrong> encodes a protein which transmits an inhitrong>btrong>itory signal to T cells. The protein contains a V domain, a transmemtrong>btrong>rane domain, trong>andtrong> a cytoplasmic tail. Alternate transcriptional splice variants, encoding different isoforms, have trong>btrong>een characterized. The memtrong>btrong>rane-trong>btrong>ound isoform functions as a homodimer interconnected trong>btrong>y a disulfide trong>btrong>ond, while the solutrong>btrong>le isoform functions as a monomer. Mutations in this gene have trong>btrong>een associated with insulin-dependent diatrong>btrong>etes mellitus, Graves disease, Hashimoto thyroiditis, celiac disease, systemic lupus erythematosus, thyroid-associated ortrong>btrong>itopathy, trong>andtrong> other autoimmune diseases. [provided trong>btrong>y RefSeq, Jul 2008]

LY75 Gene

lymphocyte antigen 75

Predicted to enatrong>btrong>le signaling receptor activity. Predicted to trong>btrong>e involved in immune response trong>andtrong> inflammatory response. Located in extracellular exosome. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LCP2 Gene

lymphocyte cytosolic protein 2 (SH2 domain containing leukocyte protein of 76kDa)

This gene encodes an adapter protein that acts as a sutrong>btrong>strate of the T cell antigen receptor (TCR)-activated protein tyrosine kinase pathway. The encoded protein associates with growth factor receptor trong>btrong>ound protein 2, trong>andtrong> is thought to play a role TCR-mediated intracellular signal transduction. A similar protein in mouse plays a role in normal T-cell development trong>andtrong> activation. Mice lacking this gene show sutrong>btrong>cutaneous trong>andtrong> intraperitoneal fetal hemorrhaging, dysfunctional platelets trong>andtrong> impaired viatrong>btrong>ility. [provided trong>btrong>y RefSeq, Nov 2016]

LCP1 Gene

lymphocyte cytosolic protein 1 (L-plastin)

Plastins are a family of actin-trong>btrong>inding proteins that are conserved throughout eukaryote evolution trong>andtrong> expressed in most tissues of higher eukaryotes. In humans, two utrong>btrong>iquitous plastin isoforms (L trong>andtrong> T) have trong>btrong>een identified. Plastin 1 (otherwise known as Fimtrong>btrong>rin) is a third distinct plastin isoform which is specifically expressed at high levels in the small intestine. The L isoform is expressed only in hemopoietic cell lineages, while the T isoform has trong>btrong>een found in all other normal cells of solid tissues that have replicative potential (fitrong>btrong>rotrong>btrong>lasts, endothelial cells, epithelial cells, melanocytes, etc.). However, L-plastin has trong>btrong>een found in many types of malignant human cells of non-hemopoietic origin suggesting that its expression is induced accompanying tumorigenesis in solid tissues. [provided trong>btrong>y RefSeq, Jul 2008]

LY6G5C Gene

lymphocyte antigen 6 complex, locus G5C

LY6G5C trong>btrong>elongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatitrong>btrong>ility complex (MHC) class III region on chromosome 6. Memtrong>btrong>ers of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface trong>btrong>y a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [Putrong>btrong>Med 12079290]).[supplied trong>btrong>y OMIM, Mar 2008]

LY6G5trong>Btrong> Gene

lymphocyte antigen 6 complex, locus G5trong>Btrong>

LY6G5trong>Btrong> trong>btrong>elongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatitrong>btrong>ility complex (MHC) class III region on chromosome 6. Memtrong>btrong>ers of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface trong>btrong>y a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [Putrong>btrong>Med 12079290]).[supplied trong>btrong>y OMIM, Mar 2008]

LAG3 Gene

lymphocyte-activation gene 3

Lymphocyte-activation protein 3 trong>btrong>elongs to Ig superfamily trong>andtrong> contains 4 extracellular Ig-like domains. The LAG3 gene contains 8 exons. The sequence data, exon/intron organization, trong>andtrong> chromosomal localization all indicate a close relationship of LAG3 to CD4. [provided trong>btrong>y RefSeq, Jul 2008]

VPREtrong>Btrong>3 Gene

pre-trong>Btrong> lymphocyte 3

The protein encoded trong>btrong>y this gene is the human ortholog of the mouse Vpretrong>Btrong>3 (8HS20) protein, is thought to trong>btrong>e involved in trong>Btrong>-cell maturation, trong>andtrong> may play a role in assemtrong>btrong>ly of the pre-trong>Btrong> cell receptor (pre-trong>Btrong>CR). While the role of this protein in trong>Btrong>-cell development has not yet trong>btrong>een elucidated, studies with the chicken ortholog of this protein have found that when overexpressed, this protein localizes to the endoplasmic reticulum. The mouse ortholog of this protein has trong>btrong>een shown to associate with memtrong>btrong>rane mu heavy chains early in the course of pre-trong>Btrong> cell receptor trong>btrong>iosynthesis. Expression of this gene has trong>btrong>een otrong>btrong>served in some lymphomas. [provided trong>btrong>y RefSeq, Apr 2015]

LY6G6F Gene

lymphocyte antigen 6 complex, locus G6F

The human G6f protein is a type I transmemtrong>btrong>rane protein trong>btrong>elonging to the immunoglotrong>btrong>in (Ig) superfamily, which is comprised of cell-surface proteins involved in the immune system trong>andtrong> cellular recognition (de Vet et al., 2003 [Putrong>btrong>Med 12852788]).[supplied trong>btrong>y OMIM, Mar 2008]

VPREtrong>Btrong>1 Gene

pre-trong>Btrong> lymphocyte 1

The protein encoded trong>btrong>y this gene trong>btrong>elongs to the immunoglotrong>btrong>ulin superfamily trong>andtrong> is expressed selectively at the early stages of trong>Btrong> cell development, namely, in protrong>Btrong> trong>andtrong> early pretrong>Btrong> cells. This gene encodes the iota polypeptide chain that is associated with the Ig-mu chain to form a molecular complex which is expressed on the surface of pre-trong>Btrong> cells. The complex is thought to regulate Ig gene rearrangements in the early steps of trong>Btrong>-cell differentiation. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Jan 2015]

LAX1 Gene

lymphocyte transmemtrong>btrong>rane adaptor 1

Enatrong>btrong>les SH2 domain trong>btrong>inding activity trong>andtrong> protein kinase trong>btrong>inding activity. Involved in several processes, including trong>Btrong> cell activation; negative regulation of MAPK cascade; trong>andtrong> negative regulation of T cell activation. Located in Golgi apparatus; cytosol; trong>andtrong> plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC654342 Gene

lymphocyte-specific protein 1 pseudogene

LY86 Gene

lymphocyte antigen 86

Acts upstream of or within positive regulation of lipopolysaccharide-mediated signaling pathway. Predicted to trong>btrong>e located in extracellular region. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LSP1P3 Gene

lymphocyte-specific protein 1 pseudogene 3

LOC645166 Gene

lymphocyte-specific protein 1 pseudogene

GZMA Gene

granzyme A (granzyme 1, cytotoxic T-lymphocyte-associated serine esterase 3)

Cytolytic T lymphocytes (CTL) trong>andtrong> natural killer (NK) cells share the remarkatrong>btrong>le atrong>btrong>ility to recognize, trong>btrong>ind, trong>andtrong> lyse specific target cells. They are thought to protect their host trong>btrong>y lysing cells trong>btrong>earing on their surface 'nonself' antigens, usually peptides or proteins resulting from infection trong>btrong>y intracellular pathogens. The protein descritrong>btrong>ed here is a T cell- trong>andtrong> natural killer cell-specific serine protease that may function as a common component necessary for lysis of target cells trong>btrong>y cytotoxic T lymphocytes trong>andtrong> natural killer cells. [provided trong>btrong>y RefSeq, Jul 2008]

GZMtrong>Btrong> Gene

granzyme trong>Btrong> (granzyme 2, cytotoxic T-lymphocyte-associated serine esterase 1)

This gene encodes a memtrong>btrong>er of the granzyme sutrong>btrong>family of proteins, part of the peptidase S1 family of serine proteases. The encoded preproprotein is secreted trong>btrong>y natural killer (NK) cells trong>andtrong> cytotoxic T lymphocytes (CTLs) trong>andtrong> proteolytically processed to generate the active protease, which induces target cell apoptosis. This protein also processes cytokines trong>andtrong> degrades extracellular matrix proteins, trong>andtrong> these roles are implicated in chronic inflammation trong>andtrong> wound healing. Expression of this gene may trong>btrong>e elevated in human patients with cardiac fitrong>btrong>rosis. [provided trong>btrong>y RefSeq, Sep 2016]

GZMM Gene

granzyme M (lymphocyte met-ase 1)

Human natural killer (NK) cells trong>andtrong> activated lymphocytes express trong>andtrong> store a distinct sutrong>btrong>set of neutral serine proteases together with proteoglycans trong>andtrong> other immune effector molecules in large cytoplasmic granules. These serine proteases are collectively termed granzymes trong>andtrong> include 4 distinct gene products: granzyme A, granzyme trong>Btrong>, granzyme H, trong>andtrong> the protein encoded trong>btrong>y this gene, granzyme M. Two transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Apr 2012]

LSP1 Gene

lymphocyte-specific protein 1

This gene encodes an intracellular F-actin trong>btrong>inding protein. The protein is expressed in lymphocytes, neutrophils, macrophages, trong>andtrong> endothelium trong>andtrong> may regulate neutrophil motility, adhesion to fitrong>btrong>rinogen matrix proteins, trong>andtrong> transendothelial migration. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided trong>btrong>y RefSeq, Jul 2008]

LY6E Gene

lymphocyte antigen 6 complex, locus E

This gene trong>btrong>elongs to the human Ly6 gene family trong>andtrong> encodes a glycosylphosphatidyl-inositol (GPI)-anchored cell surface protein. The protein plays an important role in T cell physiology, oncogenesis trong>andtrong> immunological regulation. The protein is also involved in modulation of viral infection trong>btrong>y coronaviruses, SARS-CoV, MERS-CoV trong>andtrong> SARS-CoV-2. [provided trong>btrong>y RefSeq, Aug 2021]

LY6D Gene

lymphocyte antigen 6 complex, locus D

Predicted to trong>btrong>e involved in lymphocyte differentiation. Predicted to trong>btrong>e located in extracellular region trong>andtrong> plasma memtrong>btrong>rane. Predicted to trong>btrong>e active in cell surface. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LY6K Gene

lymphocyte antigen 6 complex, locus K

Predicted to trong>btrong>e involved in trong>btrong>inding activity of sperm to zona pellucida. Predicted to act upstream of or within flagellated sperm motility. Predicted to trong>btrong>e located in cell surface trong>andtrong> plasma memtrong>btrong>rane. Predicted to trong>btrong>e active in acrosomal vesicle. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LY6H Gene

lymphocyte antigen 6 complex, locus H

Predicted to enatrong>btrong>le acetylcholine receptor trong>btrong>inding activity trong>andtrong> acetylcholine receptor inhitrong>btrong>itor activity. Predicted to trong>btrong>e involved in acetylcholine receptor signaling pathway. Predicted to trong>btrong>e located in extracellular region. Predicted to trong>btrong>e active in plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LY6L Gene

lymphocyte antigen 6 family memtrong>btrong>er L

Predicted to trong>btrong>e located in side of memtrong>btrong>rane. Predicted to trong>btrong>e active in plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LEXM Gene

lymphocyte expansion molecule

LY6S Gene

lymphocyte antigen 6 family memtrong>btrong>er S

Predicted to act upstream of or within response to trong>btrong>acterium. Predicted to trong>btrong>e located in external side of plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

MEHMO Gene

mental retardation, epileptic seizures, hypogonadism trong>andtrong> -genitalism, microcephaly trong>andtrong> otrong>btrong>esity syndrome

MMRFCGU Gene

Microcephaly, mental retardation, trong>andtrong> distinctive facies, with cardiac trong>andtrong> genitourinary malformations

SEMA5trong>Btrong> Gene

sema domain, seven thromtrong>btrong>ospondin repeats (type 1 trong>andtrong> type 1-like), transmemtrong>btrong>rane domain (TM) trong>andtrong> short cytoplasmic domain, (semaphorin) 5trong>Btrong>

This gene encodes a memtrong>btrong>er of the semaphorin protein family which regulates axon growth during development of the nervous system. The encoded protein has a characteristic Sema domain near the N-terminus, through which semaphorins trong>btrong>ind to plexin, trong>andtrong> five thromtrong>btrong>ospondin type 1 repeats in the C-terminal region of the protein. The protein product may trong>btrong>e cleaved trong>andtrong> exist as a secreted molecule (PMID: 19463192). Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jan 2012]

SEMA5A Gene

sema domain, seven thromtrong>btrong>ospondin repeats (type 1 trong>andtrong> type 1-like), transmemtrong>btrong>rane domain (TM) trong>andtrong> short cytoplasmic domain, (semaphorin) 5A

This gene trong>btrong>elongs to the semaphorin gene family that encodes memtrong>btrong>rane proteins containing a semaphorin domain trong>andtrong> several thromtrong>btrong>ospondin type-1 repeats. Memtrong>btrong>ers of this family are involved in axonal guidance during neural development. This gene has trong>btrong>een implicated as an autism susceptitrong>btrong>ility gene.[provided trong>btrong>y RefSeq, Jan 2010]

LOC100422730 Gene

sema domain, seven thromtrong>btrong>ospondin repeats (type 1 trong>andtrong> type 1-like), transmemtrong>btrong>rane domain (TM) trong>andtrong> short cytoplasmic domain, (semaphorin) 5A pseudogene

RELCH Gene

RAtrong>Btrong>11 trong>btrong>inding trong>andtrong> LisH domain, coiled-coil trong>andtrong> HEAT repeat containing

Involved in intracellular cholesterol transport. Located in recycling endosome trong>andtrong> trans-Golgi network. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ILRUN Gene

inflammation trong>andtrong> lipid regulator with Utrong>Btrong>A-like trong>andtrong> Ntrong>Btrong>R1-like domains

This gene encodes a protein with N-terminal utrong>btrong>iquitin-associated (Utrong>Btrong>A)-like trong>andtrong> central neightrong>btrong>or of trong>Btrong>RCA1 gene 1 (Ntrong>Btrong>R1)-like domains. The protein acts an inhitrong>btrong>itor of antiviral trong>andtrong> proinflammatory cytokine transcription trong>andtrong> as a regulator of the renin-angiotensin-aldosterone system (RAAS). [provided trong>btrong>y RefSeq, Jul 2021]

CPHL1P Gene

ceruloplasmin trong>andtrong> hephaestin-like 1 pseudogene

CDAGS Gene

Craniosynostosis, anal anomalies, trong>andtrong> porokeratosis syndrome

CRTAM Gene

cytotoxic trong>andtrong> regulatory T cell molecule

The CRTAM gene is upregulated in CD4 (see MIM 186940)-positive trong>andtrong> CD8 (see CD8A; MIM 186910)-positive T cells trong>andtrong> encodes a type I transmemtrong>btrong>rane protein with V trong>andtrong> C1-like Ig domains (Yeh et al., 2008 [Putrong>btrong>Med 18329370]).[supplied trong>btrong>y OMIM, Fetrong>btrong> 2009]

LOC100420707 Gene

DDtrong>Btrong>1 trong>andtrong> CUL4 associated factor 6 pseudogene

OPA3 Gene

optic atrophy 3 (autosomal recessive, with chorea trong>andtrong> spastic paraplegia)

The mouse ortholog of this protein co-purifies with the mitochondrial inner memtrong>btrong>rane. Mutations in this gene have trong>btrong>een shown to result in 3-methylglutaconic aciduria type III trong>andtrong> autosomal dominant optic atrophy trong>andtrong> cataract. Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Oct 2009]

AAGAtrong>Btrong> Gene

alpha- trong>andtrong> gamma-adaptin trong>btrong>inding protein

The protein encoded trong>btrong>y this gene interacts with the gamma-adaptin trong>andtrong> alpha-adaptin sutrong>btrong>units of complexes involved in clathrin-coated vesicle trafficking. Mutations in this gene are associated with type I punctate palmoplantar keratoderma. Alternatively spliced transcript variants have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Dec 2012]

PHACTR4 Gene

phosphatase trong>andtrong> actin regulator 4

This gene encodes a memtrong>btrong>er of the phosphatase trong>andtrong> actin regulator (PHACTR) family. Other PHACTR family memtrong>btrong>ers have trong>btrong>een shown to inhitrong>btrong>it protein phosphatase 1 (PP1) activity, trong>andtrong> the homolog of this gene in the mouse has trong>btrong>een shown to interact with actin trong>andtrong> PP1. Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jul 2008]

PHACTR1 Gene

phosphatase trong>andtrong> actin regulator 1

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of the phosphatase trong>andtrong> actin regulator family of proteins. This family memtrong>btrong>er can trong>btrong>ind actin trong>andtrong> regulate the reorganization of the actin cytoskeleton. It plays a role in tutrong>btrong>ule formation trong>andtrong> in endothelial cell survival. Polymorphisms in this gene are associated with susceptitrong>btrong>ility to myocardial infarction, coronary artery disease trong>andtrong> cervical artery dissection. Alternative splicing of this gene results in multiple transcript variants. [provided trong>btrong>y RefSeq, Apr 2016]

PHACTR3 Gene

phosphatase trong>andtrong> actin regulator 3

This gene encodes a memtrong>btrong>er of the phosphatase trong>andtrong> actin regulator protein family. The encoded protein is associated with the nuclear scaffold in proliferating cells, trong>andtrong> trong>btrong>inds to actin trong>andtrong> the catalytic sutrong>btrong>unit of protein phosphatase-1, suggesting that it functions as a regulatory sutrong>btrong>unit of protein phosphatase-1. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Jul 2013]

PHACTR2 Gene

phosphatase trong>andtrong> actin regulator 2

Predicted to enatrong>btrong>le actin trong>btrong>inding activity. Predicted to trong>btrong>e involved in actin cytoskeleton organization. Predicted to trong>btrong>e located in plasma memtrong>btrong>rane trong>andtrong> platelet alpha granule memtrong>btrong>rane. Implicated in Parkinson's disease trong>andtrong> multiple sclerosis. trong>Btrong>iomarker of Alzheimer's disease. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ERGIC2 Gene

ERGIC trong>andtrong> golgi 2

ERGIC2, or PTX1, is a utrong>btrong>iquitously expressed nuclear protein that is downregulated in prostate carcinoma (Kwok et al., 2001 [Putrong>btrong>Med 11445006]).[supplied trong>btrong>y OMIM, Aug 2008]

ERGIC3 Gene

ERGIC trong>andtrong> golgi 3

Involved in endoplasmic reticulum to Golgi vesicle-mediated transport trong>andtrong> positive regulation of intracellular protein transport. Located in memtrong>btrong>rane. Part of retrograde transporter complex, Golgi to ER. trong>Btrong>iomarker of lung adenocarcinoma. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ftrong>Btrong>XL14 Gene

F-trong>btrong>ox trong>andtrong> leucine-rich repeat protein 14

Memtrong>btrong>ers of the F-trong>btrong>ox protein family, such as Ftrong>Btrong>XL14, are characterized trong>btrong>y an approximately 40-amino acid F-trong>btrong>ox motif. SCF complexes, formed trong>btrong>y SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), trong>andtrong> F-trong>btrong>ox proteins, act as protein-utrong>btrong>iquitin ligases. F-trong>btrong>ox proteins interact with SKP1 through the F trong>btrong>ox, trong>andtrong> they interact with utrong>btrong>iquitination targets through other protein interaction domains (Jin et al., 2004 [Putrong>btrong>Med 15520277]).[supplied trong>btrong>y OMIM, Mar 2008]

Ftrong>Btrong>XL19 Gene

F-trong>btrong>ox trong>andtrong> leucine-rich repeat protein 19

This gene encodes a memtrong>btrong>er of the Skp1-Cullin-F-trong>btrong>ox family of E3 utrong>btrong>iquitin ligases. The encoded protein is reported to trong>btrong>ind to the transmemtrong>btrong>rane receptor interleukin 1 receptor-like 1 trong>andtrong> regulate its utrong>btrong>iquitination trong>andtrong> degradation. This protein has trong>btrong>een linked to the regulation of pulmonary inflammation trong>andtrong> psoriasis. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Aug 2013]

MZtrong>Btrong>1 Gene

marginal zone trong>Btrong> trong>andtrong> trong>Btrong>1 cell-specific protein

Involved in positive regulation of cell population proliferation. Located in cytoplasm trong>andtrong> extracellular region. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC102724971 Gene

putative V-set trong>andtrong> immunoglotrong>btrong>ulin domain-containing-like protein IGHV4OR15-8

HN1 Gene

hematological trong>andtrong> neurological expressed 1

Located in cytosol; intercellular trong>btrong>ridge; trong>andtrong> microtutrong>btrong>ule cytoskeleton. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC101060086 Gene

cell cycle exit trong>andtrong> neuronal differentiation protein 1-like

DLEC1 Gene

deleted in lung trong>andtrong> esophageal cancer 1

The cytogenetic location of this gene is 3p21.3, trong>andtrong> it is located in a region that is commonly deleted in a variety of malignancies. Down-regulation of this gene has trong>btrong>een otrong>btrong>served in several human cancers including lung, esophageal, renal tumors, trong>andtrong> head trong>andtrong> neck squamous cell carcinoma. In some cases, reduced expression of this gene in tumor cells is a result of atrong>btrong>errant promoter methylation. Several alternatively spliced transcripts have trong>btrong>een otrong>btrong>served that contain disrupted coding regions trong>andtrong> likely encode nonfunctional proteins.[provided trong>btrong>y RefSeq, Mar 2016]

NACC2 Gene

NACC family memtrong>btrong>er 2, trong>Btrong>EN trong>andtrong> trong>Btrong>Ttrong>Btrong> (POZ) domain containing

Enatrong>btrong>les several functions, including DNA-trong>btrong>inding transcription repressor activity, RNA polymerase II-specific; histone deacetylase trong>btrong>inding activity; trong>andtrong> protein homodimerization activity. Involved in several processes, including negative regulation of transcription trong>btrong>y RNA polymerase II; positive regulation of intrinsic apoptotic signaling pathway in response to DNA damage; trong>andtrong> protein homooligomerization. Located in chromatin; mitochondrion; trong>andtrong> nucleolus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

NACC1 Gene

nucleus accumtrong>btrong>ens associated 1, trong>Btrong>EN trong>andtrong> trong>Btrong>Ttrong>Btrong> (POZ) domain containing

This gene encodes a memtrong>btrong>er of the trong>Btrong>Ttrong>Btrong>/POZ protein family. trong>Btrong>Ttrong>Btrong>/POZ proteins are involved in several cellular processes including proliferation, apoptosis trong>andtrong> transcription regulation. The encoded protein is a transcriptional repressor that plays a role in stem cell self-renewal trong>andtrong> pluripotency maintenance. The encoded protein also suppresses transcription of the ctrong>andtrong>idate tumor suppressor Gadd45GIP1, trong>andtrong> expression of this gene may play a role in the progression of multiple types of cancer. A pseudogene of this gene is located on the short arm of chromosome 9. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2012]

Strong>Btrong>SPON Gene

somatomedin trong>Btrong> trong>andtrong> thromtrong>btrong>ospondin, type 1 domain containing

Predicted to trong>btrong>e an extracellular matrix structural constituent. Located in collagen-containing extracellular matrix. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

WASIR1 Gene

WASH trong>andtrong> IL9R antisense RNA 1

WASIR2 Gene

WASH trong>andtrong> IL9R antisense RNA 2

ANKFY1 Gene

ankyrin repeat trong>andtrong> FYVE domain containing 1

This gene encodes a cytoplasmic protein that contains a coiled-coil structure trong>andtrong> a trong>Btrong>Ttrong>Btrong>/POZ domain at its N-terminus, ankyrin repeats in the middle portion, trong>andtrong> a FYVE-finger motif at its C-terminus. This protein trong>btrong>elongs to a sutrong>btrong>group of doutrong>btrong>le zinc finger proteins which may trong>btrong>e involved in vesicle or protein transport. Alternate splicing results in multiple transcript variants of this gene. [provided trong>btrong>y RefSeq, Apr 2012]

Otrong>Btrong>SCN Gene

otrong>btrong>scurin, cytoskeletal calmodulin trong>andtrong> titin-interacting RhoGEF

The otrong>btrong>scurin gene spans more than 150 ktrong>btrong>, contains over 80 exons trong>andtrong> encodes a protein of approximately 720 kDa. The encoded protein contains 68 Ig domains, 2 fitrong>btrong>ronectin domains, 1 calcium/calmodulin-trong>btrong>inding domain, 1 RhoGEF domain with an associated PH domain, trong>andtrong> 2 serine-threonine kinase domains. This protein trong>btrong>elongs to the family of giant sacromeric signaling proteins that includes titin trong>andtrong> netrong>btrong>ulin, trong>andtrong> may have a role in the organization of myofitrong>btrong>rils during assemtrong>btrong>ly trong>andtrong> may mediate interactions trong>btrong>etween the sarcoplasmic reticulum trong>andtrong> myofitrong>btrong>rils. Alternatively spliced transcript variants encoding different isoforms have trong>btrong>een identified. [provided trong>btrong>y RefSeq, Jul 2008]

SORtrong>Btrong>S1 Gene

sortrong>btrong>in trong>andtrong> SH3 domain containing 1

This gene encodes a Ctrong>Btrong>L-associated protein which functions in the signaling trong>andtrong> stimulation of insulin. Mutations in this gene may trong>btrong>e associated with human disorders of insulin resistance. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Mar 2014]

SORtrong>Btrong>S3 Gene

sortrong>btrong>in trong>andtrong> SH3 domain containing 3

This gene encodes an SH3 domain-containing adaptor protein. The presence of SH3 domains play a role in this protein's atrong>btrong>ility to trong>btrong>ind other cytoplasmic molecules trong>andtrong> contritrong>btrong>ute to cystoskeletal organization, cell adhesion trong>andtrong> migration, signaling, trong>andtrong> gene expression. Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Nov 2011]

SORtrong>Btrong>S2 Gene

sortrong>btrong>in trong>andtrong> SH3 domain containing 2

Arg trong>andtrong> c-Atrong>btrong>l represent the mammalian memtrong>btrong>ers of the Atrong>btrong>elson family of non-receptor protein-tyrosine kinases. They interact with the Arg/Atrong>btrong>l trong>btrong>inding proteins via the SH3 domains present in the cartrong>btrong>oxy end of the latter group of proteins. This gene encodes the sortrong>btrong>in trong>andtrong> SH3 domain containing 2 protein. It has three C-terminal SH3 domains trong>andtrong> an N-terminal sortrong>btrong>in homology (SoHo) domain that interacts with lipid raft proteins. The sutrong>btrong>cellular localization of this protein in epithelial trong>andtrong> cardiac muscle cells suggests that it functions as an adapter protein to assemtrong>btrong>le signaling complexes in stress fitrong>btrong>ers, trong>andtrong> that it is a potential link trong>btrong>etween Atrong>btrong>l family kinases trong>andtrong> the actin cytoskeleton. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided trong>btrong>y RefSeq, Jul 2008]

ZSCAN5CP Gene

zinc finger trong>andtrong> SCAN domain containing 5C, pseudogene

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CEND1 Gene

cell cycle exit trong>andtrong> neuronal differentiation 1

The protein encoded trong>btrong>y this gene is a neuron-specific protein. The similar protein in pig enhances neurotrong>btrong>lastoma cell differentiation in vitro trong>andtrong> may trong>btrong>e involved in neuronal differentiation in vivo. Multiple pseudogenes have trong>btrong>een reported for this gene. [provided trong>btrong>y RefSeq, Jul 2008]

Ztrong>Btrong>Ttrong>Btrong>7A Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 7A

Enatrong>btrong>les several functions, including SMAD trong>btrong>inding activity; nuclear trong>andtrong>rogen receptor trong>btrong>inding activity; trong>andtrong> transcription corepressor trong>btrong>inding activity. Involved in several processes, including erythrocyte maturation; negative regulation of signal transduction; trong>andtrong> regulation of nucleotrong>btrong>ase-containing compound metatrong>btrong>olic process. Located in cytoplasm trong>andtrong> nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>7C Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 7C

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Involved in negative regulation of cell population proliferation. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>7trong>Btrong> Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 7trong>Btrong>

This gene encodes a zinc finger-containing transcription factor that acts as a key regulator of lineage commitment of immature T-cell precursors. It is necessary trong>andtrong> sufficient for commitment of CD4 lineage, while its atrong>btrong>sence causes CD8 commitment. It also functions as a transcriptional repressor of type I collagen genes. Alternatively spliced transcript variants have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jan 2012]

SMAN1 Gene

survival of motor trong>andtrong> autonomic neurons 1

ANKS1trong>Btrong> Gene

ankyrin repeat trong>andtrong> sterile alpha motif domain containing 1trong>Btrong>

This gene encodes a multi-domain protein that is predominantly expressed in trong>btrong>rain trong>andtrong> testis. This protein interacts with amyloid trong>btrong>eta protein precursor (Atrong>btrong>etaPP) trong>andtrong> may have a role in normal trong>btrong>rain development, trong>andtrong> in the pathogenesis of Alzheimer's disease. Expression of this gene has trong>btrong>een shown to trong>btrong>e elevated in patients with pre-trong>Btrong> cell acute lymphocytic leukemia associated with t(1;19) translocation. Alternatively spliced transcript variants encoding different isoforms (some with different sutrong>btrong>cellular localization, PMID:15004329) have trong>btrong>een descritrong>btrong>ed for this gene. [provided trong>btrong>y RefSeq, Aug 2011]

ANKS1A Gene

ankyrin repeat trong>andtrong> sterile alpha motif domain containing 1A

Predicted to enatrong>btrong>le ephrin receptor trong>btrong>inding activity. Predicted to trong>btrong>e involved in ephrin receptor signaling pathway; neuron remodeling; trong>andtrong> sutrong>btrong>strate-dependent cell migration. Predicted to act upstream of or within negative regulation of utrong>btrong>iquitin-dependent protein catatrong>btrong>olic process trong>andtrong> regulation of ephrin receptor signaling pathway. Located in cytosol trong>andtrong> nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

OPALIN Gene

oligodendrocytic myelin paranodal trong>andtrong> inner loop protein

Predicted to trong>btrong>e involved in regulation of oligodendrocyte differentiation. Located in Golgi apparatus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SHANK3 Gene

SH3 trong>andtrong> multiple ankyrin repeat domains 3

This gene is a memtrong>btrong>er of the Shank gene family. Shank proteins are multidomain scaffold proteins of the postsynaptic density that connect neurotransmitter receptors, ion channels, trong>andtrong> other memtrong>btrong>rane proteins to the actin cytoskeleton trong>andtrong> G-protein-coupled signaling pathways. Shank proteins also play a role in synapse formation trong>andtrong> dendritic spine maturation. Mutations in this gene are a cause of autism spectrum disorder (ASD), which is characterized trong>btrong>y impairments in social interaction trong>andtrong> communication, trong>andtrong> restricted trong>btrong>ehavioral patterns trong>andtrong> interests. Mutations in this gene also cause schizophrenia type 15, trong>andtrong> are a major causative factor in the neurological symptoms of 22q13.3 deletion syndrome, which is also known as Phelan-McDermid syndrome. Additional isoforms have trong>btrong>een descritrong>btrong>ed for this gene trong>btrong>ut they have not yet trong>btrong>een experimentally verified. [provided trong>btrong>y RefSeq, Mar 2012]

SHANK2 Gene

SH3 trong>andtrong> multiple ankyrin repeat domains 2

This gene encodes a protein that is a memtrong>btrong>er of the Shank family of synaptic proteins that may function as molecular scaffolds in the postsynaptic density of excitatory synapses. Shank proteins contain multiple domains for protein-protein interaction, including ankyrin repeats, trong>andtrong> an SH3 domain. This particular family memtrong>btrong>er contains a PDZ domain, a consensus sequence for cortactin SH3 domain-trong>btrong>inding peptides trong>andtrong> a sterile alpha motif. The alternative splicing demonstrated in Shank genes has trong>btrong>een suggested as a mechanism for regulating the molecular structure of Shank trong>andtrong> the spectrum of Shank-interacting proteins in the postsynaptic densities of the adult trong>andtrong> developing trong>btrong>rain. Alterations in the encoded protein may trong>btrong>e associated with susceptitrong>btrong>ility to autism spectrum disorder. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2014]

SHANK1 Gene

SH3 trong>andtrong> multiple ankyrin repeat domains 1

This gene encodes a memtrong>btrong>er of the SHANK (SH3 domain trong>andtrong> ankyrin repeat containing) family of proteins. Memtrong>btrong>ers of this family act as scaffold proteins that are required for the development trong>andtrong> function of neuronal synapses. Deletions in this gene may trong>btrong>e associated with autism spectrum disorder in males. [provided trong>btrong>y RefSeq, Apr 2016]

SAMSN1 Gene

SAM domain, SH3 domain trong>andtrong> nuclear localization signals 1

SAMSN1 is a memtrong>btrong>er of a novel gene family of putative adaptors trong>andtrong> scaffold proteins containing SH3 trong>andtrong> SAM (sterile alpha motif) domains (Claudio et al., 2001 [Putrong>btrong>Med 11536050]).[supplied trong>btrong>y OMIM, Mar 2008]

LOC100421259 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 14 pseudogene

SKA1 Gene

spindle trong>andtrong> kinetochore associated complex sutrong>btrong>unit 1

Enatrong>btrong>les microtutrong>btrong>ule trong>btrong>inding activity. Involved in attachment of mitotic spindle microtutrong>btrong>ules to kinetochore; negative regulation of mitotic spindle assemtrong>btrong>ly checkpoint signaling; trong>andtrong> positive regulation of microtutrong>btrong>ule polymerization. Located in intercellular trong>btrong>ridge; kinetochore; trong>andtrong> microtutrong>btrong>ule cytoskeleton. Part of SKA complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SKA3 Gene

spindle trong>andtrong> kinetochore associated complex sutrong>btrong>unit 3

This gene encodes a component of the spindle trong>andtrong> kinetochore-associated protein complex that regulates microtutrong>btrong>ule attachment to the kinetochores during mitosis. The encoded protein localizes to the outer kinetechore trong>andtrong> may trong>btrong>e required for normal chromosome segregation trong>andtrong> cell division. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Oct 2009]

SKA2 Gene

spindle trong>andtrong> kinetochore associated complex sutrong>btrong>unit 2

Enatrong>btrong>les microtutrong>btrong>ule trong>btrong>inding activity. Involved in attachment of mitotic spindle microtutrong>btrong>ules to kinetochore trong>andtrong> regulation of microtutrong>btrong>ule polymerization or depolymerization. Located in spindle microtutrong>btrong>ule. Part of SKA complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

HN1L Gene

hematological trong>andtrong> neurological expressed 1-like

Involved in endocytosis involved in viral entry into host cell trong>andtrong> regulation of calcium-mediated signaling. Located in cytosol; nucleus; trong>andtrong> plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CDADC1 Gene

cytidine trong>andtrong> dCMP deaminase domain containing 1

Enatrong>btrong>les several functions, including cytidine deaminase activity; importin-alpha family protein trong>btrong>inding activity; trong>andtrong> protein homodimerization activity. Involved in DNA cytosine deamination trong>andtrong> cytidine deamination. Located in cytoplasm trong>andtrong> nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC100420832 Gene

cysteine trong>andtrong> glycine-rich protein 2 pseudogene

NUCKS1 Gene

nuclear casein kinase trong>andtrong> cyclin-dependent kinase sutrong>btrong>strate 1

This gene encodes a nuclear protein that is highly conserved in vertetrong>btrong>rates. The conserved regions of the protein contain several consensus phosphorylation sites for casein kinase II trong>andtrong> cyclin-dependent kinases, two putative nuclear localization signals, trong>andtrong> a trong>btrong>asic DNA-trong>btrong>inding domain. It is phosphorylated in vivo trong>btrong>y Cdk1 during mitosis of the cell cycle. [provided trong>btrong>y RefSeq, Aug 2010]

RIN1 Gene

Ras trong>andtrong> Ratrong>btrong> interactor 1

Predicted to enatrong>btrong>le guanyl-nucleotide exchange factor activity trong>andtrong> small GTPase trong>btrong>inding activity. Predicted to trong>btrong>e involved in signal transduction. Predicted to act upstream of or within associative learning; memory; trong>andtrong> negative regulation of synaptic plasticity. Located in cytoplasm trong>andtrong> plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

RIN3 Gene

Ras trong>andtrong> Ratrong>btrong> interactor 3

Summary: This protein encoded trong>btrong>y this gene is a memtrong>btrong>er of the RIN family of Ras interaction-interference proteins, which are trong>btrong>inding partners to the RAtrong>Btrong>5 small GTPases. The protein functions as a guanine nucleotide exchange for RAtrong>Btrong>5trong>Btrong> trong>andtrong> RAtrong>Btrong>31. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2016]

RIN2 Gene

Ras trong>andtrong> Ratrong>btrong> interactor 2

The RAtrong>Btrong>5 protein is a small GTPase involved in memtrong>btrong>rane trafficking in the early endocytic pathway. The protein encoded trong>btrong>y this gene trong>btrong>inds the GTP-trong>btrong>ound form of the RAtrong>Btrong>5 protein preferentially over the GDP-trong>btrong>ound form, trong>andtrong> functions as a guanine nucleotide exchange factor for RAtrong>Btrong>5. The encoded protein is found primarily as a tetramer in the cytoplasm trong>andtrong> does not trong>btrong>ind other memtrong>btrong>ers of the RAtrong>Btrong> family. Mutations in this gene cause macrocephaly alopecia cutis laxa trong>andtrong> scoliosis (MACS) syndrome, an elastic tissue disorder, as well as the related connective tissue disorder, RIN2 syndrome. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Jun 2011]

LOC340268 Gene

C3 trong>andtrong> PZP-like, alpha-2-macroglotrong>btrong>ulin domain containing 8 pseudogene

LOC102724726 Gene

coxsackievirus trong>andtrong> adenovirus receptor-like

TMUtrong>Btrong>1 Gene

transmemtrong>btrong>rane trong>andtrong> utrong>btrong>iquitin-like domain containing 1

Involved in ERAD pathway. Predicted to trong>btrong>e located in several cellular components, including centrosome; postsynaptic memtrong>btrong>rane; trong>andtrong> recycling endosome. Predicted to trong>btrong>e active in postsynaptic recycling endosome memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

TMUtrong>Btrong>2 Gene

transmemtrong>btrong>rane trong>andtrong> utrong>btrong>iquitin-like domain containing 2

Predicted to trong>btrong>e involved in ERAD pathway. Predicted to trong>btrong>e located in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

RNGTT Gene

RNA guanylyltransferase trong>andtrong> 5'-phosphatase

Enatrong>btrong>les inorganic triphosphate phosphatase activity trong>andtrong> mRNA guanylyltransferase activity. Involved in 7-methylguanosine mRNA capping. Predicted to trong>btrong>e located in nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PDX1 Gene

pancreatic trong>andtrong> duodenal homeotrong>btrong>ox 1

The protein encoded trong>btrong>y this gene is a transcriptional activator of several genes, including insulin, somatostatin, glucokinase, islet amyloid polypeptide, trong>andtrong> glucose transporter type 2. The encoded nuclear protein is involved in the early development of the pancreas trong>andtrong> plays a major role in glucose-dependent regulation of insulin gene expression. Defects in this gene are a cause of pancreatic agenesis, which can lead to early-onset insulin-dependent diatrong>btrong>etes mellitus (IDDM), as well as maturity onset diatrong>btrong>etes of the young type 4 (MODY4). [provided trong>btrong>y RefSeq, Aug 2017]

PAQR9 Gene

progestin trong>andtrong> adipoQ receptor family memtrong>btrong>er IX

Predicted to enatrong>btrong>le signaling receptor activity. Predicted to trong>btrong>e located in plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

EFCC1 Gene

EF-htrong>andtrong> trong>andtrong> coiled-coil domain containing 1

Predicted to enatrong>btrong>le calcium ion trong>btrong>inding activity. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SMU1 Gene

smu-1 suppressor of mec-8 trong>andtrong> unc-52 homolog (C. elegans)

Involved in mRNA splicing, via spliceosome. Located in nucleus. Part of U2-type precatalytic spliceosome. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

RFWD2P1 Gene

ring finger trong>andtrong> WD repeat domain 2, E3 utrong>btrong>iquitin protein ligase pseudogene 1

ANKDD1A Gene

ankyrin repeat trong>andtrong> death domain containing 1A

Predicted to trong>btrong>e involved in signal transduction. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ANKDD1trong>Btrong> Gene

ankyrin repeat trong>andtrong> death domain containing 1trong>Btrong>

Predicted to trong>btrong>e involved in signal transduction. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

NMI Gene

N-myc (trong>andtrong> STAT) interactor

NMYC interactor (NMI) encodes a protein that interacts with NMYC trong>andtrong> CMYC (two memtrong>btrong>ers of the oncogene Myc family), trong>andtrong> other transcription factors containing a Zip, HLH, or HLH-Zip motif. The NMI protein also interacts with all STATs except STAT2 trong>andtrong> augments STAT-mediated transcription in response to cytokines IL2 trong>andtrong> IFN-gamma. The NMI mRNA has low expression levels in all human fetal trong>andtrong> adult tissues tested except trong>btrong>rain trong>andtrong> has high expression in cancer cell line-myeloid leukemias. [provided trong>btrong>y RefSeq, Jul 2008]

LOC101060089 Gene

cleavage trong>andtrong> polyadenylation specificity factor sutrong>btrong>unit 5-like

CFAP126 Gene

cilia trong>andtrong> flagella associated protein 126

Predicted to trong>btrong>e involved in cilium organization trong>andtrong> flagellated sperm motility. Located in axonemal microtutrong>btrong>ule. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

RFFL Gene

ring finger trong>andtrong> FYVE-like domain containing E3 utrong>btrong>iquitin protein ligase

Enatrong>btrong>les enzyme trong>btrong>inding activity; p53 trong>btrong>inding activity; trong>andtrong> utrong>btrong>iquitin protein ligase activity. Involved in several processes, including negative regulation of cysteine-type endopeptidase activity; negative regulation of signal transduction; trong>andtrong> protein K48-linked utrong>btrong>iquitination. Located in endosome memtrong>btrong>rane trong>andtrong> plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CPSF3L Gene

cleavage trong>andtrong> polyadenylation specific factor 3-like

The Integrator complex contains at least 12 sutrong>btrong>units trong>andtrong> associates with the C-terminal domain of RNA polymerase II large sutrong>btrong>unit (POLR2A; MIM 180660) trong>andtrong> mediates the 3-prime end processing of small nuclear RNAs U1 (RNU1; MIM 180680) trong>andtrong> U2 (RNU2; MIM 180690). INTS11, or CPSF3L, is the catalytic sutrong>btrong>unit of the Integrator complex (trong>Btrong>aillat et al., 2005 [Putrong>btrong>Med 16239144]).[supplied trong>btrong>y OMIM, Mar 2008]

CALCOCO1 Gene

calcium trong>btrong>inding trong>andtrong> coiled-coil domain 1

Enatrong>btrong>les RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity; trong>btrong>eta-catenin trong>btrong>inding activity; trong>andtrong> nuclear receptor coactivator activity. Involved in positive regulation of DNA-templated transcription trong>andtrong> positive regulation of gene expression. Located in cytosol trong>andtrong> nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CALCOCO2 Gene

calcium trong>btrong>inding trong>andtrong> coiled-coil domain 2

This gene encodes a coiled-coil domain-containing protein. The encoded protein functions as a receptor for utrong>btrong>iquitin-coated trong>btrong>acteria trong>andtrong> plays an important role in innate immunity trong>btrong>y mediating macroautophagy. Alternatively spliced transcript variants encoding multiple isoforms have trong>btrong>een otrong>btrong>served for this gene. [provided trong>btrong>y RefSeq, May 2012]

FSD1L Gene

fitrong>btrong>ronectin type III trong>andtrong> SPRY domain containing 1-like

Predicted to trong>btrong>e located in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

DDA1 Gene

DET1 trong>andtrong> DDtrong>Btrong>1 associated 1

Involved in protein polyutrong>btrong>iquitination. Part of Cul4-RING E3 utrong>btrong>iquitin ligase complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

HAND2 Gene

heart trong>andtrong> neural crest derivatives expressed 2

The protein encoded trong>btrong>y this gene trong>btrong>elongs to the trong>btrong>asic helix-loop-helix family of transcription factors. This gene product is one of two closely related family memtrong>btrong>ers, the HAND proteins, which are asymmetrically expressed in the developing ventricular chamtrong>btrong>ers trong>andtrong> play an essential role in cardiac morphogenesis. Working in a complementary fashion, they function in the formation of the right ventricle trong>andtrong> aortic arch arteries, implicating them as mediators of congenital heart disease. In addition, this transcription factor plays an important role in limtrong>btrong> trong>andtrong> trong>btrong>ranchial arch development. [provided trong>btrong>y RefSeq, Jul 2008]

FCHSD1 Gene

FCH trong>andtrong> doutrong>btrong>le SH3 domains 1

Predicted to enatrong>btrong>le lipid trong>btrong>inding activity. Predicted to trong>btrong>e involved in neuromuscular synaptic transmission trong>andtrong> positive regulation of actin filament polymerization. Predicted to act upstream of or within several processes, including import into nucleus; inflammatory response; trong>andtrong> response to hydrogen peroxide. Predicted to trong>btrong>e located in cuticular plate. Predicted to trong>btrong>e part of protein-containing complex. Predicted to trong>btrong>e active in cytosol; neuromuscular junction; trong>andtrong> recycling endosome. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

FCHSD2 Gene

FCH trong>andtrong> doutrong>btrong>le SH3 domains 2

Enatrong>btrong>les phosphatidylinositol-3,4,5-trisphosphate trong>btrong>inding activity trong>andtrong> phosphatidylinositol-3,4-trong>btrong>isphosphate trong>btrong>inding activity. Involved in clathrin-dependent endocytosis trong>andtrong> positive regulation of Arp2/3 complex-mediated actin nucleation. Located in clathrin-coated pit trong>andtrong> plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

AMMECR1 Gene

Alport syndrome, mental retardation, midface hypoplasia trong>andtrong> elliptocytosis chromosomal region gene 1

The exact function of this gene is not known, however, sutrong>btrong>microscopic deletion of the X chromosome including this gene, COL4A5, trong>andtrong> FACL4 genes, result in a contiguous gene deletion syndrome, the AMME complex (Alport syndrome, mental retardation, midface hypoplasia, trong>andtrong> elliptocytosis). Alternatively spliced transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jan 2010]

CXADRP3 Gene

coxsackie virus trong>andtrong> adenovirus receptor pseudogene 3

TPTE2 Gene

transmemtrong>btrong>rane phosphoinositide 3-phosphatase trong>andtrong> tensin homolog 2

TPIP is a memtrong>btrong>er of a large class of memtrong>btrong>rane-associated phosphatases with sutrong>btrong>strate specificity for the 3-position phosphate of inositol phospholipids.[supplied trong>btrong>y OMIM, Jul 2002]

TMCC1P1 Gene

transmemtrong>btrong>rane trong>andtrong> coiled-coil domain family 1 pseudogene 1

RLTPR Gene

RGD motif, leucine rich repeats, tropomodulin domain trong>andtrong> proline-rich containing

This gene encodes a memtrong>btrong>er of the CARMIL (capping protein, Arp2/3, myosin-I linker) family of proteins. The encoded protein interacts with trong>andtrong> negatively regulates the heterodimeric capping protein trong>andtrong> promotes cell migration. Reduced expression of this gene has trong>btrong>een otrong>btrong>served in human psoriasis patients. Mutations in this gene cause a human immunodeficiency syndrome characterized trong>btrong>y smooth muscle tumors trong>andtrong> impaired T-cell function. [provided trong>btrong>y RefSeq, May 2017]

TMTC2 Gene

transmemtrong>btrong>rane trong>andtrong> tetratricopeptide repeat containing 2

The protein encoded trong>btrong>y this gene is an integral memtrong>btrong>rane protein localized to the endoplasmic reticulum (ER). The encoded protein contains many tetratricopeptide repeats, sequences known for trong>btrong>eing involved in protein-protein interactions. This protein trong>btrong>inds trong>btrong>oth the calcium uptake pump SERCA2trong>Btrong> trong>andtrong> the cartrong>btrong>ohydrate-trong>btrong>inding chaperone calnexin, trong>andtrong> it appears to play a role in calcium homeostasis in the ER. Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2016]

DMRT1 Gene

doutrong>btrong>lesex trong>andtrong> matrong>btrong>-3 related transcription factor 1

This gene is found in a cluster with two other memtrong>btrong>ers of the gene family, having in common a zinc finger-like DNA-trong>btrong>inding motif (DM domain). The DM domain is an ancient, conserved component of the vertetrong>btrong>rate sex-determining pathway that is also a key regulator of male development in flies trong>andtrong> nematodes. This gene exhitrong>btrong>its a gonad-specific trong>andtrong> sexually dimorphic expression pattern. Defective testicular development trong>andtrong> XY feminization occur when this gene is hemizygous. [provided trong>btrong>y RefSeq, Jul 2008]

DMRT2 Gene

doutrong>btrong>lesex trong>andtrong> matrong>btrong>-3 related transcription factor 2

The protein encoded trong>btrong>y this gene trong>btrong>elongs to the DMRT gene family, sharing a DM DNA-trong>btrong>inding domain with Drosophila 'doutrong>btrong>lesex' (dsx) trong>andtrong> C. elegans matrong>btrong>3, genes involved in sex determination in these organisms. Also, this gene is located in a region of the human genome (chromosome 9p24.3) associated with gonadal dysgenesis trong>andtrong> XY sex reversal. Hence this gene is one of the ctrong>andtrong>idates for sex-determining gene(s) on chr 9. [provided trong>btrong>y RefSeq, Apr 2010]

DMRT3 Gene

doutrong>btrong>lesex trong>andtrong> matrong>btrong>-3 related transcription factor 3

Enatrong>btrong>les sequence-specific doutrong>btrong>le-strtrong>andtrong>ed DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in male sex differentiation trong>andtrong> regulation of transcription trong>btrong>y RNA polymerase II. Predicted to act upstream of or within several processes, including adult walking trong>btrong>ehavior; regulation of odontogenesis of dentin-containing tooth; trong>andtrong> ventral spinal cord interneuron specification. Predicted to trong>btrong>e located in chromatin. Predicted to trong>btrong>e active in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CRADD Gene

CASP2 trong>andtrong> RIPK1 domain containing adaptor with death domain

This gene encodes a protein containing a death domain (DD) motif. This protein recruits caspase 2/ICH1 to the cell death signal transduction complex, which includes tumor necrosis factor receptor 1 (TNFR1A) trong>andtrong> RIPK1/RIP kinase, trong>andtrong> acts in promoting apoptosis. A mutation in this gene was associated with cognitive disatrong>btrong>ility. A related pseudogene is found on chromosome 3. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2016]

HPPD Gene

Hypertelorism, preauricular sinus, punctal pits, trong>andtrong> deafness

AGAP1 Gene

ArfGAP with GTPase domain, ankyrin repeat trong>andtrong> PH domain 1

This gene encodes a memtrong>btrong>er of an ADP-ritrong>btrong>osylation factor GTPase-activating protein family involved in memtrong>btrong>rane trafficking trong>andtrong> cytoskeleton dynamics. This gene functions as a direct regulator of the adaptor-related protein complex 3 on endosomes. Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Oct 2011]

AGAP2 Gene

ArfGAP with GTPase domain, ankyrin repeat trong>andtrong> PH domain 2

The protein encoded trong>btrong>y this gene trong>btrong>elongs to the centaurin gamma-like family. It mediates anti-apoptotic effects of nerve growth factor trong>btrong>y activating nuclear phosphoinositide 3-kinase. It is overexpressed in cancer cells, trong>andtrong> promotes cancer cell invasion. Alternatively spliced transcript variants encoding different isoforms have trong>btrong>een descritrong>btrong>ed for this gene. [provided trong>btrong>y RefSeq, Aug 2011]

AGAP3 Gene

ArfGAP with GTPase domain, ankyrin repeat trong>andtrong> PH domain 3

This gene encodes an essential component of the N-methyl-D-aspartate (NMDA) receptor signaling complex which mediates long-term potentiation in synapses trong>btrong>y linking activation of NMDA receptor to alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor trafficking. The encoded protein contains an N-terminal GTPase-like domain, a pleckstrin homology domain, an ArfGAP domain trong>andtrong> several C-terminal ankryn repeat domains. [provided trong>btrong>y RefSeq, Apr 2017]

AGAP4 Gene

ArfGAP with GTPase domain, ankyrin repeat trong>andtrong> PH domain 4

Predicted to enatrong>btrong>le GTPase activator activity trong>andtrong> GTPase activity. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

AGAP5 Gene

ArfGAP with GTPase domain, ankyrin repeat trong>andtrong> PH domain 5

Predicted to enatrong>btrong>le GTPase activator activity trong>andtrong> GTPase activity. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

AGAP6 Gene

ArfGAP with GTPase domain, ankyrin repeat trong>andtrong> PH domain 6

Predicted to enatrong>btrong>le GTPase activator activity trong>andtrong> GTPase activity. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

AGAP9 Gene

ArfGAP with GTPase domain, ankyrin repeat trong>andtrong> PH domain 9

Predicted to enatrong>btrong>le GTPase activator activity trong>andtrong> GTPase activity. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

DRAIC Gene

downregulated RNA in cancer, inhitrong>btrong>itor of cell invasion trong>andtrong> migration

HACE1 Gene

HECT domain trong>andtrong> ankyrin repeat containing E3 utrong>btrong>iquitin protein ligase 1

This gene encodes a HECT domain trong>andtrong> ankyrin repeat-containing utrong>btrong>iquitin ligase. The encoded protein is involved in specific tagging of target proteins, leading to their sutrong>btrong>cellular localization or proteasomal degradation. The protein is a potential tumor suppressor trong>andtrong> is involved in the pathophysiology of several tumors, including Wilm's tumor. [provided trong>btrong>y RefSeq, Mar 2016]

RUSC2 Gene

RUN trong>andtrong> SH3 domain containing 2

This gene encodes a RUN trong>andtrong> SH3 domain containing protein that interacts with Ratrong>btrong>1trong>btrong> trong>andtrong> Ratrong>btrong>1-trong>btrong>inding protein GM130. Alternatively spliced transcript variants have trong>btrong>een otrong>btrong>served for this gene. [provided trong>btrong>y RefSeq, Jun 2012]

RUSC1 Gene

RUN trong>andtrong> SH3 domain containing 1

Predicted to enatrong>btrong>le actin trong>btrong>inding activity. Involved in protein polyutrong>btrong>iquitination. Located in cytosol. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LZIC Gene

leucine zipper trong>andtrong> CTNNtrong>Btrong>IP1 domain containing

Predicted to enatrong>btrong>le trong>btrong>eta-catenin trong>btrong>inding activity. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ktrong>Btrong>Ttrong>Btrong>D7 Gene

kelch repeat trong>andtrong> trong>Btrong>Ttrong>Btrong> (POZ) domain containing 7

The protein encoded trong>btrong>y this gene is a transcriptional activator, having trong>btrong>een shown to increase the transcription of activator protein-1 trong>andtrong> serum response element. The encoded protein can also form a complex with Ktrong>Btrong>Ttrong>Btrong>D6 trong>andtrong> CUL3, which regulates the utrong>btrong>iquitylation trong>andtrong> degradation of TIAM1, which is a regulator of RAC1. [provided trong>btrong>y RefSeq, Jul 2016]

Ktrong>Btrong>Ttrong>Btrong>D4 Gene

kelch repeat trong>andtrong> trong>Btrong>Ttrong>Btrong> (POZ) domain containing 4

Ktrong>Btrong>Ttrong>Btrong>D3 Gene

kelch repeat trong>andtrong> trong>Btrong>Ttrong>Btrong> (POZ) domain containing 3

Predicted to enatrong>btrong>le utrong>btrong>iquitin-like ligase-sutrong>btrong>strate adaptor activity. Predicted to trong>btrong>e involved in proteasome-mediated utrong>btrong>iquitin-dependent protein catatrong>btrong>olic process. Predicted to trong>btrong>e part of Cul3-RING utrong>btrong>iquitin ligase complex. Predicted to trong>btrong>e active in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ktrong>Btrong>Ttrong>Btrong>D2 Gene

kelch repeat trong>andtrong> trong>Btrong>Ttrong>Btrong> (POZ) domain containing 2

Enatrong>btrong>les utrong>btrong>iquitin-like ligase-sutrong>btrong>strate adaptor activity. Involved in protein K48-linked utrong>btrong>iquitination trong>andtrong> regulation of cellular response to insulin stimulus. Is active in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ktrong>Btrong>Ttrong>Btrong>D8 Gene

kelch repeat trong>andtrong> trong>Btrong>Ttrong>Btrong> (POZ) domain containing 8

Predicted to enatrong>btrong>le utrong>btrong>iquitin-like ligase-sutrong>btrong>strate adaptor activity. Involved in neural crest cell development; neural crest formation; trong>andtrong> protein monoutrong>btrong>iquitination. Part of Cul3-RING utrong>btrong>iquitin ligase complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC126860 Gene

ArfGAP with GTPase domain, ankyrin repeat trong>andtrong> PH domain 1 pseudogene

TICRR Gene

TOPtrong>Btrong>P1-interacting checkpoint trong>andtrong> replication regulator

Enatrong>btrong>les chromatin trong>btrong>inding activity. Involved in regulation of DNA-templated DNA replication initiation. Located in cytosol trong>andtrong> nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

trong>Btrong>ROX Gene

trong>Btrong>RO1 domain trong>andtrong> CAAX motif containing

Involved in mitotic nuclear memtrong>btrong>rane reassemtrong>btrong>ly. Located in nuclear envelope. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ITGtrong>Btrong>2 Gene

integrin, trong>btrong>eta 2 (complement component 3 receptor 3 trong>andtrong> 4 sutrong>btrong>unit)

This gene encodes an integrin trong>btrong>eta chain, which comtrong>btrong>ines with multiple different alpha chains to form different integrin heterodimers. Integrins are integral cell-surface proteins that participate in cell adhesion as well as cell-surface mediated signalling. The encoded protein plays an important role in immune response trong>andtrong> defects in this gene cause leukocyte adhesion deficiency. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Dec 2014]

CFAP69 Gene

cilia trong>andtrong> flagella associated protein 69

Acts upstream of or within sperm axoneme assemtrong>btrong>ly. Located in cytoplasm trong>andtrong> sperm midpiece. Implicated in spermatogenic failure 24. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP61 Gene

cilia trong>andtrong> flagella associated protein 61

Involved in sperm flagellum assemtrong>btrong>ly. Predicted to trong>btrong>e located in radial spoke stalk trong>andtrong> sperm flagellum. Implicated in spermatogenic failure 84. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ZAK Gene

sterile alpha motif trong>andtrong> leucine zipper containing kinase AZK

This gene is a memtrong>btrong>er of the MAPKKK family of signal transduction molecules trong>andtrong> encodes a protein with an N-terminal kinase catalytic domain, followed trong>btrong>y a leucine zipper motif trong>andtrong> a sterile-alpha motif (SAM). This magnesium-trong>btrong>inding protein forms homodimers trong>andtrong> is located in the cytoplasm. The protein mediates gamma radiation signaling leading to cell cycle arrest trong>andtrong> activity of this protein plays a role in cell cycle checkpoint regulation in cells. The protein also has pro-apoptotic activity. Alternate transcriptional splice variants, encoding different isoforms, have trong>btrong>een characterized. [provided trong>btrong>y RefSeq, Jul 2008]

VSTM5 Gene

V-set trong>andtrong> transmemtrong>btrong>rane domain containing 5

Predicted to trong>btrong>e involved in several processes, including filopodium assemtrong>btrong>ly; positive regulation of excitatory synapse assemtrong>btrong>ly; trong>andtrong> protein homooligomerization. Predicted to trong>btrong>e located in memtrong>btrong>rane. Predicted to trong>btrong>e active in axon; dendrite; trong>andtrong> plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

VSTM4 Gene

V-set trong>andtrong> transmemtrong>btrong>rane domain containing 4

Predicted to act upstream of or within several processes, including endothelial cell proliferation; retina trong>btrong>lood vessel maintenance; trong>andtrong> vasculature development. Predicted to trong>btrong>e located in extracellular region trong>andtrong> plasma memtrong>btrong>rane. Predicted to trong>btrong>e active in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

VSTM1 Gene

V-set trong>andtrong> transmemtrong>btrong>rane domain containing 1

Predicted to enatrong>btrong>le cytokine activity. Predicted to trong>btrong>e involved in immune response-regulating signaling pathway. Predicted to trong>btrong>e located in extracellular space trong>andtrong> memtrong>btrong>rane. Predicted to trong>btrong>e active in plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

GADD45A Gene

growth arrest trong>andtrong> DNA-damage-inducitrong>btrong>le, alpha

This gene is a memtrong>btrong>er of a group of genes whose transcript levels are increased following stressful growth arrest conditions trong>andtrong> treatment with DNA-damaging agents. The protein encoded trong>btrong>y this gene responds to environmental stresses trong>btrong>y mediating activation of the p38/JNK pathway via MTK1/MEKK4 kinase. The DNA damage-induced transcription of this gene is mediated trong>btrong>y trong>btrong>oth p53-dependent trong>andtrong> -independent mechanisms. Alternatively spliced transcript variants encoding distinct isoforms have trong>btrong>een found for this gene.[provided trong>btrong>y RefSeq, Dec 2010]

GADD45trong>Btrong> Gene

growth arrest trong>andtrong> DNA-damage-inducitrong>btrong>le, trong>btrong>eta

This gene is a memtrong>btrong>er of a group of genes whose transcript levels are increased following stressful growth arrest conditions trong>andtrong> treatment with DNA-damaging agents. The genes in this group respond to environmental stresses trong>btrong>y mediating activation of the p38/JNK pathway. This activation is mediated via their proteins trong>btrong>inding trong>andtrong> activating MTK1/MEKK4 kinase, which is an upstream activator of trong>btrong>oth p38 trong>andtrong> JNK MAPKs. The function of these genes or their protein products is involved in the regulation of growth trong>andtrong> apoptosis. These genes are regulated trong>btrong>y different mechanisms, trong>btrong>ut they are often coordinately expressed trong>andtrong> can function cooperatively in inhitrong>btrong>iting cell growth. [provided trong>btrong>y RefSeq, Jul 2008]

GADD45G Gene

growth arrest trong>andtrong> DNA-damage-inducitrong>btrong>le, gamma

This gene is a memtrong>btrong>er of a group of genes whose transcript levels are increased following stressful growth arrest conditions trong>andtrong> treatment with DNA-damaging agents. The protein encoded trong>btrong>y this gene responds to environmental stresses trong>btrong>y mediating activation of the p38/JNK pathway via MTK1/MEKK4 kinase. The GADD45G is highly expressed in placenta. [provided trong>btrong>y RefSeq, Jul 2008]

Ztrong>Btrong>Ttrong>Btrong>45P2 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 45 pseudogene 2

Ztrong>Btrong>Ttrong>Btrong>45P1 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 45 pseudogene 1

HERC1 Gene

HECT trong>andtrong> RLD domain containing E3 utrong>btrong>iquitin protein ligase family memtrong>btrong>er 1

This gen encodes a memtrong>btrong>er of the HERC protein family. This protein stimulates guanine nucleotide exchange on ARF1 trong>andtrong> Ratrong>btrong> proteins. This protein may trong>btrong>e involved in memtrong>btrong>rane transport processes. [provided trong>btrong>y RefSeq, Mar 2012]

HERC3 Gene

HECT trong>andtrong> RLD domain containing E3 utrong>btrong>iquitin protein ligase 3

This gene encodes a memtrong>btrong>er the HERC utrong>btrong>iquitin ligase family. The encoded protein is located in the cytosol trong>andtrong> trong>btrong>inds utrong>btrong>iquitin via a HECT domain. Mutations in this gene have trong>btrong>een associated with colorectal trong>andtrong> gastric carcinomas. Alternatively spliced transcript variants encoding multiple isoforms have trong>btrong>een otrong>btrong>served for this gene. [provided trong>btrong>y RefSeq, Oct 2012]

HERC2 Gene

HECT trong>andtrong> RLD domain containing E3 utrong>btrong>iquitin protein ligase 2

This gene trong>btrong>elongs to the HERC gene family that encodes a group of unusually large proteins, which contain multiple structural domains. All memtrong>btrong>ers have at least 1 copy of an N-terminal region showing homology to the cell cycle regulator RCC1 trong>andtrong> a C-terminal HECT (homologous to E6-AP C terminus) domain found in a numtrong>btrong>er of E3 utrong>btrong>iquitin protein ligases. Genetic variations in this gene are associated with skin/hair/eye pigmentation variatrong>btrong>ility. Multiple pseudogenes of this gene are located on chromosomes 15 trong>andtrong> 16. [provided trong>btrong>y RefSeq, Mar 2012]

HERC5 Gene

HECT trong>andtrong> RLD domain containing E3 utrong>btrong>iquitin protein ligase 5

This gene is a memtrong>btrong>er of the HERC family of utrong>btrong>iquitin ligases trong>andtrong> encodes a protein with a HECT domain trong>andtrong> five RCC1 repeats. Pro-inflammatory cytokines upregulate expression of this gene in endothelial cells. The protein localizes to the cytoplasm trong>andtrong> perinuclear region trong>andtrong> functions as an interferon-induced E3 protein ligase that mediates ISGylation of protein targets. The protein also acts as a modulator of the antiviral immune response. The gene lies in a cluster of HERC family genes on chromosome 4. [provided trong>btrong>y RefSeq, Aug 2021]

HERC4 Gene

HECT trong>andtrong> RLD domain containing E3 utrong>btrong>iquitin protein ligase 4

HERC4 trong>btrong>elongs to the HERC family of utrong>btrong>iquitin ligases, all of which contain a HECT domain trong>andtrong> at least 1 RCC1 (MIM 179710)-like domain (RLD). The 350-amino acid HECT domain is predicted to catalyze the formation of a thioester with utrong>btrong>iquitin trong>btrong>efore transferring it to a sutrong>btrong>strate, trong>andtrong> the RLD is predicted to act as a guanine nucleotide exchange factor for small G proteins (Hochrainer et al., 2005 [Putrong>btrong>Med 15676274]).[supplied trong>btrong>y OMIM, Mar 2008]

HERC6 Gene

HECT trong>andtrong> RLD domain containing E3 utrong>btrong>iquitin protein ligase family memtrong>btrong>er 6

HERC6 trong>btrong>elongs to the HERC family of utrong>btrong>iquitin ligases, all of which contain a HECT domain trong>andtrong> at least 1 RCC1 (MIM 179710)-like domain (RLD). The 350-amino acid HECT domain is predicted to catalyze the formation of a thioester with utrong>btrong>iquitin trong>btrong>efore transferring it to a sutrong>btrong>strate, trong>andtrong> the RLD is predicted to act as a guanine nucleotide exchange factor for small G proteins (Hochrainer et al., 2005 [Putrong>btrong>Med 15676274]).[supplied trong>btrong>y OMIM, Mar 2008]

AGGF1P10 Gene

angiogenic factor with G patch trong>andtrong> FHA domains 1 pseudogene 10

FANK1 Gene

fitrong>btrong>ronectin type III trong>andtrong> ankyrin repeat domains 1

Involved in regulation of DNA-templated transcription trong>andtrong> regulation of apoptotic process. Located in chromatin; cytosol; trong>andtrong> nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ANKMY1 Gene

ankyrin repeat trong>andtrong> MYND domain containing 1

Predicted to enatrong>btrong>le metal ion trong>btrong>inding activity. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ANKMY2 Gene

ankyrin repeat trong>andtrong> MYND domain containing 2

Predicted to enatrong>btrong>le enzyme trong>btrong>inding activity trong>andtrong> metal ion trong>btrong>inding activity. Predicted to trong>btrong>e located in cilium. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC101060637 Gene

nuclear utrong>btrong>iquitous casein trong>andtrong> cyclin-dependent kinase sutrong>btrong>strate 1-like

AARD Gene

alanine trong>andtrong> arginine rich domain containing protein

Predicted to act upstream of or within response to testosterone. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC100422352 Gene

transmemtrong>btrong>rane trong>andtrong> tetratricopeptide repeat containing 1 pseudogene

RSF1 Gene

remodeling trong>andtrong> spacing factor 1

This gene encodes a nuclear protein that interacts with hepatitis trong>Btrong> virus X protein (Htrong>Btrong>X) trong>andtrong> facilitates transcription of hepatitis trong>Btrong> virus genes trong>btrong>y the Htrong>Btrong>X transcription activator, suggesting a role for this interaction in the virus life cycle. This protein also interacts with SNF2H protein to form the RSF chromatin-remodeling complex, where the SNF2H sutrong>btrong>unit functions as the nucleosome-dependent ATPase, trong>andtrong> this protein as the histone chaperone. [provided trong>btrong>y RefSeq, Sep 2011]

LOC100130044 Gene

cilia trong>andtrong> flagella associated protein 69 pseudogene

CFAP47 Gene

cilia trong>andtrong> flagella associated protein 47

While this gene is well-supported trong>btrong>y transcript data, no functional information on its protein product is currently availatrong>btrong>le. [provided trong>btrong>y RefSeq, Dec 2009]

CFAP44 Gene

cilia trong>andtrong> flagella associated protein 44

Enatrong>btrong>les peptidase activity. Involved in sperm axoneme assemtrong>btrong>ly. Acts upstream of or within microtutrong>btrong>ule cytoskeleton organization. Predicted to trong>btrong>e located in cytoplasm; cytoskeleton; trong>andtrong> motile cilium. Implicated in spermatogenic failure 20. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ftrong>Btrong>XL20 Gene

F-trong>btrong>ox trong>andtrong> leucine-rich repeat protein 20

Memtrong>btrong>ers of the F-trong>btrong>ox protein family, such as Ftrong>Btrong>XL20, are characterized trong>btrong>y an approximately 40-amino acid F-trong>btrong>ox motif. SCF complexes, formed trong>btrong>y SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), trong>andtrong> F-trong>btrong>ox proteins, act as protein-utrong>btrong>iquitin ligases. F-trong>btrong>ox proteins interact with SKP1 through the F trong>btrong>ox, trong>andtrong> they interact with utrong>btrong>iquitination targets through other protein interaction domains (Jin et al., 2004 [Putrong>btrong>Med 15520277]).[supplied trong>btrong>y OMIM, Mar 2008]

Ftrong>Btrong>XL21 Gene

F-trong>btrong>ox trong>andtrong> leucine-rich repeat protein 21 (gene/pseudogene)

This locus represents a transcritrong>btrong>ed pseudogene that is related to genes encoding memtrong>btrong>ers of the F-trong>btrong>ox family of proteins. [provided trong>btrong>y RefSeq, Nov 2017]

Ftrong>Btrong>XL22 Gene

F-trong>btrong>ox trong>andtrong> leucine-rich repeat protein 22

This gene encodes a memtrong>btrong>er of the F-trong>btrong>ox protein family. This F-trong>btrong>ox protein interacts with S-phase kinase-associated protein 1A trong>andtrong> cullin in order to form SCF complexes which function as utrong>btrong>iquitin ligases.[provided trong>btrong>y RefSeq, Sep 2010]

LOC100419763 Gene

zinc finger with KRAtrong>Btrong> trong>andtrong> SCAN domains 8 pseudogene

CXADR Gene

coxsackie virus trong>andtrong> adenovirus receptor

The protein encoded trong>btrong>y this gene is a type I memtrong>btrong>rane receptor for group trong>Btrong> coxsackieviruses trong>andtrong> sutrong>btrong>group C adenoviruses. Several transcript variants encoding different isoforms have trong>btrong>een found for this gene. Pseudogenes of this gene are found on chromosomes 15, 18, trong>andtrong> 21. [provided trong>btrong>y RefSeq, May 2011]

MNDEC Gene

Microtia with nasolacrimal duct imperforation trong>andtrong> eye colotrong>btrong>oma

INF2 Gene

inverted formin, FH2 trong>andtrong> WH2 domain containing

This gene represents a memtrong>btrong>er of the formin family of proteins. It is considered a diaphanous formin due to the presence of a diaphanous inhitrong>btrong>itory domain located at the N-terminus of the encoded protein. Studies of a similar mouse protein indicate that the protein encoded trong>btrong>y this locus may function in polymerization trong>andtrong> depolymerization of actin filaments. Mutations at this locus have trong>btrong>een associated with focal segmental glomerulosclerosis 5.[provided trong>btrong>y RefSeq, Aug 2010]

PATE4 Gene

prostate trong>andtrong> testis expressed 4

Enatrong>btrong>les acetylcholine receptor regulator activity. Involved in regulation of neurotransmitter receptor activity. Located in acrosomal vesicle trong>andtrong> extracellular space. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PHLPP1 Gene

PH domain trong>andtrong> leucine rich repeat protein phosphatase 1

This gene encodes a memtrong>btrong>er of the serine/threonine phosphatase family. The encoded protein promotes apoptosis trong>btrong>y dephosphorylating trong>andtrong> inactivating the serine/threonine kinase Akt, trong>andtrong> functions as a tumor suppressor in multiple types of cancer. Increased expression of this gene may also play a role in otrong>btrong>esity trong>andtrong> type 2 diatrong>btrong>etes trong>btrong>y interfering with Akt-mediated insulin signaling. [provided trong>btrong>y RefSeq, Dec 2011]

DIS3 Gene

DIS3 exosome endoritrong>btrong>onuclease trong>andtrong> 3'-5' exoritrong>btrong>onuclease

Enatrong>btrong>les 3'-5'-RNA exonuclease activity; endonuclease activity; trong>andtrong> guanyl-nucleotide exchange factor activity. Involved in CUT catatrong>btrong>olic process; RNA processing; trong>andtrong> rRNA catatrong>btrong>olic process. Located in cytosol trong>andtrong> nucleoplasm. Part of nuclear exosome (RNase complex). [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ANKS4trong>Btrong> Gene

ankyrin repeat trong>andtrong> sterile alpha motif domain containing 4trong>Btrong>

Involved in trong>btrong>rush trong>btrong>order assemtrong>btrong>ly; protein localization to microvillus; trong>andtrong> protein-containing complex assemtrong>btrong>ly. Located in trong>btrong>rush trong>btrong>order trong>andtrong> microvillus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SKA2P1 Gene

spindle trong>andtrong> kinetochore associated complex sutrong>btrong>unit 2 pseudogene 1

IGSF6-DREV1 Gene

region containing immunoglotrong>btrong>ulin superfamily, memtrong>btrong>er 6 trong>andtrong> DREV1

SNED1 Gene

sushi, nidogen trong>andtrong> EGF-like domains 1

Predicted to enatrong>btrong>le Notch trong>btrong>inding activity. Predicted to trong>btrong>e involved in cell-matrix adhesion. Located in extracellular matrix. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

MLSM7 Gene

Myelodysplasia trong>andtrong> leukemia syndrome with monosomy 7

TCEANC2 Gene

transcription elongation factor A (SII) N-terminal trong>andtrong> central domain containing 2

Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e active in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

GPKOW Gene

G patch domain trong>andtrong> KOW motifs

This gene encodes a putative RNA-trong>btrong>inding protein containing G-patch trong>andtrong> KOW (Kyprides, Ouzounis, Woese) domains. The encoded protein interacts directly with protein kinase A trong>andtrong> protein kinase X trong>andtrong> is also found associated with the spliceosome. [provided trong>btrong>y RefSeq, Aug 2013]

CUZD1 Gene

CUtrong>Btrong> trong>andtrong> zona pellucida-like domains 1

Predicted to trong>btrong>e involved in trypsinogen activation. Located in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC100288437 Gene

ring finger trong>andtrong> WD repeat domain 2, E3 utrong>btrong>iquitin protein ligase pseudogene

CCL18 Gene

chemokine (C-C motif) ligtrong>andtrong> 18 (pulmonary trong>andtrong> activation-regulated)

This antimicrotrong>btrong>ial gene is one of several Cys-Cys (CC) cytokine genes clustered on the q arm of chromosome 17. Cytokines are a family of secreted proteins involved in immunoregulatory trong>andtrong> inflammatory processes. The CC cytokines are proteins characterized trong>btrong>y two adjacent cysteines. The cytokine encoded trong>btrong>y this gene displays chemotactic activity for naive T cells, CD4+ trong>andtrong> CD8+ T cells trong>andtrong> nonactivated lymphocytes, trong>btrong>ut not for monocytes or granulocytes. This chemokine attracts naive T lymphocytes toward dendritic cells trong>andtrong> activated macrophages in lymph nodes. It may play a role in trong>btrong>oth humoral trong>andtrong> cell-mediated immunity responses. [provided trong>btrong>y RefSeq, Sep 2014]

STAT5trong>Btrong> Gene

signal transducer trong>andtrong> activator of transcription 5trong>Btrong>

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of the STAT family of transcription factors. In response to cytokines trong>andtrong> growth factors, STAT family memtrong>btrong>ers are phosphorylated trong>btrong>y the receptor associated kinases, trong>andtrong> then form homo- or heterodimers that translocate to the cell nucleus where they act as transcription activators. This protein mediates the signal transduction triggered trong>btrong>y various cell ligtrong>andtrong>s, such as IL2, IL4, CSF1, trong>andtrong> different growth hormones. It has trong>btrong>een shown to trong>btrong>e involved in diverse trong>btrong>iological processes, such as TCR signaling, apoptosis, adult mammary gltrong>andtrong> development, trong>andtrong> sexual dimorphism of liver gene expression. This gene was found to fuse to retinoic acid receptor-alpha (RARA) gene in a small sutrong>btrong>set of acute promyelocytic leukemias (APLL). The dysregulation of the signaling pathways mediated trong>btrong>y this protein may trong>btrong>e the cause of the APLL. [provided trong>btrong>y RefSeq, Jul 2008]

STAT5A Gene

signal transducer trong>andtrong> activator of transcription 5A

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of the STAT family of transcription factors. In response to cytokines trong>andtrong> growth factors, STAT family memtrong>btrong>ers are phosphorylated trong>btrong>y the receptor associated kinases, trong>andtrong> then form homo- or heterodimers that translocate to the cell nucleus where they act as transcription activators. This protein is activated trong>btrong>y, trong>andtrong> mediates the responses of many cell ligtrong>andtrong>s, such as IL2, IL3, IL7 GM-CSF, erythropoietin, thromtrong>btrong>opoietin, trong>andtrong> different growth hormones. Activation of this protein in myeloma trong>andtrong> lymphoma associated with a TEL/JAK2 gene fusion is independent of cell stimulus trong>andtrong> has trong>btrong>een shown to trong>btrong>e essential for tumorigenesis. The mouse counterpart of this gene is found to induce the expression of trong>Btrong>CL2L1/trong>Btrong>CL-X(L), which suggests the antiapoptotic function of this gene in cells. Alternatively spliced transcript variants have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Dec 2013]

RASGRP2 Gene

RAS guanyl releasing protein 2 (calcium trong>andtrong> DAG-regulated)

The protein encoded trong>btrong>y this gene is a trong>btrong>rain-enriched nucleotide exchanged factor that contains an N-terminal GEF domain, 2 ttrong>andtrong>em repeats of EF-htrong>andtrong> calcium-trong>btrong>inding motifs, trong>andtrong> a C-terminal diacylglycerol/phortrong>btrong>ol ester-trong>btrong>inding domain. This protein can activate small GTPases, including RAS trong>andtrong> RAP1/RAS3. The nucleotide exchange activity of this protein can trong>btrong>e stimulated trong>btrong>y calcium trong>andtrong> diacylglycerol. Four alternatively spliced transcript variants encoding two different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jan 2016]

RASGRP3 Gene

RAS guanyl releasing protein 3 (calcium trong>andtrong> DAG-regulated)

The protein encoded trong>btrong>y this gene is a guanine nucleotide exchange factor that activates the oncogenes HRAS trong>andtrong> RAP1A. Defects in this gene have trong>btrong>een associated with systemic lupus erythematosus trong>andtrong> several cancers. [provided trong>btrong>y RefSeq, Mar 2017]

RASGRP1 Gene

RAS guanyl releasing protein 1 (calcium trong>andtrong> DAG-regulated)

This gene is a memtrong>btrong>er of a family of genes characterized trong>btrong>y the presence of a Ras superfamily guanine nucleotide exchange factor (GEF) domain. It functions as a diacylglycerol (DAG)-regulated nucleotide exchange factor specifically activating Ras through the exchange of trong>btrong>ound GDP for GTP. It activates the Erk/MAP kinase cascade trong>andtrong> regulates T-cells trong>andtrong> trong>Btrong>-cells development, homeostasis trong>andtrong> differentiation. Alternatively spliced transcript variants encoding different isoforms have trong>btrong>een identified. Altered expression of the different isoforms of this protein may trong>btrong>e a cause of susceptitrong>btrong>ility to systemic lupus erythematosus (SLE). [provided trong>btrong>y RefSeq, Jul 2008]

LOC100421197 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 10 pseudogene

LOC102723312 Gene

angiogenic factor with G patch trong>andtrong> FHA domains 1 pseudogene

ANKFN1 Gene

ankyrin-repeat trong>andtrong> fitrong>btrong>ronectin type III domain containing 1

Predicted to trong>btrong>e involved in estatrong>btrong>lishment of mitotic spindle orientation trong>andtrong> regulation of estatrong>btrong>lishment of trong>btrong>ipolar cell polarity. Predicted to act upstream of or within trong>btrong>ehavioral fear response; equilitrong>btrong>rioception; trong>andtrong> locomotor rhythm. Predicted to trong>btrong>e active in spindle. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

POROK2 Gene

Porokeratosis, palmar, plantar, trong>andtrong> disseminated 1

LIMCH1 Gene

LIM trong>andtrong> calponin homology domains 1

Enatrong>btrong>les myosin II head/neck trong>btrong>inding activity. Involved in several processes, including cytoplasmic actin-trong>btrong>ased contraction involved in cell motility; positive regulation of stress fitrong>btrong>er assemtrong>btrong>ly; trong>andtrong> regulation of focal adhesion assemtrong>btrong>ly. Located in myosin II complex trong>andtrong> stress fitrong>btrong>er. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

trong>Btrong>AHCC1 Gene

trong>Btrong>AH domain trong>andtrong> coiled-coil containing 1

Predicted to enatrong>btrong>le chromatin trong>btrong>inding activity. Predicted to act upstream of or within chromatin organization; locomotory trong>btrong>ehavior; trong>andtrong> neuron differentiation. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

WWC2 Gene

WW trong>andtrong> C2 domain containing 2

This gene encodes a memtrong>btrong>er of the WW-trong>andtrong>-C2-domain-containing family of proteins. Memtrong>btrong>ers of this family have two N-terminal WW domains that mediate trong>btrong>inding to target proteins hartrong>btrong>oring L/PPxY motifs, an internal C2 domain for memtrong>btrong>rane association, trong>andtrong> C-terminal alpha protein kinase C trong>btrong>inding sites trong>andtrong> class III PDZ domain-interaction motifs. Proteins of this family are atrong>btrong>le to form homo- trong>andtrong> heterodimers trong>andtrong> to modulate hippo pathway signaling. [provided trong>btrong>y RefSeq, Sep 2016]

MIEN1 Gene

migration trong>andtrong> invasion enhancer 1

Involved in negative regulation of apoptotic process; positive regulation of cell migration; trong>andtrong> positive regulation of filopodium assemtrong>btrong>ly. Located in cytoplasmic side of plasma memtrong>btrong>rane trong>andtrong> cytosol. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC100862682 Gene

nucleus accumtrong>btrong>ens associated 1, trong>Btrong>EN trong>andtrong> trong>Btrong>Ttrong>Btrong> (POZ) domain containing pseudogene

TMEFF1 Gene

transmemtrong>btrong>rane protein with EGF-like trong>andtrong> two follistatin-like domains 1

Enatrong>btrong>les receptor ligtrong>andtrong> inhitrong>btrong>itor activity. Involved in negative regulation of viral entry into host cell. Is active in plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

TMEFF2 Gene

transmemtrong>btrong>rane protein with EGF-like trong>andtrong> two follistatin-like domains 2

This gene encodes a memtrong>btrong>er of the tomoregulin family of transmemtrong>btrong>rane proteins. This protein has trong>btrong>een shown to function as trong>btrong>oth an oncogene trong>andtrong> a tumor suppressor depending on the cellular context trong>andtrong> may regulate prostate cancer cell invasion. Multiple solutrong>btrong>le forms of this protein have trong>btrong>een identified that arise from trong>btrong>oth an alternative splice variant trong>andtrong> ectodomain shedding. Additionally, this gene has trong>btrong>een found to trong>btrong>e hypermethylated in multiple cancer types. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2015]

PROSER1 Gene

proline trong>andtrong> serine rich 1

This gene encodes a conserved protein containing proline trong>andtrong> serine rich regions. These regions may trong>btrong>e important in protein-protein interactions. [provided trong>btrong>y RefSeq, Aug 2012]

PROSER2 Gene

proline trong>andtrong> serine rich 2

PROSER3 Gene

proline trong>andtrong> serine rich 3

Located in centrosome. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SARM1 Gene

sterile alpha trong>andtrong> TIR motif containing 1

Enatrong>btrong>les NAD+ nucleosidase activity; NAD+ nucleotidase, cyclic ADP-ritrong>btrong>ose generating; trong>andtrong> identical protein trong>btrong>inding activity. Involved in NAD catatrong>btrong>olic process trong>andtrong> response to axon injury. Is active in mitochondrion. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CVMRF Gene

cutrong>btrong>itus valgus with mental retardation trong>andtrong> unusual facies

PRIMPOL Gene

primase trong>andtrong> polymerase (DNA-directed)

This gene encodes a DNA primase-polymerase that trong>btrong>elongs to a superfamily of archaeao-eukaryotic primases. Memtrong>btrong>ers of this family have primase activity, catalyzing the synthesis of short RNA primers that serve as starting points for DNA synthesis, as well as DNA polymerase activity. The encoded protein facilitates DNA damage tolerance trong>btrong>y mediating uninterrupted fork progression after UV irradiation trong>andtrong> reinitiating DNA synthesis. An allelic variant in this gene is associated with myopia 22. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Sep 2016]

EGFEM1P Gene

EGF-like trong>andtrong> EMI domain containing 1, pseudogene

Predicted to enatrong>btrong>le scavenger receptor activity. Predicted to trong>btrong>e involved in vesicle-mediated transport. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LIMS3L Gene

LIM trong>andtrong> senescent cell antigen-like domains 3-like

Predicted to enatrong>btrong>le metal ion trong>btrong>inding activity. Predicted to trong>btrong>e located in cytoplasm; focal adhesion; trong>andtrong> plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC100419574 Gene

HECT trong>andtrong> RLD domain containing E3 utrong>btrong>iquitin protein ligase 2 pseudogene

SIGIRR Gene

single immunoglotrong>btrong>ulin trong>andtrong> toll-interleukin 1 receptor (TIR) domain

Involved in negative regulation of Toll signaling pathway. Located in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ELMSAN1 Gene

ELM2 trong>andtrong> Mytrong>btrong>/SANT-like domain containing 1

Predicted to enatrong>btrong>le transcription corepressor activity. Predicted to trong>btrong>e involved in negative regulation of DNA-templated transcription trong>andtrong> regulation of transcription trong>btrong>y RNA polymerase II. Located in nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

AGGF1 Gene

angiogenic factor with G patch trong>andtrong> FHA domains 1

This gene encodes an angiogenic factor that promotes proliferation of endothelial cells. Mutations in this gene are associated with a susceptitrong>btrong>ility to Klippel-Trenaunay syndrome. Pseudogenes of this gene are found on chromosomes 3, 4, 10 trong>andtrong> 16.[provided trong>btrong>y RefSeq, Sep 2010]

SLC47A2 Gene

solute carrier family 47 (multidrug trong>andtrong> toxin extrusion), memtrong>btrong>er 2

This gene encodes a protein trong>btrong>elonging to a family of transporters involved in excretion of toxic electrolytes, trong>btrong>oth endogenous trong>andtrong> exogenous, through urine trong>andtrong> trong>btrong>ile. This transporter family shares homology with the trong>btrong>acterial MATE (multidrug trong>andtrong> toxin extrusion) protein family responsitrong>btrong>le for drug resistance. This gene is one of two memtrong>btrong>ers of the MATE transporter family located near each other on chromosome 17. Alternatively spliced transcript variants encoding different isoforms have trong>btrong>een identified for this gene. [provided trong>btrong>y RefSeq, Jul 2008]

SLC47A1 Gene

solute carrier family 47 (multidrug trong>andtrong> toxin extrusion), memtrong>btrong>er 1

This gene is located within the Smith-Magenis syndrome region on chromosome 17. It encodes a protein of unknown function. [provided trong>btrong>y RefSeq, Jul 2008]

LOC100130466 Gene

nuclear utrong>btrong>iquitous casein trong>andtrong> cyclin-dependent kinase sutrong>btrong>strate 1-like

Atrong>Btrong>Ttrong>Btrong>1 Gene

ankyrin repeat trong>andtrong> trong>Btrong>Ttrong>Btrong> (POZ) domain containing 1

This gene encodes a protein with an ankyrin repeat region trong>andtrong> two trong>Btrong>Ttrong>Btrong>/POZ domains, which are thought to trong>btrong>e involved in protein-protein interactions. Expression of this gene is activated trong>btrong>y the phosphatase trong>andtrong> tensin homolog, a tumor suppressor. Alternate splicing results in three transcript variants. [provided trong>btrong>y RefSeq, Mar 2010]

Atrong>Btrong>Ttrong>Btrong>2 Gene

ankyrin repeat trong>andtrong> trong>Btrong>Ttrong>Btrong> (POZ) domain containing 2

Predicted to enatrong>btrong>le protein heterodimerization activity. Predicted to act upstream of or within cellular response to toxic sutrong>btrong>stance. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

DCAF7 Gene

DDtrong>Btrong>1 trong>andtrong> CUL4 associated factor 7

This gene encodes a protein with multiple WD40 repeats which facilitate protein-protein interactions trong>andtrong> theretrong>btrong>y enatrong>btrong>le the assemtrong>btrong>ly of multiprotein complexes. This protein has trong>btrong>een shown to function as a scaffold protein for protein complexes involved in kinase signaling. This highly conserved gene is present in eukaryotic plants, fungi, trong>andtrong> animals. The ortholog of this gene was first identified in plants as a key regulator of anthocyanin trong>btrong>iosynthesis trong>andtrong> flower pigmentation. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2014]

DCAF6 Gene

DDtrong>Btrong>1 trong>andtrong> CUL4 associated factor 6

The protein encoded trong>btrong>y this gene is a ligtrong>andtrong>-dependent coactivator of nuclear receptors, including nuclear receptor sutrong>btrong>family 3 group C memtrong>btrong>er 1 (NR3C1), glucocorticoid receptor (GR), trong>andtrong> trong>andtrong>rogen receptor (AR). The encoded protein trong>andtrong> DNA damage trong>btrong>inding protein 2 (DDtrong>Btrong>2) may act as tumor promoters trong>andtrong> tumor suppressors, respectively, trong>btrong>y regulating the level of trong>andtrong>rogen receptor in prostate tissues. In addition, this protein can act with glucocorticoid receptor to promote human papillomavirus gene expression. [provided trong>btrong>y RefSeq, Mar 2017]

DCAF5 Gene

DDtrong>Btrong>1 trong>andtrong> CUL4 associated factor 5

Predicted to trong>btrong>e involved in negative regulation of fatty acid trong>btrong>iosynthetic process. Part of Cul4-RING E3 utrong>btrong>iquitin ligase complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

DCAF4 Gene

DDtrong>Btrong>1 trong>andtrong> CUL4 associated factor 4

This gene encodes a WD repeat-containing protein that interacts with the Cul4-Ddtrong>btrong>1 E3 ligase macromolecular complex. Multiple alternatively spliced transcript variants have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jul 2009]

DCAF8 Gene

DDtrong>Btrong>1 trong>andtrong> CUL4 associated factor 8

This gene encodes a WD repeat-containing protein that interacts with the Cul4-Ddtrong>btrong>1 E3 ligase macromolecular complex. Multiple alternatively spliced transcript variants have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jul 2009]

Rtrong>Btrong>CK1 Gene

Rantrong>Btrong>P-type trong>andtrong> C3HC4-type zinc finger containing 1

Enatrong>btrong>les several functions, including protein sequestering activity; transcription coactivator activity; trong>andtrong> utrong>btrong>iquitin trong>btrong>inding activity. Involved in several processes, including positive regulation of canonical NF-kappatrong>Btrong> signal transduction; protein linear polyutrong>btrong>iquitination; trong>andtrong> regulation of DNA-trong>btrong>inding transcription factor activity. Part of LUtrong>Btrong>AC complex. Implicated in glycogen storage disease. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC101930027 Gene

FERM trong>andtrong> PDZ domain-containing protein 2-like

PAXtrong>Btrong>P1 Gene

PAX3 trong>andtrong> PAX7 trong>btrong>inding protein 1

Predicted to enatrong>btrong>le DNA trong>btrong>inding activity trong>andtrong> histone methyltransferase trong>btrong>inding activity. Predicted to trong>btrong>e involved in positive regulation of transcription trong>btrong>y RNA polymerase II. Predicted to act upstream of or within positive regulation of myotrong>btrong>last proliferation trong>andtrong> regulation of skeletal muscle satellite cell proliferation. Located in cytosol. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

trong>Btrong>RWD3 Gene

trong>btrong>romodomain trong>andtrong> WD repeat domain containing 3

The protein encoded trong>btrong>y this gene contains a trong>btrong>romodomain trong>andtrong> several WD repeats. It is thought to have a chromatin-modifying function, trong>andtrong> may thus play a role in transcription. Mutations in this gene are associated with a spectrum of cognitive disatrong>btrong>ilities trong>andtrong> X-linked macrocephaly. This gene is also associated with translocations in patients with trong>Btrong>-cell chronic lymphocytic leukemia. [provided trong>btrong>y RefSeq, Jul 2017]

trong>Btrong>RWD1 Gene

trong>btrong>romodomain trong>andtrong> WD repeat domain containing 1

This gene encodes a memtrong>btrong>er of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically trong>btrong>racketed trong>btrong>y gly-his trong>andtrong> trp-asp (GH-WD) residues which may facilitate formation of heterotrimeric or multiprotein complexes. Memtrong>btrong>ers of this family are involved in a variety of cellular processes including cell cycle progression, signal transduction, apoptosis, trong>andtrong> gene regulation. This protein contains 2 trong>btrong>romodomains trong>andtrong> multiple WD repeats. This gene is located within the Down syndrome region-2 on chromosome 21. Alternative splicing of this gene generates multiple transcript variants encoding distinct isoforms. In mouse, this gene encodes a nuclear protein that has a polyglutamine-containing region that functions as a transcriptional activation domain which may regulate chromatin remodelling trong>andtrong> associates with a component of the SWI/SNF chromatin remodelling complex.[provided trong>btrong>y RefSeq, Jun 2011]

ZSCAN18 Gene

zinc finger trong>andtrong> SCAN domain containing 18

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ZSCAN10 Gene

zinc finger trong>andtrong> SCAN domain containing 10

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in negative regulation of DNA-templated transcription trong>andtrong> regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleoplasm. Predicted to trong>btrong>e active in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ZSCAN12 Gene

zinc finger trong>andtrong> SCAN domain containing 12

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ZSCAN16 Gene

zinc finger trong>andtrong> SCAN domain containing 16

Enatrong>btrong>les sequence-specific doutrong>btrong>le-strtrong>andtrong>ed DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

JAKMIP3 Gene

Janus kinase trong>andtrong> microtutrong>btrong>ule interacting protein 3

Predicted to enatrong>btrong>le kinase trong>btrong>inding activity trong>andtrong> microtutrong>btrong>ule trong>btrong>inding activity. Predicted to trong>btrong>e located in Golgi apparatus trong>andtrong> memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

JAKMIP2 Gene

janus kinase trong>andtrong> microtutrong>btrong>ule interacting protein 2

The protein encoded trong>btrong>y this gene is reported to trong>btrong>e a component of the Golgi matrix. It may act as a golgin protein trong>btrong>y negatively regulating transit of secretory cargo trong>andtrong> trong>btrong>y acting as a structural scaffold of the Golgi. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Aug 2012]

JAKMIP1 Gene

janus kinase trong>andtrong> microtutrong>btrong>ule interacting protein 1

Enatrong>btrong>les GAtrong>Btrong>A receptor trong>btrong>inding activity trong>andtrong> RNA trong>btrong>inding activity. Involved in cognition. Located in memtrong>btrong>rane. Part of ritrong>btrong>onucleoprotein complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LRRIQ3 Gene

leucine-rich repeats trong>andtrong> IQ motif containing 3

CCAR1 Gene

cell division cycle trong>andtrong> apoptosis regulator 1

Enatrong>btrong>les RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity; nuclear receptor coactivator activity; trong>andtrong> transcription corepressor activity. Involved in positive regulation of cell migration trong>andtrong> positive regulation of cell population proliferation. Acts upstream of or within positive regulation of apoptotic process. Located in nuclear envelope lumen. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CCAR2 Gene

cell cycle trong>andtrong> apoptosis regulator 2

Enatrong>btrong>les RNA polymerase II complex trong>btrong>inding activity trong>andtrong> enzyme inhitrong>btrong>itor activity. Involved in several processes, including mitochondrial fragmentation involved in apoptotic process; regulation of primary metatrong>btrong>olic process; trong>andtrong> regulation of signal transduction. Located in several cellular components, including mitochondrial matrix; nucleoplasm; trong>andtrong> spindle. Part of Dtrong>Btrong>IRD complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>8A Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 8A

Enatrong>btrong>les several functions, including DNA-trong>btrong>inding transcription repressor activity, RNA polymerase II-specific; RNA polymerase II-specific DNA-trong>btrong>inding transcription factor trong>btrong>inding activity; trong>andtrong> transcription coactivator trong>btrong>inding activity. Involved in negative regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>8trong>Btrong> Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 8trong>Btrong>

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in chromatin. Predicted to trong>btrong>e active in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

AMMEC Gene

Alport syndrome, mental retardation, midface hypoplasia, trong>andtrong> elliptocytosis

RCtrong>Btrong>Ttrong>Btrong>2P1 Gene

regulator of chromosome condensation (RCC1) trong>andtrong> trong>Btrong>Ttrong>Btrong> (POZ) domain containing protein 2 pseudogene 1

CPSF4L Gene

cleavage trong>andtrong> polyadenylation specific factor 4-like

Predicted to enatrong>btrong>le RNA trong>btrong>inding activity trong>andtrong> metal ion trong>btrong>inding activity. Predicted to trong>btrong>e involved in mRNA 3'-end processing. Predicted to trong>btrong>e located in nucleus. Predicted to trong>btrong>e part of mRNA cleavage trong>andtrong> polyadenylation specificity factor complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

trong>Btrong>HMG1 Gene

trong>btrong>asic helix-loop-helix trong>andtrong> HMG trong>btrong>ox domain containing 1

Predicted to enatrong>btrong>le DNA trong>btrong>inding activity trong>andtrong> protein dimerization activity. Predicted to trong>btrong>e involved in several processes, including activation of meiosis; cellular response to retinoic acid; trong>andtrong> regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PKHD1L1 Gene

polycystic kidney trong>andtrong> hepatic disease 1 (autosomal recessive)-like 1

Predicted to enatrong>btrong>le signaling receptor activity. Predicted to trong>btrong>e involved in immune response. Predicted to act upstream of or within sensory perception of sound. Predicted to trong>btrong>e located in cytosol; extracellular space; trong>andtrong> memtrong>btrong>rane. Implicated in autosomal recessive nonsyndromic deafness. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

AStrong>Btrong>9P1 Gene

ankyrin repeat trong>andtrong> SOCS trong>btrong>ox containing 9 pseudogene 1

UHRF1 Gene

utrong>btrong>iquitin-like with PHD trong>andtrong> ring finger domains 1

This gene encodes a memtrong>btrong>er of a sutrong>btrong>family of RING-finger type E3 utrong>btrong>iquitin ligases. The protein trong>btrong>inds to specific DNA sequences, trong>andtrong> recruits a histone deacetylase to regulate gene expression. Its expression peaks at late G1 phase trong>andtrong> continues during G2 trong>andtrong> M phases of the cell cycle. It plays a major role in the G1/S transition trong>btrong>y regulating topoisomerase IIalpha trong>andtrong> retinotrong>btrong>lastoma gene expression, trong>andtrong> functions in the p53-dependent DNA damage checkpoint. It is regarded as a hutrong>btrong> protein for the integration of epigenetic information. This gene is up-regulated in various cancers, trong>andtrong> it is therefore considered to trong>btrong>e a therapeutic target. Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. A related pseudogene exists on chromosome 12. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2014]

UHRF2 Gene

utrong>btrong>iquitin-like with PHD trong>andtrong> ring finger domains 2, E3 utrong>btrong>iquitin protein ligase

This gene encodes a nuclear protein which is involved in cell-cycle regulation. The encoded protein is a utrong>btrong>iquitin-ligase capatrong>btrong>le of utrong>btrong>iquinating PCNP (PEST-containing nuclear protein), trong>andtrong> together they may play a role in tumorigenesis. The encoded protein contains an NIRF_N domain, a PHD finger, a set- trong>andtrong> ring-associated (SRA) domain, trong>andtrong> a RING finger domain trong>andtrong> several of these domains have trong>btrong>een shown to trong>btrong>e essential for the regulation of cell proliferation. This protein may also have a role in intranuclear degradation of polyglutamine aggregates. Alternative splicing results in multiple transcript variants some of which are non-protein coding. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2012]

DSCC1 Gene

DNA replication trong>andtrong> sister chromatid cohesion 1

CHTF18 (MIM 613201), CHTF8 (MIM 613202), trong>andtrong> DSCC1 are components of an alternative replication factor C (RFC) (see MIM 600404) complex that loads PCNA (MIM 176740) onto DNA during S phase of the cell cycle (Merkle et al., 2003 [Putrong>btrong>Med 12766176]; trong>Btrong>ermudez et al., 2003 [Putrong>btrong>Med 12930902]).[supplied trong>btrong>y OMIM, Dec 2009]

LOC100130171 Gene

hematological trong>andtrong> neurological expressed 1 pseudogene

FHL2 Gene

four trong>andtrong> a half LIM domains 2

This gene encodes a memtrong>btrong>er of the four-trong>andtrong>-a-half-LIM-only protein family. Family memtrong>btrong>ers contain two highly conserved, ttrong>andtrong>emly arranged, zinc finger domains with four highly conserved cysteines trong>btrong>inding a zinc atom in each zinc finger. This protein is thought to have a role in the assemtrong>btrong>ly of extracellular memtrong>btrong>ranes. Also, this gene is down-regulated during transformation of normal myotrong>btrong>lasts to rhatrong>btrong>domyosarcoma cells trong>andtrong> the encoded protein may function as a link trong>btrong>etween presenilin-2 trong>andtrong> an intracellular signaling pathway. Multiple alternatively spliced variants encoding different isoforms have trong>btrong>een identified. [provided trong>btrong>y RefSeq, Jan 2016]

FHL3 Gene

four trong>andtrong> a half LIM domains 3

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of a family of proteins containing a four-trong>andtrong>-a-half LIM domain, which is a highly conserved doutrong>btrong>le zinc finger motif. The encoded protein has trong>btrong>een shown to interact with the cancer developmental regulators SMAD2, SMAD3, trong>andtrong> SMAD4, the skeletal muscle myogenesis protein MyoD, trong>andtrong> the high-affinity IgE trong>btrong>eta chain regulator MZF-1. This protein may trong>btrong>e involved in tumor suppression, repression of MyoD expression, trong>andtrong> repression of IgE receptor expression. Two transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Aug 2011]

FHL1 Gene

four trong>andtrong> a half LIM domains 1

This gene encodes a memtrong>btrong>er of the four-trong>andtrong>-a-half-LIM-only protein family. Family memtrong>btrong>ers contain two highly conserved, ttrong>andtrong>emly arranged, zinc finger domains with four highly conserved cysteines trong>btrong>inding a zinc atom in each zinc finger. Expression of these family memtrong>btrong>ers occurs in a cell- trong>andtrong> tissue-specific mode trong>andtrong> these proteins are involved in many cellular processes. Mutations in this gene have trong>btrong>een found in patients with Emery-Dreifuss muscular dystrophy. Multiple alternately spliced transcript variants which encode different protein isoforms have trong>btrong>een descritrong>btrong>ed.[provided trong>btrong>y RefSeq, Nov 2009]

FATE1 Gene

fetal trong>andtrong> adult testis expressed 1

This gene encodes a cancer-testis antigen that is highly expressed in hepatocellular carcinomas trong>andtrong> other tumors trong>andtrong> weakly expressed in normal tissues except testis. The protein is strongly expressed in spermatogonia, primary spermatocytes, trong>andtrong> Sertoli cells in seminiferous tutrong>btrong>ules. This protein may have a role in the control of early testicular differentiation trong>andtrong> cell proliferation. [provided trong>btrong>y RefSeq, Jan 2010]

ZNRF4 Gene

zinc trong>andtrong> ring finger 4

Enatrong>btrong>les utrong>btrong>iquitin protein ligase activity. Involved in negative regulation of nucleotide-trong>btrong>inding activity oligomerization domain containing 2 signaling pathway trong>andtrong> proteasome-mediated utrong>btrong>iquitin-dependent protein catatrong>btrong>olic process. Is active in endoplasmic reticulum memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ZNRF1 Gene

zinc trong>andtrong> ring finger 1, E3 utrong>btrong>iquitin protein ligase

This gene encodes an E3 utrong>btrong>iquitin-protein ligase that plays a role in neural-cell differentiation. Overexpression of this gene causes neurite-like elongation. The encoded protein contains trong>btrong>oth a zinc finger trong>andtrong> a RING finger motif trong>andtrong> is localized in the endosome/lysosome compartment, indicating that it may trong>btrong>e involved in utrong>btrong>iquitin-mediated protein modification, trong>andtrong> in synaptic vessicle memtrong>btrong>ranes in neurons. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2012]

ZNRF3 Gene

zinc trong>andtrong> ring finger 3

Enatrong>btrong>les frizzled trong>btrong>inding activity trong>andtrong> utrong>btrong>iquitin-protein transferase activity. Involved in negative regulation of Wnt signaling pathway; protein utrong>btrong>iquitination; trong>andtrong> utrong>btrong>iquitin-dependent protein catatrong>btrong>olic process. Located in plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ZNRF2 Gene

zinc trong>andtrong> ring finger 2, E3 utrong>btrong>iquitin protein ligase

Enatrong>btrong>les utrong>btrong>iquitin protein ligase activity. Involved in positive regulation of autophagosome-lysosome fusion. Located in cytoplasmic vesicle memtrong>btrong>rane; nuclear lumen; trong>andtrong> plasma memtrong>btrong>rane. Part of protein-containing complex. Is active in intracellular memtrong>btrong>rane-trong>btrong>ounded organelle. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC100421674 Gene

kelch repeat trong>andtrong> trong>Btrong>Ttrong>Btrong> (POZ) domain containing 2 pseudogene

TCEANC Gene

transcription elongation factor A (SII) N-terminal trong>andtrong> central domain containing

Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e active in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC105370944 Gene

inositol hexakisphosphate trong>andtrong> diphosphoinositol-pentakisphosphate kinase 1-like

LOC100129391 Gene

zinc finger (CCCH type), RNA-trong>btrong>inding motif trong>andtrong> serine/arginine rich 2 pseudogene

CDT1 Gene

chromatin licensing trong>andtrong> DNA replication factor 1

The protein encoded trong>btrong>y this gene is involved in the formation of the pre-replication complex that is necessary for DNA replication. The encoded protein can trong>btrong>ind geminin, which prevents replication trong>andtrong> may function to prevent this protein from initiating replication at inappropriate origins. Phosphorylation of this protein trong>btrong>y cyclin A-dependent kinases results in degradation of the protein. [provided trong>btrong>y RefSeq, Mar 2011]

PTENP1 Gene

phosphatase trong>andtrong> tensin homolog pseudogene 1 (functional)

PTENP1 represents a highly homologous processed pseudogene of PTEN (phosphatase trong>andtrong> tensin homolog), a protein that encodes a tumor suppressor that functions trong>btrong>y negatively regulating the AKT/PKtrong>Btrong> signaling pathway. PTENP1 is found on chromosome 9 trong>andtrong> regulates PTEN trong>btrong>y trong>btrong>oth sense trong>andtrong> antisense RNAs (Gene ID: 101243555). This long-noncoding RNA (lncRNA) acts as a decoy for PTEN targeting microRNAs trong>andtrong> also exerts a tumor suppressive activity. [provided trong>btrong>y RefSeq, Jun 2020]

LRTM2 Gene

leucine-rich repeats trong>andtrong> transmemtrong>btrong>rane domains 2

Predicted to enatrong>btrong>le Roundatrong>btrong>out trong>btrong>inding activity trong>andtrong> heparin trong>btrong>inding activity. Predicted to trong>btrong>e involved in axon guidance trong>andtrong> negative chemotaxis. Predicted to act upstream of or within positive regulation of synapse assemtrong>btrong>ly. Predicted to trong>btrong>e located in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC727896 Gene

cysteine trong>andtrong> histidine-rich domain (CHORD) containing 1 pseudogene

RSPRY1 Gene

ring finger trong>andtrong> SPRY domain containing 1

This gene encodes a glycoprotein that contains a RING-type zinc finger domain trong>andtrong> an SPRY domain of unknown function. Alternative splicing of this gene results in multiple transcript variants. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2015]

ANKAR Gene

ankyrin trong>andtrong> armadillo repeat containing

Predicted to trong>btrong>e located in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC100422426 Gene

CASP2 trong>andtrong> RIPK1 domain containing adaptor with death domain pseudogene

GTSE1 Gene

G-2 trong>andtrong> S-phase expressed 1

The protein encoded trong>btrong>y this gene is only expressed in the S trong>andtrong> G2 phases of the cell cycle, where it colocalizes with cytoplasmic tutrong>btrong>ulin trong>andtrong> microtutrong>btrong>ules. In response to DNA damage, the encoded protein accumulates in the nucleus trong>andtrong> trong>btrong>inds the tumor suppressor protein p53, shuttling it out of the nucleus trong>andtrong> repressing its atrong>btrong>ility to induce apoptosis. [provided trong>btrong>y RefSeq, Jul 2008]

FYCO1 Gene

FYVE trong>andtrong> coiled-coil domain containing 1

The gene encodes a Ratrong>btrong>7 adapter protein that is implicated in the microtutrong>btrong>ule transport of autophagosomes. The encoded protein contains a RUN domain, a FYVE-type zinc finger domain, trong>andtrong> Golgi dynamics (GOLD) domain. The encoded protein plays a role in microtutrong>btrong>ule plus end-directed transport of autophagic vesicles through interactions with the small GTPase Ratrong>btrong>7, phosphatidylinositol-3-phosphate (PI3P), the autophagosome marker LC3, trong>andtrong> the kinesin KIF5. Mutations in this gene are associated with inclusion trong>btrong>ody myositis (Itrong>Btrong>M) trong>andtrong> autosomal recessive congenital cataracts (CATC2). [provided trong>btrong>y RefSeq, Aug 2020]

HERC2P1 Gene

hect domain trong>andtrong> RLD 2 pseudogene 1

HERC2P3 Gene

hect domain trong>andtrong> RLD 2 pseudogene 3

Predicted to enatrong>btrong>le utrong>btrong>iquitin protein ligase activity. Predicted to trong>btrong>e involved in protein utrong>btrong>iquitination. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

HERC2P2 Gene

hect domain trong>andtrong> RLD 2 pseudogene 2

HERC2P5 Gene

hect domain trong>andtrong> RLD 2 pseudogene 5

HERC2P4 Gene

hect domain trong>andtrong> RLD 2 pseudogene 4

HERC2P7 Gene

hect domain trong>andtrong> RLD 2 pseudogene 7

HERC2P6 Gene

hect domain trong>andtrong> RLD 2 pseudogene 6

HERC2P9 Gene

hect domain trong>andtrong> RLD 2 pseudogene 9

HERC2P8 Gene

hect domain trong>andtrong> RLD 2 pseudogene 8

CHFR Gene

checkpoint with forkhead trong>andtrong> ring finger domains, E3 utrong>btrong>iquitin protein ligase

This gene encodes an E3 utrong>btrong>iquitin-protein ligase required for the maintenance of the antephase checkpoint that regulates cell cycle entry into mitosis trong>andtrong>, therefore, may play a key role in cell cycle progression trong>andtrong> tumorigenesis. The encoded protein has an N-terminal forkhead-associated domain, a central RING-finger domain, trong>andtrong> a cysteine-rich C-terminal region. Alternatively spliced transcript variants that encode different protein isoforms have trong>btrong>een descritrong>btrong>ed. [provided trong>btrong>y RefSeq, Mar 2014]

MECOM Gene

MDS1 trong>andtrong> EVI1 complex locus

The protein encoded trong>btrong>y this gene is a transcriptional regulator trong>andtrong> oncoprotein that may trong>btrong>e involved in hematopoiesis, apoptosis, development, trong>andtrong> cell differentiation trong>andtrong> proliferation. The encoded protein can interact with CTtrong>Btrong>P1, SMAD3, CREtrong>Btrong>trong>Btrong>P, KAT2trong>Btrong>, MAPK8, trong>andtrong> MAPK9. This gene can undergo translocation with the AML1 gene, resulting in overexpression of this gene trong>andtrong> the onset of leukemia. Several transcript variants encoding a few different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Mar 2011]

ZKSCAN7P1 Gene

zinc finger with KRAtrong>Btrong> trong>andtrong> SCAN domains 7 pseudogene 1

ZSCAN9 Gene

zinc finger trong>andtrong> SCAN domain containing 9

Enatrong>btrong>les sequence-specific doutrong>btrong>le-strtrong>andtrong>ed DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ZSCAN4 Gene

zinc finger trong>andtrong> SCAN domain containing 4

The ZSCAN4 gene encodes a protein involved in telomere maintenance trong>andtrong> with a key role in the critical feature of mouse emtrong>btrong>ryonic stem (ES) cells, namely, defying cellular senescence trong>andtrong> maintaining normal karyotype for many cell divisions in culture (Zalzman et al., 2010 [Putrong>btrong>Med 20336070]).[supplied trong>btrong>y OMIM, May 2010]

ZSCAN1 Gene

zinc finger trong>andtrong> SCAN domain containing 1

Enatrong>btrong>les sequence-specific doutrong>btrong>le-strtrong>andtrong>ed DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in chromatin. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ZSCAN2 Gene

zinc finger trong>andtrong> SCAN domain containing 2

The protein encoded trong>btrong>y this gene contains several copies of zinc finger motif, which is commonly found in transcriptional regulatory proteins. Studies in mice show that this gene is expressed during emtrong>btrong>ryonic development, trong>andtrong> specifically in the testis in adult mice, suggesting that it may play a role in regulating genes in germ cells. Alternative splicing of this gene results in several transcript variants encoding different isoforms. [provided trong>btrong>y RefSeq, Jul 2008]

PSD Gene

pleckstrin trong>andtrong> Sec7 domain containing

This gene encodes a Plekstrin homology trong>andtrong> SEC7 domains-containing protein that functions as a guanine nucleotide exchange factor. The encoded protein regulates signal transduction trong>btrong>y activating ADP-ritrong>btrong>osylation factor 6. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Aug 2012]

SAMM50P1 Gene

SAMM50 sorting trong>andtrong> assemtrong>btrong>ly machinery component pseudogene 1

CFAP36 Gene

cilia trong>andtrong> flagella associated protein 36

Located in ciliary transition zone. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ASAP1 Gene

ArfGAP with SH3 domain, ankyrin repeat trong>andtrong> PH domain 1

This gene encodes an ADP-ritrong>btrong>osylation factor (ARF) GTPase-activating protein. The GTPase-activating activity is stimulated trong>btrong>y phosphatidylinositol 4,5-trong>btrong>iphosphate (PIP2), trong>andtrong> is greater towards ARF1 trong>andtrong> ARF5, trong>andtrong> lesser for ARF6. This gene maytrong>btrong>e involved in regulation of memtrong>btrong>rane trafficking trong>andtrong> cytoskeleton remodeling. Alternatively spliced transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Oct 2011]

ASAP2 Gene

ArfGAP with SH3 domain, ankyrin repeat trong>andtrong> PH domain 2

This gene encodes a multidomain protein containing an N-terminal alpha-helical region with a coiled-coil motif, followed trong>btrong>y a pleckstrin homology (PH) domain, an Arf-GAP domain, an ankyrin homology region, a proline-rich region, trong>andtrong> a C-terminal Src homology 3 (SH3) domain. The protein localizes in the Golgi apparatus trong>andtrong> at the plasma memtrong>btrong>rane, where it colocalizes with protein tyrosine kinase 2-trong>btrong>eta (PYK2). The encoded protein forms a statrong>btrong>le complex with PYK2 in vivo. This interaction appears to trong>btrong>e mediated trong>btrong>y trong>btrong>inding of its SH3 domain to the C-terminal proline-rich domain of PYK2. The encoded protein is tyrosine phosphorylated trong>btrong>y activated PYK2. It has catalytic activity for class I trong>andtrong> II ArfGAPs in vitro, trong>andtrong> can trong>btrong>ind the class III Arf ARF6 without immediate GAP activity. The encoded protein is trong>btrong>elieved to function as an ARF GAP that controls ARF-mediated vesicle trong>btrong>udding when recruited to Golgi memtrong>btrong>ranes. In addition, it functions as a sutrong>btrong>strate trong>andtrong> downstream target for PYK2 trong>andtrong> SRC, a pathway that may trong>btrong>e involved in the regulation of vesicular transport. Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Sep 2008]

ASAP3 Gene

ArfGAP with SH3 domain, ankyrin repeat trong>andtrong> PH domain 3

This gene encodes a memtrong>btrong>er of a sutrong>btrong>family of ADP-ritrong>btrong>osylation factor(Arf) GTPase-activating proteins that contain additional ankyrin repeat trong>andtrong> pleckstrin homology domains. The Arf GAP domain of this protein catalyzes the hydrolysis of GTP trong>btrong>ound to Arf proteins. The encoded protein promotes cell differentiation trong>andtrong> migration trong>andtrong> has trong>btrong>een implicated in cancer cell invasion. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Jan 2009]

ANKLE1 Gene

ankyrin repeat trong>andtrong> LEM domain containing 1

Enatrong>btrong>les endonuclease activity. Involved in DNA damage response trong>andtrong> protein export from nucleus. Located in cytosol trong>andtrong> nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ANKLE2 Gene

ankyrin repeat trong>andtrong> LEM domain containing 2

This gene encodes a memtrong>btrong>er of the LEM family of inner nuclear memtrong>btrong>rane proteins. The encoded protein functions as a mitotic regulator through postmitotic formation of the nuclear envelope. Mutations in this gene cause morphology defects in the nuclear envelope trong>andtrong> trong>Btrong>AF hyperphosphorylation. [provided trong>btrong>y RefSeq, Mar 2014]

SPG7 Gene

spastic paraplegia 7 (pure trong>andtrong> complicated autosomal recessive)

This gene encodes a mitochondrial metalloprotease protein that is a memtrong>btrong>er of the AAA family. Memtrong>btrong>ers of this protein family share an ATPase domain trong>andtrong> have roles in diverse cellular processes including memtrong>btrong>rane trafficking, intracellular motility, organelle trong>btrong>iogenesis, protein folding, trong>andtrong> proteolysis. Mutations in this gene cause autosomal recessive spastic paraplegia 7. Two transcript variants encoding distinct isoforms have trong>btrong>een identified. [provided trong>btrong>y RefSeq, Mar 2014]

VWDE Gene

von Willetrong>btrong>rtrong>andtrong> factor D trong>andtrong> EGF domains

Predicted to enatrong>btrong>le signaling receptor trong>btrong>inding activity. Predicted to trong>btrong>e active in cell surface trong>andtrong> extracellular region. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

RINL Gene

Ras trong>andtrong> Ratrong>btrong> interactor-like

Predicted to enatrong>btrong>le guanyl-nucleotide exchange factor activity trong>andtrong> small GTPase trong>btrong>inding activity. Predicted to trong>btrong>e involved in endocytosis. Predicted to trong>btrong>e located in ruffle. Predicted to trong>btrong>e active in cytosol trong>andtrong> endocytic vesicle. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

DEL11P13 Gene

Wilms tumor, aniridia, genitourinary anomalies trong>andtrong> mental retardation syndrome

STAT6 Gene

signal transducer trong>andtrong> activator of transcription 6, interleukin-4 induced

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of the STAT family of transcription factors. In response to cytokines trong>andtrong> growth factors, STAT family memtrong>btrong>ers are phosphorylated trong>btrong>y the receptor associated kinases, trong>andtrong> then form homo- or heterodimers that translocate to the cell nucleus where they act as transcription activators. This protein plays a central role in exerting IL4 mediated trong>btrong>iological responses. It is found to induce the expression of trong>Btrong>CL2L1/trong>Btrong>CL-X(L), which is responsitrong>btrong>le for the anti-apoptotic activity of IL4. Knockout studies in mice suggested the roles of this gene in differentiation of T helper 2 (Th2) cells, expression of cell surface markers, trong>andtrong> class switch of immunoglotrong>btrong>ulins. Alternative splicing results in multiple transcript variants.[provided trong>btrong>y RefSeq, May 2010]

TMCC1 Gene

transmemtrong>btrong>rane trong>andtrong> coiled-coil domain family 1

Enatrong>btrong>les identical protein trong>btrong>inding activity. Involved in several processes, including endosome fission; endosome memtrong>btrong>rane tutrong>btrong>ulation; trong>andtrong> memtrong>btrong>rane fission. Located in cytosol; endoplasmic reticulum-endosome memtrong>btrong>rane contact site; trong>andtrong> rough endoplasmic reticulum. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

TMCC2 Gene

transmemtrong>btrong>rane trong>andtrong> coiled-coil domain family 2

Involved in amyloid precursor protein metatrong>btrong>olic process. Located in endoplasmic reticulum. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

TMCC3 Gene

transmemtrong>btrong>rane trong>andtrong> coiled-coil domain family 3

Enatrong>btrong>les 14-3-3 protein trong>btrong>inding activity trong>andtrong> identical protein trong>btrong>inding activity. Located in endoplasmic reticulum. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SAMHD1 Gene

SAM domain trong>andtrong> HD domain 1

This gene may play a role in regulation of the innate immune response. The encoded protein is upregulated in response to viral infection trong>andtrong> may trong>btrong>e involved in mediation of tumor necrosis factor-alpha proinflammatory responses. Mutations in this gene have trong>btrong>een associated with Aicardi-Goutieres syndrome. [provided trong>btrong>y RefSeq, Mar 2010]

PYCARD Gene

PYD trong>andtrong> CARD domain containing

This gene encodes an adaptor protein that is composed of two protein-protein interaction domains: a N-terminal PYRIN-PAAD-DAPIN domain (PYD) trong>andtrong> a C-terminal caspase-recruitment domain (CARD). The PYD trong>andtrong> CARD domains are memtrong>btrong>ers of the six-helix trong>btrong>undle death domain-fold superfamily that mediates assemtrong>btrong>ly of large signaling complexes in the inflammatory trong>andtrong> apoptotic signaling pathways via the activation of caspase. In normal cells, this protein is localized to the cytoplasm; however, in cells undergoing apoptosis, it forms trong>btrong>all-like aggregates near the nuclear periphery. Two transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jul 2008]

EDIL3 Gene

EGF-like repeats trong>andtrong> discoidin I-like domains 3

The protein encoded trong>btrong>y this gene is an integrin ligtrong>andtrong>. It plays an important role in mediating angiogenesis trong>andtrong> may trong>btrong>e important in vessel wall remodeling trong>andtrong> development. It also influences endothelial cell trong>btrong>ehavior. [provided trong>btrong>y RefSeq, Jul 2008]

TIGIT Gene

T cell immunoreceptor with Ig trong>andtrong> ITIM domains

This gene encodes a memtrong>btrong>er of the PVR (poliovirus receptor) family of immunoglotrong>btrong>in proteins. The product of this gene is expressed on several classes of T cells including follicular trong>Btrong> helper T cells (TFH). The protein has trong>btrong>een shown to trong>btrong>ind PVR with high affinity; this trong>btrong>inding is thought to assist interactions trong>btrong>etween TFH trong>andtrong> dendritic cells to regulate T cell dependent trong>Btrong> cell responses.[provided trong>btrong>y RefSeq, Sep 2009]

AGAP7P Gene

ArfGAP with GTPase domain, ankyrin repeat trong>andtrong> PH domain 7, pseudogene

Predicted to enatrong>btrong>le GTPase activator activity trong>andtrong> GTPase activity. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC101059974 Gene

p53 trong>andtrong> DNA damage-regulated protein 1 pseudogene

CCSAP Gene

centriole, cilia trong>andtrong> spindle-associated protein

Enatrong>btrong>les microtutrong>btrong>ule trong>btrong>inding activity. Involved in mitotic spindle microtutrong>btrong>ule depolymerization trong>andtrong> regulation of mitotic spindle assemtrong>btrong>ly. Located in axon; ciliary transition zone; trong>andtrong> cytoskeleton. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

MCIDAS Gene

multiciliate differentiation trong>andtrong> DNA synthesis associated cell cycle protein

This gene encodes a memtrong>btrong>er of the geminin family of proteins. The encoded nuclear protein is required for the generation of multiciliated cells in respiratory epithelium. Mutations in this gene cause a rare mucociliary clearance disorder associated with recurring respiratory infections in human patients, known as reduced generation of multiple motile cilia (RGMC). [provided trong>btrong>y RefSeq, Sep 2016]

WDHD1 Gene

WD repeat trong>andtrong> HMG-trong>btrong>ox DNA trong>btrong>inding protein 1

The protein encoded trong>btrong>y this gene contains multiple N-terminal WD40 domains trong>andtrong> a C-terminal high motrong>btrong>ility group (HMG) trong>btrong>ox. WD40 domains are found in a variety of eukaryotic proteins trong>andtrong> may function as adaptor/regulatory modules in signal transduction, pre-mRNA processing trong>andtrong> cytoskeleton assemtrong>btrong>ly. HMG trong>btrong>oxes are found in many eukaryotic proteins involved in chromatin assemtrong>btrong>ly, transcription trong>andtrong> replication. Alternative splicing results in two transcript variants encoding different isoforms. [provided trong>btrong>y RefSeq, Jul 2008]

PYHIN1 Gene

pyrin trong>andtrong> HIN domain family, memtrong>btrong>er 1

The protein encoded trong>btrong>y this gene trong>btrong>elongs to the HIN-200 family of interferon-inducitrong>btrong>le proteins that share a 200-amino acid signature motif at their C-termini. HIN200 proteins are primarily nuclear trong>andtrong> are involved in transcriptional regulation of genes important for cell cycle control, differentiation, trong>andtrong> apoptosis. Downregulation of this gene is associated with trong>btrong>reast cancer. This protein acts as a tumor suppressor trong>btrong>y promoting utrong>btrong>iquitination trong>andtrong> sutrong>btrong>sequent degradation of MDM2, which leads to statrong>btrong>ilization of p53/TP53. Alternatively spliced transcript variants encoding different isoforms have trong>btrong>een descritrong>btrong>ed for this gene. [provided trong>btrong>y RefSeq, Aug 2011]

WFIKKN2 Gene

WAP, follistatin/kazal, immunoglotrong>btrong>ulin, kunitz trong>andtrong> netrin domain containing 2

The WFIKKN1 protein contains a WAP domain, follistatin domain, immunoglotrong>btrong>ulin domain, two ttrong>andtrong>em Kunitz domains, trong>andtrong> an NTR domain. This gene encodes a WFIKKN1-related protein which has the same domain organization as the WFIKKN1 protein. The WAP-type, follistatin type, Kunitz-type, trong>andtrong> NTR-type protease inhitrong>btrong>itory domains may control the action of multiple types of proteases. [provided trong>btrong>y RefSeq, Jul 2008]

WFIKKN1 Gene

WAP, follistatin/kazal, immunoglotrong>btrong>ulin, kunitz trong>andtrong> netrin domain containing 1

This gene encodes a secreted multidomain protein consisting of a signal peptide, a WAP domain, a follistatin domain, an immunoglotrong>btrong>ulin domain, two ttrong>andtrong>em Kunitz domains, trong>andtrong> an NTR domain. These domains have trong>btrong>een implicated frequently in inhitrong>btrong>ition of various types of proteases, suggesting that the encoded protein may trong>btrong>e a multivalent protease inhitrong>btrong>itor trong>andtrong> may control the action of multiple types of serine proteases as well as metalloproteinases. [provided trong>btrong>y RefSeq, Jul 2008]

DCAF12L2 Gene

DDtrong>Btrong>1 trong>andtrong> CUL4 associated factor 12-like 2

This gene encodes a memtrong>btrong>er of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically trong>btrong>racketed trong>btrong>y Gly-His trong>andtrong> Trp-Asp (GH-WD), which may facilitate formation of heterotrimeric or multi-protein complexes. Memtrong>btrong>ers of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, trong>andtrong> gene regulation. This gene appears to represent an intronless retrocopy of a related multi-exon gene located on chromosome 9. However, the CDS of this intronless gene remains intact, it is conserved in other mammalian species, it is known to trong>btrong>e transcritrong>btrong>ed, trong>andtrong> it is therefore thought to encode a functional protein. [provided trong>btrong>y RefSeq, May 2010]

DCAF12L1 Gene

DDtrong>Btrong>1 trong>andtrong> CUL4 associated factor 12-like 1

This gene encodes a memtrong>btrong>er of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically trong>btrong>racketed trong>btrong>y gly-his trong>andtrong> trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Memtrong>btrong>ers of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, trong>andtrong> gene regulation. [provided trong>btrong>y RefSeq, Jul 2008]

ZHX2 Gene

zinc fingers trong>andtrong> homeotrong>btrong>oxes 2

The memtrong>btrong>ers of the zinc fingers trong>andtrong> homeotrong>btrong>oxes gene family are nuclear homodimeric transcriptional repressors that interact with the A sutrong>btrong>unit of nuclear factor-Y (NF-YA) trong>andtrong> contain two C2H2-type zinc fingers trong>andtrong> five homeotrong>btrong>ox DNA-trong>btrong>inding domains. This gene encodes memtrong>btrong>er 2 of this gene family. In addition to forming homodimers, this protein heterodimerizes with memtrong>btrong>er 1 of the zinc fingers trong>andtrong> homeotrong>btrong>oxes family. [provided trong>btrong>y RefSeq, Jul 2008]

ZHX3 Gene

zinc fingers trong>andtrong> homeotrong>btrong>oxes 3

This gene encodes a memtrong>btrong>er of the zinc fingers trong>andtrong> homeotrong>btrong>oxes (ZHX) gene family. The encoded protein contains two C2H2-type zinc fingers trong>andtrong> five homeodomains trong>andtrong> forms a dimer with itself or with zinc fingers trong>andtrong> homeotrong>btrong>oxes family memtrong>btrong>er 1. In the nucleus, the dimerized protein interacts with the A sutrong>btrong>unit of the utrong>btrong>iquitous transcription factor nuclear factor-Y trong>andtrong> may function as a transcriptional repressor. [provided trong>btrong>y RefSeq, Jul 2008]

ZHX1 Gene

zinc fingers trong>andtrong> homeotrong>btrong>oxes 1

The memtrong>btrong>ers of the zinc fingers trong>andtrong> homeotrong>btrong>oxes gene family are nuclear homodimeric transcriptional repressors that interact with the A sutrong>btrong>unit of nuclear factor-Y (NF-YA) trong>andtrong> contain two C2H2-type zinc fingers trong>andtrong> five homeotrong>btrong>ox DNA-trong>btrong>inding domains. This gene encodes memtrong>btrong>er 1 of this gene family. In addition to forming homodimers, this protein heterodimerizes with memtrong>btrong>ers 2 trong>andtrong> 3 of the zinc fingers trong>andtrong> homeotrong>btrong>oxes family. Alternative splicing results in multiple transcript variants. Read-through transcription also exists trong>btrong>etween this gene trong>andtrong> the downstream chromosome 8 open reading frame 76 (C8orf76) gene. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2011]

APPL1 Gene

adaptor protein, phosphotyrosine interaction, PH domain trong>andtrong> leucine zipper containing 1

The protein encoded trong>btrong>y this gene has trong>btrong>een shown to trong>btrong>e involved in the regulation of cell proliferation, trong>andtrong> in the crosstalk trong>btrong>etween the adiponectin signalling trong>andtrong> insulin signalling pathways. The encoded protein trong>btrong>inds many other proteins, including RAtrong>Btrong>5A, DCC, AKT2, PIK3CA, adiponectin receptors, trong>andtrong> proteins of the NuRD/MeCP1 complex. This protein is found associated with endosomal memtrong>btrong>ranes, trong>btrong>ut can trong>btrong>e released trong>btrong>y EGF trong>andtrong> translocated to the nucleus. [provided trong>btrong>y RefSeq, Jul 2008]

APPL2 Gene

adaptor protein, phosphotyrosine interaction, PH domain trong>andtrong> leucine zipper containing 2

The protein encoded trong>btrong>y this gene is one of two effectors of the small GTPase RAtrong>Btrong>5A/Ratrong>btrong>5, which are involved in a signal transduction pathway. trong>Btrong>oth effectors contain an N-terminal trong>Btrong>in/Amphiphysin/Rvs (trong>Btrong>AR) domain, a central pleckstrin homology (PH) domain, trong>andtrong> a C-terminal phosphotyrosine trong>btrong>inding (PTtrong>Btrong>) domain, trong>andtrong> they trong>btrong>ind the Ratrong>btrong>5 through the trong>Btrong>AR domain. They are associated with endosomal memtrong>btrong>ranes trong>andtrong> can trong>btrong>e translocated to the nucleus in response to the EGF stimulus. They interact with the NuRD/MeCP1 complex (nucleosome remodeling trong>andtrong> deacetylase /methyl-CpG-trong>btrong>inding protein 1 complex) trong>andtrong> are required for efficient cell proliferation. A chromosomal atrong>btrong>erration t(12;22)(q24.1;q13.3) involving this gene trong>andtrong> the PSAP2 gene results in 22q13.3 deletion syndrome, also known as Phelan-McDermid syndrome. [provided trong>btrong>y RefSeq, Oct 2011]

LOC100421809 Gene

LON peptidase N-terminal domain trong>andtrong> ring finger 2 pseudogene

Ftrong>Btrong>XL3 Gene

F-trong>btrong>ox trong>andtrong> leucine-rich repeat protein 3

This gene encodes a memtrong>btrong>er of the F-trong>btrong>ox protein family which is characterized trong>btrong>y an approximately 40 amino acid motif, the F-trong>btrong>ox. The F-trong>btrong>ox proteins constitute one of the four sutrong>btrong>units of utrong>btrong>iquitin protein ligase complex called SCFs (SKP1-cullin-F-trong>btrong>ox), which function in phosphorylation-dependent utrong>btrong>iquitination. The F-trong>btrong>ox proteins are divided into 3 classes: Ftrong>btrong>ws containing WD-40 domains, Ftrong>btrong>ls containing leucine-rich repeats, trong>andtrong> Ftrong>btrong>xs containing either different protein-protein interaction modules or no recognizatrong>btrong>le motifs. The protein encoded trong>btrong>y this gene trong>btrong>elongs to the Ftrong>btrong>ls class trong>andtrong>, in addition to an F-trong>btrong>ox, contains several ttrong>andtrong>em leucine-rich repeats trong>andtrong> is localized in the nucleus. [provided trong>btrong>y RefSeq, Jul 2008]

Ftrong>Btrong>XL5 Gene

F-trong>btrong>ox trong>andtrong> leucine-rich repeat protein 5

This gene encodes a memtrong>btrong>er of the F-trong>btrong>ox protein family which is characterized trong>btrong>y an approximately 40 amino acid motif, the F-trong>btrong>ox. The F-trong>btrong>ox proteins constitute one of the four sutrong>btrong>units of utrong>btrong>iquitin protein ligase complex called SCFs (SKP1-cullin-F-trong>btrong>ox), which function in phosphorylation-dependent utrong>btrong>iquitination. The F-trong>btrong>ox proteins are divided into 3 classes: Ftrong>btrong>ws containing WD-40 domains, Ftrong>btrong>ls containing leucine-rich repeats, trong>andtrong> Ftrong>btrong>xs containing either different protein-protein interaction modules or no recognizatrong>btrong>le motifs. The protein encoded trong>btrong>y this gene trong>btrong>elongs to the Ftrong>btrong>ls class trong>andtrong>, in addition to an F-trong>btrong>ox, contains several ttrong>andtrong>em leucine-rich repeats. Alternatively spliced transcript variants have trong>btrong>een descritrong>btrong>ed for this locus. [provided trong>btrong>y RefSeq, Aug 2010]

LOC345571 Gene

RUN trong>andtrong> FYVE domain containing 3 pseudogene

CLP1 Gene

cleavage trong>andtrong> polyadenylation factor I sutrong>btrong>unit 1

This gene encodes a memtrong>btrong>er of the Clp1 family. The encoded protein is a multifunctional kinase which is a component of the tRNA splicing endonuclease complex trong>andtrong> a component of the pre-mRNA cleavage complex II. This protein is implicated in tRNA, mRNA, trong>andtrong> siRNA maturation. Mutations in this gene are associated with pontoceretrong>btrong>ellar hypoplasia type 10 (PCH10). Alternatively splice transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Sep 2014]

PKLR Gene

pyruvate kinase, liver trong>andtrong> Rtrong>Btrong>C

The protein encoded trong>btrong>y this gene is a pyruvate kinase that catalyzes the transphosphorylation of phohsphoenolpyruvate into pyruvate trong>andtrong> ATP, which is the rate-limiting step of glycolysis. Defects in this enzyme, due to gene mutations or genetic variations, are the common cause of chronic hereditary nonspherocytic hemolytic anemia (CNSHA or HNSHA). Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jul 2008]

LOC105369175 Gene

cilia- trong>andtrong> flagella-associated protein 54-like

CHRFAM7A Gene

CHRNA7 (cholinergic receptor, nicotinic, alpha 7, exons 5-10) trong>andtrong> FAM7A (family with sequence similarity 7A, exons A-E) fusion

The nicotinic acetylcholine receptors (nAChRs) are memtrong>btrong>ers of a superfamily of ligtrong>andtrong>-gated ion channels that mediate fast signal transmission at synapses. The family memtrong>btrong>er CHRNA7, which is located on chromosome 15 in a region associated with several neuropsychiatric disorders, is partially duplicated trong>andtrong> forms a hytrong>btrong>rid with a novel gene from the family with sequence similarity 7 (FAM7A). Alternative splicing has trong>btrong>een otrong>btrong>served, trong>andtrong> two variants exist, for this hytrong>btrong>rid gene. The N-terminally truncated products predicted trong>btrong>y the largest open reading frames for each variant would lack the majority of the neurotransmitter-gated ion-channel ligtrong>andtrong> trong>btrong>inding domain trong>btrong>ut retain the transmemtrong>btrong>rane region that forms the ion channel. Although current evidence supports transcription of this hytrong>btrong>rid gene, translation of the nicotinic acetylcholine receptor-like protein-encoding open reading frames has not trong>btrong>een confirmed. [provided trong>btrong>y RefSeq, Jul 2008]

LOC100420693 Gene

solute carrier family 47 (multidrug trong>andtrong> toxin extrusion), memtrong>btrong>er 2 pseudogene

SMYD4 Gene

SET trong>andtrong> MYND domain containing 4

Predicted to enatrong>btrong>le histone deacetylase trong>btrong>inding activity. Involved in heart development. Predicted to trong>btrong>e active in cytoplasm trong>andtrong> nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SMYD1 Gene

SET trong>andtrong> MYND domain containing 1

Predicted to enatrong>btrong>le several functions, including histone H3K4 trimethyltransferase activity; metal ion trong>btrong>inding activity; trong>andtrong> transcription corepressor activity. Involved in positive regulation of myotrong>btrong>last differentiation trong>andtrong> positive regulation of myotutrong>btrong>e differentiation. Predicted to trong>btrong>e located in cytoplasm. Predicted to trong>btrong>e active in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SMYD2 Gene

SET trong>andtrong> MYND domain containing 2

SET domain-containing proteins, such as SMYD2, catalyze lysine methylation (trong>Btrong>rown et al., 2006 [Putrong>btrong>Med 16805913]).[supplied trong>btrong>y OMIM, Nov 2008]

SMYD3 Gene

SET trong>andtrong> MYND domain containing 3

This gene encodes a histone methyltransferase which functions in RNA polymerase II complexes trong>btrong>y an interaction with a specific RNA helicase. Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Dec 2011]

SETMAR Gene

SET domain trong>andtrong> mariner transposase fusion gene

This gene encodes a fusion protein that contains an N-terminal histone-lysine N-methyltransferase domain trong>andtrong> a C-terminal mariner transposase domain. The encoded protein trong>btrong>inds DNA trong>andtrong> functions in DNA repair activities including non-homologous end joining trong>andtrong> doutrong>btrong>le strtrong>andtrong> trong>btrong>reak repair. The SET domain portion of this protein specifically methylates histone H3 lysines 4 trong>andtrong> 36. This gene exists as a fusion gene only in anthropoid primates, other organisms lack mariner transposase domain. Alternate splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Jan 2013]

ZKSCAN1 Gene

zinc finger with KRAtrong>Btrong> trong>andtrong> SCAN domains 1

This gene encodes a memtrong>btrong>er of the Kruppel C2H2-type zinc-finger family of proteins. This encoded protein may function as a transcription factor that regulates the expression of GAtrong>Btrong>A type-A receptors in the trong>btrong>rain. Transcripts from this gene have trong>btrong>een shown to form statrong>btrong>le trong>andtrong> atrong>btrong>undant circular RNAs. Elevated expression of this gene has trong>btrong>een otrong>btrong>served in gastric cancer trong>andtrong> the encoded protein may stimulate migration trong>andtrong> invasion of human gastric cancer cells. [provided trong>btrong>y RefSeq, Oct 2016]

ZKSCAN3 Gene

zinc finger with KRAtrong>Btrong> trong>andtrong> SCAN domains 3

Enatrong>btrong>les DNA-trong>btrong>inding transcription repressor activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity; trong>andtrong> chromatin trong>btrong>inding activity. Involved in lysosome organization; negative regulation of metatrong>btrong>olic process; trong>andtrong> regulation of DNA-templated transcription. Located in cytoplasm trong>andtrong> nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ZKSCAN2 Gene

zinc finger with KRAtrong>Btrong> trong>andtrong> SCAN domains 2

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ZKSCAN5 Gene

zinc finger with KRAtrong>Btrong> trong>andtrong> SCAN domains 5

This gene encodes a zinc finger protein of the Kruppel family. The protein contains a SCAN trong>btrong>ox trong>andtrong> a KRAtrong>Btrong> A domain trong>andtrong> may trong>btrong>e involved in transcriptional regulation. A similar protein in mouse is differentially expressed in spermatogenesis. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Dec 2015]

ZKSCAN4 Gene

zinc finger with KRAtrong>Btrong> trong>andtrong> SCAN domains 4

Enatrong>btrong>les identical protein trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Located in nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ZKSCAN7 Gene

zinc finger with KRAtrong>Btrong> trong>andtrong> SCAN domains 7

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e active in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ZKSCAN8 Gene

zinc finger with KRAtrong>Btrong> trong>andtrong> SCAN domains 8

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

INDX Gene

Immunoneurologic syndrome X-linked, of Wood, trong>Btrong>lack, trong>andtrong> Nortrong>btrong>ury

TOPAZ1 Gene

testis trong>andtrong> ovary specific PAZ domain containing 1

Predicted to trong>btrong>e involved in spermatocyte division. Predicted to act upstream of or within apoptotic process; ectopic germ cell programmed cell death; trong>andtrong> lncRNA transcription. Predicted to trong>btrong>e located in cytosol. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

VAPtrong>Btrong> Gene

VAMP (vesicle-associated memtrong>btrong>rane protein)-associated protein trong>Btrong> trong>andtrong> C

The protein encoded trong>btrong>y this gene is a type IV memtrong>btrong>rane protein found in plasma trong>andtrong> intracellular vesicle memtrong>btrong>ranes. The encoded protein is found as a homodimer trong>andtrong> as a heterodimer with VAPA. This protein also can interact with VAMP1 trong>andtrong> VAMP2 trong>andtrong> may trong>btrong>e involved in vesicle trafficking. [provided trong>btrong>y RefSeq, Jul 2008]

PCF11 Gene

PCF11 cleavage trong>andtrong> polyadenylation factor sutrong>btrong>unit

The protein encoded trong>btrong>y this gene trong>btrong>inds to CLP1 to form pre-mRNA cleavage factor IIm. The encoded protein is necessary for efficient Pol II transcription termination trong>andtrong> may trong>btrong>e involved in degradation of the 3' product of polyA site cleavage. [provided trong>btrong>y RefSeq, Oct 2016]

trong>Btrong>Atrong>Btrong>AM1 Gene

trong>Btrong>RISC trong>andtrong> trong>Btrong>RCA1 A complex memtrong>btrong>er 1

Enatrong>btrong>les identical protein trong>btrong>inding activity. Involved in several processes, including DNA repair-dependent chromatin remodeling; mitotic G2 DNA damage checkpoint signaling; trong>andtrong> positive regulation of DNA repair. Located in cytosol trong>andtrong> nuclear trong>btrong>ody. Part of trong>Btrong>RCA1-A complex trong>andtrong> trong>Btrong>RISC complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

RUFY1 Gene

RUN trong>andtrong> FYVE domain containing 1

This gene encodes a protein that contains a RUN domain trong>andtrong> a FYVE-type zinc finger domain. The encoded protein trong>btrong>inds to phosphatidylinositol-3-phosphate (PI3P) trong>andtrong> plays a role in early endosomal trafficking, tethering trong>andtrong> fusion through interactions with small GTPases including Ratrong>btrong>4, Ratrong>btrong>5 trong>andtrong> Ratrong>btrong>14. Alternatively spliced transcript variants encoding multiple isoforms have trong>btrong>een otrong>btrong>served for this gene. [provided trong>btrong>y RefSeq, Dec 2011]

RUFY3 Gene

RUN trong>andtrong> FYVE domain containing 3

This gene encodes a RPIP8, UNC-14, trong>andtrong> NESCA domain-containing protein that is required for maintenance of neuronal polarity. In addition, it has trong>btrong>een implicated in mediation of gastric cancer cell migration trong>andtrong> invasion via interaction with P21-activated kinase-1, which promotes its expression. The encoded protein localizes to F-actin-enriched invadopodia to induce formation of protrusions, theretrong>btrong>y facilitating cell migration. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Sep 2016]

RUFY2 Gene

RUN trong>andtrong> FYVE domain containing 2

Enatrong>btrong>les SH3 domain trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of endocytosis. Located in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

RUFY4 Gene

RUN trong>andtrong> FYVE domain containing 4

Enatrong>btrong>les phosphatidylinositol-3-phosphate trong>btrong>inding activity. Involved in autophagosome assemtrong>btrong>ly; cellular response to interleukin-4; trong>andtrong> positive regulation of macroautophagy. Located in autophagosome. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LAMTOR3P1 Gene

late endosomal/lysosomal adaptor, MAPK trong>andtrong> MTOR activator 3 pseudogene 1

PPDPF Gene

pancreatic progenitor cell differentiation trong>andtrong> proliferation factor

Predicted to trong>btrong>e involved in cell differentiation. Predicted to act upstream of or within TORC1 signaling trong>andtrong> liver development. Located in mitochondrion. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ECM2 Gene

extracellular matrix protein 2, female organ trong>andtrong> adipocyte specific

ECM2 encodes extracellular matrix protein 2, so named trong>btrong>ecause it shares extensive similarity with known extracelluar matrix proteins. Three transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Oct 2010]

KANK4 Gene

KN motif trong>andtrong> ankyrin repeat domains 4

Predicted to trong>btrong>e involved in negative regulation of actin filament polymerization. Located in cytosol trong>andtrong> microtutrong>btrong>ule cytoskeleton. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

KANK2 Gene

KN motif trong>andtrong> ankyrin repeat domains 2

This gene encodes a memtrong>btrong>er of the KN motif trong>andtrong> ankyrin repeat domains (KANK) family of proteins, which play a role in cytoskeletal formation trong>btrong>y regulating actin polymerization. The encoded protein functions in the sequestration of steroid receptor coactivators trong>andtrong> possitrong>btrong>ly other proteins. Mutations in this gene are associated with impaired kidney podocyte function trong>andtrong> nephrotic syndrome, trong>andtrong> keratoderma trong>andtrong> woolly hair. [provided trong>btrong>y RefSeq, Jul 2016]

KANK3 Gene

KN motif trong>andtrong> ankyrin repeat domains 3

Predicted to trong>btrong>e involved in negative regulation of actin filament polymerization. Predicted to trong>btrong>e active in cytoplasm trong>andtrong> cytoskeleton. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

KANK1 Gene

KN motif trong>andtrong> ankyrin repeat domains 1

The protein encoded trong>btrong>y this gene trong>btrong>elongs to the Kank family of proteins, which contain multiple ankyrin repeat domains. This family memtrong>btrong>er functions in cytoskeleton formation trong>btrong>y regulating actin polymerization. This gene is a ctrong>andtrong>idate tumor suppressor for renal cell carcinoma. Mutations in this gene cause ceretrong>btrong>ral palsy spastic quadriplegic type 2, a central nervous system development disorder. A t(5;9) translocation results in fusion of the platelet-derived growth factor receptor trong>btrong>eta gene (PDGFRtrong>Btrong>) on chromosome 5 with this gene in a myeloproliferative neoplasm featuring severe thromtrong>btrong>ocythemia. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has trong>btrong>een identified on chromosome 20. [provided trong>btrong>y RefSeq, Dec 2014]

TMIGD3 Gene

transmemtrong>btrong>rane trong>andtrong> immunoglotrong>btrong>ulin domain containing 3

This gene encodes a transmemtrong>btrong>rane trong>andtrong> immunoglotrong>btrong>ulin domain-containing protein. Alternative splicing results in multiple transcript variants, one of which shares its 5' terminal exon with that of the overlapping adenosine A3 receptor gene (GeneID:140), thus resulting in a fusion product. [provided trong>btrong>y RefSeq, Nov 2014]

TMIGD2 Gene

transmemtrong>btrong>rane trong>andtrong> immunoglotrong>btrong>ulin domain containing 2

Enatrong>btrong>les coreceptor activity. Involved in positive regulation of T cell activation; positive regulation of angiogenesis; trong>andtrong> positive regulation of cytokine production. Predicted to trong>btrong>e located in plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

WDFY3 Gene

WD repeat trong>andtrong> FYVE domain containing 3

This gene encodes a phosphatidylinositol 3-phosphate-trong>btrong>inding protein that functions as a master conductor for aggregate clearance trong>btrong>y autophagy. This protein shuttles from the nuclear memtrong>btrong>rane to colocalize with aggregated proteins, where it complexes with other autophagic components to achieve macroautophagy-mediated clearance of these aggregated proteins. However, it is not necessary for starvation-induced macroautophagy. [provided trong>btrong>y RefSeq, May 2010]

WDFY2 Gene

WD repeat trong>andtrong> FYVE domain containing 2

This gene encodes a protein that contains two WD domains trong>andtrong> an FYVE zinc finger region. The function of this gene is unknown. An alternatively spliced transcript variant of this gene may exist. [provided trong>btrong>y RefSeq, Jul 2008]

WDFY1 Gene

WD repeat trong>andtrong> FYVE domain containing 1

The protein encoded trong>btrong>y this gene is a phosphatidylinositol 3-phosphate trong>btrong>inding protein, which contains a FYVE zinc finger domain trong>andtrong> multiple WD-40 repeat domains. When exogenously expressed, it localizes to early endosomes. Mutagenesis analysis demonstrates that this endosomal localization is mediated trong>btrong>y the FYVE domain. [provided trong>btrong>y RefSeq, Jan 2015]

CHORDC2P Gene

cysteine trong>andtrong> histidine-rich domain (CHORD) containing 2 pseudogene

SPECC1 Gene

sperm antigen with calponin homology trong>andtrong> coiled-coil domains 1

The protein encoded trong>btrong>y this gene trong>btrong>elongs to the cytospin-A family. It is localized in the nucleus, trong>andtrong> highly expressed in testis trong>andtrong> some cancer cell lines. A chromosomal translocation involving this gene trong>andtrong> platelet-derived growth factor receptor, trong>btrong>eta gene (PDGFRtrong>Btrong>) may trong>btrong>e a cause of juvenile myelomonocytic leukemia. Alternatively spliced transcript variants encoding different isoforms have trong>btrong>een descritrong>btrong>ed for this gene. [provided trong>btrong>y RefSeq, Aug 2011]

LIMS2 Gene

LIM trong>andtrong> senescent cell antigen-like domains 2

This gene encodes a memtrong>btrong>er of a small family of focal adhesion proteins which interacts with ILK (integrin-linked kinase), a protein which effects protein-protein interactions with the extraceullar matrix. The encoded protein has five LIM domains, each domain forming two zinc fingers, which permit interactions which regulate cell shape trong>andtrong> migration. A pseudogene of this gene is located on chromosome 4. Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Nov 2011]

LIMS3 Gene

LIM trong>andtrong> senescent cell antigen-like domains 3

Predicted to enatrong>btrong>le metal ion trong>btrong>inding activity. Predicted to trong>btrong>e located in cytoplasm; focal adhesion; trong>andtrong> plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LIMS1 Gene

LIM trong>andtrong> senescent cell antigen-like domains 1

The protein encoded trong>btrong>y this gene is an adaptor protein which contains five LIM domains, or doutrong>btrong>le zinc fingers. The protein is likely involved in integrin signaling through its LIM domain-mediated interaction with integrin-linked kinase, found in focal adhesion plaques. It is also thought to act as a trong>btrong>ridge linking integrin-linked kinase to NCK adaptor protein 2, which is involved in growth factor receptor kinase signaling pathways. Its localization to the periphery of spreading cells also suggests that this protein may play a role in integrin-mediated cell adhesion or spreading. Several transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jul 2010]

SUN2 Gene

Sad1 trong>andtrong> UNC84 domain containing 2

SUN1 (MIM 607723) trong>andtrong> SUN2 are inner nuclear memtrong>btrong>rane (INM) proteins that play a major role in nuclear-cytoplasmic connection trong>btrong>y formation of a 'trong>btrong>ridge' across the nuclear envelope, known as the LINC complex, via interaction with the conserved luminal KASH domain of nesprins (e.g., SYNE1; MIM 608441) located in the outer nuclear memtrong>btrong>rane (ONM). The LINC complex provides a direct connection trong>btrong>etween the nuclear lamina trong>andtrong> the cytoskeleton, which contritrong>btrong>utes to nuclear positioning trong>andtrong> cellular rigidity (summary trong>btrong>y Haque et al., 2010 [Putrong>btrong>Med 19933576]).[supplied trong>btrong>y OMIM, Nov 2010]

SUN3 Gene

Sad1 trong>andtrong> UNC84 domain containing 3

Predicted to enatrong>btrong>le protein-memtrong>btrong>rane adaptor activity. Predicted to trong>btrong>e located in nuclear inner memtrong>btrong>rane. Predicted to trong>btrong>e part of meiotic nuclear memtrong>btrong>rane microtutrong>btrong>ule tethering complex. Predicted to trong>btrong>e active in nuclear envelope. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SUN1 Gene

Sad1 trong>andtrong> UNC84 domain containing 1

This gene is a memtrong>btrong>er of the unc-84 homolog family trong>andtrong> encodes a nuclear envelope protein with an Unc84 (SUN) domain. The protein is involved in nuclear anchorage trong>andtrong> migration. Alternatively spliced transcript variants have trong>btrong>een descritrong>btrong>ed. [provided trong>btrong>y RefSeq, Jan 2019]

SUN5 Gene

Sad1 trong>andtrong> UNC84 domain containing 5

The protein encoded trong>btrong>y this gene appears to play a role in the meiotic stage of spermatogenesis. The encoded protein localizes to the junction trong>btrong>etween the sperm head trong>andtrong> trong>btrong>ody trong>andtrong> may trong>btrong>e involved in nuclear envelope reconstitution trong>andtrong> nuclear migration. Mutations in this gene have trong>btrong>een implicated in acephalic spermatozoa syndrome. [provided trong>btrong>y RefSeq, May 2017]

LOC100421332 Gene

zinc finger with KRAtrong>Btrong> trong>andtrong> SCAN domains 1 pseudogene

AOCH Gene

Acromegaloid features, overgrowth, cleft palate, trong>andtrong> hernia

DCAF8L1 Gene

DDtrong>Btrong>1 trong>andtrong> CUL4 associated factor 8-like 1

This gene encodes a memtrong>btrong>er of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically trong>btrong>racketed trong>btrong>y Gly-His trong>andtrong> Trp-Asp (GH-WD), which may facilitate the formation of heterotrimeric or multi-protein complexes. Memtrong>btrong>ers of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, trong>andtrong> gene regulation. This gene appears to represent an intronless retrocopy of a related multi-exon gene located on chromosome 1. However, the CDS of this intronless gene remains intact, it is conserved in other primate species, it is known to trong>btrong>e transcritrong>btrong>ed, trong>andtrong> it is therefore thought to encode a functional protein. [provided trong>btrong>y RefSeq, May 2010]

DCAF8L2 Gene

DDtrong>Btrong>1 trong>andtrong> CUL4 associated factor 8-like 2

Predicted to trong>btrong>e located in nucleus. Predicted to trong>btrong>e part of Cul4-RING E3 utrong>btrong>iquitin ligase complex. Predicted to trong>btrong>e active in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PAQR8 Gene

progestin trong>andtrong> adipoQ receptor family memtrong>btrong>er VIII

Predicted to enatrong>btrong>le nuclear steroid receptor activity trong>andtrong> steroid trong>btrong>inding activity. Predicted to trong>btrong>e involved in response to steroid hormone. Located in Golgi apparatus trong>andtrong> plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PAQR3 Gene

progestin trong>andtrong> adipoQ receptor family memtrong>btrong>er III

This gene encodes a seven-transmemtrong>btrong>rane protein localized in the Golgi apparatus in mammalian cells. The encoded protein trong>btrong>elongs to the progestin trong>andtrong> adipoQ receptor (PAQR) family. This protein functions as a tumor suppressor trong>btrong>y inhitrong>btrong>iting the Raf/MEK/ERK signaling cascade. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Apr 2017]

PAQR5 Gene

progestin trong>andtrong> adipoQ receptor family memtrong>btrong>er V

Predicted to enatrong>btrong>le signaling receptor activity. Predicted to trong>btrong>e involved in oogenesis. Predicted to trong>btrong>e located in plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PAQR4 Gene

progestin trong>andtrong> adipoQ receptor family memtrong>btrong>er IV

Enatrong>btrong>les molecular adaptor activity. Involved in protein statrong>btrong>ilization trong>andtrong> regulation of ceramide trong>btrong>iosynthetic process. Located in Golgi memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PAQR7 Gene

progestin trong>andtrong> adipoQ receptor family memtrong>btrong>er VII

Predicted to enatrong>btrong>le nuclear steroid receptor activity trong>andtrong> steroid trong>btrong>inding activity. Predicted to trong>btrong>e involved in response to steroid hormone. Predicted to trong>btrong>e located in memtrong>btrong>rane. Predicted to trong>btrong>e active in plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PAQR6 Gene

progestin trong>andtrong> adipoQ receptor family memtrong>btrong>er VI

Predicted to enatrong>btrong>le signaling receptor activity. Predicted to trong>btrong>e located in plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC102723407 Gene

putative V-set trong>andtrong> immunoglotrong>btrong>ulin domain-containing-like protein IGHV4OR15-8

SLITRK6 Gene

SLIT trong>andtrong> NTRK-like family, memtrong>btrong>er 6

This gene encodes a memtrong>btrong>er of the SLITRK protein family. Memtrong>btrong>ers of this family are integral memtrong>btrong>rane proteins that are characterized trong>btrong>y two N-terminal leucine-rich repeat (LRR) domains trong>andtrong> a C-terminal region that shares homology with trk neurotrophin receptors. This protein functions as a regulator of neurite outgrowth required for normal hearing trong>andtrong> vision. Mutations in this gene are a cause of myopia trong>andtrong> deafness. [provided trong>btrong>y RefSeq, Dec 2014]

SLITRK4 Gene

SLIT trong>andtrong> NTRK-like family, memtrong>btrong>er 4

This gene encodes a transmemtrong>btrong>rane protein trong>btrong>elonging to the the SLITRK family. These family memtrong>btrong>ers include two N-terminal leucine-rich repeat domains similar to those found in the axonal growth-controlling protein SLIT, as well as C-terminal regions similar to neurotrophin receptors. Studies of an homologous protein in mouse suggest that this family memtrong>btrong>er functions to suppress neurite outgrowth. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, May 2010]

SLITRK5 Gene

SLIT trong>andtrong> NTRK-like family, memtrong>btrong>er 5

Memtrong>btrong>ers of the SLITRK family, such as SLITRK5, are integral memtrong>btrong>rane proteins with 2 N-terminal leucine-rich repeat (LRR) domains similar to those of SLIT proteins (see SLIT1; MIM 603742). Most SLITRKs, including SLITRK5, also have C-terminal regions that share homology with neurotrophin receptors (see NTRK1; MIM 191315). SLITRKs are expressed predominantly in neural tissues trong>andtrong> have neurite-modulating activity (Aruga et al., 2003 [Putrong>btrong>Med 14557068]).[supplied trong>btrong>y OMIM, Mar 2008]

SLITRK2 Gene

SLIT trong>andtrong> NTRK-like family, memtrong>btrong>er 2

This gene encodes an integral memtrong>btrong>rane protein that contains two N-terminal leucine-rich repeats domains trong>andtrong> contains C-terminal regions similar to neurotrophin receptors. The encoded protein may play a role in modulating neurite activity. Alternatively spliced transcript variants encoding the same protein have trong>btrong>een descritrong>btrong>ed.[provided trong>btrong>y RefSeq, Fetrong>btrong> 2010]

SLITRK3 Gene

SLIT trong>andtrong> NTRK-like family, memtrong>btrong>er 3

This gene encodes a memtrong>btrong>er of the Slitrk family of structurally related transmemtrong>btrong>rane proteins that are involved in controlling neurite outgrowth. The encoded protein contains two leucine-rich repeat (LRR) domains trong>andtrong> a C-terminal domain that is partially similar to Trk neurotrophin receptor protein. Enhanced expression of this gene was found in tissue from several different types of tumors. Alternative splicing results in multiple transcript variants, all encoding the same protein. [provided trong>btrong>y RefSeq, Jan 2016]

SLITRK1 Gene

SLIT trong>andtrong> NTRK-like family, memtrong>btrong>er 1

This gene encodes a memtrong>btrong>er of the SLITRK protein family. Memtrong>btrong>ers of this family are integral memtrong>btrong>rane proteins that are characterized trong>btrong>y two N-terminal leucine-rich repeat (LRR) domains trong>andtrong> a C-terminal region that shares homology with trk neurotrophin receptors. However, the protein encoded trong>btrong>y this gene lacks the region of homology to neurotrophin receptors. This protein is thought to trong>btrong>e involved in neurite outgrowth. Mutations in this gene may trong>btrong>e associated with Tourette syndrome. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Jul 2013]

LOC400927 Gene

TPTE trong>andtrong> PTEN homologous inositol lipid phosphatase pseudogene

ETL4 Gene

epilepsy, occipitotemporal lotrong>btrong>e, trong>andtrong> migraine with aura

R3HCC1L Gene

R3H domain trong>andtrong> coiled-coil containing 1-like

Located in exon-exon junction complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

HMSN5 Gene

Hereditary motor trong>andtrong> sensory neuropathy V

LOC100421641 Gene

zinc finger CCHC-type trong>andtrong> RNA trong>btrong>inding motif 1 pseudogene

CSPP1 Gene

centrosome trong>andtrong> spindle pole associated protein 1

This gene encodes a centrosome trong>andtrong> spindle pole associated protein. The encoded protein plays a role in cell-cycle progression trong>andtrong> spindle organization, regulates cytokinesis, interacts with Nephrocystin 8 trong>andtrong> is required for cilia formation. Mutations in this gene result in primary cilia atrong>btrong>normalities trong>andtrong> classical Joutrong>btrong>ert syndrome. Alternatively spliced transcript variants encoding distinct isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Apr 2014]

GNPTAtrong>Btrong> Gene

N-acetylglucosamine-1-phosphate transferase, alpha trong>andtrong> trong>btrong>eta sutrong>btrong>units

This gene encodes two of three sutrong>btrong>unit types of the memtrong>btrong>rane-trong>btrong>ound enzyme N-acetylglucosamine-1-phosphotransferase, a heterohexameric complex composed of two alpha, two trong>btrong>eta, trong>andtrong> two gamma sutrong>btrong>units. The encoded protein is proteolytically cleaved at the Lys928-Asp929 trong>btrong>ond to yield mature alpha trong>andtrong> trong>btrong>eta polypeptides while the gamma sutrong>btrong>units are the product of a distinct gene (GeneID 84572). In the Golgi apparatus, the heterohexameric complex catalyzes the first step in the synthesis of mannose 6-phosphate recognition markers on certain oligosaccharides of newly synthesized lysosomal enzymes. These recognition markers are essential for appropriate trafficking of lysosomal enzymes. Mutations in this gene have trong>btrong>een associated with trong>btrong>oth mucolipidosis II trong>andtrong> mucolipidosis IIIA.[provided trong>btrong>y RefSeq, May 2010]

QSER1 Gene

glutamine trong>andtrong> serine rich 1

Predicted to trong>btrong>e located in chromosome. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

NMSR Gene

Neuropathy, hereditary motor trong>andtrong> sensory, Russe type

ANKUtrong>Btrong>1 Gene

ankyrin repeat trong>andtrong> utrong>btrong>iquitin domain containing 1

MSTO1 Gene

misato 1, mitochondrial distritrong>btrong>ution trong>andtrong> morphology regulator

Involved in mitochondrion distritrong>btrong>ution; mitochondrion organization; trong>andtrong> positive regulation of mitochondrial fusion. Located in mitochondrial outer memtrong>btrong>rane. Is active in cytosol. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>3 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 3

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e active in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PATE1 Gene

prostate trong>andtrong> testis expressed 1

Predicted to enatrong>btrong>le acetylcholine receptor regulator activity. Predicted to trong>btrong>e located in extracellular region. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PATE3 Gene

prostate trong>andtrong> testis expressed 3

Predicted to trong>btrong>e located in extracellular region. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PATE2 Gene

prostate trong>andtrong> testis expressed 2

Located in extracellular space. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>1 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 1

Enatrong>btrong>les K63-linked polyutrong>btrong>iquitin modification-dependent protein trong>btrong>inding activity; protein heterodimerization activity; trong>andtrong> protein homodimerization activity. Involved in several processes, including negative regulation of transcription trong>btrong>y RNA polymerase II; nucleotrong>btrong>ase-containing compound trong>btrong>iosynthetic process; trong>andtrong> protein homooligomerization. Located in nuclear trong>btrong>ody trong>andtrong> nuclear memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

HECW1 Gene

HECT, C2 trong>andtrong> WW domain containing E3 utrong>btrong>iquitin protein ligase 1

Predicted to enatrong>btrong>le utrong>btrong>iquitin protein ligase activity. Predicted to trong>btrong>e involved in regulation of dendrite morphogenesis trong>andtrong> utrong>btrong>iquitin-dependent protein catatrong>btrong>olic process. Predicted to trong>btrong>e located in cytosol. Predicted to trong>btrong>e active in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

HECW2 Gene

HECT, C2 trong>andtrong> WW domain containing E3 utrong>btrong>iquitin protein ligase 2

This gene encodes a memtrong>btrong>er of a family of E3 utrong>btrong>iquitin ligases which plays an important role in the proliferation, migration trong>andtrong> differentiation of neural crest cells as a regulator of glial cell line-derived neurotrophic factor (GDNF)/Ret signaling. This gene also plays an important role in angiogenesis through statrong>btrong>ilization of endothelial cell-to-cell junctions as a regulator of angiomotin-like 1 statrong>btrong>ility. The encoded protein contains an N-terminal calcium/lipid-trong>btrong>inding (C2) domain involved in memtrong>btrong>rane targeting, two-four WW domains responsitrong>btrong>le for cellular localization trong>andtrong> sutrong>btrong>strate recognition, trong>andtrong> a C-terminal homologous with E6-associated protein C-terminus (HECT) catalytic domain. Naturally occurring mutations in this gene are associated with neurodevelopmental delay, hypotonia, trong>andtrong> epilepsy. The decreased expression of this gene in the aganglionic colon is associated with Hirschsprung's disease. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2017]

LOC101929203 Gene

RING finger trong>andtrong> transmemtrong>btrong>rane domain-containing protein 1-like

HPRHP Gene

Hypophosphatemic rickets trong>andtrong> hyperparathyroidism

PSIP1P2 Gene

PC4 trong>andtrong> SFRS1 interacting protein 1 pseudogene 2

PSIP1P1 Gene

PC4 trong>andtrong> SFRS1 interacting protein 1 pseudogene 1

RADIL Gene

Ras association trong>andtrong> DIL domains

Predicted to enatrong>btrong>le GTPase trong>btrong>inding activity. Acts upstream of or within sutrong>btrong>strate adhesion-dependent cell spreading. Located in microtutrong>btrong>ule. Part of protein-containing complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

NHS Gene

Nance-Horan syndrome (congenital cataracts trong>andtrong> dental anomalies)

This gene encodes a protein containing four conserved nuclear localization signals. The encoded protein functions in eye, tooth, craniofacial trong>andtrong> trong>btrong>rain development, trong>andtrong> it can regulate actin remodeling trong>andtrong> cell morphology. Mutations in this gene have trong>btrong>een shown to cause Nance-Horan syndrome, trong>andtrong> also X-linked cataract-40. Alternatively spliced transcript variants encoding different isoforms have trong>btrong>een descritrong>btrong>ed for this gene. [provided trong>btrong>y RefSeq, May 2014]

VSIG10L Gene

V-set trong>andtrong> immunoglotrong>btrong>ulin domain containing 10 like

Located in nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

MMEDF Gene

Macrocephaly with multiple epiphyseal dysplasia trong>andtrong> distinctive facies

LOC102723478 Gene

coxsackievirus trong>andtrong> adenovirus receptor pseudogene

CFAP221 Gene

cilia trong>andtrong> flagella associated protein 221

Predicted to enatrong>btrong>le calmodulin trong>btrong>inding activity. Predicted to trong>btrong>e involved in motile cilium assemtrong>btrong>ly. Predicted to act upstream of or within epithelial cilium movement involved in extracellular fluid movement; estatrong>btrong>lishment of localization in cell; trong>andtrong> sperm flagellum assemtrong>btrong>ly. Predicted to trong>btrong>e located in axoneme; glial cell projection; trong>andtrong> manchette. Predicted to trong>btrong>e active in 9+2 motile cilium. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC105369258 Gene

arf-GAP with GTPase, ANK repeat trong>andtrong> PH domain-containing protein 4

DLEC1P1 Gene

deleted in lung trong>andtrong> esophageal cancer 1 pseudogene 1

ASOtrong>Btrong>S Gene

Asthma trong>andtrong> otrong>btrong>esity susceptitrong>btrong>ility, chromosome 16p11 inversion related

CItrong>Btrong>2 Gene

calcium trong>andtrong> integrin trong>btrong>inding family memtrong>btrong>er 2

The protein encoded trong>btrong>y this gene is similar to that of KIP/CItrong>Btrong>, calcineurin trong>Btrong>, trong>andtrong> calmodulin. The encoded protein is a calcium-trong>btrong>inding regulatory protein that interacts with DNA-dependent protein kinase catalytic sutrong>btrong>units (DNA-PKcs), trong>andtrong> it is involved in photoreceptor cell maintenance. Mutations in this gene cause deafness, autosomal recessive, 48 (DFNtrong>Btrong>48), trong>andtrong> also Usher syndrome 1J (USH1J). Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Jul 2014]

CItrong>Btrong>3 Gene

calcium trong>andtrong> integrin trong>btrong>inding family memtrong>btrong>er 3

This gene product shares a high degree of sequence similarity with DNA-dependent protein kinase catalytic sutrong>btrong>unit-interacting protein 2 in human trong>andtrong> mouse, trong>andtrong> like them may trong>btrong>ind the catalytic sutrong>btrong>unit of DNA-dependent protein kinases. The exact function of this gene is not known. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Jul 2014]

CItrong>Btrong>1 Gene

calcium trong>andtrong> integrin trong>btrong>inding 1 (calmyrin)

This gene encodes a memtrong>btrong>er of the EF-htrong>andtrong> domain-containing calcium-trong>btrong>inding superfamily. The encoded protein interacts with many other proteins, including the platelet integrin alpha-IItrong>btrong>-trong>btrong>eta-3, DNA-dependent protein kinase, presenilin-2, focal adhesion kinase, p21 activated kinase, trong>andtrong> protein kinase D. The encoded protein may trong>btrong>e involved in cell survival trong>andtrong> proliferation, trong>andtrong> is associated with several disease states including cancer trong>andtrong> Alzheimer's disease. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Apr 2013]

CItrong>Btrong>4 Gene

calcium trong>andtrong> integrin trong>btrong>inding family memtrong>btrong>er 4

Enatrong>btrong>les calcium ion trong>btrong>inding activity trong>andtrong> magnesium ion trong>btrong>inding activity. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

RASEF Gene

RAS trong>andtrong> EF-htrong>andtrong> domain containing

This gene is a memtrong>btrong>er of the Ratrong>btrong> family of GTPases that are involved in regulation of memtrong>btrong>rane traffic. The encoded protein contains an N-terminal EF-htrong>andtrong> domain, a coiled-coil motif trong>andtrong> a C-terminal Ratrong>btrong> domain. A potential role as tumor suppressor has trong>btrong>een indicated for this gene. [provided trong>btrong>y RefSeq, Nov 2012]

LOC100422376 Gene

ArfGAP with GTPase domain, ankyrin repeat trong>andtrong> PH domain 1 pseudogene

NAMA Gene

non-protein coding RNA, associated with MAP kinase pathway trong>andtrong> growth arrest

JMY Gene

junction mediating trong>andtrong> regulatory protein, p53 cofactor

Enatrong>btrong>les microtutrong>btrong>ule trong>btrong>inding activity. Involved in cellular response to starvation. Located in autophagosome memtrong>btrong>rane; cell leading edge; trong>andtrong> cytoplasmic vesicle. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LRIG3 Gene

leucine-rich repeats trong>andtrong> immunoglotrong>btrong>ulin-like domains 3

Predicted to act upstream of or within otolith morphogenesis. Located in extracellular space. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LRIG2 Gene

leucine-rich repeats trong>andtrong> immunoglotrong>btrong>ulin-like domains 2

This gene encodes a transmemtrong>btrong>rane protein containing leucine-rich repeats trong>andtrong> immunoglotrong>btrong>ulin-like domains. The encoded protein promotes epidermal growth factor signalling, resulting in increased proliferation. Its expression in the cytoplasm of glioma cells is correlated with poor survival. Mutations in this gene can cause urofacial syndrome. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Aug 2015]

LRIG1 Gene

leucine-rich repeats trong>andtrong> immunoglotrong>btrong>ulin-like domains 1

Predicted to act upstream of or within several processes, including innervation; otolith morphogenesis; trong>andtrong> sensory perception of sound. Predicted to trong>btrong>e located in plasma memtrong>btrong>rane. Predicted to trong>btrong>e active in extracellular matrix trong>andtrong> extracellular space. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

RGPD5 Gene

RANtrong>Btrong>P2-like trong>andtrong> GRIP domain containing 5

RAN is a small GTP-trong>btrong>inding protein of the RAS superfamily that is associated with the nuclear memtrong>btrong>rane trong>andtrong> is thought to control a variety of cellular functions through its interactions with other proteins. This gene shares a high degree of sequence identity with RANtrong>Btrong>P2, a large RAN-trong>btrong>inding protein localized at the cytoplasmic side of the nuclear pore complex. It is trong>btrong>elieved that this RANtrong>Btrong>P2 gene family memtrong>btrong>er arose from a duplication event 3 Mtrong>btrong> distal to RANtrong>Btrong>P2. Alternative splicing has trong>btrong>een otrong>btrong>served for this locus trong>andtrong> two variants are descritrong>btrong>ed. Additional splicing is suggested trong>btrong>ut complete sequence for further transcripts has not trong>btrong>een determined. [provided trong>btrong>y RefSeq, Jul 2008]

FRMPD4 Gene

FERM trong>andtrong> 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 trong>andtrong> density, trong>andtrong> is required for the maintenance of excitatory synaptic transmission. [provided trong>btrong>y RefSeq, Jan 2010]

FRMPD1 Gene

FERM trong>andtrong> PDZ domain containing 1

Involved in estatrong>btrong>lishment of protein localization to memtrong>btrong>rane trong>andtrong> regulation of G protein-coupled receptor signaling pathway. Located in cell cortex trong>andtrong> plasma memtrong>btrong>rane. Part of protein-containing complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

FRMPD3 Gene

FERM trong>andtrong> PDZ domain containing 3

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

FRMPD2 Gene

FERM trong>andtrong> PDZ domain containing 2

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

PDLIM1P4 Gene

PDZ trong>andtrong> LIM domain 1 pseudogene 4

XPR1 Gene

xenotropic trong>andtrong> polytropic retrovirus receptor 1

The protein encoded trong>btrong>y this gene is a receptor for the xenotropic trong>andtrong> polytropic classes of murine leukemia viruses. The encoded protein is involved in phosphate homeostasis trong>btrong>y mediating phosphate export from the cell. Defects in this gene have trong>btrong>een associated with idiopathic trong>btrong>asal ganglia calcification-6. [provided trong>btrong>y RefSeq, Jun 2016]

PDLIM1P3 Gene

PDZ trong>andtrong> LIM domain 1 pseudogene 3

PDLIM1P2 Gene

PDZ trong>andtrong> LIM domain 1 pseudogene 2

PDLIM1P1 Gene

PDZ trong>andtrong> LIM domain 1 pseudogene 1

HOMEZ Gene

homeotrong>btrong>ox trong>andtrong> leucine zipper encoding

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Located in cytosol; nucleolus; trong>andtrong> nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

HEPACAM Gene

hepatic trong>andtrong> glial cell adhesion molecule

The protein encoded trong>btrong>y this gene is a single-pass type I memtrong>btrong>rane protein that localizes to the cytoplasmic side of the cell memtrong>btrong>rane. The encoded protein acts as a homodimer trong>andtrong> is involved in cell motility trong>andtrong> cell-matrix interactions. The expression of this gene is downregulated or undetectatrong>btrong>le in many cancer cell lines, so this may trong>btrong>e a tumor suppressor gene. [provided trong>btrong>y RefSeq, Jul 2011]

trong>Btrong>AMtrong>Btrong>I Gene

trong>Btrong>MP trong>andtrong> activin memtrong>btrong>rane-trong>btrong>ound inhitrong>btrong>itor

This gene encodes a transmemtrong>btrong>rane glycoprotein related to the type I receptors of the transforming growth factor-trong>btrong>eta (TGF-trong>btrong>eta) family, whose memtrong>btrong>ers play important roles in signal transduction in many developmental trong>andtrong> pathological processes. The encoded protein however is a pseudoreceptor, lacking an intracellular serine/threonine kinase domain required for signaling. Similar proteins in frog, mouse trong>andtrong> zetrong>btrong>rafish function as negative regulators of TGF-trong>btrong>eta, which has led to the suggestion that the encoded protein may function to limit the signaling range of the TGF-trong>btrong>eta family during early emtrong>btrong>ryogenesis. [provided trong>btrong>y RefSeq, Jul 2008]

LOC100421246 Gene

D4, zinc trong>andtrong> doutrong>btrong>le PHD fingers family 2 pseudogene

LOC100288929 Gene

coxsackievirus trong>andtrong> adenovirus receptor-like

LOC391230 Gene

KN motif trong>andtrong> ankyrin repeat domain-containing protein 1-like

DELXQ21 Gene

Choroideremia, deafness, trong>andtrong> mental retardation

SCLT1 Gene

sodium channel trong>andtrong> clathrin linker 1

This gene encodes an adaptor protein. Studies of a related gene in rat suggest that the encoded protein functions to link clathrin to the sodium channel protein type 10 sutrong>btrong>unit alpha protein. The encoded protein has also trong>btrong>een identified as a component of distal appendages of centrioles that is necessary for ciliogenesis. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Jul 2014]

SPOAN Gene

spastic paraplegia, optic atrophy, trong>andtrong> neuropathy

DEL15Q15.3 Gene

Deafness trong>andtrong> male infertility

GCSAML Gene

germinal center-associated, signaling trong>andtrong> motility-like

This gene encodes a protein thought to trong>btrong>e a signaling molecule associated with germinal centers, the sites of proliferation trong>andtrong> differentiation of mature trong>Btrong> lymphocytes. Alternate splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Aug 2013]

SH3YL1 Gene

SH3 trong>andtrong> SYLF domain containing 1

Enatrong>btrong>les phosphatase trong>btrong>inding activity trong>andtrong> phosphatidylinositol trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of ruffle assemtrong>btrong>ly. Predicted to act upstream of or within phosphatidylinositol trong>btrong>iosynthetic process. Located in ruffle memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC646071 Gene

disintegrin trong>andtrong> metalloproteinase domain-containing protein 21-like

DCAF13 Gene

DDtrong>Btrong>1 trong>andtrong> CUL4 associated factor 13

Enatrong>btrong>les nuclear estrogen receptor trong>btrong>inding activity trong>andtrong> utrong>btrong>iquitin-like ligase-sutrong>btrong>strate adaptor activity. Involved in several processes, including decidualization; epigenetic programming in the zygotic pronuclei; trong>andtrong> spindle assemtrong>btrong>ly involved in female meiosis. Located in several cellular components, including centrosome; cytosol; trong>andtrong> nuclear lumen. Part of Cul4-RING E3 utrong>btrong>iquitin ligase complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

DCAF12 Gene

DDtrong>Btrong>1 trong>andtrong> CUL4 associated factor 12

This gene encodes a WD repeat-containing protein that interacts with the COP9 signalosome, a macromolecular complex that interacts with cullin-RING E3 ligases trong>andtrong> regulates their activity trong>btrong>y hydrolyzing cullin-Nedd8 conjugates. [provided trong>btrong>y RefSeq, Jul 2009]

DCAF11 Gene

DDtrong>Btrong>1 trong>andtrong> CUL4 associated factor 11

This gene encodes a WD repeat-containing protein that interacts with the COP9 signalosome, a macromolecular complex that interacts with cullin-RING E3 ligases trong>andtrong> regulates their activity trong>btrong>y hydrolyzing cullin-Nedd8 conjugates. Multiple alternatively spliced transcript variants have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jul 2009]

DCAF10 Gene

DDtrong>Btrong>1 trong>andtrong> CUL4 associated factor 10

Predicted to trong>btrong>e involved in protein utrong>btrong>iquitination. Part of Cul4-RING E3 utrong>btrong>iquitin ligase complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

DCAF17 Gene

DDtrong>Btrong>1 trong>andtrong> CUL4 associated factor 17

This gene encodes a nuclear transmemtrong>btrong>rane protein that associates with cullin 4A/damaged DNA trong>btrong>inding protein 1 utrong>btrong>iquitin ligase complex. Mutations in this gene are associated with Woodhouse-Sakati syndrome. Alternate splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Sep 2009]

DCAF16 Gene

DDtrong>Btrong>1 trong>andtrong> CUL4 associated factor 16

Predicted to trong>btrong>e involved in protein utrong>btrong>iquitination. Part of Cul4-RING E3 utrong>btrong>iquitin ligase complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

DCAF15 Gene

DDtrong>Btrong>1 trong>andtrong> CUL4 associated factor 15

Enatrong>btrong>les small molecule trong>btrong>inding activity. Involved in protein polyutrong>btrong>iquitination trong>andtrong> regulation of natural killer cell activation. Part of Cul4-RING E3 utrong>btrong>iquitin ligase complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

AGGF1P3 Gene

angiogenic factor with G patch trong>andtrong> FHA domains 1 pseudogene 3

AGGF1P2 Gene

angiogenic factor with G patch trong>andtrong> FHA domains 1 pseudogene 2

AGGF1P1 Gene

angiogenic factor with G patch trong>andtrong> FHA domains 1 pseudogene 1

AGGF1P7 Gene

angiogenic factor with G patch trong>andtrong> FHA domains 1 pseudogene 7

AGGF1P5 Gene

angiogenic factor with G patch trong>andtrong> FHA domains 1 pseudogene 5

AGGF1P4 Gene

angiogenic factor with G patch trong>andtrong> FHA domains 1 pseudogene 4

AGGF1P9 Gene

angiogenic factor with G patch trong>andtrong> FHA domains 1 pseudogene 9

AGGF1P8 Gene

angiogenic factor with G patch trong>andtrong> FHA domains 1 pseudogene 8

LOC101930080 Gene

GPS, PLAT trong>andtrong> transmemtrong>btrong>rane domain-containing protein FLJ00285-like

LMCD1 Gene

LIM trong>andtrong> cysteine-rich domains 1

This gene encodes a memtrong>btrong>er of the LIM-domain family of zinc finger proteins. The encoded protein contains an N-terminal cysteine-rich domain trong>andtrong> two C-terminal LIM domains. The presence of LIM domains suggests involvement in protein-protein interactions. The protein may act as a co-regulator of transcription along with other transcription factors. Alternate splicing results in multiple transcript variants of this gene. [provided trong>btrong>y RefSeq, May 2013]

Ztrong>Btrong>Ttrong>Btrong>8OSP2 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 8 opposite strtrong>andtrong> pseudogene 2

ACAP2 Gene

ArfGAP with coiled-coil, ankyrin repeat trong>andtrong> PH domains 2

Enatrong>btrong>les GTPase activator activity. Acts upstream of or within actin filament-trong>btrong>ased process. Located in ruffle. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SPATC1L Gene

spermatogenesis trong>andtrong> centriole associated 1-like

Enatrong>btrong>les identical protein trong>btrong>inding activity. Predicted to trong>btrong>e involved in spermatogenesis. Predicted to act upstream of or within actin polymerization or depolymerization; positive regulation of cAMP-dependent protein kinase activity; trong>andtrong> positive regulation of cAMP/PKA signal transduction. Predicted to trong>btrong>e active in centrosome trong>andtrong> sperm head-tail coupling apparatus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

R3HCC1 Gene

R3H domain trong>andtrong> coiled-coil containing 1

Predicted to enatrong>btrong>le nucleic acid trong>btrong>inding activity. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

IQSEC1 Gene

IQ motif trong>andtrong> Sec7 domain 1

Predicted to enatrong>btrong>le protein kinase trong>btrong>inding activity. Predicted to trong>btrong>e involved in several processes, including positive regulation of focal adhesion disassemtrong>btrong>ly; positive regulation of keratinocyte migration; trong>andtrong> regulation of postsynaptic neurotransmitter receptor internalization. Located in nucleolus. Implicated in intellectual developmental disorder with short stature trong>andtrong> trong>btrong>ehavioral atrong>btrong>normalities trong>andtrong> lung adenocarcinoma. trong>Btrong>iomarker of lung non-small cell carcinoma. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

IQSEC3 Gene

IQ motif trong>andtrong> Sec7 domain 3

Predicted to enatrong>btrong>le guanyl-nucleotide exchange factor activity. Predicted to trong>btrong>e involved in several processes, including activation of GTPase activity; postsynapse organization; trong>andtrong> regulation of small GTPase mediated signal transduction. Located in cytosol trong>andtrong> nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

IQSEC2 Gene

IQ motif trong>andtrong> Sec7 domain 2

This gene encodes a guanine nucleotide exchange factor for the ARF family of small GTP-trong>btrong>inding proteins. The encoded protein is a component of the postsynaptic density at excitatory synapses, trong>andtrong> may play a critical role in cytoskeletal trong>andtrong> synaptic organization through the activation of selected ARF sutrong>btrong>strates including ARF1 trong>andtrong> ARF6. Mutations in this gene have trong>btrong>een implicated in nonsyndromic X-linked cognitive disatrong>btrong>ility. Alternatively spliced transcript variants encoding multiple isoforms have trong>btrong>een otrong>btrong>served for this gene. [provided trong>btrong>y RefSeq, Aug 2011]

NOLC1 Gene

nucleolar trong>andtrong> coiled-trong>btrong>ody phosphoprotein 1

Enatrong>btrong>les molecular function inhitrong>btrong>itor activity; protein heterodimerization activity; trong>andtrong> protein-macromolecule adaptor activity. Involved in neural crest cell development; neural crest formation; trong>andtrong> regulation of translation. Acts upstream of or within axonogenesis trong>andtrong> regulation of synaptic plasticity. Located in fitrong>btrong>rillar center. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

MYRIP Gene

myosin VIIA trong>andtrong> Ratrong>btrong> interacting protein

Predicted to enatrong>btrong>le actin trong>btrong>inding activity; myosin trong>btrong>inding activity; trong>andtrong> protein kinase A trong>btrong>inding activity. Predicted to trong>btrong>e involved in positive regulation of insulin secretion. Predicted to trong>btrong>e located in several cellular components, including cytoplasmic vesicle; perinuclear region of cytoplasm; trong>andtrong> photoreceptor outer segment. Predicted to trong>btrong>e part of exocyst. Predicted to trong>btrong>e active in cortical actin cytoskeleton. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

MNX1 Gene

motor neuron trong>andtrong> pancreas homeotrong>btrong>ox 1

This gene encodes a nuclear protein, which contains a homeotrong>btrong>ox domain trong>andtrong> is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Sep 2009]

LOC105372412 Gene

phospholipase A2 inhitrong>btrong>itor trong>andtrong> Ly6/PLAUR domain-containing protein-like

PSD2 Gene

pleckstrin trong>andtrong> Sec7 domain containing 2

Predicted to enatrong>btrong>le guanyl-nucleotide exchange factor activity trong>andtrong> phospholipid trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of ARF protein signal transduction. Predicted to trong>btrong>e located in cleavage furrow trong>andtrong> ruffle memtrong>btrong>rane. Predicted to trong>btrong>e active in glutamatergic synapse trong>andtrong> postsynapse. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PSD4 Gene

pleckstrin trong>andtrong> Sec7 domain containing 4

Predicted to enatrong>btrong>le guanyl-nucleotide exchange factor activity trong>andtrong> phospholipid trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of ARF protein signal transduction. Located in ruffle memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

UEVLD Gene

UEV trong>andtrong> lactate/malate dehyrogenase domains

Predicted to enatrong>btrong>le utrong>btrong>iquitin trong>btrong>inding activity. Predicted to trong>btrong>e involved in endosome to lysosome transport. Located in extracellular exosome. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

EYA4 Gene

EYA transcriptional coactivator trong>andtrong> phosphatase 4

This gene encodes a memtrong>btrong>er of the eyes atrong>btrong>sent (EYA) family of proteins. The encoded protein may act as a transcriptional activator through its protein phosphatase activity, trong>andtrong> it may trong>btrong>e important for eye development, trong>andtrong> for continued function of the mature organ of Corti. Mutations in this gene are associated with postlingual, progressive, autosomal dominant hearing loss at the deafness, autosomal dominant non-syndromic sensorineural 10 locus. The encoded protein is also a putative oncogene that mediates DNA repair, apoptosis, trong>andtrong> innate immunity following DNA damage, cellular damage, trong>andtrong> viral attack. Defects in this gene are also associated with dilated cardiomyopathy 1J. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided trong>btrong>y RefSeq, Jul 2014]

EYA1 Gene

EYA transcriptional coactivator trong>andtrong> phosphatase 1

This gene encodes a memtrong>btrong>er of the eyes atrong>btrong>sent (EYA) family of proteins. The encoded protein may play a role in the developing kidney, trong>btrong>ranchial arches, eye, trong>andtrong> ear. Mutations of this gene have trong>btrong>een associated with trong>btrong>ranchiootorenal dysplasia syndrome, trong>btrong>ranchiootic syndrome, trong>andtrong> sporadic cases of congenital cataracts trong>andtrong> ocular anterior segment anomalies. A similar protein in mice can act as a transcriptional activator. Alternatively spliced transcript variants have trong>btrong>een identified for this gene. [provided trong>btrong>y RefSeq, Dec 2013]

EYA3 Gene

EYA transcriptional coactivator trong>andtrong> phosphatase 3

This gene encodes a memtrong>btrong>er of the eyes atrong>btrong>sent (EYA) family of proteins. The encoded protein may act as a transcriptional activator trong>andtrong> have a role during development. It can act as a mediator of chemoresistance trong>andtrong> cell survival in Ewing sarcoma cells, where this gene is up-regulated via a micro-RNA that trong>btrong>inds to the 3' UTR of the transcript. A similar protein in mice acts as a transcriptional activator. Alternative splicing of this gene results in multiple transcript variants. [provided trong>btrong>y RefSeq, Sep 2013]

EYA2 Gene

EYA transcriptional coactivator trong>andtrong> phosphatase 2

This gene encodes a memtrong>btrong>er of the eyes atrong>btrong>sent (EYA) family of proteins. The encoded protein may trong>btrong>e post-translationally modified trong>andtrong> may play a role in eye development. A similar protein in mice can act as a transcriptional activator. Alternative splicing results in multiple transcript variants, trong>btrong>ut the full-length natures of all of these variants have not yet trong>btrong>een determined. [provided trong>btrong>y RefSeq, Jul 2009]

IGFN1 Gene

immunoglotrong>btrong>ulin-like trong>andtrong> fitrong>btrong>ronectin type III domain containing 1

Predicted to trong>btrong>e located in Z disc trong>andtrong> nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

OGFOD1 Gene

2-oxoglutarate trong>andtrong> iron-dependent oxygenase domain containing 1

Enatrong>btrong>les peptidyl-proline 3-dioxygenase activity. Involved in several processes, including peptidyl-proline hydroxylation; regulation of translational termination; trong>andtrong> stress granule assemtrong>btrong>ly. Located in cytoplasmic stress granule; cytosol; trong>andtrong> nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

OGFOD3 Gene

2-oxoglutarate trong>andtrong> iron-dependent oxygenase domain containing 3

Predicted to enatrong>btrong>le several functions, including L-ascortrong>btrong>ic acid trong>btrong>inding activity; dioxygenase activity; trong>andtrong> iron ion trong>btrong>inding activity. Located in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

OGFOD2 Gene

2-oxoglutarate trong>andtrong> iron-dependent oxygenase domain containing 2

Predicted to enatrong>btrong>le several functions, including L-ascortrong>btrong>ic acid trong>btrong>inding activity; dioxygenase activity; trong>andtrong> iron ion trong>btrong>inding activity. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC100421368 Gene

zinc finger trong>andtrong> SCAN domain containing 5A pseudogene

LOC100288803 Gene

F-trong>btrong>ox trong>andtrong> WD repeat domain containing 2 pseudogene

LOC402076 Gene

F-trong>btrong>ox trong>andtrong> leucine-rich repeat protein 12 pseudogene

DHTKD1 Gene

dehydrogenase E1 trong>andtrong> transketolase domain containing 1

This gene encodes a component of a mitochondrial 2-oxoglutarate-dehydrogenase-complex-like protein involved in the degradation pathways of several amino acids, including lysine. Mutations in this gene are associated with 2-aminoadipic 2-oxoadipic aciduria trong>andtrong> Charcot-Marie-Tooth Disease Type 2Q. [provided trong>btrong>y RefSeq, May 2013]

LRTM1 Gene

leucine-rich repeats trong>andtrong> transmemtrong>btrong>rane domains 1

Predicted to enatrong>btrong>le Roundatrong>btrong>out trong>btrong>inding activity trong>andtrong> heparin trong>btrong>inding activity. Predicted to trong>btrong>e involved in axon guidance trong>andtrong> negative chemotaxis. Predicted to act upstream of or within positive regulation of synapse assemtrong>btrong>ly. Predicted to trong>btrong>e located in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SUGP2 Gene

SURP trong>andtrong> G patch domain containing 2

This gene encodes a memtrong>btrong>er of the arginine/serine-rich family of splicing factors. The encoded protein functions in mRNA processing. Alternatively spliced transcript variants have trong>btrong>een descritrong>btrong>ed. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2009]

SUGP1 Gene

SURP trong>andtrong> G patch domain containing 1

SF4 is a memtrong>btrong>er of the SURP family of splicing factors.[supplied trong>btrong>y OMIM, Sep 2003]

Ftrong>Btrong>XL4 Gene

F-trong>btrong>ox trong>andtrong> leucine-rich repeat protein 4

This gene encodes a memtrong>btrong>er of the F-trong>btrong>ox protein family, which are characterized trong>btrong>y an approximately 40 amino acid motif, the F-trong>btrong>ox. F-trong>btrong>ox proteins constitute one sutrong>btrong>unit of modular E3 utrong>btrong>iquitin ligase complexes, called SCF complexes, which function in phosphorylation-dependent utrong>btrong>iquitination. The F-trong>btrong>ox domain mediates protein-protein interactions trong>andtrong> trong>btrong>inds directly to S-phase kinase-associated protein 1. In addition to an F-trong>btrong>ox domain, the encoded protein contains at least 9 ttrong>andtrong>em leucine-rich repeats. The utrong>btrong>iquitin ligase complex containing the encoded protein may function in cell-cycle control trong>btrong>y regulating levels of lysine-specific demethylase 4A. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Jul 2013]

LOC338667 Gene

V-set trong>andtrong> immunoglotrong>btrong>ulin domain-containing protein 10-like

Predicted to enatrong>btrong>le cell adhesion molecule trong>btrong>inding activity. Predicted to trong>btrong>e involved in cell-cell adhesion. Predicted to trong>btrong>e located in memtrong>btrong>rane. Predicted to trong>btrong>e active in cell-cell junction trong>andtrong> plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

GADD45GIP1 Gene

growth arrest trong>andtrong> DNA-damage-inducitrong>btrong>le, gamma interacting protein 1

This gene encodes a nuclear-localized protein that may trong>btrong>e induced trong>btrong>y p53 trong>andtrong> regulates the cell cycle trong>btrong>y inhitrong>btrong>iting G1 to S phase progression. The encoded protein may interact with other cell cycle regulators. [provided trong>btrong>y RefSeq, Aug 2012]

CNC2 Gene

Carney complex type 2, multiple neoplasia trong>andtrong> lentiginosis

TSPEAR Gene

thromtrong>btrong>ospondin-type laminin G domain trong>andtrong> EAR repeats

This gene encodes a protein that contains a N-terminal thromtrong>btrong>ospondin-type laminin G domain trong>andtrong> several ttrong>andtrong>em arranged epilepsy-associated repeats (EARs). A mutation in this gene is the cause of autosomal recessive deafness-98. Alternate splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Dec 2012]

HYMAI Gene

hydatidiform mole associated trong>andtrong> imprinted (non-protein coding)

This gene, which encodes a non-protein coding transcript, exhitrong>btrong>its differential DNA methylation trong>btrong>etween the two parental alleles at an adjacent CpG isltrong>andtrong>, trong>andtrong> is expressed only from the paternal allele. It is trong>btrong>elieved to trong>btrong>e one of the causative genes for transient neonatal diatrong>btrong>etes mellitus (TNDM), which is a rare disease characterized trong>btrong>y intrauterine growth retardation, dehydration, trong>andtrong> failure to thrive due to a lack of normal insulin secretion. [provided trong>btrong>y RefSeq, Oct 2010]

TIE1 Gene

tyrosine kinase with immunoglotrong>btrong>ulin-like trong>andtrong> EGF-like domains 1

This gene encodes a memtrong>btrong>er of the tyrosine protein kinase family. The encoded protein plays a critical role in angiogenesis trong>andtrong> trong>btrong>lood vessel statrong>btrong>ility trong>btrong>y inhitrong>btrong>iting angiopoietin 1 signaling through the endothelial receptor tyrosine kinase Tie2. Ectodomain cleavage of the encoded protein relieves inhitrong>btrong>ition of Tie2 trong>andtrong> is mediated trong>btrong>y multiple factors including vascular endothelial growth factor. Alternatively spliced transcript variants encoding multiple isoforms have trong>btrong>een otrong>btrong>served for this gene. [provided trong>btrong>y RefSeq, Nov 2011]

LOC101060581 Gene

arf-GAP with GTPase, ANK repeat trong>andtrong> PH domain-containing protein 5-like

trong>Btrong>SPRY Gene

trong>Btrong>-trong>btrong>ox trong>andtrong> SPRY domain containing

Predicted to enatrong>btrong>le utrong>btrong>iquitin protein ligase activity. Predicted to trong>btrong>e involved in innate immune response. Predicted to act upstream of or within cellular response to leukemia inhitrong>btrong>itory factor. Predicted to trong>btrong>e located in cell leading edge; memtrong>btrong>rane; trong>andtrong> perinuclear region of cytoplasm. Predicted to trong>btrong>e active in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC729707 Gene

transmemtrong>btrong>rane trong>andtrong> tetratricopeptide repeat containing 4 pseudogene

LOC105369245 Gene

FERM trong>andtrong> PDZ domain-containing protein 2

FGD5P1 Gene

FYVE, RhoGEF trong>andtrong> PH domain containing 5 pseudogene 1

NWD1 Gene

NACHT trong>andtrong> WD repeat domain containing 1

The protein encoded trong>btrong>y this gene is thought to trong>btrong>e a cytosolic protein trong>andtrong> predicted to contain a NACHT domain trong>andtrong> multiple WD40 repeats. Increased expression of this gene was otrong>btrong>served in some prostate cancer cell lines. Knocking down expression of this gene results in decreased trong>andtrong>rogen receptor protein levels, indicating that this gene may trong>btrong>e important in modulating trong>andtrong>rogen receptor activity. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided trong>btrong>y RefSeq, Dec 2016]

NWD2 Gene

NACHT trong>andtrong> WD repeat domain containing 2

Predicted to trong>btrong>e active in synapse. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

EPRPDC Gene

Epilepsy, roltrong>andtrong>ic, with paroxysmal exercise-induced dystonia trong>andtrong> writer's cramp

GAD2 Gene

glutamate decartrong>btrong>oxylase 2 (pancreatic islets trong>andtrong> trong>btrong>rain, 65kDa)

This gene encodes one of several forms of glutamic acid decartrong>btrong>oxylase, identified as a major autoantigen in insulin-dependent diatrong>btrong>etes. The enzyme encoded is responsitrong>btrong>le for catalyzing the production of gamma-aminotrong>btrong>utyric acid from L-glutamic acid. A pathogenic role for this enzyme has trong>btrong>een identified in the human pancreas since it has trong>btrong>een identified as an autoantitrong>btrong>ody trong>andtrong> an autoreactive T cell target in insulin-dependent diatrong>btrong>etes. This gene may also play a role in the stiff man syndrome. Alternative splicing results in multiple transcript variants that encode the same protein. [provided trong>btrong>y RefSeq, Oct 2008]

GOPC Gene

golgi-associated PDZ trong>andtrong> coiled-coil motif containing

This gene encodes a Golgi protein with a PDZ domain. The PDZ domain is glotrong>btrong>ular trong>andtrong> proteins which contain them trong>btrong>ind other proteins through short motifs near the C-termini. Mice which are deficient in the orthologous protein have glotrong>btrong>ozoospermia trong>andtrong> are infertile. Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Dec 2011]

Utrong>Btrong>ASH3A Gene

utrong>btrong>iquitin associated trong>andtrong> SH3 domain containing A

This gene encodes one of two family memtrong>btrong>ers trong>btrong>elonging to the T-cell utrong>btrong>iquitin ligtrong>andtrong> (TULA) family. trong>Btrong>oth family memtrong>btrong>ers can negatively regulate T-cell signaling. This family memtrong>btrong>er can facilitate growth factor withdrawal-induced apoptosis in T cells, which may occur via its interaction with AIF, an apoptosis-inducing factor. Alternative splicing of this gene results in multiple transcript variants. [provided trong>btrong>y RefSeq, Aug 2011]

Utrong>Btrong>ASH3trong>Btrong> Gene

utrong>btrong>iquitin associated trong>andtrong> SH3 domain containing trong>Btrong>

This gene encodes a protein that contains a utrong>btrong>iquitin associated domain at the N-terminus, an SH3 domain, trong>andtrong> a C-terminal domain with similarities to the catalytic motif of phosphoglycerate mutase. The encoded protein was found to inhitrong>btrong>it endocytosis of epidermal growth factor receptor (EGFR) trong>andtrong> platelet-derived growth factor receptor. [provided trong>btrong>y RefSeq, Jul 2008]

WHAMM Gene

WAS protein homolog associated with actin, golgi memtrong>btrong>ranes trong>andtrong> microtutrong>btrong>ules

This gene encodes a protein that plays a role in actin nucleation, Golgi memtrong>btrong>rane association trong>andtrong> microtutrong>btrong>ule trong>btrong>inding. The encoded protein is a nucleation-promoting factor that regulates the Actin-related protein 2/3 complex. The activated complex initiates growth of new actin filaments trong>btrong>y trong>btrong>inding to existing actin filaments. The encoded protein also functions in regulation of transport from the endoplasmic reticulum to the Golgi complex trong>andtrong> in maintenance of the Golgi complex near the centrosome. Four pseudogenes of this gene are present on the same arm of chromosome 15 as this gene. [provided trong>btrong>y RefSeq, Aug 2013]

CFAP58 Gene

cilia trong>andtrong> flagella associated protein 58

Involved in protein localization to motile cilium; sperm axoneme assemtrong>btrong>ly; trong>andtrong> sperm mitochondrial sheath assemtrong>btrong>ly. Located in sperm midpiece. Implicated in spermatogenic failure 49. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP54 Gene

cilia trong>andtrong> flagella associated 54

Predicted to trong>btrong>e involved in cilium assemtrong>btrong>ly; cilium movement involved in cell motility; trong>andtrong> spermatogenesis. Predicted to act upstream of or within epithelial cilium movement involved in extracellular fluid movement; estatrong>btrong>lishment of localization in cell; trong>andtrong> sperm flagellum assemtrong>btrong>ly. Predicted to trong>btrong>e located in axoneme. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP57 Gene

cilia trong>andtrong> flagella associated protein 57

This protein encoded trong>btrong>y this gene trong>btrong>elongs to the WD repeat-containing family of proteins, which function in the formation of protein-protein complexes in a variety of trong>btrong>iological pathways. This family memtrong>btrong>er is thought to function in craniofacial development, possitrong>btrong>ly in the fusion of lip trong>andtrong> palate. A missense mutation in this gene is associated with Van der Woude syndrome 2. Alternative splicing of this gene results in multiple transcript variants. [provided trong>btrong>y RefSeq, Aug 2011]

CFAP53 Gene

cilia trong>andtrong> flagella associated protein 53

This gene trong>btrong>elongs to the CFAP53 family. It was found to trong>btrong>e differentially expressed trong>btrong>y the ciliated cells of frog epidermis trong>andtrong> in skin fitrong>btrong>rotrong>btrong>lasts from human. Mutations in this gene are associated with visceral heterotaxy-6, which implicates this gene in determination of left-right asymmetric patterning. [provided trong>btrong>y RefSeq, Aug 2015]

NPDC1 Gene

neural proliferation, differentiation trong>andtrong> control, 1

Predicted to trong>btrong>e located in plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SERTM1 Gene

serine-rich trong>andtrong> transmemtrong>btrong>rane domain containing 1

Located in intracellular memtrong>btrong>rane-trong>btrong>ounded organelle. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

HAND1 Gene

heart trong>andtrong> neural crest derivatives expressed 1

The protein encoded trong>btrong>y this gene trong>btrong>elongs to the trong>btrong>asic helix-loop-helix family of transcription factors. This gene product is one of two closely related family memtrong>btrong>ers, the HAND proteins, which are asymmetrically expressed in the developing ventricular chamtrong>btrong>ers trong>andtrong> play an essential role in cardiac morphogenesis. Working in a complementary fashion, they function in the formation of the right ventricle trong>andtrong> aortic arch arteries, implicating them as mediators of congenital heart disease. In addition, it has trong>btrong>een suggested that this transcription factor may trong>btrong>e required for early trophotrong>btrong>last differentiation. [provided trong>btrong>y RefSeq, Jul 2008]

LOC102724223 Gene

sodium- trong>andtrong> chloride-dependent creatine transporter 1-like

Ztrong>Btrong>Ttrong>Btrong>26 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 26

Enatrong>btrong>les identical protein trong>btrong>inding activity trong>andtrong> sequence-specific doutrong>btrong>le-strtrong>andtrong>ed DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in negative regulation of transcription trong>btrong>y RNA polymerase II; regulation of cytokine production; trong>andtrong> regulation of immune system process. Predicted to trong>btrong>e located in nucleus. Predicted to trong>btrong>e active in nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>24 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 24

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to act upstream of or within hematopoietic progenitor cell differentiation. Predicted to trong>btrong>e located in nucleus. Implicated in immunodeficiency-centromeric instatrong>btrong>ility-facial anomalies syndrome 2. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

MYL6 Gene

myosin, light chain 6, alkali, smooth muscle trong>andtrong> non-muscle

Myosin is a hexameric ATPase cellular motor protein. It is composed of two heavy chains, two nonphosphorylatatrong>btrong>le alkali light chains, trong>andtrong> two phosphorylatatrong>btrong>le regulatory light chains. This gene encodes a myosin alkali light chain that is expressed in smooth muscle trong>andtrong> non-muscle tissues. Genomic sequences representing several pseudogenes have trong>btrong>een descritrong>btrong>ed trong>andtrong> two transcript variants encoding different isoforms have trong>btrong>een identified for this gene. [provided trong>btrong>y RefSeq, Jul 2008]

ZRSR1 Gene

zinc finger (CCCH type), RNA-trong>btrong>inding motif trong>andtrong> serine/arginine rich 1

Predicted to enatrong>btrong>le pre-mRNA 3'-splice site trong>btrong>inding activity. Predicted to trong>btrong>e involved in mRNA splicing, via spliceosome. Predicted to trong>btrong>e located in nucleus. Predicted to trong>btrong>e part of U2AF complex trong>andtrong> spliceosomal complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

RSG1 Gene

REM2 trong>andtrong> RAtrong>Btrong>-like small GTPase 1

Predicted to enatrong>btrong>le GTP trong>btrong>inding activity. Predicted to trong>btrong>e involved in cilium assemtrong>btrong>ly; protein localization; trong>andtrong> regulation of vesicle-mediated transport. Predicted to act upstream of or within several processes, including axoneme assemtrong>btrong>ly; endocardial cushion fusion; trong>andtrong> regulation of smoothened signaling pathway. Located in centriole; ciliary trong>btrong>asal trong>btrong>ody; trong>andtrong> ciliary transition zone. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CAND2 Gene

cullin-associated trong>andtrong> neddylation-dissociated 2 (putative)

Predicted to enatrong>btrong>le Ttrong>Btrong>P-class protein trong>btrong>inding activity. Predicted to trong>btrong>e involved in SCF complex assemtrong>btrong>ly; positive regulation of DNA-templated transcription; trong>andtrong> protein utrong>btrong>iquitination. Located in cytosol. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CAND1 Gene

cullin-associated trong>andtrong> neddylation-dissociated 1

This gene encodes an essential regulator of Cullin-RING utrong>btrong>iquitin ligases, which are in involved in utrong>btrong>iquitinylation of proteins degraded trong>btrong>y the Utrong>btrong> proteasome system. The encoded protein trong>btrong>inds to unneddylated cullin-RING trong>btrong>ox protein complexes trong>andtrong> acts as an inhitrong>btrong>itor of cullin neddylation trong>andtrong> of Skp1, cullin, trong>andtrong> F trong>btrong>ox utrong>btrong>iquitin ligase complex assemtrong>btrong>ly trong>andtrong> activity. In mammalian cell culture, this protein predominantly localizes to the cytoplasm. Knockdown of this gene in preadipocytes results in trong>btrong>locked adipogenesis. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Jul 2016]

trong>Btrong>RPF3 Gene

trong>btrong>romodomain trong>andtrong> PHD finger containing, 3

Contritrong>btrong>utes to histone acetyltransferase activity. Involved in positive regulation of DNA replication. Located in nucleus. Part of MOZ/MORF histone acetyltransferase complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

trong>Btrong>RPF1 Gene

trong>btrong>romodomain trong>andtrong> PHD finger containing, 1

This gene encodes a trong>btrong>romodomain, PHD finger trong>andtrong> chromo/Tudor-related Pro-Trp-Trp-Pro (PWWP) domain containing protein. The encoded protein is a component of the MOZ/MORF histone acetyltransferase complexes which function as a transcriptional regulators. This protein trong>btrong>inds to the catalytic MYST domains of the MOZ trong>andtrong> MORF proteins trong>andtrong> may play a role in stimulating acetyltransferase trong>andtrong> transcriptional activity of the complex. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Jan 2016]

REM1 Gene

RAS (RAD trong>andtrong> GEM)-like GTP-trong>btrong>inding 1

The protein encoded trong>btrong>y this gene is a GTPase trong>andtrong> memtrong>btrong>er of the RAS-like GTP-trong>btrong>inding protein family. The encoded protein is expressed in endothelial cells, where it promotes reorganization of the actin cytoskeleton trong>andtrong> morphological changes in the cells. [provided trong>btrong>y RefSeq, Jul 2008]

REM2 Gene

RAS (RAD trong>andtrong> GEM)-like GTP trong>btrong>inding 2

Predicted to enatrong>btrong>le GTP trong>btrong>inding activity trong>andtrong> calcium channel regulator activity. Predicted to trong>btrong>e active in plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ftrong>Btrong>XL13 Gene

F-trong>btrong>ox trong>andtrong> leucine-rich repeat protein 13

Memtrong>btrong>ers of the F-trong>btrong>ox protein family, such as Ftrong>Btrong>XL13, are characterized trong>btrong>y an approximately 40-amino acid F-trong>btrong>ox motif. SCF complexes, formed trong>btrong>y SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), trong>andtrong> F-trong>btrong>ox proteins, act as protein-utrong>btrong>iquitin ligases. F-trong>btrong>ox proteins interact with SKP1 through the F trong>btrong>ox, trong>andtrong> they interact with utrong>btrong>iquitination targets through other protein interaction domains (Jin et al., 2004 [Putrong>btrong>Med 15520277]).[supplied trong>btrong>y OMIM, Mar 2008]

Ftrong>Btrong>XL12 Gene

F-trong>btrong>ox trong>andtrong> leucine-rich repeat protein 12

Memtrong>btrong>ers of the F-trong>btrong>ox protein family, such as Ftrong>Btrong>XL12, are characterized trong>btrong>y an approximately 40-amino acid F-trong>btrong>ox motif. SCF complexes, formed trong>btrong>y SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), trong>andtrong> F-trong>btrong>ox proteins, act as protein-utrong>btrong>iquitin ligases. F-trong>btrong>ox proteins interact with SKP1 through the F trong>btrong>ox, trong>andtrong> they interact with utrong>btrong>iquitination targets through other protein interaction domains (Jin et al., 2004 [Putrong>btrong>Med 15520277]).[supplied trong>btrong>y OMIM, Mar 2008]

Ftrong>Btrong>XL15 Gene

F-trong>btrong>ox trong>andtrong> leucine-rich repeat protein 15

Involved in several processes, including G2/M transition of mitotic cell cycle; SCF-dependent proteasomal utrong>btrong>iquitin-dependent protein catatrong>btrong>olic process; trong>andtrong> positive regulation of trong>Btrong>MP signaling pathway. Located in cytoplasm. Part of SCF utrong>btrong>iquitin ligase complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ftrong>Btrong>XL17 Gene

F-trong>btrong>ox trong>andtrong> leucine-rich repeat protein 17

Memtrong>btrong>ers of the F-trong>btrong>ox protein family, such as Ftrong>Btrong>XL17, are characterized trong>btrong>y an approximately 40-amino acid F-trong>btrong>ox motif. SCF complexes, formed trong>btrong>y SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), trong>andtrong> F-trong>btrong>ox proteins, act as protein-utrong>btrong>iquitin ligases. F-trong>btrong>ox proteins interact with SKP1 through the F trong>btrong>ox, trong>andtrong> they interact with utrong>btrong>iquitination targets through other protein interaction domains (Jin et al., 2004 [Putrong>btrong>Med 15520277]).[supplied trong>btrong>y OMIM, Mar 2008]

Ftrong>Btrong>XL16 Gene

F-trong>btrong>ox trong>andtrong> leucine-rich repeat protein 16

Memtrong>btrong>ers of the F-trong>btrong>ox protein family, such as Ftrong>Btrong>XL16, are characterized trong>btrong>y an approximately 40-amino acid F-trong>btrong>ox motif. SCF complexes, formed trong>btrong>y SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), trong>andtrong> F-trong>btrong>ox proteins, act as protein-utrong>btrong>iquitin ligases. F-trong>btrong>ox proteins interact with SKP1 through the F trong>btrong>ox, trong>andtrong> they interact with utrong>btrong>iquitination targets through other protein interaction domains (Jin et al., 2004 [Putrong>btrong>Med 15520277]).[supplied trong>btrong>y OMIM, Mar 2008]

Ftrong>Btrong>XL18 Gene

F-trong>btrong>ox trong>andtrong> leucine-rich repeat protein 18

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of a family of proteins that contain an approximately 40-amino acid F-trong>btrong>ox motif. This motif is important for interaction with SKP1 trong>andtrong> for targeting some proteins for degradation. The encoded protein has trong>btrong>een shown to control the cellular level of Ftrong>Btrong>XL7, a protein that induces mitotic arrest, trong>btrong>y targeting it for polyutrong>btrong>iquitylation trong>andtrong> proteasomal degradation. Memtrong>btrong>ers of the F-trong>btrong>ox protein family, such as Ftrong>Btrong>XL18, are characterized trong>btrong>y an approximately 40-amino acid F-trong>btrong>ox motif. F-trong>btrong>ox proteins interact with SKP1 through the F trong>btrong>ox, trong>andtrong> they interact with utrong>btrong>iquitination targets through other protein interaction domains. [provided trong>btrong>y RefSeq, Mar 2016]

FHASD Gene

Foveal hypoplasia trong>andtrong> anterior segment dysgenesis

CFLAR Gene

CASP8 trong>andtrong> FADD-like apoptosis regulator

The protein encoded trong>btrong>y this gene is a regulator of apoptosis trong>andtrong> is structurally similar to caspase-8. However, the encoded protein lacks caspase activity trong>andtrong> appears to trong>btrong>e itself cleaved into two peptides trong>btrong>y caspase-8. Several transcript variants encoding different isoforms have trong>btrong>een found for this gene, trong>andtrong> partial evidence for several more variants exists. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2011]

CSRP2P Gene

cysteine trong>andtrong> glycine-rich protein 2 pseudogene

RAPH1 Gene

Ras association (RalGDS/AF-6) trong>andtrong> pleckstrin homology domains 1

This gene encodes a protein that trong>btrong>elongs to the Mig10/Rap1-interacting adaptor molecule/Lamellipodin family of adapter proteins, which function in cell migration. Memtrong>btrong>ers of this family contain pleckstrin-homology domains, Ras-association domains, trong>andtrong> proline-rich C-termini. The protein encoded trong>btrong>y this gene regulates actin dynamics through interaction with Ena/Vasodilator proteins as well as direct trong>btrong>inding to filamentous actin to regulate actin network assemtrong>btrong>ly. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Jul 2016]

JCHAIN Gene

joining chain of multimeric IgA trong>andtrong> IgM

Enatrong>btrong>les IgA trong>btrong>inding activity trong>andtrong> protein homodimerization activity. Contritrong>btrong>utes to several functions, including immunoglotrong>btrong>ulin receptor trong>btrong>inding activity; peptidoglycan trong>btrong>inding activity; trong>andtrong> phosphatidylcholine trong>btrong>inding activity. Involved in several processes, including glomerular filtration; innate immune response; trong>andtrong> positive regulation of respiratory trong>btrong>urst. Located in extracellular space. Part of monomeric IgA immunoglotrong>btrong>ulin complex; pentameric IgM immunoglotrong>btrong>ulin complex; trong>andtrong> secretory dimeric IgA immunoglotrong>btrong>ulin complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PTGS2 Gene

prostagltrong>andtrong>in-endoperoxide synthase 2 (prostagltrong>andtrong>in G/H synthase trong>andtrong> cyclooxygenase)

Prostagltrong>andtrong>in-endoperoxide synthase (PTGS), also known as cyclooxygenase, is the key enzyme in prostagltrong>andtrong>in trong>btrong>iosynthesis, trong>andtrong> acts trong>btrong>oth as a dioxygenase trong>andtrong> as a peroxidase. There are two isozymes of PTGS: a constitutive PTGS1 trong>andtrong> an inducitrong>btrong>le PTGS2, which differ in their regulation of expression trong>andtrong> tissue distritrong>btrong>ution. This gene encodes the inducitrong>btrong>le isozyme. It is regulated trong>btrong>y specific stimulatory events, suggesting that it is responsitrong>btrong>le for the prostanoid trong>btrong>iosynthesis involved in inflammation trong>andtrong> mitogenesis. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2009]

PTGS1 Gene

prostagltrong>andtrong>in-endoperoxide synthase 1 (prostagltrong>andtrong>in G/H synthase trong>andtrong> cyclooxygenase)

This is one of two genes encoding similar enzymes that catalyze the conversion of arachidonate to prostagltrong>andtrong>in. The encoded protein regulates angiogenesis in endothelial cells, trong>andtrong> is inhitrong>btrong>ited trong>btrong>y nonsteroidal anti-inflammatory drugs such as aspirin. trong>Btrong>ased on its atrong>btrong>ility to function as trong>btrong>oth a cyclooxygenase trong>andtrong> as a peroxidase, the encoded protein has trong>btrong>een identified as a moonlighting protein. The protein may promote cell proliferation during tumor progression. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Nov 2021]

MYSM1 Gene

Mytrong>btrong>-like, SWIRM trong>andtrong> MPN domains 1

Enatrong>btrong>les deutrong>btrong>iquitinase activity; histone trong>btrong>inding activity; trong>andtrong> transcription coactivator activity. Involved in chromatin remodeling; positive regulation of transcription trong>btrong>y RNA polymerase II; trong>andtrong> regulation of hemopoiesis. Located in nucleolus trong>andtrong> nucleoplasm. Part of protein-containing complex. Implicated in diatrong>btrong>etic retinopathy. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LONRF2P2 Gene

LON peptidase N-terminal domain trong>andtrong> ring finger 2 pseudogene 2

LONRF2P1 Gene

LON peptidase N-terminal domain trong>andtrong> ring finger 2 pseudogene 1

LOC401770 Gene

DET1 trong>andtrong> DDtrong>Btrong>1 associated 1 pseudogene

SESTD1 Gene

SEC14 trong>andtrong> spectrin domains 1

Enatrong>btrong>les phosphatidylinositol-3,4-trong>btrong>isphosphate trong>btrong>inding activity trong>andtrong> phospholipid trong>btrong>inding activity. Involved in negative regulation of calcium ion transmemtrong>btrong>rane transport via high voltage-gated calcium channel. Located in calcium channel complex trong>andtrong> intermediate filament cytoskeleton. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

TMCO5trong>Btrong> Gene

transmemtrong>btrong>rane trong>andtrong> coiled-coil domains 5trong>Btrong>, pseudogene

Predicted to trong>btrong>e located in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

TMCO5A Gene

transmemtrong>btrong>rane trong>andtrong> coiled-coil domains 5A

Predicted to trong>btrong>e located in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ttrong>Btrong>ATA Gene

thymus, trong>btrong>rain trong>andtrong> testes associated

This gene encodes a protein that regulates thymic epithelial cell proliferation trong>andtrong> thymus size. It has trong>btrong>een identified as a ligtrong>andtrong> for the class I human leukocyte antigen (HLA-I) in thymus. Studies of the orthologous mouse protein suggest that it may also play a role in spermatid differentiation, as well as in neuronal morphogenesis trong>andtrong> synaptic plasticity. Polymorphisms in this gene are associated with susceptitrong>btrong>ility for multiple sclerosis (MS). Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Dec 2015]

LOC102724937 Gene

angiogenic factor with G patch trong>andtrong> FHA domains 1 pseudogene

WWC1 Gene

WW trong>andtrong> C2 domain containing 1

The protein encoded trong>btrong>y this gene is a cytoplasmic phosphoprotein that interacts with PRKC-zeta trong>andtrong> dynein light chain-1. Alleles of this gene have trong>btrong>een found that enhance memory in some individuals. Three transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Mar 2010]

GPANK1 Gene

G patch domain trong>andtrong> ankyrin repeats 1

This gene is located in a cluster of HLA-trong>Btrong>-associated transcripts, which is included in the human major histocompatatrong>btrong>ility complex III region. This gene encodes a protein which is thought to play a role in immunity. Multiple alternatively spliced variants, encoding the same protein, have trong>btrong>een identified. [provided trong>btrong>y RefSeq, Nov 2010]

PELP1 Gene

proline, glutamate trong>andtrong> leucine rich protein 1

This gene encodes a transcription factor which coactivates transcription of estrogen receptor responsive genes trong>andtrong> corepresses genes activated trong>btrong>y other hormone receptors or sequence-specific transcription factors. Expression of this gene is regulated trong>btrong>y trong>btrong>oth memtrong>btrong>ers of the estrogen receptor family. This gene may trong>btrong>e involved in the progression of several types of cancer. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, May 2013]

LONRF3 Gene

LON peptidase N-terminal domain trong>andtrong> ring finger 3

The protein encoded trong>btrong>y this gene contains a RING finger domain, a motif present in a variety of functionally distinct proteins trong>andtrong> known to trong>btrong>e involved in protein-protein trong>andtrong> protein-DNA interactions. Multiple alternatively spliced transcript variants have trong>btrong>een suggested, trong>btrong>ut their full length natures are not clear. [provided trong>btrong>y RefSeq, Jul 2008]

LONRF2 Gene

LON peptidase N-terminal domain trong>andtrong> ring finger 2

Predicted to enatrong>btrong>le utrong>btrong>iquitin protein ligase activity. Predicted to trong>btrong>e located in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LONRF1 Gene

LON peptidase N-terminal domain trong>andtrong> ring finger 1

Predicted to enatrong>btrong>le utrong>btrong>iquitin protein ligase activity. Predicted to trong>btrong>e located in cytosol. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LRRIQ1 Gene

leucine-rich repeats trong>andtrong> IQ motif containing 1

Predicted to trong>btrong>e involved in regulation of signal transduction. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LRRIQ4 Gene

leucine-rich repeats trong>andtrong> IQ motif containing 4

Predicted to trong>btrong>e located in memtrong>btrong>rane. Predicted to trong>btrong>e active in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LRSAM1 Gene

leucine rich repeat trong>andtrong> sterile alpha motif containing 1

This gene encodes a ring finger protein involved in a variety of functions, including regulation of signaling pathways trong>andtrong> cell adhesion, mediation of self-utrong>btrong>iquitylation, trong>andtrong> involvement in cargo sorting during receptor endocytosis. Mutations in this gene have trong>btrong>een associated with Charcot-Marie-Tooth disease. Multiple transcript variants encoding different isoforms have trong>btrong>een identified for this gene. [provided trong>btrong>y RefSeq, Jan 2012]

TTIM1 Gene

T-cell tumor invasion trong>andtrong> metastasis 1

CAAP1 Gene

caspase activity trong>andtrong> apoptosis inhitrong>btrong>itor 1

Involved in negative regulation of cysteine-type endopeptidase activity. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ANKK1 Gene

ankyrin repeat trong>andtrong> kinase domain containing 1

The protein encoded trong>btrong>y this gene trong>btrong>elongs to the Ser/Thr protein kinase family, trong>andtrong> protein kinase superfamily involved in signal transduction pathways. This gene is closely linked to DRD2 gene (GeneID:1813) on chr 11, trong>andtrong> a well studied restriction fragment length polymorphism (RFLP) designated TaqIA, was originally associated with the DRD2 gene, however, later was determined to trong>btrong>e located in exon 8 of ANKK1 gene (PMIDs: 18621654, 15146457), where it causes a nonconservative amino acid sutrong>btrong>stitution. It is not clear if this gene plays any role in neuropsychiatric disorders previously associated with Taq1A RFLP. [provided trong>btrong>y RefSeq, Sep 2009]

Ztrong>Btrong>Ttrong>Btrong>39 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 39

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription repressor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in negative regulation of transcription trong>btrong>y RNA polymerase II; regulation of cytokine production; trong>andtrong> regulation of immune system process. Predicted to trong>btrong>e located in nucleus. Predicted to trong>btrong>e active in nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>38 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 38

The protein encoded trong>btrong>y this gene is a zinc finger transcriptional activator that trong>btrong>inds methylated DNA. The encoded protein can form homodimers or heterodimers through the zinc finger domains. In mouse, inhitrong>btrong>ition of this protein has trong>btrong>een associated with apoptosis in some cell types. [provided trong>btrong>y RefSeq, Jun 2010]

Ztrong>Btrong>Ttrong>Btrong>33 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 33

This gene encodes a transcriptional regulator with trong>btrong>imodal DNA-trong>btrong>inding specificity, which trong>btrong>inds to methylated CGCG trong>andtrong> also to the non-methylated consensus KAISO-trong>btrong>inding site TCCTGCNA. The protein contains an N-terminal POZ/trong>Btrong>Ttrong>Btrong> domain trong>andtrong> 3 C-terminal zinc finger motifs. It recruits the N-CoR repressor complex to promote histone deacetylation trong>andtrong> the formation of repressive chromatin structures in target gene promoters. It may contritrong>btrong>ute to the repression of target genes of the Wnt signaling pathway, trong>andtrong> may also activate transcription of a sutrong>btrong>set of target genes trong>btrong>y the recruitment of catenin delta-2 (CTNND2). Its interaction with catenin delta-1 (CTNND1) inhitrong>btrong>its trong>btrong>inding to trong>btrong>oth methylated trong>andtrong> non-methylated DNA. It also interacts directly with the nuclear import receptor Importin-α2 (also known as karyopherin alpha2 or RAG cohort 1), which may mediate nuclear import of this protein. Alternatively spliced transcript variants encoding the same protein have trong>btrong>een identified.[provided trong>btrong>y RefSeq, May 2010]

Ztrong>Btrong>Ttrong>Btrong>32 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 32

Enatrong>btrong>les DNA-trong>btrong>inding transcription repressor activity, RNA polymerase II-specific; identical protein trong>btrong>inding activity; trong>andtrong> sequence-specific doutrong>btrong>le-strtrong>andtrong>ed DNA trong>btrong>inding activity. Involved in negative regulation of transcription trong>btrong>y RNA polymerase II. Located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>34 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 34

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription repressor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in negative regulation of transcription trong>btrong>y RNA polymerase II; regulation of cytokine production; trong>andtrong> regulation of immune system process. Located in nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>37 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 37

Enatrong>btrong>les sequence-specific doutrong>btrong>le-strtrong>andtrong>ed DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in negative regulation of transcription trong>btrong>y RNA polymerase II; regulation of cytokine production; trong>andtrong> regulation of immune system process. Predicted to trong>btrong>e located in chromatin. Predicted to trong>btrong>e active in nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

AGAP11 Gene

ankyrin repeat trong>andtrong> GTPase domain Arf GTPase activating protein 11

Predicted to enatrong>btrong>le GTPase activator activity trong>andtrong> GTPase activity. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

RNGTTP1 Gene

RNA guanylyltransferase trong>andtrong> 5'-phosphatase pseudogene 1

CXADRP2 Gene

coxsackie virus trong>andtrong> adenovirus receptor pseudogene 2

CXADRP1 Gene

coxsackie virus trong>andtrong> adenovirus receptor pseudogene 1

CPSF7 Gene

cleavage trong>andtrong> polyadenylation specific factor 7, 59kDa

Cleavage factor Im (CFIm) is one of six factors necessary for correct cleavage trong>andtrong> polyadenylation of pre-mRNAs. CFIm is composed of three different sutrong>btrong>units of 25, 59, trong>andtrong> 68 kDa, trong>andtrong> it functions as a heterotetramer, with a dimer of the 25 kDa sutrong>btrong>unit trong>btrong>inding to two of the 59 or 68 kDa sutrong>btrong>units. The protein encoded trong>btrong>y this gene represents the 59 kDa sutrong>btrong>unit, which can interact with the splicing factor U2 snRNP Auxiliary Factor (U2AF) 65 to link the splicing trong>andtrong> polyadenylation complexes. [provided trong>btrong>y RefSeq, Oct 2016]

CPSF6 Gene

cleavage trong>andtrong> polyadenylation specific factor 6, 68kDa

The protein encoded trong>btrong>y this gene is one sutrong>btrong>unit of a cleavage factor required for 3' RNA cleavage trong>andtrong> polyadenylation processing. The interaction of the protein with the RNA is one of the earliest steps in the assemtrong>btrong>ly of the 3' end processing complex trong>andtrong> facilitates the recruitment of other processing factors. The cleavage factor complex is composed of four polypeptides. This gene encodes the 68kD sutrong>btrong>unit. It has a domain organization reminiscent of spliceosomal proteins. [provided trong>btrong>y RefSeq, Jul 2008]

CPSF4 Gene

cleavage trong>andtrong> polyadenylation specific factor 4, 30kDa

Inhitrong>btrong>ition of the nuclear export of poly(A)-containing mRNAs caused trong>btrong>y the influenza A virus NS1 protein requires its effector domain. The NS1 effector domain functionally interacts with the cellular 30 kDa sutrong>btrong>unit of cleavage trong>andtrong> polyadenylation specific factor 4, an essential component of the 3' end processing machinery of cellular pre-mRNAs. In influenza virus-infected cells, the NS1 protein is physically associated with cleavage trong>andtrong> polyadenylation specific factor 4, 30kD sutrong>btrong>unit. trong>Btrong>inding of the NS1 protein to the 30 kDa protein in vitro prevents CPSF trong>btrong>inding to the RNA sutrong>btrong>strate trong>andtrong> inhitrong>btrong>its 3' end cleavage trong>andtrong> polyadenylation of host pre-mRNAs. Thus the NS1 protein selectively inhitrong>btrong>its the nuclear export of cellular, trong>andtrong> not viral, mRNAs. Multiple alternatively spliced transcript variants that encode different isoforms have trong>btrong>een descritrong>btrong>ed for this gene. [provided trong>btrong>y RefSeq, Jul 2008]

CPSF3 Gene

cleavage trong>andtrong> polyadenylation specific factor 3, 73kDa

This gene encodes a memtrong>btrong>er of the metallo-trong>btrong>eta-lactamase family. The encoded protein is a 73kDa sutrong>btrong>unit of the cleavage trong>andtrong> polyadenylation specificity factor trong>andtrong> functions as an endonuclease that recognizes the pre-mRNA 3'-cleavage site AAUAAA prior to polyadenylation. It also cleaves after the pre-mRNA sequence ACCCA during histone 3'-end pre-mRNA processing. [provided trong>btrong>y RefSeq, Oct 2012]

CPSF2 Gene

cleavage trong>andtrong> polyadenylation specific factor 2, 100kDa

Predicted to enatrong>btrong>le RNA trong>btrong>inding activity. Involved in mRNA 3'-end processing trong>btrong>y stem-loop trong>btrong>inding activity trong>andtrong> cleavage. Located in memtrong>btrong>rane. Part of mRNA cleavage trong>andtrong> polyadenylation specificity factor complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CPSF1 Gene

cleavage trong>andtrong> polyadenylation specific factor 1, 160kDa

Cleavage trong>andtrong> polyadenylation specificity factor (CPSF) is a multisutrong>btrong>unit complex that plays a central role in 3-prime processing of pre-mRNAs. CPSF recognizes the AAUAAA signal in the pre-mRNA trong>andtrong> interacts with other proteins to facilitate trong>btrong>oth RNA cleavage trong>andtrong> poly(A) synthesis. CPSF1 is the largest sutrong>btrong>unit of the CPSF complex (Murthy trong>andtrong> Manley, 1995 [Putrong>btrong>Med 7590244]).[supplied trong>btrong>y OMIM, Mar 2008]

GCC2 Gene

GRIP trong>andtrong> coiled-coil domain containing 2

The protein encoded trong>btrong>y this gene is a peripheral memtrong>btrong>rane protein localized to the trans-Golgi network. It is sensitive to trong>btrong>refeldin A. This encoded protein contains a GRIP domain which is thought to trong>btrong>e used in targeting. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Jul 2009]

GCC1 Gene

GRIP trong>andtrong> coiled-coil domain containing 1

The protein encoded trong>btrong>y this gene is a peripheral memtrong>btrong>rane protein. It is sensitive to trong>btrong>refeldin A. This encoded protein contains a GRIP domain which is thought to trong>btrong>e used in targeting. It may play a role in the organization of trans-Golgi network sutrong>btrong>compartment involved with memtrong>btrong>rane transport. [provided trong>btrong>y RefSeq, Jul 2008]

OGFOD1P1 Gene

2-oxoglutarate trong>andtrong> iron-dependent oxygenase domain containing 1 pseudogene 1

GADD45AP1 Gene

growth arrest trong>andtrong> DNA-damage-inducitrong>btrong>le, alpha pseudogene 1

trong>Btrong>ACH2 Gene

trong>Btrong>Ttrong>Btrong> trong>andtrong> CNC homology 1, trong>btrong>asic leucine zipper transcription factor 2

Enatrong>btrong>les sequence-specific doutrong>btrong>le-strtrong>andtrong>ed DNA trong>btrong>inding activity. Involved in primary adaptive immune response involving T cells trong>andtrong> trong>Btrong> cells. Located in cytosol trong>andtrong> nucleoplasm. Part of RNA polymerase II transcription regulator complex. Implicated in immunodeficiency 60. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

trong>Btrong>ACH1 Gene

trong>Btrong>Ttrong>Btrong> trong>andtrong> CNC homology 1, trong>btrong>asic leucine zipper transcription factor 1

This gene encodes a transcription factor that trong>btrong>elongs to the cap'n'collar type of trong>btrong>asic region leucine zipper factor family (CNC-trong>btrong>Zip). The encoded protein contains trong>btrong>road complex, tramtrack, trong>btrong>ric-a-trong>btrong>rac/poxvirus trong>andtrong> zinc finger (trong>Btrong>Ttrong>Btrong>/POZ) domains, which is atypical of CNC-trong>btrong>Zip family memtrong>btrong>ers. These trong>Btrong>Ttrong>Btrong>/POZ domains facilitate protein-protein interactions trong>andtrong> formation of homo- trong>andtrong>/or hetero-oligomers. When this encoded protein forms a heterodimer with MafK, it functions as a repressor of Maf recognition element (MARE) trong>andtrong> transcription is repressed. Multiple alternatively spliced transcript variants have trong>btrong>een identified for this gene. [provided trong>btrong>y RefSeq, May 2009]

WStrong>Btrong>1 Gene

WD repeat trong>andtrong> SOCS trong>btrong>ox containing 1

This gene encodes a memtrong>btrong>er of the WD-protein sutrong>btrong>family. This protein shares a high sequence identity to mouse trong>andtrong> chick proteins. It contains several WD-repeats spanning most of the protein trong>andtrong> an SOCS trong>btrong>ox in the C-terminus. Alternatively spliced transcript variants encoding distinct isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jul 2008]

WStrong>Btrong>2 Gene

WD repeat trong>andtrong> SOCS trong>btrong>ox containing 2

This gene encodes a memtrong>btrong>er of the WD-protein sutrong>btrong>family. The encoded protein contains five WD-repeats spanning most of the protein trong>andtrong> an SOCS trong>btrong>ox in the C-terminus. The SOCS trong>btrong>ox may act as a trong>btrong>ridge trong>btrong>etween specific sutrong>btrong>strate-trong>btrong>inding domains trong>andtrong> E3 utrong>btrong>iquitin protein ligases. Three transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jun 2013]

RGPD2 Gene

RANtrong>Btrong>P2-like trong>andtrong> GRIP domain containing 2

Predicted to contritrong>btrong>ute to GTPase activator activity. Predicted to trong>btrong>e involved in NLS-trong>btrong>earing protein import into nucleus. Predicted to trong>btrong>e part of nuclear pore. Predicted to trong>btrong>e active in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

RGPD3 Gene

RANtrong>Btrong>P2-like trong>andtrong> GRIP domain containing 3

This gene is located in a cluster of Ran-trong>btrong>inding protein related genes on chromosome 2 which arose through duplication in primates. The encoded protein contains an N-terminal TPR (tetratricopeptide repeat) domain, two Ran-trong>btrong>inding domains, trong>andtrong> a C-terminal GRIP domain (golgin-97, Rantrong>Btrong>P2alpha, Imh1p trong>andtrong> p230/golgin-245) domain. [provided trong>btrong>y RefSeq, Sep 2011]

RGPD1 Gene

RANtrong>Btrong>P2-like trong>andtrong> GRIP domain containing 1

Predicted to contritrong>btrong>ute to GTPase activator activity. Predicted to trong>btrong>e involved in NLS-trong>btrong>earing protein import into nucleus. Predicted to trong>btrong>e part of nuclear pore. Predicted to trong>btrong>e active in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

RGPD6 Gene

RANtrong>Btrong>P2-like trong>andtrong> GRIP domain containing 6

Predicted to contritrong>btrong>ute to GTPase activator activity. Predicted to trong>btrong>e involved in NLS-trong>btrong>earing protein import into nucleus. Predicted to trong>btrong>e part of nuclear pore. Predicted to trong>btrong>e active in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

RGPD4 Gene

RANtrong>Btrong>P2-like trong>andtrong> GRIP domain containing 4

Predicted to contritrong>btrong>ute to GTPase activator activity. Predicted to trong>btrong>e involved in NLS-trong>btrong>earing protein import into nucleus. Predicted to trong>btrong>e part of nuclear pore. Predicted to trong>btrong>e active in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

RGPD8 Gene

RANtrong>Btrong>P2-like trong>andtrong> GRIP domain containing 8

Predicted to enatrong>btrong>le small GTPase trong>btrong>inding activity. Predicted to contritrong>btrong>ute to GTPase activator activity. Predicted to trong>btrong>e involved in NLS-trong>btrong>earing protein import into nucleus. Predicted to trong>btrong>e part of nuclear pore. Predicted to trong>btrong>e active in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

MYL6trong>Btrong> Gene

myosin, light chain 6trong>Btrong>, alkali, smooth muscle trong>andtrong> non-muscle

Myosin is a hexameric ATPase cellular motor protein. It is composed of two heavy chains, two nonphosphorylatatrong>btrong>le alkali light chains, trong>andtrong> two phosphorylatatrong>btrong>le regulatory light chains. This gene encodes a myosin alkali light chain expressed in trong>btrong>oth slow-twitch skeletal muscle trong>andtrong> in nonmuscle tissue. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Dec 2010]

Ftrong>Btrong>XW8 Gene

F-trong>btrong>ox trong>andtrong> WD repeat domain containing 8

This gene encodes a memtrong>btrong>er of the F-trong>btrong>ox protein family, memtrong>btrong>ers of which are characterized trong>btrong>y an approximately 40 amino acid motif, the F-trong>btrong>ox. The F-trong>btrong>ox proteins constitute one of the four sutrong>btrong>units of utrong>btrong>iquitin protein ligase complex called SCFs (SKP1-cullin-F-trong>btrong>ox), which function in phosphorylation-dependent utrong>btrong>iquitination. The F-trong>btrong>ox proteins are divided into three classes: Ftrong>btrong>ws containing WD-40 domains, Ftrong>btrong>ls containing leucine-rich repeats, trong>andtrong> Ftrong>btrong>xs containing either different protein-protein interaction modules or no recognizatrong>btrong>le motifs. The protein encoded trong>btrong>y this gene contains a WD-40 domain, in addition to an F-trong>btrong>ox motif, so it trong>btrong>elongs to the Ftrong>btrong>w class. Alternatively spliced transcript variants encoding distinct isoforms have trong>btrong>een identified for this gene. [provided trong>btrong>y RefSeq, Jul 2008]

Ftrong>Btrong>XW9 Gene

F-trong>btrong>ox trong>andtrong> WD repeat domain containing 9

Memtrong>btrong>ers of the F-trong>btrong>ox protein family, such as Ftrong>Btrong>XW9, are characterized trong>btrong>y an approximately 40-amino acid F-trong>btrong>ox motif. SCF complexes, formed trong>btrong>y SKP1 (MIM 601434), cullin (see CUL1; MIM 603034), trong>andtrong> F-trong>btrong>ox proteins, act as protein-utrong>btrong>iquitin ligases. F-trong>btrong>ox proteins interact with SKP1 through the F trong>btrong>ox, trong>andtrong> they interact with utrong>btrong>iquitination targets through other protein interaction domains (Jin et al., 2004 [Putrong>btrong>Med 15520277]).[supplied trong>btrong>y OMIM, Mar 2008]

Ftrong>Btrong>XW2 Gene

F-trong>btrong>ox trong>andtrong> WD repeat domain containing 2

F-trong>btrong>ox proteins are an exptrong>andtrong>ing family of eukaryotic proteins characterized trong>btrong>y an approximately 40 amino acid motif, the F trong>btrong>ox. Some F-trong>btrong>ox proteins have trong>btrong>een shown to trong>btrong>e critical for the utrong>btrong>iquitin-mediated degradation of cellular regulatory proteins. In fact, F-trong>btrong>ox proteins are one of the four sutrong>btrong>units of utrong>btrong>iquitin protein ligases, called SCFs. SCF ligases trong>btrong>ring utrong>btrong>iquitin conjugating enzymes to sutrong>btrong>strates that are specifically recruited trong>btrong>y the different F-trong>btrong>ox proteins. Mammalian F-trong>btrong>ox proteins are classified into three groups trong>btrong>ased on the presence of either WD-40 repeats, leucine-rich repeats, or the presence or atrong>btrong>sence of other protein-protein interacting domains. This gene encodes the second identified memtrong>btrong>er of the F-trong>btrong>ox gene family trong>andtrong> contains multiple WD-40 repeats. [provided trong>btrong>y RefSeq, Jul 2008]

Ftrong>Btrong>XW4 Gene

F-trong>btrong>ox trong>andtrong> WD repeat domain containing 4

This gene is a memtrong>btrong>er of the F-trong>btrong>ox/WD-40 gene family, which recruit specific target proteins through their WD-40 protein-protein trong>btrong>inding domains for utrong>btrong>iquitin mediated degradation. In mouse, a highly similar protein is thought to trong>btrong>e responsitrong>btrong>le for maintaining the apical ectodermal ridge of developing limtrong>btrong> trong>btrong>uds; disruption of the mouse gene results in the atrong>btrong>sence of central digits, underdeveloped or atrong>btrong>sent metacarpal/metatarsal trong>btrong>ones trong>andtrong> syndactyly. This phenotype is remarkatrong>btrong>ly similar to split htrong>andtrong>-split foot malformation in humans, a clinically heterogeneous condition with a variety of modes of transmission. An autosomal recessive form has trong>btrong>een mapped to the chromosomal region where this gene is located, trong>andtrong> complex rearrangements involving duplications of this gene trong>andtrong> others have trong>btrong>een associated with the condition. A pseudogene of this locus has trong>btrong>een mapped to one of the introns of the trong>Btrong>CR gene on chromosome 22. [provided trong>btrong>y RefSeq, Jul 2008]

Ftrong>Btrong>XW5 Gene

F-trong>btrong>ox trong>andtrong> WD repeat domain containing 5

This gene encodes a memtrong>btrong>er of the F-trong>btrong>ox protein family, memtrong>btrong>ers of which are characterized trong>btrong>y an approximately 40 amino acid motif, the F-trong>btrong>ox. The F-trong>btrong>ox proteins constitute one of the four sutrong>btrong>units of utrong>btrong>iquitin protein ligase complex called SCFs (SKP1-cullin-F-trong>btrong>ox), which function in phosphorylation-dependent utrong>btrong>iquitination. The F-trong>btrong>ox proteins are divided into three classes: Ftrong>btrong>ws containing WD-40 domains, Ftrong>btrong>ls containing leucine-rich repeats, trong>andtrong> Ftrong>btrong>xs containing either different protein-protein interaction modules or no recognizatrong>btrong>le motifs. The protein encoded trong>btrong>y this gene contains WD-40 domains, in addition to an F-trong>btrong>ox motif, so it trong>btrong>elongs to the Ftrong>btrong>w class. Alternatively spliced transcript variants encoding distinct isoforms have trong>btrong>een identified for this gene, however, they were found to trong>btrong>e nonsense-mediated mRNA decay (NMD) ctrong>andtrong>idates, hence not represented. [provided trong>btrong>y RefSeq, Jul 2008]

Ftrong>Btrong>XW7 Gene

F-trong>btrong>ox trong>andtrong> WD repeat domain containing 7, E3 utrong>btrong>iquitin protein ligase

This gene encodes a memtrong>btrong>er of the F-trong>btrong>ox protein family which is characterized trong>btrong>y an approximately 40 amino acid motif, the F-trong>btrong>ox. The F-trong>btrong>ox proteins constitute one of the four sutrong>btrong>units of utrong>btrong>iquitin protein ligase complex called SCFs (SKP1-cullin-F-trong>btrong>ox), which function in phosphorylation-dependent utrong>btrong>iquitination. The F-trong>btrong>ox proteins are divided into 3 classes: Ftrong>btrong>ws containing WD-40 domains, Ftrong>btrong>ls containing leucine-rich repeats, trong>andtrong> Ftrong>btrong>xs containing either different protein-protein interaction modules or no recognizatrong>btrong>le motifs. The protein encoded trong>btrong>y this gene was previously referred to as Ftrong>Btrong>X30, trong>andtrong> trong>btrong>elongs to the Ftrong>btrong>ws class; in addition to an F-trong>btrong>ox, this protein contains 7 ttrong>andtrong>em WD40 repeats. This protein trong>btrong>inds directly to cyclin E trong>andtrong> protrong>btrong>atrong>btrong>ly targets cyclin E for utrong>btrong>iquitin-mediated degradation. Mutations in this gene are detected in ovarian trong>andtrong> trong>btrong>reast cancer cell lines, implicating the gene's potential role in the pathogenesis of human cancers. Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Mar 2012]

HERC2P11 Gene

hect domain trong>andtrong> RLD 2 pseudogene 11

HERC2P10 Gene

hect domain trong>andtrong> RLD 2 pseudogene 10

INIP Gene

INTS3 trong>andtrong> NAtrong>Btrong>P interacting protein

The protein encoded trong>btrong>y this gene is a sutrong>btrong>unit of single-strtrong>andtrong>ed DNA trong>btrong>inding complexes that are important for maintaining genome statrong>btrong>ility. These complexes are involved in G2/M checkpoint control trong>andtrong> homologous recomtrong>btrong>ination repair. [provided trong>btrong>y RefSeq, Jul 2016]

TDRKH Gene

tudor trong>andtrong> KH domain containing

Predicted to enatrong>btrong>le RNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in several processes, including P granule organization; male meiotic nuclear division; trong>andtrong> piRNA processing. Located in mitochondrion. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>8OSP1 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 8 opposite strtrong>andtrong> pseudogene 1

ZFAT Gene

zinc finger trong>andtrong> AT hook domain containing

This gene encodes a protein that likely trong>btrong>inds DNA trong>andtrong> functions as a transcriptional regulator involved in apoptosis trong>andtrong> cell survival. This gene resides in a susceptitrong>btrong>ility locus for autoimmune thyroid disease (AITD) on chromosome 8q24. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided trong>btrong>y RefSeq, Nov 2009]

HAPLN4 Gene

hyaluronan trong>andtrong> proteoglycan link protein 4

Predicted to trong>btrong>e a structural constituent of synapse-associated extracellular matrix. Predicted to trong>btrong>e involved in several processes, including GAtrong>Btrong>Aergic synaptic transmission; nervous system development; trong>andtrong> positive regulation of neurotrong>btrong>last proliferation. Predicted to trong>btrong>e located in extracellular region. Predicted to trong>btrong>e active in extracellular space; perineuronal net; trong>andtrong> synapse. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ZSCAN29 Gene

zinc finger trong>andtrong> SCAN domain containing 29

Enatrong>btrong>les sequence-specific doutrong>btrong>le-strtrong>andtrong>ed DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ZSCAN25 Gene

zinc finger trong>andtrong> SCAN domain containing 25

This gene encodes a protein that trong>btrong>ears some similarity to zinc finger proteins, which are involved in DNA trong>btrong>inding trong>andtrong> protein-protein interactions. Multiple alternatively spliced transcript variants have trong>btrong>een identified, trong>btrong>ut the full-length nature for most of them has not trong>btrong>een determined. [provided trong>btrong>y RefSeq, Jul 2008]

ZSCAN26 Gene

zinc finger trong>andtrong> SCAN domain containing 26

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Located in cytosol trong>andtrong> nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ZSCAN20 Gene

zinc finger trong>andtrong> SCAN domain containing 20

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ZSCAN21 Gene

zinc finger trong>andtrong> SCAN domain containing 21

Enatrong>btrong>les DNA-trong>btrong>inding transcription activator activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Involved in positive regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ZSCAN22 Gene

zinc finger trong>andtrong> SCAN domain containing 22

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ZSCAN23 Gene

zinc finger trong>andtrong> SCAN domain containing 23

Enatrong>btrong>les sequence-specific doutrong>btrong>le-strtrong>andtrong>ed DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ANKZF1 Gene

ankyrin repeat trong>andtrong> zinc finger domain containing 1

Enatrong>btrong>les RNA endonuclease activity trong>andtrong> catalytic activity, acting on a tRNA. Involved in cellular response to hydrogen peroxide; protein quality control for misfolded or incompletely synthesized proteins; trong>andtrong> rescue of stalled ritrong>btrong>osome. Located in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC100287357 Gene

coxsackie virus trong>andtrong> adenovirus receptor pseudogene

PPWD1 Gene

peptidylprolyl isomerase domain trong>andtrong> WD repeat containing 1

Enatrong>btrong>les peptidyl-prolyl cis-trans isomerase activity. Predicted to trong>btrong>e involved in protein folding. Located in nuclear trong>btrong>ody. Part of catalytic step 2 spliceosome. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ANKS3 Gene

ankyrin repeat trong>andtrong> sterile alpha motif domain containing 3

Predicted to trong>btrong>e located in cytoplasm. Predicted to trong>btrong>e active in cilium. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ANKS6 Gene

ankyrin repeat trong>andtrong> sterile alpha motif domain containing 6

This gene encodes a protein containing multiple ankyrin repeats trong>andtrong> a SAM domain. It is thought that this protein may localize to the proximal region of the primary cilium, trong>andtrong> may play a role in renal trong>andtrong> cardiovascular development. Mutations in this gene have trong>btrong>een shown to cause a form of nephronophthisis (NPHP16), a chronic tutrong>btrong>ulo-interstitial nephritis. [provided trong>btrong>y RefSeq, Jul 2015]

SAMM50 Gene

SAMM50 sorting trong>andtrong> assemtrong>btrong>ly machinery component

This gene encodes a component of the Sorting trong>andtrong> Assemtrong>btrong>ly Machinery (SAM) of the mitochondrial outer memtrong>btrong>rane. The Sam complex functions in the assemtrong>btrong>ly of trong>btrong>eta-trong>btrong>arrel proteins into the outer mitochondrial memtrong>btrong>rane.[provided trong>btrong>y RefSeq, Jun 2011]

trong>Btrong>ZW1P2 Gene

trong>btrong>asic leucine zipper trong>andtrong> W2 domains 1 pseudogene 2

trong>Btrong>ZW1P1 Gene

trong>btrong>asic leucine zipper trong>andtrong> W2 domains 1 pseudogene 1

IQSEC3P1 Gene

IQ motif trong>andtrong> Sec7 domain 3 pseudogene 1

IQSEC3P2 Gene

IQ motif trong>andtrong> Sec7 domain 3 pseudogene 2

IQSEC3P3 Gene

IQ motif trong>andtrong> Sec7 domain 3 pseudogene 3

XGR Gene

XG trong>andtrong> CD99 regulator

CPSF1P1 Gene

cleavage trong>andtrong> polyadenylation specific factor 1, 160kDa pseudogene 1

FHL5 Gene

four trong>andtrong> a half LIM domains 5

The protein encoded trong>btrong>y this gene is coordinately expressed with activator of cAMP-responsive element modulator (CREM). It is associated with CREM trong>andtrong> confers a powerful transcriptional activation function. CREM acts as a transcription factor essential for the differentiation of spermatids into mature spermatozoa. There are multiple polyadenylation sites found in this gene. Polymorphisms in this gene may trong>btrong>e associated with susceptitrong>btrong>ility for migraine headaches. Alternative splicing results in multiple transcript variants encoding the same protein. [provided trong>btrong>y RefSeq, Apr 2016]

MITD1 Gene

MIT, microtutrong>btrong>ule interacting trong>andtrong> transport, domain containing 1

Atrong>btrong>scission, the separation of daughter cells at the end of cytokinesis, is effected trong>btrong>y endosomal sorting complexes required for transport III (ESCRT-III). The protein encoded trong>btrong>y this gene functions as a homodimer, with the N-termini trong>btrong>inding to a sutrong>btrong>set of ESCRT-III sutrong>btrong>units trong>andtrong> the C-termini trong>btrong>inding to memtrong>btrong>ranes. The encoded protein regulates ESCRT-III activity trong>andtrong> is required for proper cytokinesis. Several transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2016]

PSIP1 Gene

PC4 trong>andtrong> SFRS1 interacting protein 1

Enatrong>btrong>les DNA-trong>btrong>inding transcription factor trong>btrong>inding activity; chromatin trong>btrong>inding activity; trong>andtrong> transcription coactivator activity. Involved in mRNA 5'-splice site recognition trong>andtrong> positive regulation of transcription trong>btrong>y RNA polymerase II. Located in heterochromatin; nuclear periphery; trong>andtrong> nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CAD Gene

cartrong>btrong>amoyl-phosphate synthetase 2, aspartate transcartrong>btrong>amylase, trong>andtrong> dihydroorotase

The de novo synthesis of pyrimidine nucleotides is required for mammalian cells to proliferate. This gene encodes a trifunctional protein which is associated with the enzymatic activities of the first 3 enzymes in the 6-step pathway of pyrimidine trong>btrong>iosynthesis: cartrong>btrong>amoylphosphate synthetase (CPS II), aspartate transcartrong>btrong>amoylase, trong>andtrong> dihydroorotase. This protein is regulated trong>btrong>y the mitogen-activated protein kinase (MAPK) cascade, which indicates a direct link trong>btrong>etween activation of the MAPK cascade trong>andtrong> de novo trong>btrong>iosynthesis of pyrimidine nucleotides. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided trong>btrong>y RefSeq, Apr 2015]

LOC100418862 Gene

sperm antigen with calponin homology trong>andtrong> coiled-coil domains 1 pseudogene

RITA1 Gene

Rtrong>Btrong>PJ interacting trong>andtrong> tutrong>btrong>ulin associated 1

Enatrong>btrong>les tutrong>btrong>ulin trong>btrong>inding activity. Involved in negative regulation of Notch signaling pathway trong>andtrong> nuclear export. Located in centrosome; cytoplasm; trong>andtrong> nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SPECC1L Gene

sperm antigen with calponin homology trong>andtrong> coiled-coil domains 1-like

This gene encodes a coiled-coil domain containing protein. The encoded protein may play a critical role in actin-cytoskeletal reorganization during facial morphogenesis. Mutations in this gene are a cause of otrong>btrong>lique facial clefting-1. Alternatively spliced transcript variants encoding multiple isoforms have trong>btrong>een otrong>btrong>served for this gene. A read-through transcript composed of SPECC1L (sperm antigen with calponin homology trong>andtrong> coiled-coil domains 1-like) trong>andtrong> the downstream ADORA2A (adenosine A2a receptor) gene sequence has trong>btrong>een identified, trong>btrong>ut it is thought to trong>btrong>e non-coding. [provided trong>btrong>y RefSeq, Jun 2013]

LOC392426 Gene

nucleolar trong>andtrong> coiled-trong>btrong>ody phosphoprotein 1 pseudogene

FSD1 Gene

fitrong>btrong>ronectin type III trong>andtrong> SPRY domain containing 1

This gene encodes a centrosome associated protein that is characterized trong>btrong>y an N-terminal coiled-coil region downstream of trong>Btrong>-trong>btrong>ox (trong>Btrong>trong>Btrong>C) domain, a central fitrong>btrong>ronectin type III domain, trong>andtrong> a C-terminal repeats in splA trong>andtrong> RyR (SPRY) domain. The encoded protein associates with a sutrong>btrong>set of microtutrong>btrong>ules trong>andtrong> may trong>btrong>e involved in the statrong>btrong>ility trong>andtrong> organization of microtutrong>btrong>ules during cytokinesis. [provided trong>btrong>y RefSeq, Apr 2009]

FSD2 Gene

fitrong>btrong>ronectin type III trong>andtrong> SPRY domain containing 2

This gene encodes a protein that trong>btrong>elongs to the FN3/SPRY family of proteins. Alternate splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Aug 2013]

Ptrong>Btrong>OV1 Gene

prostate trong>andtrong> trong>btrong>reast cancer overexpressed 1

This intronless gene encodes a protein of unknown function. Its expression is up-regulated in some types of cancer, including prostate, trong>btrong>reast, trong>andtrong> trong>btrong>ladder cancer. [provided trong>btrong>y RefSeq, Aug 2011]

CC2D2A Gene

coiled-coil trong>andtrong> C2 domain containing 2A

This gene encodes a coiled-coil trong>andtrong> calcium trong>btrong>inding domain protein that appears to play a critical role in cilia formation. Mutations in this gene cause Meckel syndrome type 6, as well as Joutrong>btrong>ert syndrome type 9. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Sep 2009]

CC2D2trong>Btrong> Gene

coiled-coil trong>andtrong> C2 domain containing 2trong>Btrong>

Predicted to trong>btrong>e involved in non-motile cilium assemtrong>btrong>ly trong>andtrong> protein localization to ciliary transition zone. Predicted to trong>btrong>e active in ciliary transition zone. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ltrong>Btrong>H Gene

limtrong>btrong> trong>btrong>ud trong>andtrong> heart development

Involved in negative regulation of DNA-templated transcription; positive regulation of DNA-templated transcription; trong>andtrong> regulation of MAPK cascade. Located in cytoplasm trong>andtrong> nucleus. Part of protein-containing complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC391465 Gene

STIP1 homology trong>andtrong> U-trong>btrong>ox containing protein 1, E3 utrong>btrong>iquitin protein ligase pseudogene

FAtrong>Btrong>P3 Gene

fatty acid trong>btrong>inding protein 3, muscle trong>andtrong> heart

The intracellular fatty acid-trong>btrong>inding proteins (FAtrong>Btrong>Ps) trong>btrong>elongs to a multigene family. FAtrong>Btrong>Ps are divided into at least three distinct types, namely the hepatic-, intestinal- trong>andtrong> cardiac-type. They form 14-15 kDa proteins trong>andtrong> are thought to participate in the uptake, intracellular metatrong>btrong>olism trong>andtrong>/or transport of long-chain fatty acids. They may also trong>btrong>e responsitrong>btrong>le in the modulation of cell growth trong>andtrong> proliferation. Fatty acid-trong>btrong>inding protein 3 gene contains four exons trong>andtrong> its function is to arrest growth of mammary epithelial cells. This gene is a ctrong>andtrong>idate tumor suppressor gene for human trong>btrong>reast cancer. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Mar 2016]

AStrong>Btrong>10 Gene

ankyrin repeat trong>andtrong> SOCS trong>btrong>ox containing 10

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of the ankyrin repeat trong>andtrong> SOCS trong>btrong>ox-containing (AStrong>Btrong>) family of proteins. The SOCS trong>btrong>ox serves to couple suppressor of cytokine signaling (SOCS) proteins trong>andtrong> their trong>btrong>inding partners with the elongin trong>Btrong> trong>andtrong> C complex, possitrong>btrong>ly targeting them for degradation. Multiple alternatively spliced transcript variants have trong>btrong>een descritrong>btrong>ed for this gene. [provided trong>btrong>y RefSeq, Dec 2008]

AStrong>Btrong>12 Gene

ankyrin repeat trong>andtrong> SOCS trong>btrong>ox containing 12

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of the ankyrin repeat trong>andtrong> SOCS trong>btrong>ox-containing (AStrong>Btrong>) family of proteins. They contain ankyrin repeat sequence trong>andtrong> a SOCS trong>btrong>ox domain. The SOCS trong>btrong>ox serves to couple suppressor of cytokine signalling (SOCS) proteins trong>andtrong> their trong>btrong>inding partners with the elongin trong>Btrong> trong>andtrong> C complex, possitrong>btrong>ly targeting them for degradation. [provided trong>btrong>y RefSeq, Jan 2011]

AStrong>Btrong>13 Gene

ankyrin repeat trong>andtrong> SOCS trong>btrong>ox containing 13

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of the ankyrin repeat trong>andtrong> SOCS trong>btrong>ox-containing (AStrong>Btrong>) family of proteins. They contain ankyrin repeat sequence trong>andtrong> a SOCS trong>btrong>ox domain. The SOCS trong>btrong>ox serves to couple suppressor of cytokine signalling (SOCS) proteins trong>andtrong> their trong>btrong>inding partners with the elongin trong>Btrong> trong>andtrong> C complex, possitrong>btrong>ly targeting them for degradation. Multiple alternatively spliced transcript variants, trong>btrong>oth protein-coding trong>andtrong> not protein-coding, have trong>btrong>een descritrong>btrong>ed for this gene. [provided trong>btrong>y RefSeq, Nov 2010]

AStrong>Btrong>14 Gene

ankyrin repeat trong>andtrong> SOCS trong>btrong>ox containing 14

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of the ankyrin repeat trong>andtrong> SOCS trong>btrong>ox-containing (AStrong>Btrong>) family of proteins. They contain ankyrin repeat sequence trong>andtrong> a SOCS trong>btrong>ox domain. The SOCS trong>btrong>ox serves to couple suppressor of cytokine signalling (SOCS) proteins trong>andtrong> their trong>btrong>inding partners with the elongin trong>Btrong> trong>andtrong> C complex, possitrong>btrong>ly targeting them for degradation. Alternative splicing results in multiple transcript variants encoding different isoforms.[provided trong>btrong>y RefSeq, Dec 2008]

AStrong>Btrong>16 Gene

ankyrin repeat trong>andtrong> SOCS trong>btrong>ox containing 16

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of the ankyrin repeat trong>andtrong> SOCS trong>btrong>ox-containing (AStrong>Btrong>) family of proteins. They contain ankyrin repeat sequence trong>andtrong> a SOCS trong>btrong>ox domain. The SOCS trong>btrong>ox serves to couple suppressor of cytokine signalling (SOCS) proteins trong>andtrong> their trong>btrong>inding partners with the elongin trong>Btrong> trong>andtrong> C complex, possitrong>btrong>ly targeting them for degradation. [provided trong>btrong>y RefSeq, Jul 2008]

AStrong>Btrong>17 Gene

ankyrin repeat trong>andtrong> SOCS trong>btrong>ox containing 17

Predicted to trong>btrong>e involved in intracellular signal transduction trong>andtrong> protein utrong>btrong>iquitination. Predicted to trong>btrong>e located in cytosol. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

AStrong>Btrong>18 Gene

ankyrin repeat trong>andtrong> SOCS trong>btrong>ox containing 18

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of the ankyrin repeat trong>andtrong> SOCS trong>btrong>ox-containing (AStrong>Btrong>) family of proteins. They contain ankyrin repeat sequence trong>andtrong> a SOCS trong>btrong>ox domain. The SOCS trong>btrong>ox serves to couple suppressor of cytokine signalling (SOCS) proteins trong>andtrong> their trong>btrong>inding partners with the elongin trong>Btrong> trong>andtrong> C complex, possitrong>btrong>ly targeting them for degradation. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2017]

NSMF Gene

NMDA receptor synaptonuclear signaling trong>andtrong> neuronal migration factor

The protein encoded trong>btrong>y this gene is involved in guidance of olfactory axon projections trong>andtrong> migration of luteinizing hormone-releasing hormone neurons. Defects in this gene are a cause of idiopathic hypogonadotropic hypogonadism (IHH). Several transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, May 2010]

CCZ1trong>Btrong> Gene

CCZ1 vacuolar protein trafficking trong>andtrong> trong>btrong>iogenesis associated homolog trong>Btrong> (S. cerevisiae)

Enatrong>btrong>les guanyl-nucleotide exchange factor activity. Predicted to trong>btrong>e involved in vesicle-mediated transport. Located in intracellular memtrong>btrong>rane-trong>btrong>ounded organelle. Part of Mon1-Ccz1 complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LILRtrong>Btrong>5 Gene

leukocyte immunoglotrong>btrong>ulin-like receptor, sutrong>btrong>family trong>Btrong> (with TM trong>andtrong> ITIM domains), memtrong>btrong>er 5

This gene is a memtrong>btrong>er of the leukocyte immunoglotrong>btrong>ulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein trong>btrong>elongs to the sutrong>btrong>family trong>Btrong> class of LIR receptors which contain two or four extracellular immunoglotrong>btrong>ulin domains, a transmemtrong>btrong>rane domain, trong>andtrong> two to four cytoplasmic immunoreceptor tyrosine-trong>btrong>ased inhitrong>btrong>itory motifs (ITIMs). Several other LIR sutrong>btrong>family trong>Btrong> receptors are expressed on immune cells where they trong>btrong>ind to MHC class I molecules on antigen-presenting cells trong>andtrong> inhitrong>btrong>it stimulation of an immune response. Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jul 2008]

LILRtrong>Btrong>4 Gene

leukocyte immunoglotrong>btrong>ulin-like receptor, sutrong>btrong>family trong>Btrong> (with TM trong>andtrong> ITIM domains), memtrong>btrong>er 4

This gene is a memtrong>btrong>er of the leukocyte immunoglotrong>btrong>ulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein trong>btrong>elongs to the sutrong>btrong>family trong>Btrong> class of LIR receptors which contain two or four extracellular immunoglotrong>btrong>ulin domains, a transmemtrong>btrong>rane domain, trong>andtrong> two to four cytoplasmic immunoreceptor tyrosine-trong>btrong>ased inhitrong>btrong>itory motifs (ITIMs). The receptor is expressed on immune cells where it trong>btrong>inds to MHC class I molecules on antigen-presenting cells trong>andtrong> transduces a negative signal that inhitrong>btrong>its stimulation of an immune response. The receptor can also function in antigen capture trong>andtrong> presentation. It is thought to control inflammatory responses trong>andtrong> cytotoxicity to help focus the immune response trong>andtrong> limit autoreactivity. Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jul 2008]

LILRtrong>Btrong>3 Gene

leukocyte immunoglotrong>btrong>ulin-like receptor, sutrong>btrong>family trong>Btrong> (with TM trong>andtrong> ITIM domains), memtrong>btrong>er 3

This gene is a memtrong>btrong>er of the leukocyte immunoglotrong>btrong>ulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein trong>btrong>elongs to the sutrong>btrong>family trong>Btrong> class of LIR receptors which contain two or four extracellular immunoglotrong>btrong>ulin domains, a transmemtrong>btrong>rane domain, trong>andtrong> two to four cytoplasmic immunoreceptor tyrosine-trong>btrong>ased inhitrong>btrong>itory motifs (ITIMs). The receptor is expressed on immune cells where it trong>btrong>inds to MHC class I molecules on antigen-presenting cells trong>andtrong> transduces a negative signal that inhitrong>btrong>its stimulation of an immune response. It is thought to control inflammatory responses trong>andtrong> cytotoxicity to help focus the immune response trong>andtrong> limit autoreactivity. Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jul 2008]

LILRtrong>Btrong>2 Gene

leukocyte immunoglotrong>btrong>ulin-like receptor, sutrong>btrong>family trong>Btrong> (with TM trong>andtrong> ITIM domains), memtrong>btrong>er 2

This gene is a memtrong>btrong>er of the leukocyte immunoglotrong>btrong>ulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein trong>btrong>elongs to the sutrong>btrong>family trong>Btrong> class of LIR receptors which contain two or four extracellular immunoglotrong>btrong>ulin domains, a transmemtrong>btrong>rane domain, trong>andtrong> two to four cytoplasmic immunoreceptor tyrosine-trong>btrong>ased inhitrong>btrong>itory motifs (ITIMs). The receptor is expressed on immune cells where it trong>btrong>inds to MHC class I molecules on antigen-presenting cells trong>andtrong> transduces a negative signal that inhitrong>btrong>its stimulation of an immune response. It is thought to control inflammatory responses trong>andtrong> cytotoxicity to help focus the immune response trong>andtrong> limit autoreactivity. Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jul 2008]

LILRtrong>Btrong>1 Gene

leukocyte immunoglotrong>btrong>ulin-like receptor, sutrong>btrong>family trong>Btrong> (with TM trong>andtrong> ITIM domains), memtrong>btrong>er 1

This gene is a memtrong>btrong>er of the leukocyte immunoglotrong>btrong>ulin-like receptor (LIR) family, which is found in a gene cluster at chromosomal region 19q13.4. The encoded protein trong>btrong>elongs to the sutrong>btrong>family trong>Btrong> class of LIR receptors which contain two or four extracellular immunoglotrong>btrong>ulin domains, a transmemtrong>btrong>rane domain, trong>andtrong> two to four cytoplasmic immunoreceptor tyrosine-trong>btrong>ased inhitrong>btrong>itory motifs (ITIMs). The receptor is expressed on immune cells where it trong>btrong>inds to MHC class I molecules on antigen-presenting cells trong>andtrong> transduces a negative signal that inhitrong>btrong>its stimulation of an immune response. It is thought to control inflammatory responses trong>andtrong> cytotoxicity to help focus the immune response trong>andtrong> limit autoreactivity. Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jul 2008]

LOC105375116 Gene

TRIO trong>andtrong> F-actin-trong>btrong>inding protein-like

LOC100418722 Gene

cilia trong>andtrong> flagella associated protein 97 pseudogene

CLPTM1 Gene

cleft lip trong>andtrong> palate associated transmemtrong>btrong>rane protein 1

Predicted to enatrong>btrong>le GAtrong>Btrong>A receptor trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of T cell differentiation in thymus. Located in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

HSD3trong>Btrong>7 Gene

hydroxy-delta-5-steroid dehydrogenase, 3 trong>btrong>eta- trong>andtrong> steroid delta-isomerase 7

This gene encodes an enzyme which is involved in the initial stages of the synthesis of trong>btrong>ile acids from cholesterol trong>andtrong> a memtrong>btrong>er of the short-chain dehydrogenase/reductase superfamily. The encoded protein is a memtrong>btrong>rane-associated endoplasmic reticulum protein which is active against 7-alpha hydrosylated sterol sutrong>btrong>strates. Mutations in this gene are associated with a congenital trong>btrong>ile acid synthesis defect which leads to neonatal cholestasis, a form of progressive liver disease. Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Dec 2008]

HSD3trong>Btrong>1 Gene

hydroxy-delta-5-steroid dehydrogenase, 3 trong>btrong>eta- trong>andtrong> steroid delta-isomerase 1

The protein encoded trong>btrong>y this gene is an enzyme that catalyzes the oxidative conversion of delta-5-3-trong>btrong>eta-hydroxysteroid precursors into delta-4-ketosteroids, which leads to the production of all classes of steroid hormones. The encoded protein also catalyzes the interconversion of 3-trong>btrong>eta-hydroxy- trong>andtrong> 3-keto-5-alpha-trong>andtrong>rostane steroids. [provided trong>btrong>y RefSeq, Jun 2016]

HSD3trong>Btrong>2 Gene

hydroxy-delta-5-steroid dehydrogenase, 3 trong>btrong>eta- trong>andtrong> steroid delta-isomerase 2

The protein encoded trong>btrong>y this gene is a trong>btrong>ifunctional enzyme that catalyzes the oxidative conversion of delta(5)-ene-3-trong>btrong>eta-hydroxy steroid, trong>andtrong> the oxidative conversion of ketosteroids. It plays a crucial role in the trong>btrong>iosynthesis of all classes of hormonal steroids. This gene is predominantly expressed in the adrenals trong>andtrong> the gonads. Mutations in this gene are associated with 3-trong>btrong>eta-hydroxysteroid dehydrogenase, type II, deficiency. Alternatively spliced transcript variants have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Oct 2009]

CSMD2 Gene

CUtrong>Btrong> trong>andtrong> Sushi multiple domains 2

The protein encoded trong>btrong>y this gene is thought to trong>btrong>e involved in the control of complement cascade of the immune system. Defects in this gene have trong>btrong>een associated with schizophrenia. This gene may act as a tumor suppressor for colorectal cancer. [provided trong>btrong>y RefSeq, Jan 2020]

CSMD3 Gene

CUtrong>Btrong> trong>andtrong> Sushi multiple domains 3

Predicted to trong>btrong>e involved in regulation of dendrite development. Predicted to trong>btrong>e located in plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CSMD1 Gene

CUtrong>Btrong> trong>andtrong> Sushi multiple domains 1

Predicted to act upstream of or within several processes, including learning or memory; mammary gltrong>andtrong> trong>btrong>ranching involved in pregnancy; trong>andtrong> reproductive structure development. Predicted to trong>btrong>e located in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP20 Gene

cilia trong>andtrong> flagella associated protein 20

Enatrong>btrong>les RNA trong>btrong>inding activity. Involved in several processes, including positive regulation of feeding trong>btrong>ehavior; protein polyglutamylation; trong>andtrong> regulation of cilium trong>btrong>eat frequency involved in ciliary motility. Located in microtutrong>btrong>ule cytoskeleton trong>andtrong> nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LRCH4 Gene

leucine-rich repeats trong>andtrong> calponin homology (CH) domain containing 4

This gene encodes a protein that contains leucine-rich repeats (LRR) at its amino terminus trong>andtrong> that is known to trong>btrong>e involved in ligtrong>andtrong> trong>btrong>inding. The cartrong>btrong>oxyl terminus may act as a memtrong>btrong>rane anchor. Identified structural elements suggest that the encoded protein resemtrong>btrong>les a receptor. [provided trong>btrong>y RefSeq, Jul 2008]

LRCH1 Gene

leucine-rich repeats trong>andtrong> calponin homology (CH) domain containing 1

This gene encodes a protein with a leucine-rich repeat trong>andtrong> a calponin homology domain. Polymorphism in this gene may trong>btrong>e associated with susceptitrong>btrong>ililty to knee osteoarthritis. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided trong>btrong>y RefSeq, Mar 2010]

LRCH2 Gene

leucine-rich repeats trong>andtrong> calponin homology (CH) domain containing 2

This gene encodes a memtrong>btrong>er of the leucine-rich repeat trong>andtrong> calponin homology domain-containing protein family. These family memtrong>btrong>ers contain multiple N-terminal leucine-rich repeats, in addition to a C-terminal calponin homology domain, a type of domain that mediates interactions with actin filaments. These proteins are conserved across animal species, trong>andtrong> studies of a similar Drosophila protein indicate a function as a cytoskeletal scaffolding protein. Alternative splicing of this gene results in multiple transcript variants. [provided trong>btrong>y RefSeq, Sep 2011]

LRCH3 Gene

leucine-rich repeats trong>andtrong> calponin homology (CH) domain containing 3

Involved in septin cytoskeleton organization. Located in cytosol. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC102724962 Gene

angiogenic factor with G patch trong>andtrong> FHA domains 1-like

ELMO2P1 Gene

engulfment trong>andtrong> cell motility 2 pseudogene 1

DAPP1 Gene

dual adaptor of phosphotyrosine trong>andtrong> 3-phosphoinositides

Enatrong>btrong>les phosphatidylinositol-3,4,5-trisphosphate trong>btrong>inding activity trong>andtrong> phosphatidylinositol-3,4-trong>btrong>isphosphate trong>btrong>inding activity. Predicted to trong>btrong>e involved in protein dephosphorylation trong>andtrong> signal transduction. Located in plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ktrong>Btrong>Ttrong>Btrong>D6 Gene

kelch repeat trong>andtrong> trong>Btrong>Ttrong>Btrong> (POZ) domain containing 6

Predicted to enatrong>btrong>le utrong>btrong>iquitin-like ligase-sutrong>btrong>strate adaptor activity. Involved in proteasome-mediated utrong>btrong>iquitin-dependent protein catatrong>btrong>olic process; protein K48-linked utrong>btrong>iquitination; trong>andtrong> regulation of Rac protein signal transduction. Located in cytoplasm trong>andtrong> nucleus. Part of Cul3-RING utrong>btrong>iquitin ligase complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CCtrong>Btrong>E1 Gene

collagen trong>andtrong> calcium trong>btrong>inding EGF domains 1

This gene is thought to function in extracellular matrix remodeling trong>andtrong> migration. It is predominantly expressed in the ovary, trong>btrong>ut down regulated in ovarian cancer cell lines trong>andtrong> primary carcinomas, suggesting its role as a tumour suppressor. Mutations in this gene have trong>btrong>een associated with Hennekam lymphangiectasia-lymphedema syndrome, a generalized lymphatic dysplasia in humans. [provided trong>btrong>y RefSeq, Mar 2010]

PERM1 Gene

PPARGC1 trong>andtrong> ESRR induced regulator, muscle 1

Involved in response to muscle activity. Predicted to trong>btrong>e active in cytoplasm trong>andtrong> nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC651644 Gene

LIM trong>andtrong> senescent cell antigen-like domains 2 pseudogene

TIAM1 Gene

T-cell lymphoma invasion trong>andtrong> metastasis 1

This gene encodes a RAC1-specific guanine nucleotide exchange factor (GEF). GEFs mediate the exchange of guanosine diphosphate (GDP) for guanosine triphosphate (GTP). The trong>btrong>inding of GTP induces a conformational change in RAC1 that allows downstream effectors to trong>btrong>ind trong>andtrong> transduce a signal. This gene thus regulates RAC1 signaling pathways that affect cell shape, migration, adhesion, growth, survival, trong>andtrong> polarity, as well as influencing actin cytoskeletal formation, endocytosis, trong>andtrong> memtrong>btrong>rane trafficking. This gene thus plays an important role in cell invasion, metastasis, trong>andtrong> carcinogenesis. In addition to RAC1, the encoded protein activates additional Rho-like GTPases such as CDC42, RAC2, RAC3 trong>andtrong> RHOA. This gene encodes multiple protein isoforms that experience a diverse array of intramolecular, protein-protein, trong>andtrong> phosphorylation interactions as well as phosphoinositide trong>btrong>inding. trong>Btrong>oth the longer trong>andtrong> shorter isoforms have C-terminal Dtrong>btrong>l homology (DH) trong>andtrong> pleckstrin homology (PH) domains while only the longer isoforms of this gene have the N-terminal myristoylation site trong>andtrong> the downstream N-terminal PH domain, ras-trong>btrong>inding domain (Rtrong>Btrong>D), trong>andtrong> PSD-95/DlgA/ZO-1 (PDZ) domain. [provided trong>btrong>y RefSeq, Jul 2017]

TIAM2 Gene

T-cell lymphoma invasion trong>andtrong> metastasis 2

This gene encodes a guanine nucleotide exchange factor. A highly similar mouse protein specifically activates ras-related C3 trong>btrong>otulinum sutrong>btrong>strate 1, converting this Rho-like guanosine triphosphatase (GTPase) from a guanosine diphosphate-trong>btrong>ound inactive state to a guanosine triphosphate-trong>btrong>ound active state. The encoded protein may play a role in neural cell development. Alternatively spliced transcript variants encoding different isoforms have trong>btrong>een descritrong>btrong>ed. [provided trong>btrong>y RefSeq, Jul 2008]

VSTM2L Gene

V-set trong>andtrong> transmemtrong>btrong>rane domain containing 2 like

Involved in negative regulation of neuron apoptotic process. Located in cytoplasm trong>andtrong> extracellular region. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

VSTM2A Gene

V-set trong>andtrong> transmemtrong>btrong>rane domain containing 2A

Predicted to enatrong>btrong>le identical protein trong>btrong>inding activity. Involved in several processes, including positive regulation of trong>btrong>rown fat cell differentiation; positive regulation of lipid storage; trong>andtrong> positive regulation of white fat cell proliferation. Predicted to trong>btrong>e located in extracellular region. Predicted to trong>btrong>e active in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

VSTM2trong>Btrong> Gene

V-set trong>andtrong> transmemtrong>btrong>rane domain containing 2trong>Btrong>

Predicted to trong>btrong>e active in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SPICE1 Gene

spindle trong>andtrong> centriole associated protein 1

Involved in metaphase chromosome alignment; mitotic spindle assemtrong>btrong>ly; trong>andtrong> regulation of centriole replication. Located in centriole; centrosome; trong>andtrong> spindle. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

RCHY1 Gene

ring finger trong>andtrong> CHY zinc finger domain containing 1, E3 utrong>btrong>iquitin protein ligase

The protein encoded trong>btrong>y this gene has utrong>btrong>iquitin ligase activity. It mediates E3-dependent utrong>btrong>iquitination trong>andtrong> proteasomal degradation of target proteins, including tumor protein 53, histone deacetylase 1, trong>andtrong> cyclin-dependent kinase inhitrong>btrong>itor 1trong>Btrong>, thus regulating their levels trong>andtrong> cell cycle progression. Alternatively spliced transcript variants encoding different isoforms have trong>btrong>een descritrong>btrong>ed for this gene. [provided trong>btrong>y RefSeq, Jun 2013]

APLF Gene

aprataxin trong>andtrong> PNKP like factor

Enatrong>btrong>les several functions, including ADP-D-ritrong>btrong>ose modification-dependent protein trong>btrong>inding activity; nuclease activity; trong>andtrong> poly-ADP-D-ritrong>btrong>ose trong>btrong>inding activity. Involved in DNA repair; DNA repair-dependent chromatin remodeling; trong>andtrong> protein localization to chromatin. Acts upstream of or within positive regulation of DNA ligation. Located in nucleoplasm. Is active in site of doutrong>btrong>le-strtrong>andtrong> trong>btrong>reak. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ANKEF1 Gene

ankyrin repeat trong>andtrong> EF-htrong>andtrong> domain containing 1

Predicted to enatrong>btrong>le calcium ion trong>btrong>inding activity. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CAtrong>Btrong>LES1 Gene

Cdk5 trong>andtrong> Atrong>btrong>l enzyme sutrong>btrong>strate 1

This gene encodes a protein involved in regulation of the cell cycle through interactions with several cyclin-dependent kinases. One study (PMID: 16177568) reported atrong>btrong>errant splicing of transcripts from this gene which results in removal of the cyclin trong>btrong>inding domain only in human cancer cells, trong>andtrong> reduction in gene expression was shown in colorectal cancers (PMID: 17982127).Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jan 2012]

CAtrong>Btrong>LES2 Gene

Cdk5 trong>andtrong> Atrong>btrong>l enzyme sutrong>btrong>strate 2

Predicted to trong>btrong>e involved in cell division trong>andtrong> regulation of cell cycle. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>40 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 40

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific. Involved in DNA damage response. Located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>41 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 41

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>42 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 42

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of the C2H2 zinc finger protein family. This protein is predicted to have a pox virus trong>andtrong> zinc finger (POZ) domain at the N-terminus trong>andtrong> four zinc finger domains at the C-terminus. In human trong>andtrong> mouse, the protein localizes to the nuclei of skeletal muscle cells. Knockdown of this gene in zetrong>btrong>rafish results in atrong>btrong>normal skeletal muscle development trong>andtrong> myofitrong>btrong>rillar disorganization. A novel homozygous variant of the human gene has trong>btrong>een associated with lethal congenital contracture syndrome, an autosomal recessive disorder that results in muscle wasting. [provided trong>btrong>y RefSeq, Mar 2015]

Ztrong>Btrong>Ttrong>Btrong>43 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 43

Enatrong>btrong>les RNA polymerase III general transcription initiation factor trong>btrong>inding activity trong>andtrong> sequence-specific doutrong>btrong>le-strtrong>andtrong>ed DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in chromatin. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>44 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 44

Predicted to enatrong>btrong>le DNA trong>btrong>inding activity trong>andtrong> metal ion trong>btrong>inding activity. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>45 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 45

Enatrong>btrong>les sequence-specific doutrong>btrong>le-strtrong>andtrong>ed DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in negative regulation of transcription trong>btrong>y RNA polymerase II; regulation of cytokine production; trong>andtrong> regulation of immune system process. Predicted to trong>btrong>e located in nucleus. Predicted to trong>btrong>e active in nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>46 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 46

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription repressor activity, RNA polymerase II-specific trong>andtrong> transcription cis-regulatory region trong>btrong>inding activity. Involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in chromatin. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>47 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 47

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e active in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>48 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 48

Enatrong>btrong>les doutrong>btrong>le-strtrong>andtrong>ed telomeric DNA trong>btrong>inding activity; identical protein trong>btrong>inding activity; trong>andtrong> transcription cis-regulatory region trong>btrong>inding activity. Involved in positive regulation of DNA-templated transcription trong>andtrong> telomere maintenance via telomere lengthening. Located in chromosome, telomeric region. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>49 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 49

Enatrong>btrong>les DNA-trong>btrong>inding transcription factor trong>btrong>inding activity; sequence-specific DNA trong>btrong>inding activity; trong>andtrong> transcription coactivator trong>btrong>inding activity. Involved in negative regulation of cell population proliferation; positive regulation of transcription trong>btrong>y RNA polymerase II; trong>andtrong> regulation of cell cycle. Located in cytosol; microtutrong>btrong>ule cytoskeleton; trong>andtrong> nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

WDTC1 Gene

WD trong>andtrong> tetratricopeptide repeats 1

Predicted to enatrong>btrong>le enzyme inhitrong>btrong>itor activity; histone trong>btrong>inding activity; trong>andtrong> histone deacetylase trong>btrong>inding activity. Predicted to trong>btrong>e involved in negative regulation of fatty acid trong>btrong>iosynthetic process. Predicted to act upstream of or within several processes, including cellular response to insulin stimulus; glucose metatrong>btrong>olic process; trong>andtrong> negative regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleoplasm. Predicted to trong>btrong>e part of Cul4-RING E3 utrong>btrong>iquitin ligase complex. Predicted to trong>btrong>e active in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

DSTYK Gene

dual serine/threonine trong>andtrong> tyrosine protein kinase

This gene encodes a dual serine/threonine trong>andtrong> tyrosine protein kinase which is expressed in multiple tissues. It is thought to function as a regulator of cell death. Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Dec 2008]

LASP1 Gene

LIM trong>andtrong> SH3 protein 1

This gene encodes a memtrong>btrong>er of a sutrong>btrong>family of LIM proteins, characterized trong>btrong>y a LIM motif trong>andtrong> a domain of Src homology region 3, trong>andtrong> also a memtrong>btrong>er of the netrong>btrong>ulin family of actin-trong>btrong>inding proteins. The encoded protein is a cAMP trong>andtrong> cGMP dependent signaling protein trong>andtrong> trong>btrong>inds to the actin cytoskeleton at extensions of the cell memtrong>btrong>rane. The encoded protein has trong>btrong>een linked to metastatic trong>btrong>reast cancer, hematopoetic tumors such as trong>Btrong>-cell lymphomas, trong>andtrong> colorectal cancer. [provided trong>btrong>y RefSeq, Oct 2012]

LIMA1 Gene

LIM domain trong>andtrong> actin trong>btrong>inding 1

This gene encodes a cytoskeleton-associated protein that inhitrong>btrong>its actin filament depolymerization trong>andtrong> cross-links filaments in trong>btrong>undles. It is downregulated in some cancer cell lines. Alternatively spliced transcript variants encoding different isoforms have trong>btrong>een descritrong>btrong>ed for this gene, trong>andtrong> expression of some of the variants maytrong>btrong>e independently regulated. [provided trong>btrong>y RefSeq, Aug 2011]

LOC283804 Gene

disintegrin trong>andtrong> metalloproteinase domain-containing protein 21-like

PDRG1 Gene

p53 trong>andtrong> DNA-damage regulated 1

Predicted to enatrong>btrong>le unfolded protein trong>btrong>inding activity. Predicted to trong>btrong>e involved in protein statrong>btrong>ilization. Part of RPAP3/R2TP/prefoldin-like complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

IFNAR2 Gene

interferon (alpha, trong>btrong>eta trong>andtrong> omega) receptor 2

The protein encoded trong>btrong>y this gene is a type I memtrong>btrong>rane protein that forms one of the two chains of a receptor for interferons alpha trong>andtrong> trong>btrong>eta. trong>Btrong>inding trong>andtrong> activation of the receptor stimulates Janus protein kinases, which in turn phosphorylate several proteins, including STAT1 trong>andtrong> STAT2. The protein trong>btrong>elongs to the type II cytokine receptor family. Mutations in this gene are associated with Immunodeficiency 45. [provided trong>btrong>y RefSeq, Jul 2020]

IFNAR1 Gene

interferon (alpha, trong>btrong>eta trong>andtrong> omega) receptor 1

The protein encoded trong>btrong>y this gene is a type I memtrong>btrong>rane protein that forms one of the two chains of a receptor for interferons alpha trong>andtrong> trong>btrong>eta. trong>Btrong>inding trong>andtrong> activation of the receptor stimulates Janus protein kinases, which in turn phosphorylate several proteins, including STAT1 trong>andtrong> STAT2. The protein trong>btrong>elongs to the type II cytokine receptor family trong>andtrong> functions as an antiviral factor. [provided trong>btrong>y RefSeq, Jul 2020]

PDLIM4 Gene

PDZ trong>andtrong> LIM domain 4

Enatrong>btrong>les alpha-actinin trong>btrong>inding activity; protein homodimerization activity; trong>andtrong> protein phosphatase trong>btrong>inding activity. Involved in actin cytoskeleton organization. Located in several cellular components, including lamellipodium; perinuclear region of cytoplasm; trong>andtrong> stress fitrong>btrong>er. Part of filamentous actin. Implicated in osteoporosis. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PDLIM5 Gene

PDZ trong>andtrong> LIM domain 5

This gene encodes a memtrong>btrong>er of a family of proteins that possess a 100-amino acid PDZ domain at the N terminus trong>andtrong> one to three LIM domains at the C-terminus. This family memtrong>btrong>er functions as a scaffold protein that tethers protein kinases to the Z-disk in striated muscles. It is thought to function in cardiomyocyte expansion trong>andtrong> in restraining postsynaptic growth of excitatory synapses. Alternative splicing of this gene results in multiple transcript variants. [provided trong>btrong>y RefSeq, Jan 2012]

PDLIM7 Gene

PDZ trong>andtrong> LIM domain 7 (enigma)

The protein encoded trong>btrong>y this gene is representative of a family of proteins composed of conserved PDZ trong>andtrong> LIM domains. LIM domains are proposed to function in protein-protein recognition in a variety of contexts including gene transcription trong>andtrong> development trong>andtrong> in cytoskeletal interaction. The LIM domains of this protein trong>btrong>ind to protein kinases, whereas the PDZ domain trong>btrong>inds to actin filaments. The gene product is involved in the assemtrong>btrong>ly of an actin filament-associated complex essential for transmission of ret/ptc2 mitogenic signaling. The trong>btrong>iological function is likely to trong>btrong>e that of an adapter, with the PDZ domain localizing the LIM-trong>btrong>inding proteins to actin filaments of trong>btrong>oth skeletal muscle trong>andtrong> nonmuscle tissues. Alternative splicing of this gene results in multiple transcript variants. [provided trong>btrong>y RefSeq, Jul 2008]

PDLIM1 Gene

PDZ trong>andtrong> LIM domain 1

This gene encodes a memtrong>btrong>er of the enigma protein family. The protein contains two protein interacting domains, a PDZ domain at the amino terminal end trong>andtrong> one to three LIM domains at the cartrong>btrong>oxyl terminal. It is a cytoplasmic protein associated with the cytoskeleton. The protein may function as an adapter to trong>btrong>ring other LIM-interacting proteins to the cytoskeleton. Pseudogenes associated with this gene are located on chromosomes 3, 14 trong>andtrong> 17. [provided trong>btrong>y RefSeq, Oct 2012]

PDLIM2 Gene

PDZ trong>andtrong> LIM domain 2 (mystique)

This gene encodes a memtrong>btrong>er of the ALP sutrong>btrong>family of PDZ-LIM domain proteins. The encoded protein suppresses anchorage-dependent growth trong>andtrong> promotes cell migration trong>andtrong> adhesion through interactions with the actin cytoskeleton via the PDZ domain. The encoded protein is also a putative tumor suppressor protein, trong>andtrong> decreased expression of this gene is associated with several malignancies including trong>btrong>reast cancer trong>andtrong> adult T-cell leukemia. Alternatively spliced transcript variants encoding multiple isoforms have trong>btrong>een otrong>btrong>served for this gene. [provided trong>btrong>y RefSeq, Oct 2011]

PDLIM3 Gene

PDZ trong>andtrong> LIM domain 3

The protein encoded trong>btrong>y this gene contains a PDZ domain trong>andtrong> a LIM domain, indicating that it may trong>btrong>e involved in cytoskeletal assemtrong>btrong>ly. In support of this, the encoded protein has trong>btrong>een shown to trong>btrong>ind the spectrin-like repeats of alpha-actinin-2 trong>andtrong> to colocalize with alpha-actinin-2 at the Z lines of skeletal muscle. Alternatively spliced transcript variants encoding multiple isoforms have trong>btrong>een otrong>btrong>served for this gene. Atrong>btrong>errant alternative splicing of this gene may play a role in myotonic dystrophy. [provided trong>btrong>y RefSeq, Apr 2012]

FTO Gene

fat mass trong>andtrong> otrong>btrong>esity associated

This gene is a nuclear protein of the Alktrong>Btrong> related non-haem iron trong>andtrong> 2-oxoglutarate-dependent oxygenase superfamily trong>btrong>ut the exact physiological function of this gene is not known. Other non-heme iron enzymes function to reverse alkylated DNA trong>andtrong> RNA damage trong>btrong>y oxidative demethylation. Studies in mice trong>andtrong> humans indicate a role in nervous trong>andtrong> cardiovascular systems trong>andtrong> a strong association with trong>btrong>ody mass index, otrong>btrong>esity risk, trong>andtrong> type 2 diatrong>btrong>etes. [provided trong>btrong>y RefSeq, Jul 2011]

PSD3 Gene

pleckstrin trong>andtrong> Sec7 domain containing 3

Predicted to enatrong>btrong>le guanyl-nucleotide exchange factor activity trong>andtrong> phospholipid trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of ARF protein signal transduction. Predicted to trong>btrong>e located in memtrong>btrong>rane. Predicted to trong>btrong>e active in glutamatergic synapse; postsynapse; trong>andtrong> ruffle memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

RYtrong>Btrong>P Gene

RING1 trong>andtrong> YY1 trong>btrong>inding protein

Enatrong>btrong>les nucleic acid trong>btrong>inding activity. Involved in several processes, including negative regulation of proteasomal utrong>btrong>iquitin-dependent protein catatrong>btrong>olic process; positive regulation of DNA-templated transcription; trong>andtrong> positive regulation of apoptotic process. Located in nucleoplasm. Part of PcG protein complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

HUWE1 Gene

HECT, Utrong>Btrong>A trong>andtrong> WWE domain containing 1, E3 utrong>btrong>iquitin protein ligase

This gene encodes a protein containing a C-terminal HECT (E6AP type E3 utrong>btrong>iquitin protein ligase) domain that functions as an E3 utrong>btrong>iquitin ligase. The encoded protein is required for the utrong>btrong>iquitination trong>andtrong> sutrong>btrong>sequent degradation of the anti-apoptotic protein Mcl1 (myeloid cell leukemia sequence 1 (trong>Btrong>CL2-related)). This protein also utrong>btrong>iquitinates the p53 tumor suppressor, core histones, trong>andtrong> DNA polymerase trong>btrong>eta. Mutations in this gene are associated with Turner type X-linked syndromic cognitive disatrong>btrong>ility. [provided trong>btrong>y RefSeq, Aug 2013]

ELMO1 Gene

engulfment trong>andtrong> cell motility 1

This gene encodes a memtrong>btrong>er of the engulfment trong>andtrong> cell motility protein family. These proteins interact with dedicator of cytokinesis proteins to promote phagocytosis trong>andtrong> cell migration. Increased expression of this gene trong>andtrong> dedicator of cytokinesis 1 may promote glioma cell invasion, trong>andtrong> single nucleotide polymorphisms in this gene may trong>btrong>e associated with diatrong>btrong>etic nephropathy. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Aug 2013]

ELMO2 Gene

engulfment trong>andtrong> cell motility 2

The protein encoded trong>btrong>y this gene interacts with the dedicator of cyto-kinesis 1 protein. Similarity to a C. elegans protein suggests that this protein may function in phagocytosis of apoptotic cells trong>andtrong> in cell migration. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Dec 2015]

ELMO3 Gene

engulfment trong>andtrong> cell motility 3

The protein encoded trong>btrong>y this gene is similar to a C. elegans protein that functions in phagocytosis of apoptotic cells trong>andtrong> in cell migration. Other memtrong>btrong>ers of this small family of engulfment trong>andtrong> cell motility (ELMO) proteins have trong>btrong>een shown to interact with the dedicator of cyto-kinesis 1 protein to promote phagocytosis trong>andtrong> effect cell shape changes. [provided trong>btrong>y RefSeq, Jul 2008]

CPtrong>Btrong>HM Gene

Chondrodysplasia with platyspondyly, distinctive trong>btrong>rachydactyly, hydrocephaly, trong>andtrong> microphthalmia

LOC100128048 Gene

cysteine trong>andtrong> histidine-rich domain (CHORD) containing 1 pseudogene

ECSCR Gene

endothelial cell surface expressed chemotaxis trong>andtrong> apoptosis regulator

The protein encoded trong>btrong>y this gene is primarily found in endothelial cells trong>andtrong> trong>btrong>lood vessels, where it is involved in cell shape changes trong>andtrong> EGF-induced cell migration. It can enhance the activation of vascular endothelial growth factor receptor-2/kinase insert domain receptor trong>andtrong> also promote the proteolysis of internalized kinase insert domain receptor. This gene may play a role in angiogenesis-related diseases. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Jun 2014]

DCtrong>Btrong>LD2 Gene

discoidin, CUtrong>Btrong> trong>andtrong> LCCL domain containing 2

Predicted to enatrong>btrong>le signaling receptor activity. Involved in negative regulation of cell growth trong>andtrong> wound healing. Located in cell surface trong>andtrong> plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

DCtrong>Btrong>LD1 Gene

discoidin, CUtrong>Btrong> trong>andtrong> LCCL domain containing 1

Predicted to enatrong>btrong>le signaling receptor activity. Predicted to trong>btrong>e located in memtrong>btrong>rane. Predicted to trong>btrong>e active in plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

MIIP Gene

migration trong>andtrong> invasion inhitrong>btrong>itory protein

This gene encodes a protein that interacts with the oncogene protein insulin-like growth factor trong>btrong>inding protein 2 trong>andtrong> may function as an inhitrong>btrong>itor of cell migration trong>andtrong> invasion. This protein also interacts with the cell division protein 20 trong>andtrong> may trong>btrong>e involved in regulating mitotic progression. This protein may function as a tumor suppressor trong>btrong>y inhitrong>btrong>iting the growth or certain cancers. [provided trong>btrong>y RefSeq, Sep 2011]

LOC100420617 Gene

FERM trong>andtrong> PDZ domain containing 2 pseudogene

LRTOMT Gene

leucine rich transmemtrong>btrong>rane trong>andtrong> O-methyltransferase domain containing

This locus represents naturally occurring readthrough transcription trong>btrong>etween the neightrong>btrong>oring LRRC51 (leucine-rich repeat containing 51) trong>andtrong> TOMT (transmemtrong>btrong>rane O-methyltransferase) genes on chromosome 11. The readthrough transcript encodes a fusion protein that shares sequence identity with each individual gene product. Multiple reports implicate mutations in this gene in nonsyndromic deafness.[provided trong>btrong>y RefSeq, Fetrong>btrong> 2021]

TMTC4 Gene

transmemtrong>btrong>rane trong>andtrong> tetratricopeptide repeat containing 4

This gene encodes a transmemtrong>btrong>rane protein that trong>btrong>elongs to family of proteins containing an N-terminal transmemtrong>btrong>rane domain trong>andtrong> a C-terminal tetratricopeptide repeat (TPR) domain. TPR domains mediate protein-protein interactions in various cellular processes, such as synaptic vesicle fusion, protein folding, trong>andtrong> protein translocation. A pseudogene of this gene has trong>btrong>een defined on chromosome 5. [provided trong>btrong>y RefSeq, Apr 2017]

TMTC3 Gene

transmemtrong>btrong>rane trong>andtrong> tetratricopeptide repeat containing 3

This gene encodes a protein that trong>btrong>elongs to the transmemtrong>btrong>rane trong>andtrong> tetratricopeptide repeat-containing protein family. [provided trong>btrong>y RefSeq, May 2010]

RAX Gene

retina trong>andtrong> anterior neural fold homeotrong>btrong>ox

This gene encodes a homeotrong>btrong>ox-containing transcription factor that functions in eye development. The gene is expressed early in the eye primordia, trong>andtrong> is required for retinal cell fate determination trong>andtrong> also regulates stem cell proliferation. Mutations in this gene have trong>btrong>een reported in patients with defects in ocular development, including microphthalmia, anophthalmia, trong>andtrong> colotrong>btrong>oma.[provided trong>btrong>y RefSeq, Oct 2009]

TMTC1 Gene

transmemtrong>btrong>rane trong>andtrong> tetratricopeptide repeat containing 1

Enatrong>btrong>les dolichyl-phosphate-mannose-protein mannosyltransferase activity. Involved in protein O-linked mannosylation. Predicted to trong>btrong>e located in endoplasmic reticulum trong>andtrong> memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

DCAF4L1 Gene

DDtrong>Btrong>1 trong>andtrong> CUL4 associated factor 4-like 1

Predicted to trong>btrong>e part of Cul4-RING E3 utrong>btrong>iquitin ligase complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

DCAF4L2 Gene

DDtrong>Btrong>1 trong>andtrong> CUL4 associated factor 4-like 2

Predicted to trong>btrong>e part of Cul4-RING E3 utrong>btrong>iquitin ligase complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>12P1 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 12 pseudogene 1

LOC728688 Gene

utrong>btrong>iquitin-like, containing PHD trong>andtrong> RING finger domains, 1 pseudogene

ADIPOQ Gene

adiponectin, C1Q trong>andtrong> collagen domain containing

This gene is expressed in adipose tissue exclusively. It encodes a protein with similarity to collagens X trong>andtrong> VIII trong>andtrong> complement factor C1q. The encoded protein circulates in the plasma trong>andtrong> is involved with metatrong>btrong>olic trong>andtrong> hormonal processes. Mutations in this gene are associated with adiponectin deficiency. Multiple alternatively spliced variants, encoding the same protein, have trong>btrong>een identified. [provided trong>btrong>y RefSeq, Apr 2010]

FIP1L1 Gene

factor interacting with PAPOLA trong>andtrong> CPSF1

This gene encodes a sutrong>btrong>unit of the CPSF (cleavage trong>andtrong> polyadenylation specificity factor) complex that polyadenylates the 3' end of mRNA precursors. This gene, the homolog of yeast Fip1 (factor interacting with PAP), trong>btrong>inds to U-rich sequences of pre-mRNA trong>andtrong> stimulates poly(A) polymerase activity. Its N-terminus contains a PAP-trong>btrong>inding site trong>andtrong> its C-terminus an RNA-trong>btrong>inding domain. An interstitial chromosomal deletion on 4q12 creates an in-frame fusion of human genes FIP1L1 trong>andtrong> PDGFRA (platelet-derived growth factor receptor, alpha). The FIP1L1-PDGFRA fusion gene encodes a constitutively activated tyrosine kinase that joins the first 233 amino acids of FIP1L1 to the last 523 amino acids of PDGFRA. This gene fusion trong>andtrong> chromosomal deletion is the cause of some forms of idiopathic hypereosinophilic syndrome (HES). This syndrome, recently reclassified as chronic eosinophilic leukemia (CEL), is responsive to treatment with tyrosine kinase inhitrong>btrong>itors. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided trong>btrong>y RefSeq, Oct 2008]

Ftrong>Btrong>XW4P1 Gene

F-trong>btrong>ox trong>andtrong> WD repeat domain containing 4 pseudogene 1

RCtrong>Btrong>Ttrong>Btrong>2 Gene

regulator of chromosome condensation (RCC1) trong>andtrong> trong>Btrong>Ttrong>Btrong> (POZ) domain containing protein 2

This gene encodes a protein containing two C-terminal trong>Btrong>Ttrong>Btrong>/POZ domains that is related to regulator of chromosome condensation (RCC). The encoded protein may act as a guanine nucleotide exchange factor. This gene is otrong>btrong>served to trong>btrong>e lost or underexpressed in prostate cancers. There is a pseudogene of this gene on chromosome 10. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Nov 2013]

RCtrong>Btrong>Ttrong>Btrong>1 Gene

regulator of chromosome condensation (RCC1) trong>andtrong> trong>Btrong>Ttrong>Btrong> (POZ) domain containing protein 1

This gene encodes a protein with an N-terminal RCC1 domain trong>andtrong> a C-terminal trong>Btrong>Ttrong>Btrong> (trong>btrong>road complex, tramtrack trong>andtrong> trong>btrong>ric-a-trong>btrong>rac) domain. In rat, over-expression of this gene in vascular smooth muscle cells induced cellular hypertrophy. In rat, the C-terminus of RCtrong>Btrong>Ttrong>Btrong>1 interacts with the angiotensin II receptor-1A. In humans, this gene maps to a region of chromosome 13q that is frequently deleted in trong>Btrong>-cell chronic lymphocytic leukemia trong>andtrong> other lymphoid malignancies. [provided trong>btrong>y RefSeq, Jul 2008]

KHNYN Gene

KH trong>andtrong> NYN domain containing

The protein encoded trong>btrong>y this gene contains a ritrong>btrong>onuclease NYN domain trong>andtrong> trong>btrong>elongs to the N4trong>Btrong>P1 family. The protein is a cofactor for the zinc finger antiviral protein (ZAP protein) which targets viral RNA for degradation trong>andtrong> restricts SARS-CoV-2 infection. [provided trong>btrong>y RefSeq, Sep 2021]

FTOP1 Gene

fat mass trong>andtrong> otrong>btrong>esity associated pseudogene 1

LOC100419579 Gene

HECT trong>andtrong> RLD domain containing E3 utrong>btrong>iquitin protein ligase 2 pseudogene

SPStrong>Btrong>4 Gene

splA/ryanodine receptor domain trong>andtrong> SOCS trong>btrong>ox containing 4

Enatrong>btrong>les utrong>btrong>iquitin-like ligase-sutrong>btrong>strate adaptor activity. Involved in several processes, including positive regulation of protein polyutrong>btrong>iquitination; protein utrong>btrong>iquitination; trong>andtrong> utrong>btrong>iquitin-dependent protein catatrong>btrong>olic process. Located in cytosol. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

TANGO6 Gene

transport trong>andtrong> golgi organization 6 homolog (Drosophila)

Predicted to trong>btrong>e involved in protein secretion. Predicted to trong>btrong>e located in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

TANGO2 Gene

transport trong>andtrong> golgi organization 2 homolog (Drosophila)

This gene trong>btrong>elongs to the transport trong>andtrong> Golgi organization family, whose memtrong>btrong>ers are predicted to play roles in secretory protein loading in the endoplasmic reticulum. Depletion of this gene in Drosophila S2 cells causes fusion of the Golgi with the ER. In mouse tissue culture cells, this protein co-localizes with a mitochondrially targeted mCherry protein trong>andtrong> displays very low levels of co-localization with Golgi trong>andtrong> peroxisomes. Allelic variants of this gene are associated with rhatrong>btrong>domyolysis, metatrong>btrong>olic crises with encephalopathy, trong>andtrong> cardiac arrhythmia. [provided trong>btrong>y RefSeq, Apr 2016]

SEMA6D Gene

sema domain, transmemtrong>btrong>rane domain (TM), trong>andtrong> cytoplasmic domain, (semaphorin) 6D

Semaphorins are a large family, including trong>btrong>oth secreted trong>andtrong> memtrong>btrong>rane associated proteins, many of which have trong>btrong>een implicated as inhitrong>btrong>itors or chemorepellents in axon pathfinding, fasciculation trong>andtrong> trong>btrong>ranching, trong>andtrong> target selection. All semaphorins possess a semaphorin (Sema) domain trong>andtrong> a PSI domain (found in plexins, semaphorins trong>andtrong> integrins) in the N-terminal extracellular portion. Additional sequence motifs C-terminal to the semaphorin domain allow classification into distinct sutrong>btrong>families. Results demonstrate that transmemtrong>btrong>rane semaphorins, like the secreted ones, can act as repulsive axon guidance cues. This gene encodes a class 6 vertetrong>btrong>rate transmemtrong>btrong>rane semaphorin that demonstrates alternative splicing. Several transcript variants have trong>btrong>een identified trong>andtrong> expression of the distinct encoded isoforms is thought to trong>btrong>e regulated in a tissue- trong>andtrong> development-dependent manner. [provided trong>btrong>y RefSeq, Nov 2010]

SEMA6trong>Btrong> Gene

sema domain, transmemtrong>btrong>rane domain (TM), trong>andtrong> cytoplasmic domain, (semaphorin) 6trong>Btrong>

This gene encodes a memtrong>btrong>er of the semaphorin family, a group of proteins characterized trong>btrong>y the presence of a conserved semaphorin (sema) domain. Whereas some semaphorins are transmemtrong>btrong>rane proteins, others are secreted. Semaphorins play a major role in axon guidance. The protein encoded trong>btrong>y this gene may trong>btrong>e involved in trong>btrong>oth peripheral trong>andtrong> central nervous system development. [provided trong>btrong>y RefSeq, Jul 2008]

SEMA6C Gene

sema domain, transmemtrong>btrong>rane domain (TM), trong>andtrong> cytoplasmic domain, (semaphorin) 6C

This gene encodes a memtrong>btrong>er of the semaphorin family. Semaphorins represent important molecular signals controlling multiple aspects of the cellular response that follows CNS injury, trong>andtrong> thus may play an important role in neural regeneration. [provided trong>btrong>y RefSeq, May 2010]

SEMA6A Gene

sema domain, transmemtrong>btrong>rane domain (TM), trong>andtrong> cytoplasmic domain, (semaphorin) 6A

Predicted to enatrong>btrong>le identical protein trong>btrong>inding activity; signaling receptor trong>btrong>inding activity; trong>andtrong> transmemtrong>btrong>rane signaling receptor activity. Involved in cellular response to vascular endothelial growth factor stimulus; negative regulation of cell adhesion involved in sprouting angiogenesis; trong>andtrong> negative regulation of signal transduction. Predicted to trong>btrong>e located in axon trong>andtrong> memtrong>btrong>rane. Predicted to trong>btrong>e active in plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

trong>Btrong>RE Gene

trong>btrong>rain trong>andtrong> reproductive organ-expressed (TNFRSF1A modulator)

This gene encodes an anti-apoptotic, death receptor-associated protein that interacts with tumor necrosis factor-receptor-1. The encoded protein acts as an adapter in several protein complexes, including the trong>Btrong>RCA1-A complex trong>andtrong> the trong>Btrong>RISC complex. The trong>Btrong>RCA1-A complex possesses utrong>btrong>iquitinase activity trong>andtrong> targets sites of doutrong>btrong>le strtrong>andtrong> DNA trong>btrong>reaks, while the trong>Btrong>RISC complex exhitrong>btrong>its deutrong>btrong>iquitinase activity trong>andtrong> is involved in mitotic spindle assemtrong>btrong>ly. This gene is upregulated in several types of cancer. [provided trong>btrong>y RefSeq, Jun 2016]

PALtrong>Btrong>2 Gene

partner trong>andtrong> localizer of trong>Btrong>RCA2

This gene encodes a protein that may function in tumor suppression. This protein trong>btrong>inds to trong>andtrong> colocalizes with the trong>btrong>reast cancer 2 early onset protein (trong>Btrong>RCA2) in nuclear foci trong>andtrong> likely permits the statrong>btrong>le intranuclear localization trong>andtrong> accumulation of trong>Btrong>RCA2. [provided trong>btrong>y RefSeq, Jul 2008]

Ftrong>Btrong>XL8 Gene

F-trong>btrong>ox trong>andtrong> leucine-rich repeat protein 8

This gene encodes a memtrong>btrong>er of the F-trong>btrong>ox protein family which is characterized trong>btrong>y an approximately 40 amino acid motif, the F-trong>btrong>ox. The F-trong>btrong>ox proteins constitute one of the four sutrong>btrong>units of the utrong>btrong>iquitin protein ligase complex called SCFs (SKP1-cullin-F-trong>btrong>ox), which function in phosphorylation-dependent utrong>btrong>iquitination. The F-trong>btrong>ox proteins are divided into 3 classes: Ftrong>btrong>ws containing WD-40 domains, Ftrong>btrong>ls containing leucine-rich repeats, trong>andtrong> Ftrong>btrong>xs containing either different protein-protein interaction modules or no recognizatrong>btrong>le motifs. The protein encoded trong>btrong>y this gene trong>btrong>elongs to the Ftrong>btrong>ls class. It shares 78% sequence identity with the mouse protein. [provided trong>btrong>y RefSeq, Jul 2008]

Ftrong>Btrong>XL2 Gene

F-trong>btrong>ox trong>andtrong> leucine-rich repeat protein 2

This gene encodes a memtrong>btrong>er of the F-trong>btrong>ox protein family which is characterized trong>btrong>y an approximately 40 amino acid motif, the F-trong>btrong>ox. The F-trong>btrong>ox proteins constitute one of the four sutrong>btrong>units of utrong>btrong>iquitin protein ligase complex called SCFs (SKP1-cullin-F-trong>btrong>ox), which function in phosphorylation-dependent utrong>btrong>iquitination. The F-trong>btrong>ox proteins are divided into 3 classes: Ftrong>btrong>ws containing WD-40 domains, Ftrong>btrong>ls containing leucine-rich repeats, trong>andtrong> Ftrong>btrong>xs containing either different protein-protein interaction modules or no recognizatrong>btrong>le motifs. The protein encoded trong>btrong>y this gene trong>btrong>elongs to the Ftrong>btrong>ls class trong>andtrong>, in addition to an F-trong>btrong>ox, contains 12 ttrong>andtrong>em leucine-rich repeats. Alternatively spliced transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jan 2010]

Ftrong>Btrong>XL7 Gene

F-trong>btrong>ox trong>andtrong> leucine-rich repeat protein 7

This gene encodes a memtrong>btrong>er of the F-trong>btrong>ox protein family which is characterized trong>btrong>y a 42-48 amino acid motif, the F-trong>btrong>ox, which trong>btrong>inds to the S-phase kinase-associated protein 1 (Skp1) protein. The F-trong>btrong>ox proteins constitute one of the four sutrong>btrong>units of E3 utrong>btrong>iquitin protein ligases called SCFs (SKP1-Cul1-F-trong>btrong>ox), which play a role in phosphorylation-dependent utrong>btrong>iquitination of proteins. The F-trong>btrong>ox proteins are divided into 3 sutrong>btrong>families trong>btrong>ased on the other domain in the protein: F-trong>btrong>ox proteins that also have a WD-40 domain (Ftrong>btrong>ws sutrong>btrong>family), F-trong>btrong>ox proteins that also have leucine-rich repeats (Ftrong>btrong>ls sutrong>btrong>family) trong>andtrong> F-trong>btrong>ox proteins that contain other motifs or lack known protein-interaction domains (Ftrong>btrong>xs sutrong>btrong>family). The protein encoded trong>btrong>y this gene trong>btrong>elongs to the Ftrong>btrong>ls sutrong>btrong>family. Alternative splicing results in multiple transcript variants of this gene. [provided trong>btrong>y RefSeq, May 2013]

Ftrong>Btrong>XL6 Gene

F-trong>btrong>ox trong>andtrong> leucine-rich repeat protein 6

This gene encodes a memtrong>btrong>er of a family of proteins that are characterized trong>btrong>y an F-trong>btrong>ox motif. The encoded protein also contains leucine-rich repeats. F-trong>btrong>ox-containing proteins comprise one of the sutrong>btrong>units of the SCF (SKP1-cullin-F-trong>btrong>ox) complex, which functions in phosphorylation-dependent utrong>btrong>iquitination. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Jul 2013]

ZSCAN5D Gene

zinc finger trong>andtrong> SCAN domain containing 5D

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ZSCAN5A Gene

zinc finger trong>andtrong> SCAN domain containing 5A

Enatrong>btrong>les sequence-specific doutrong>btrong>le-strtrong>andtrong>ed DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ZSCAN5trong>Btrong> Gene

zinc finger trong>andtrong> SCAN domain containing 5trong>Btrong>

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC105377064 Gene

aspartate, glycine, lysine trong>andtrong> serine-rich protein-like

NETO1 Gene

neuropilin (NRP) trong>andtrong> tolloid (TLL)-like 1

This gene encodes a transmemtrong>btrong>rane protein containing two extracellular CUtrong>Btrong> domains followed trong>btrong>y a low-density lipoprotein class A (LDLa) domain. This protein is thought to play a critical role in spatial learning trong>andtrong> memory trong>btrong>y regulating the function of synaptic N-methyl-D-aspartic acid receptor complexes in the hippocampus. Alternatively spliced transcript variants encoding multiple isoforms have trong>btrong>een otrong>btrong>served for this gene. [provided trong>btrong>y RefSeq, Aug 2017]

NETO2 Gene

neuropilin (NRP) trong>andtrong> tolloid (TLL)-like 2

This gene encodes a predicted transmemtrong>btrong>rane protein containing two extracellular CUtrong>Btrong> domains followed trong>btrong>y a low-density lipoprotein class A (LDLa) domain. A similar gene in rats encodes a protein that modulates glutamate signaling in the trong>btrong>rain trong>btrong>y regulating kainate receptor function. Expression of this gene may trong>btrong>e a trong>btrong>iomarker for proliferating infantile hemangiomas. A pseudogene of this gene is located on the long arm of chromosome 8. Alternatively spliced transcript variants encoding multiple isoforms have trong>btrong>een otrong>btrong>served for this gene. [provided trong>btrong>y RefSeq, Jan 2011]

FGD5 Gene

FYVE, RhoGEF trong>andtrong> PH domain containing 5

Predicted to enatrong>btrong>le guanyl-nucleotide exchange factor activity trong>andtrong> small GTPase trong>btrong>inding activity. Predicted to trong>btrong>e involved in actin cytoskeleton organization; filopodium assemtrong>btrong>ly; trong>andtrong> regulation of cell shape. Located in plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

FGD4 Gene

FYVE, RhoGEF trong>andtrong> PH domain containing 4

This gene encodes a protein that is involved in the regulation of the actin cytoskeleton trong>andtrong> cell shape. This protein contains an actin filament-trong>btrong>inding domain, which together with its Dtrong>btrong>l homology domain trong>andtrong> one of its pleckstrin homology domains, can form microspikes. This protein can activate MAPK8 independently of the actin filament-trong>btrong>inding domain, trong>andtrong> it is also involved in the activation of CDC42 via the exchange of trong>btrong>ound GDP for free GTP. The activation of CDC42 also enatrong>btrong>les this protein to play a role in mediating the cellular invasion of Cryptosporidium parvum, an intracellular parasite that infects the gastrointestinal tract. Mutations in this gene can cause Charcot-Marie-Tooth disease type 4H (CMT4H), a disorder of the peripheral nervous system. Multiple alternatively spliced transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jan 2015]

FGD6 Gene

FYVE, RhoGEF trong>andtrong> PH domain containing 6

Predicted to enatrong>btrong>le guanyl-nucleotide exchange factor activity trong>andtrong> small GTPase trong>btrong>inding activity. Predicted to trong>btrong>e involved in actin cytoskeleton organization; filopodium assemtrong>btrong>ly; trong>andtrong> regulation of cell shape. Predicted to trong>btrong>e located in Golgi apparatus; lamellipodium; trong>andtrong> ruffle. Predicted to trong>btrong>e active in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

FGD1 Gene

FYVE, RhoGEF trong>andtrong> PH domain containing 1

This gene encodes a protein that contains Dtrong>btrong>l (DH) trong>andtrong> pleckstrin (PH) homology domains trong>andtrong> is similar to the Rho family of small GTP-trong>btrong>inding proteins. The encoded protein specifically trong>btrong>inds to the Rho family GTPase Cdc42Hs trong>andtrong> can stimulate the GDP-GTP exchange of the isoprenylated form of Cdc42Hs. It also stimulates the mitogen activated protein kinase cascade leading to c-Jun kinase SAPK/JNK1 activation. Defects in this gene are the cause of the faciogenital dysplasia in Aarskog-Scott syndrome trong>andtrong> a syndromatic form of X-linked cognitive disatrong>btrong>ility. [provided trong>btrong>y RefSeq, Jul 2017]

FGD3 Gene

FYVE, RhoGEF trong>andtrong> PH domain containing 3

Predicted to enatrong>btrong>le guanyl-nucleotide exchange factor activity trong>andtrong> small GTPase trong>btrong>inding activity. Predicted to trong>btrong>e involved in actin cytoskeleton organization; filopodium assemtrong>btrong>ly; trong>andtrong> regulation of cell shape. Predicted to trong>btrong>e located in Golgi apparatus; lamellipodium; trong>andtrong> ruffle. Predicted to trong>btrong>e active in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

FGD2 Gene

FYVE, RhoGEF trong>andtrong> PH domain containing 2

The protein encoded trong>btrong>y this gene trong>btrong>elongs to a family of guanine nucleotide exchange factors (GEFs) which control cytoskeleton-dependent memtrong>btrong>rane rearrangements trong>btrong>y activating the cell division cycle 42 (CDC42) protein. This gene is expressed in trong>Btrong> lymphocytes, macrophages, trong>andtrong> dendritic cells. The encoded protein may play a role in leukocyte signaling trong>andtrong> vesicle trafficking in antigen-presenting cells in the immune system. [provided trong>btrong>y RefSeq, Oct 2016]

SLC5A6 Gene

solute carrier family 5 (sodium/multivitamin trong>andtrong> iodide cotransporter), memtrong>btrong>er 6

Enatrong>btrong>les trong>btrong>iotin transmemtrong>btrong>rane transporter activity; iodide transmemtrong>btrong>rane transporter activity; trong>andtrong> pantothenate transmemtrong>btrong>rane transporter activity. Involved in iodide transmemtrong>btrong>rane transport; transport across trong>btrong>lood-trong>btrong>rain trong>btrong>arrier; trong>andtrong> vitamin transmemtrong>btrong>rane transport. Located in apical plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>2 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 2

Enatrong>btrong>les DNA-trong>btrong>inding transcription repressor activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity; trong>andtrong> identical protein trong>btrong>inding activity. Involved in negative regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. Predicted to trong>btrong>e active in nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>6 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 6

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription repressor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in negative regulation of transcription trong>btrong>y RNA polymerase II; regulation of cytokine production; trong>andtrong> regulation of immune system process. Located in mitochondrion trong>andtrong> nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>5 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 5

Enatrong>btrong>les DNA-trong>btrong>inding transcription repressor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II transcription regulatory region sequence-specific DNA trong>btrong>inding activity. Involved in negative regulation of transcription trong>btrong>y RNA polymerase II. Located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>4 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 4

Enatrong>btrong>les several functions, including DNA-trong>btrong>inding transcription repressor activity, RNA polymerase II-specific; nucleotide trong>btrong>inding activity; trong>andtrong> protein homodimerization activity. Involved in DNA damage response trong>andtrong> negative regulation of transcription trong>btrong>y RNA polymerase II. Located in cytosol trong>andtrong> nuclear trong>btrong>ody. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>9 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 9

Enatrong>btrong>les identical protein trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

AStrong>Btrong>15 Gene

ankyrin repeat trong>andtrong> SOCS trong>btrong>ox containing 15

This gene encodes a memtrong>btrong>er of the suppressor of cytokine signaling trong>btrong>ox superfamily. The proteins in this superfamily participate in the utrong>btrong>iquitin-proteasome system for the degradation of proteins in the cell cycle trong>andtrong> signal transduction pathways. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Mar 2014]

PATZ1 Gene

POZ (trong>Btrong>Ttrong>Btrong>) trong>andtrong> AT hook containing zinc finger 1

The protein encoded trong>btrong>y this gene contains an A-T hook DNA trong>btrong>inding motif which usually trong>btrong>inds to other DNA trong>btrong>inding structures to play an important role in chromatin modeling trong>andtrong> transcription regulation. Its Poz domain is thought to function as a site for protein-protein interaction trong>andtrong> is required for transcriptional repression, trong>andtrong> the zinc-fingers comprise the DNA trong>btrong>inding domain. Since the encoded protein has typical features of a transcription factor, it is postulated to trong>btrong>e a repressor of gene expression. In small round cell sarcoma, this gene is fused to EWS trong>btrong>y a small inversion of 22q, then the hytrong>btrong>rid is thought to trong>btrong>e translocated (t(1;22)(p36.1;q12). The rearrangement of chromosome 22 involves intron 8 of EWS trong>andtrong> exon 1 of this gene creating a chimeric sequence containing the transactivation domain of EWS fused to zinc finger domain of this protein. This is a distinct example of an intra-chromosomal rearrangement of chromosome 22. Four alternatively spliced transcript variants are descritrong>btrong>ed for this gene. [provided trong>btrong>y RefSeq, Jul 2008]

CEND1P1 Gene

cell cycle exit trong>andtrong> neuronal differentiation 1 pseudogene 1

CEND1P2 Gene

cell cycle exit trong>andtrong> neuronal differentiation 1 pseudogene 2

STAM2 Gene

signal transducing adaptor molecule (SH3 domain trong>andtrong> ITAM motif) 2

The protein encoded trong>btrong>y this gene is closely related to STAM, an adaptor protein involved in the downstream signaling of cytokine receptors, trong>btrong>oth of which contain a SH3 domain trong>andtrong> the immunoreceptor tyrosine-trong>btrong>ased activation motif (ITAM). Similar to STAM, this protein acts downstream of JAK kinases, trong>andtrong> is phosphorylated in response to cytokine stimulation. This protein trong>andtrong> STAM thus are thought to exhitrong>btrong>it compensatory effects on the signaling pathway downstream of JAK kinases upon cytokine stimulation. [provided trong>btrong>y RefSeq, Jul 2008]

LRRD1 Gene

leucine-rich repeats trong>andtrong> death domain containing 1

Predicted to trong>btrong>e involved in signal transduction. Predicted to trong>btrong>e active in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC100130891 Gene

PDZ trong>andtrong> LIM domain 7 (enigma) pseudogene

SPOCK1 Gene

sparc/osteonectin, cwcv trong>andtrong> kazal-like domains proteoglycan (testican) 1

This gene encodes the protein core of a seminal plasma proteoglycan containing chondroitin- trong>andtrong> heparan-sulfate chains. The protein's function is unknown, although similarity to thyropin-type cysteine protease-inhitrong>btrong>itors suggests its function may trong>btrong>e related to protease inhitrong>btrong>ition. [provided trong>btrong>y RefSeq, Jul 2008]

SPOCK2 Gene

sparc/osteonectin, cwcv trong>andtrong> kazal-like domains proteoglycan (testican) 2

This gene encodes a protein which trong>btrong>inds with glycosaminoglycans to form part of the extracellular matrix. The protein contains thyroglotrong>btrong>ulin type-1, follistatin-like, trong>andtrong> calcium-trong>btrong>inding domains, trong>andtrong> has glycosaminoglycan attachment sites in the acidic C-terminal region. Three alternatively spliced transcript variants that encode different protein isoforms have trong>btrong>een descritrong>btrong>ed for this gene. [provided trong>btrong>y RefSeq, Oct 2011]

SPOCK3 Gene

sparc/osteonectin, cwcv trong>andtrong> kazal-like domains proteoglycan (testican) 3

This gene encodes a memtrong>btrong>er of a novel family of calcium-trong>btrong>inding proteoglycan proteins that contain thyroglotrong>btrong>ulin type-1 trong>andtrong> Kazal-like domains. The encoded protein trong>andtrong> may play a role in adult T-cell leukemia trong>btrong>y inhitrong>btrong>iting the activity of memtrong>btrong>rane-type matrix metalloproteinases. Alternatively spliced transcript variants encoding multiple isoforms have trong>btrong>een otrong>btrong>served for this gene. [provided trong>btrong>y RefSeq, Oct 2011]

CSRP1 Gene

cysteine trong>andtrong> glycine-rich protein 1

This gene encodes a memtrong>btrong>er of the cysteine-rich protein (CSRP) family. This gene family includes a group of LIM domain proteins, which may trong>btrong>e involved in regulatory processes important for development trong>andtrong> cellular differentiation. The LIM/doutrong>btrong>le zinc-finger motif found in this gene product occurs in proteins with critical functions in gene regulation, cell growth, trong>andtrong> somatic differentiation. Alternatively spliced transcript variants have trong>btrong>een descritrong>btrong>ed. [provided trong>btrong>y RefSeq, Aug 2010]

CSRP3 Gene

cysteine trong>andtrong> glycine-rich protein 3 (cardiac LIM protein)

This gene encodes a memtrong>btrong>er of the CSRP family of LIM domain proteins, which may trong>btrong>e involved in regulatory processes important for development trong>andtrong> cellular differentiation. The LIM/doutrong>btrong>le zinc-finger motif found in this protein is found in a group of proteins with critical functions in gene regulation, cell growth, trong>andtrong> somatic differentiation. Mutations in this gene are thought to cause heritatrong>btrong>le forms of hypertrophic cardiomyopathy (HCM) trong>andtrong> dilated cardiomyopathy (DCM) in humans. Alternatively spliced transcript variants with different 5' UTR, trong>btrong>ut encoding the same protein, have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jul 2008]

CSRP2 Gene

cysteine trong>andtrong> glycine-rich protein 2

CSRP2 is a memtrong>btrong>er of the CSRP family of genes, encoding a group of LIM domain proteins, which may trong>btrong>e involved in regulatory processes important for development trong>andtrong> cellular differentiation. CRP2 contains two copies of the cysteine-rich amino acid sequence motif (LIM) with putative zinc-trong>btrong>inding activity, trong>andtrong> may trong>btrong>e involved in regulating ordered cell growth. Other genes in the family include CSRP1 trong>andtrong> CSRP3. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Jul 2014]

EGFLAM Gene

EGF-like, fitrong>btrong>ronectin type III trong>andtrong> laminin G domains

Predicted to enatrong>btrong>le calcium ion trong>btrong>inding activity trong>andtrong> glycosaminoglycan trong>btrong>inding activity. Predicted to act upstream of or within extracellular matrix organization trong>andtrong> positive regulation of cell-sutrong>btrong>strate adhesion. Part of cell surface. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ARAP3 Gene

ArfGAP with RhoGAP domain, ankyrin repeat trong>andtrong> PH domain 3

This gene encodes a phosphoinositide trong>btrong>inding protein containing ARF-GAP, RHO-GAP, RAS-associating, trong>andtrong> pleckstrin homology domains. The ARF-GAP trong>andtrong> RHO-GAP domains cooperate in mediating rearrangements in the cell cytoskeleton trong>andtrong> cell shape. It is a specific PtdIns(3,4,5)P3/PtdIns(3,4)P2-stimulated Arf6-GAP protein. An alternatively spliced transcript has trong>btrong>een found for this gene, trong>btrong>ut its trong>btrong>iological validity has not trong>btrong>een determined. [provided trong>btrong>y RefSeq, Sep 2015]

ARAP2 Gene

ArfGAP with RhoGAP domain, ankyrin repeat trong>andtrong> PH domain 2

The protein encoded trong>btrong>y this gene contains ARF-GAP, RHO-GAP, ankyrin repeat, RAS-associating, trong>andtrong> pleckstrin homology domains. The protein is a phosphatidylinositol (3,4,5)-trisphosphate-dependent Arf6 GAP that trong>btrong>inds RhoA-GTP, trong>btrong>ut it lacks the predicted catalytic arginine in the RHO-GAP domain trong>andtrong> does not have RHO-GAP activity. The protein associates with focal adhesions trong>andtrong> functions downstream of RhoA to regulate focal adhesion dynamics. [provided trong>btrong>y RefSeq, Sep 2008]

SRMS Gene

src-related kinase lacking C-terminal regulatory tyrosine trong>andtrong> N-terminal myristylation sites

Enatrong>btrong>les protein tyrosine kinase activity. Involved in peptidyl-tyrosine autophosphorylation trong>andtrong> positive regulation of TORC1 signaling. Located in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

THRIL Gene

TNF trong>andtrong> HNRNPL related immunoregulatory long non-coding RNA

CFAP74 Gene

cilia trong>andtrong> flagella associated protein 74

Predicted to trong>btrong>e involved in axoneme assemtrong>btrong>ly. Located in cytoplasm; nucleus; trong>andtrong> sperm flagellum. Implicated in primary ciliary dyskinesia. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP70 Gene

cilia trong>andtrong> flagella associated protein 70

Predicted to trong>btrong>e involved in cilium assemtrong>btrong>ly trong>andtrong> cilium movement. Predicted to act upstream of or within several processes, including maintenance of cell numtrong>btrong>er; single fertilization; trong>andtrong> spermatid development. Located in ciliary trong>btrong>asal trong>btrong>ody trong>andtrong> sperm flagellum. Part of outer dynein arm. Implicated in spermatogenic failure 41. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

NUSAP1 Gene

nucleolar trong>andtrong> spindle associated protein 1

NUSAP1 is a nucleolar-spindle-associated protein that plays a role in spindle microtutrong>btrong>ule organization (Raemaekers et al., 2003 [Putrong>btrong>Med 12963707]).[supplied trong>btrong>y OMIM, Jun 2009]

LOC100288203 Gene

WAS protein homolog associated with actin, golgi memtrong>btrong>ranes trong>andtrong> microtutrong>btrong>ules pseudogene

LOC100421273 Gene

F-trong>btrong>ox trong>andtrong> WD repeat domain containing 11 pseudogene

ZRSR2 Gene

zinc finger (CCCH type), RNA-trong>btrong>inding motif trong>andtrong> serine/arginine rich 2

This gene encodes an essential splicing factor. The encoded protein associates with the U2 auxiliary factor heterodimer, which is required for the recognition of a functional 3' splice site in pre-mRNA splicing, trong>andtrong> may play a role in network interactions during spliceosome assemtrong>btrong>ly. [provided trong>btrong>y RefSeq, Jul 2008]

CHMRQ Gene

Ceretrong>btrong>ellar hypoplasia, mental retardation, trong>andtrong> quadrupedal locomotion

trong>Btrong>PESC1 Gene

trong>btrong>lepharophimosis, epicanthus inversus trong>andtrong> ptosis, ctrong>andtrong>idate 1 (non-protein coding)

LRGUK Gene

leucine-rich repeats trong>andtrong> guanylate kinase domain containing

Predicted to enatrong>btrong>le guanylate kinase activity. Predicted to trong>btrong>e involved in axoneme assemtrong>btrong>ly trong>andtrong> spermatogenesis. Predicted to trong>btrong>e located in acrosomal vesicle trong>andtrong> manchette. Predicted to trong>btrong>e active in cytosol. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

MAMSTR Gene

MEF2 activating motif trong>andtrong> SAP domain containing transcriptional regulator

Predicted to enatrong>btrong>le transcription coregulator activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to act upstream of or within positive regulation of myotutrong>btrong>e differentiation trong>andtrong> positive regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e active in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LRFN5 Gene

leucine rich repeat trong>andtrong> fitrong>btrong>ronectin type III domain containing 5

This gene encodes a protein that trong>btrong>elongs to the leucine-rich repeat trong>andtrong> fitrong>btrong>ronectin type III domain-containing family of proteins. A similar protein in mouse, a glycosylated transmemtrong>btrong>rane protein, is thought to function in presynaptic differentiation. [provided trong>btrong>y RefSeq, Sep 2016]

ZSCAN12P1 Gene

zinc finger trong>andtrong> SCAN domain containing 12 pseudogene 1

PHRF1 Gene

PHD trong>andtrong> ring finger domains 1

Predicted to enatrong>btrong>le RNA polymerase trong>btrong>inding activity. Predicted to trong>btrong>e involved in protein utrong>btrong>iquitination. Located in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

DZANK1 Gene

doutrong>btrong>le zinc ritrong>btrong>trong>btrong>on trong>andtrong> ankyrin repeat domains 1

This gene contains two ankyrin repeat-encoding regions. Ankyrin repeats are ttrong>andtrong>emly repeated modules of atrong>btrong>out 33 amino acids descritrong>btrong>ed as L-shaped structures consisting of a trong>btrong>eta-hairpin trong>andtrong> two alpha-helices. Ankyrin repeats occur in a large numtrong>btrong>er of functionally diverse proteins, mainly from eukaryotes, trong>andtrong> are known to function as protein-protein interaction domains. [provided trong>btrong>y RefSeq, Dec 2018]

DUPD1 Gene

dual specificity phosphatase trong>andtrong> pro isomerase domain containing 1

Enatrong>btrong>les protein homodimerization activity trong>andtrong> protein tyrosine/serine/threonine phosphatase activity. Involved in protein dephosphorylation. Part of protein-containing complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

TANC1 Gene

tetratricopeptide repeat, ankyrin repeat trong>andtrong> coiled-coil containing 1

Predicted to trong>btrong>e involved in regulation of postsynapse organization. Predicted to act upstream of or within dendritic spine maintenance; myotrong>btrong>last fusion; trong>andtrong> visual learning. Predicted to trong>btrong>e located in several cellular components, including axon terminus; neuronal cell trong>btrong>ody; trong>andtrong> postsynaptic density. Predicted to trong>btrong>e active in glutamatergic synapse trong>andtrong> postsynaptic density, intracellular component. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

TANC2 Gene

tetratricopeptide repeat, ankyrin repeat trong>andtrong> coiled-coil containing 2

Predicted to trong>btrong>e a structural constituent of postsynaptic density. Predicted to trong>btrong>e involved in dense core granule cytoskeletal transport; regulation of dendritic spine development; trong>andtrong> regulation of dendritic spine morphogenesis. Predicted to act upstream of or within in utero emtrong>btrong>ryonic development. Located in dendritic spine. Implicated in intellectual developmental disorder with autistic features trong>andtrong> language delay, with or without seizures. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ktrong>Btrong>Ttrong>Btrong>D13 Gene

kelch repeat trong>andtrong> trong>Btrong>Ttrong>Btrong> (POZ) domain containing 13

The gene trong>btrong>elongs to a family of genes encoding proteins containing a trong>Btrong>Ttrong>Btrong> domain trong>andtrong> several kelch repeats. The trong>Btrong>Ttrong>Btrong> domain functions as a protein-protein interaction module, which includes an atrong>btrong>ility to self-associate or to interact with non-trong>Btrong>Ttrong>Btrong> domain-containing proteins. The kelch motif typically occurs in groups of five to seven repeats, trong>andtrong> has trong>btrong>een found in proteins with diverse functions. Known functions of these family memtrong>btrong>ers include transcription regulation, ion channel tetramerization trong>andtrong> gating, protein utrong>btrong>iquitination or degradation, trong>andtrong> cytoskeleton regulation. The exact function of this family memtrong>btrong>er has yet to trong>btrong>e determined. [provided trong>btrong>y RefSeq, Jun 2010]

Ktrong>Btrong>Ttrong>Btrong>D12 Gene

kelch repeat trong>andtrong> trong>Btrong>Ttrong>Btrong> (POZ) domain containing 12

Predicted to enatrong>btrong>le utrong>btrong>iquitin-like ligase-sutrong>btrong>strate adaptor activity. Predicted to trong>btrong>e involved in proteasome-mediated utrong>btrong>iquitin-dependent protein catatrong>btrong>olic process. Predicted to trong>btrong>e part of Cul3-RING utrong>btrong>iquitin ligase complex. Predicted to trong>btrong>e active in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ktrong>Btrong>Ttrong>Btrong>D11 Gene

kelch repeat trong>andtrong> trong>Btrong>Ttrong>Btrong> (POZ) domain containing 11

TRANK1 Gene

tetratricopeptide repeat trong>andtrong> ankyrin repeat containing 1

DEFA1A3 Gene

defensin, alpha 1 trong>andtrong> alpha 3, variatrong>btrong>le copy numtrong>btrong>er locus

DPF2 Gene

D4, zinc trong>andtrong> doutrong>btrong>le PHD fingers family 2

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of the d4 domain family, characterized trong>btrong>y a zinc finger-like structural motif. This protein functions as a transcription factor which is necessary for the apoptotic response following deprivation of survival factors. It likely serves a regulatory role in rapid hematopoietic cell growth trong>andtrong> turnover. This gene is considered a ctrong>andtrong>idate gene for multiple endocrine neoplasia type I, an inherited cancer syndrome involving multiple parathyroid, enteropancreatic, trong>andtrong> pituitary tumors. [provided trong>btrong>y RefSeq, Jul 2008]

DPF3 Gene

D4, zinc trong>andtrong> doutrong>btrong>le PHD fingers, family 3

This gene encodes a memtrong>btrong>er of the D4 protein family. The encoded protein is a transcription regulator that trong>btrong>inds acetylated histones trong>andtrong> is a component of the trong>Btrong>AF chromatin remodeling complex. Alternate splicing results in multiple transcript variants encoding different isoforms. [provided trong>btrong>y RefSeq, Jul 2013]

DPF1 Gene

D4, zinc trong>andtrong> doutrong>btrong>le PHD fingers family 1

Enatrong>btrong>les sequence-specific doutrong>btrong>le-strtrong>andtrong>ed DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in nervous system development. Predicted to trong>btrong>e located in nucleoplasm. Predicted to trong>btrong>e part of ntrong>Btrong>AF complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

MICAL1 Gene

microtutrong>btrong>ule associated monooxygenase, calponin trong>andtrong> LIM domain containing 1

This gene encodes an enzyme that oxidizes methionine residues on actin, theretrong>btrong>y promoting depolymerization of actin filaments. This protein interacts with trong>andtrong> regulates signalling trong>btrong>y NEDD9/CAS-L (neural precursor cell expressed, developmentally down-regulated 9). Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Aug 2015]

MICAL2 Gene

microtutrong>btrong>ule associated monooxygenase, calponin trong>andtrong> LIM domain containing 2

The protein encoded trong>btrong>y this gene is a monooxygenase that enhances depolymerization of F-actin trong>andtrong> is therefore involved in cytoskeletal dynamics. The encoded protein is a regulator of the SRF signaling pathway. Increased expression of this gene has trong>btrong>een associated with cancer progression trong>andtrong> metastasis. [provided trong>btrong>y RefSeq, Oct 2016]

MICAL3 Gene

microtutrong>btrong>ule associated monooxygenase, calponin trong>andtrong> LIM domain containing 3

Enatrong>btrong>les actin trong>btrong>inding activity trong>andtrong> molecular adaptor activity. Involved in actin filament depolymerization. Located in several cellular components, including Flemming trong>btrong>ody; intercellular trong>btrong>ridge; trong>andtrong> nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

AGAP10P Gene

ArfGAP with GTPase domain, ankyrin repeat trong>andtrong> PH domain 10 pseudogene

CPED1 Gene

cadherin-like trong>andtrong> PC-esterase domain containing 1

Located in endoplasmic reticulum. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SNRPtrong>Btrong> Gene

small nuclear ritrong>btrong>onucleoprotein polypeptides trong>Btrong> trong>andtrong> trong>Btrong>1

The protein encoded trong>btrong>y this gene is one of several nuclear proteins that are found in common among U1, U2, U4/U6, trong>andtrong> U5 small ritrong>btrong>onucleoprotein particles (snRNPs). These snRNPs are involved in pre-mRNA splicing, trong>andtrong> the encoded protein may also play a role in pre-mRNA splicing or snRNP structure. Autoantitrong>btrong>odies from patients with systemic lupus erythematosus frequently recognize epitopes on the encoded protein. Two transcript variants encoding different isoforms (trong>Btrong> trong>andtrong> trong>Btrong>') have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jul 2008]

PTEN Gene

phosphatase trong>andtrong> tensin homolog

This gene was identified as a tumor suppressor that is mutated in a large numtrong>btrong>er of cancers at high frequency. The protein encoded trong>btrong>y this gene is a phosphatidylinositol-3,4,5-trisphosphate 3-phosphatase. It contains a tensin like domain as well as a catalytic domain similar to that of the dual specificity protein tyrosine phosphatases. Unlike most of the protein tyrosine phosphatases, this protein preferentially dephosphorylates phosphoinositide sutrong>btrong>strates. It negatively regulates intracellular levels of phosphatidylinositol-3,4,5-trisphosphate in cells trong>andtrong> functions as a tumor suppressor trong>btrong>y negatively regulating AKT/PKtrong>Btrong> signaling pathway. The use of a non-canonical (CUG) upstream initiation site produces a longer isoform that initiates translation with a leucine, trong>andtrong> is thought to trong>btrong>e preferentially associated with the mitochondrial inner memtrong>btrong>rane. This longer isoform may help regulate energy metatrong>btrong>olism in the mitochondria. A pseudogene of this gene is found on chromosome 9. Alternative splicing trong>andtrong> the use of multiple translation start codons results in multiple transcript variants encoding different isoforms. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2015]

PHACTR2P1 Gene

phosphatase trong>andtrong> actin regulator 2 pseudogene 1

SPStrong>Btrong>3 Gene

splA/ryanodine receptor domain trong>andtrong> SOCS trong>btrong>ox containing 3

Enatrong>btrong>les utrong>btrong>iquitin-like ligase-sutrong>btrong>strate adaptor activity. Involved in several processes, including negative regulation of cGAS/STING signaling pathway; negative regulation of epithelial to mesenchymal transition; trong>andtrong> protein K48-linked utrong>btrong>iquitination. Part of Cul5-RING utrong>btrong>iquitin ligase complex. Is active in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SPStrong>Btrong>2 Gene

splA/ryanodine receptor domain trong>andtrong> SOCS trong>btrong>ox containing 2

This gene encodes a memtrong>btrong>er of a sutrong>btrong>family of proteins containing a central SPRY (repeats in splA trong>andtrong> RyR) domain trong>andtrong> a C-terminal suppressor of cytokine signaling (SOCS) trong>btrong>ox. This protein plays a role in cell signaling. This gene is present in a gene-rich cluster on chromosome 12p13 in the vicinity of the CD4 antigen trong>andtrong> triosephosphate isomerase genes. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2016]

SPStrong>Btrong>1 Gene

splA/ryanodine receptor domain trong>andtrong> SOCS trong>btrong>ox containing 1

Enatrong>btrong>les utrong>btrong>iquitin-like ligase-sutrong>btrong>strate adaptor activity. Involved in protein utrong>btrong>iquitination trong>andtrong> utrong>btrong>iquitin-dependent protein catatrong>btrong>olic process. Located in cytosol. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

RTCtrong>Btrong> Gene

RNA 2',3'-cyclic phosphate trong>andtrong> 5'-OH ligase

Enatrong>btrong>les RNA ligase (GTP) activity trong>andtrong> vinculin trong>btrong>inding activity. Involved in tRNA splicing, via endonucleolytic cleavage trong>andtrong> ligation. Located in cytosol trong>andtrong> nucleoplasm. Part of tRNA-splicing ligase complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

FEZ1 Gene

fasciculation trong>andtrong> elongation protein zeta 1 (zygin I)

This gene is an ortholog of the C. elegans unc-76 gene, which is necessary for normal axonal trong>btrong>undling trong>andtrong> elongation within axon trong>btrong>undles. Expression of this gene in C. elegans unc-76 mutants can restore to the mutants partial locomotion trong>andtrong> axonal fasciculation, suggesting that it also functions in axonal outgrowth. The N-terminal half of the gene product is highly acidic. Alternatively spliced transcript variants encoding different isoforms of this protein have trong>btrong>een descritrong>btrong>ed. [provided trong>btrong>y RefSeq, Jul 2008]

FEZ2 Gene

fasciculation trong>andtrong> elongation protein zeta 2 (zygin II)

This gene is an ortholog of the C. elegans unc-76 gene, which is necessary for normal axonal trong>btrong>undling trong>andtrong> elongation within axon trong>btrong>undles. Other orthologs include the rat gene that encodes zygin II, which can trong>btrong>ind to synaptotagmin. [provided trong>btrong>y RefSeq, Jul 2008]

SECTM1 Gene

secreted trong>andtrong> transmemtrong>btrong>rane 1

This gene encodes a transmemtrong>btrong>rane trong>andtrong> secreted protein with characteristics of a type 1a transmemtrong>btrong>rane protein. It is found in a perinuclear Golgi-like pattern trong>andtrong> thought to trong>btrong>e involved in hematopoietic trong>andtrong>/or immune system processes. [provided trong>btrong>y RefSeq, Jul 2008]

RALGPS2 Gene

Ral GEF with PH domain trong>andtrong> SH3 trong>btrong>inding motif 2

Predicted to enatrong>btrong>le guanyl-nucleotide exchange factor activity. Predicted to trong>btrong>e involved in Ras protein signal transduction. Predicted to trong>btrong>e located in cytoplasm. Predicted to trong>btrong>e active in plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

RALGPS1 Gene

Ral GEF with PH domain trong>andtrong> SH3 trong>btrong>inding motif 1

Enatrong>btrong>les guanyl-nucleotide exchange factor activity. Involved in regulation of Ral protein signal transduction. Predicted to trong>btrong>e located in cytoplasm. Predicted to trong>btrong>e active in plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LRtrong>Btrong>A Gene

LPS-responsive vesicle trafficking, trong>btrong>each trong>andtrong> anchor containing

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of the WDL-trong>Btrong>EACH-WD (Wtrong>Btrong>W) gene family. Its expression is induced in trong>Btrong> cells trong>andtrong> macrophages trong>btrong>y trong>btrong>acterial lipopolysaccharides (LPS). The encoded protein associates with protein kinase A trong>andtrong> may trong>btrong>e involved in leading intracellular vesicles to activated receptor complexes, which aids in the secretion trong>andtrong>/or memtrong>btrong>rane deposition of immune effector molecules. Defects in this gene are associated with the disorder common variatrong>btrong>le immunodeficiency-8 with autoimmunity. Two transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Dec 2012]

CHORDC1 Gene

cysteine trong>andtrong> histidine-rich domain (CHORD) containing 1

Enatrong>btrong>les Hsp90 protein trong>btrong>inding activity. Predicted to trong>btrong>e involved in several processes, including centrosome duplication; chaperone-mediated protein folding; trong>andtrong> negative regulation of Rho-dependent protein serine/threonine kinase activity. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LRFN3 Gene

leucine rich repeat trong>andtrong> fitrong>btrong>ronectin type III domain containing 3

Predicted to trong>btrong>e involved in regulation of presynapse assemtrong>btrong>ly; regulation of synaptic memtrong>btrong>rane adhesion; trong>andtrong> synaptic memtrong>btrong>rane adhesion. Predicted to trong>btrong>e located in plasma memtrong>btrong>rane. Predicted to trong>btrong>e active in cell surface; glutamatergic synapse; trong>andtrong> synaptic memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LRFN2 Gene

leucine rich repeat trong>andtrong> fitrong>btrong>ronectin type III domain containing 2

Predicted to trong>btrong>e involved in modulation of chemical synaptic transmission trong>andtrong> regulation of postsynapse organization. Predicted to trong>btrong>e located in plasma memtrong>btrong>rane. Predicted to trong>btrong>e active in several cellular components, including Schaffer collateral - CA1 synapse; cell surface; trong>andtrong> postsynaptic density memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LRFN1 Gene

leucine rich repeat trong>andtrong> fitrong>btrong>ronectin type III domain containing 1

Predicted to trong>btrong>e involved in regulation of postsynaptic density assemtrong>btrong>ly. Predicted to trong>btrong>e located in plasma memtrong>btrong>rane. Predicted to trong>btrong>e active in cell surface; postsynaptic density memtrong>btrong>rane; trong>andtrong> presynaptic active zone memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LRFN4 Gene

leucine rich repeat trong>andtrong> fitrong>btrong>ronectin type III domain containing 4

Predicted to trong>btrong>e involved in regulation of postsynaptic density assemtrong>btrong>ly; regulation of presynapse assemtrong>btrong>ly; trong>andtrong> synaptic memtrong>btrong>rane adhesion. Predicted to trong>btrong>e located in plasma memtrong>btrong>rane. Predicted to trong>btrong>e active in several cellular components, including GAtrong>Btrong>A-ergic synapse; glutamatergic synapse; trong>andtrong> postsynaptic density memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

OASD Gene

ocular altrong>btrong>inism trong>andtrong> sensorineural deafness

LOC100421064 Gene

sushi, nidogen trong>andtrong> EGF-like domains 1 pseudogene

SVEP1 Gene

sushi, von Willetrong>btrong>rtrong>andtrong> factor type A, EGF trong>andtrong> pentraxin domain containing 1

Enatrong>btrong>les integrin trong>btrong>inding activity. Involved in negative regulation of vasoconstriction trong>andtrong> positive regulation of platelet activation. Located in cytoplasm trong>andtrong> nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

GAPVD1 Gene

GTPase activating protein trong>andtrong> VPS9 domains 1

Enatrong>btrong>les GTPase activating protein trong>btrong>inding activity trong>andtrong> guanyl-nucleotide exchange factor activity. Involved in regulation of protein transport. Located in cytosol trong>andtrong> plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

RC3H1 Gene

ring finger trong>andtrong> CCCH-type domains 1

This gene encodes a protein containing RING-type trong>andtrong> C3H1-type zinc finger motifs. The encoded protein recognizes trong>andtrong> trong>btrong>inds to a constitutive decay element (CDE) in the 3' UTR of mRNAs, leading to mRNA deadenylation trong>andtrong> degradation. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Jul 2014]

RC3H2 Gene

ring finger trong>andtrong> CCCH-type domains 2

Enatrong>btrong>les nucleic acid trong>btrong>inding activity trong>andtrong> utrong>btrong>iquitin protein ligase activity. Involved in protein polyutrong>btrong>iquitination. Located in cell surface; intracellular memtrong>btrong>rane-trong>btrong>ounded organelle; trong>andtrong> memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

AUNIP Gene

aurora kinase A trong>andtrong> ninein interacting protein

Enatrong>btrong>les damaged DNA trong>btrong>inding activity. Involved in doutrong>btrong>le-strtrong>andtrong> trong>btrong>reak repair via homologous recomtrong>btrong>ination; negative regulation of doutrong>btrong>le-strtrong>andtrong> trong>btrong>reak repair via nonhomologous end joining; trong>andtrong> spindle organization. Located in centrosome; site of DNA damage; trong>andtrong> spindle pole. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC100129367 Gene

nucleolar trong>andtrong> coiled-trong>btrong>ody phosphoprotein 1 pseudogene

CFAP99 Gene

cilia trong>andtrong> flagella associated protein 99

Predicted to trong>btrong>e located in motile cilium. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LRWD1 Gene

leucine-rich repeats trong>andtrong> WD repeat domain containing 1

The protein encoded trong>btrong>y this gene interacts with components of the origin recognition complex (ORC) trong>andtrong> regulates the formation of the prereplicative complex. The encoded protein statrong>btrong>ilizes the ORC trong>andtrong> therefore aids in DNA replication. This protein is required for the G1/S phase transition of the cell cycle. In addition, the encoded protein trong>btrong>inds to trimethylated histone H3 in heterochromatin trong>andtrong> recruits the ORC trong>andtrong> lysine methyltransferases, which help maintain the repressive heterochromatic state. Two transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Dec 2015]

STAC Gene

SH3 trong>andtrong> cysteine rich domain

Predicted to enatrong>btrong>le transmemtrong>btrong>rane transporter trong>btrong>inding activity. Predicted to trong>btrong>e involved in positive regulation of protein localization to plasma memtrong>btrong>rane; positive regulation of voltage-gated calcium channel activity; trong>andtrong> skeletal muscle contraction. Predicted to act upstream of or within cellular response to heat; muscle contraction; trong>andtrong> regulation of voltage-gated calcium channel activity. Predicted to trong>btrong>e located in cytoplasmic side of plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

STAM Gene

signal transducing adaptor molecule (SH3 domain trong>andtrong> ITAM motif) 1

This gene encodes a memtrong>btrong>er of the signal-transducing adaptor molecule family. These proteins mediate downstream signaling of cytokine receptors trong>andtrong> also play a role in ER to Golgi trafficking trong>btrong>y interacting with the coat protein II complex. The encoded protein also associates with hepatocyte growth factor-regulated sutrong>btrong>strate to form the endosomal sorting complex required for transport-0 (ESCRT-0), which sorts utrong>btrong>iquitinated memtrong>btrong>rane proteins to the ESCRT-1 complex for lysosomal degradation. Alternatively spliced transcript variants have trong>btrong>een otrong>btrong>served for this gene. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2011]

Ztrong>Btrong>Ttrong>Btrong>12 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 12

Enatrong>btrong>les sequence-specific doutrong>btrong>le-strtrong>andtrong>ed DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in negative regulation of transcription trong>btrong>y RNA polymerase II; regulation of cytokine production; trong>andtrong> regulation of immune system process. Located in nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>11 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 11

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of DNA-templated transcription. Located in nucleoplasm. Implicated in autosomal recessive intellectual developmental disorder 69. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>17 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 17

This gene encodes a zinc finger protein involved in the regulation of c-myc. The symtrong>btrong>ol MIZ1 has also trong>btrong>een associated with PIAS2 which is a different gene located on chromosome 18. [provided trong>btrong>y RefSeq, Jul 2008]

Ztrong>Btrong>Ttrong>Btrong>16 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 16

This gene is a memtrong>btrong>er of the Krueppel C2H2-type zinc-finger protein family trong>andtrong> encodes a zinc finger transcription factor that contains nine Kruppel-type zinc finger domains at the cartrong>btrong>oxyl terminus. This protein is located in the nucleus, is involved in cell cycle progression, trong>andtrong> interacts with a histone deacetylase. Specific instances of atrong>btrong>errant gene rearrangement at this locus have trong>btrong>een associated with acute promyelocytic leukemia (APL). Alternate transcriptional splice variants have trong>btrong>een characterized. [provided trong>btrong>y RefSeq, Jul 2008]

Ztrong>Btrong>Ttrong>Btrong>14 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 14

Enatrong>btrong>les DNA-trong>btrong>inding transcription factor activity trong>andtrong> transcription cis-regulatory region trong>btrong>inding activity. Involved in negative regulation of DNA-templated transcription. Located in aggresome; cytosol; trong>andtrong> nuclear lumen. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>18 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 18

This gene encodes a C2H2-type zinc finger protein which acts a transcriptional repressor of genes involved in neuronal development. The encoded protein recognizes a specific sequence motif trong>andtrong> recruits components of chromatin to target genes. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, May 2013]

ARAP1 Gene

ArfGAP with RhoGAP domain, ankyrin repeat trong>andtrong> PH domain 1

The protein encoded trong>btrong>y this gene contains SAM, ARF-GAP, RHO-GAP, ankyrin repeat, RAS-associating, trong>andtrong> pleckstrin homology (PH) domains. In vitro, this protein displays RHO-GAP trong>andtrong> phosphatidylinositol (3,4,5) trisphosphate (PIP3)-dependent ARF-GAP activity. The encoded protein associates with the Golgi, trong>andtrong> the ARF-GAP activity mediates changes in the Golgi trong>andtrong> the formation of filopodia. It is thought to regulate the cell-specific trafficking of a receptor protein involved in apoptosis. Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Sep 2008]

NXPE1 Gene

neurexophilin trong>andtrong> PC-esterase domain family, memtrong>btrong>er 1

Predicted to trong>btrong>e located in extracellular region trong>andtrong> memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

NXPE2 Gene

neurexophilin trong>andtrong> PC-esterase domain family, memtrong>btrong>er 2

Predicted to trong>btrong>e located in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

NXPE3 Gene

neurexophilin trong>andtrong> PC-esterase domain family, memtrong>btrong>er 3

This gene encodes a memtrong>btrong>er of the neurexophilin family of neuropeptide-like glycoproteins. The encoded protein contains a variatrong>btrong>le N-terminal domain, a highly conserved neurexophilin trong>andtrong> PC-esterase (NXPE) central domain, a short linker region, trong>andtrong> a cysteine-rich C-terminal domain. This protein trong>btrong>inds alpha neurexins, a group of presynaptic transmemtrong>btrong>rane receptors that promote adhesion trong>btrong>etween dendrites trong>andtrong> axons. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2017]

NXPE4 Gene

neurexophilin trong>andtrong> PC-esterase domain family, memtrong>btrong>er 4

Located in extracellular exosome. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

KIN Gene

Kin17 DNA trong>andtrong> RNA trong>btrong>inding protein

The protein encoded trong>btrong>y this gene is a nuclear protein that forms intranuclear foci during proliferation trong>andtrong> is redistritrong>btrong>uted in the nucleoplasm during the cell cycle. Short-wave ultraviolet light provokes the relocalization of the protein, suggesting its participation in the cellular response to DNA damage. Originally selected trong>btrong>ased on protein-trong>btrong>inding with RecA antitrong>btrong>odies, the mouse protein presents a limited similarity with a functional domain of the trong>btrong>acterial RecA protein, a characteristic shared trong>btrong>y this human ortholog. Alternative splicing of this gene results in multiple transcript variants. [provided trong>btrong>y RefSeq, Jan 2012]

TPTE2P5 Gene

transmemtrong>btrong>rane phosphoinositide 3-phosphatase trong>andtrong> tensin homolog 2 pseudogene 5

LOC100421184 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 2 pseudogene

FRMPD2trong>Btrong> Gene

FERM trong>andtrong> PDZ domain containing 2trong>Btrong>, pseudogene

This gene represents a pseudogene of the FERM trong>andtrong> 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 trong>btrong>y RefSeq, Dec 2014]

LOC100128164 Gene

four trong>andtrong> a half LIM domains 1 pseudogene

LAMTOR3P2 Gene

late endosomal/lysosomal adaptor, MAPK trong>andtrong> MTOR activator 3 pseudogene 2

MAA Gene

microphthalmia or anophthalmia trong>andtrong> associated anomalies

Ztrong>Btrong>Ttrong>Btrong>10 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 10

Enatrong>btrong>les telomeric DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in negative regulation of transcription trong>btrong>y RNA polymerase II. Located in chromosome, telomeric region trong>andtrong> nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ARGLU1 Gene

arginine trong>andtrong> glutamate rich 1

Enatrong>btrong>les nuclear receptor coactivator activity trong>andtrong> pre-mRNA trong>btrong>inding activity. Involved in regulation of alternative mRNA splicing, via spliceosome. Located in cytosol; mitochondrion; trong>andtrong> nuclear speck. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC391048 Gene

cysteine trong>andtrong> histidine-rich domain (CHORD) containing 1 pseudogene

DCAF13P2 Gene

DDtrong>Btrong>1 trong>andtrong> CUL4 associated factor 13 pseudogene 2

DCAF13P1 Gene

DDtrong>Btrong>1 trong>andtrong> CUL4 associated factor 13 pseudogene 1

SH3PXD2trong>Btrong> Gene

SH3 trong>andtrong> PX domains 2trong>Btrong>

This gene encodes an adapter protein that is characterized trong>btrong>y a PX domain trong>andtrong> four Src homology 3 domains. The encoded protein is required for podosome formation trong>andtrong> is involved in cell adhesion trong>andtrong> migration of numerous cell types. Mutations in this gene are the cause of Frank-ter Haar syndrome (FTHS), trong>andtrong> also trong>Btrong>orrone Dermato-Cardio-Skeletal (trong>Btrong>DCS) syndrome. Alternative splicing of this gene results in multiple transcript variants. [provided trong>btrong>y RefSeq, Apr 2015]

SH3PXD2A Gene

SH3 trong>andtrong> PX domains 2A

Predicted to enatrong>btrong>le superoxide-generating NADPH oxidase activator activity. Involved in osteoclast fusion trong>andtrong> superoxide metatrong>btrong>olic process. Located in podosome. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC646377 Gene

pyrin trong>andtrong> HIN domain family, memtrong>btrong>er 1 pseudogene

POMZP3 Gene

POM121 trong>andtrong> ZP3 fusion

This gene appears to have resulted from a fusion of DNA sequences derived from 2 distinct loci, specifically through the duplication of two internal exons from the POM121 gene trong>andtrong> four 3' exons from the ZP3 gene. The 5' end of this gene is similar to the 5` coding region of the POM121 gene which encodes an integral nuclear pore memtrong>btrong>rane protein. However, the protein encoded trong>btrong>y this gene lacks the nuclear pore localization motif. The 3' end of this gene is similar to the last 4 exons of the zona pellucida glycoprotein 3 (ZP3) gene trong>andtrong> the encoded protein retains one zona pellucida domain. Multiple protein isoforms are encoded trong>btrong>y transcript variants of this gene. [provided trong>btrong>y RefSeq, Jul 2008]

APOtrong>Btrong>EC3A_trong>Btrong> Gene

APOtrong>Btrong>EC3A trong>andtrong> APOtrong>Btrong>EC3trong>Btrong> deletion hytrong>btrong>rid

This gene is a memtrong>btrong>er of the cytidine deaminase gene family. It is one of seven related genes or pseudogenes found in a cluster, thought to result from gene duplication, on chromosome 22. Memtrong>btrong>ers of the cluster encode proteins that are structurally trong>andtrong> functionally related to the C to U RNA-editing cytidine deaminase APOtrong>Btrong>EC1. The protein encoded trong>btrong>y this gene lacks the zinc trong>btrong>inding activity of other family memtrong>btrong>ers. The protein plays a role in immunity, trong>btrong>y restricting transmission of foreign DNA such as viruses. One mechanism of foreign DNA restriction is deamination of foreign doutrong>btrong>le-strtrong>andtrong>ed DNA cytidines to uridines, which leads to DNA degradation. However, other mechanisms are also thought to trong>btrong>e involved, as anti-viral effect is not dependent on deaminase activity. The protein encoded trong>btrong>y this gene is the same as that encoded trong>btrong>y APOtrong>Btrong>EC3A; however, this gene is a hytrong>btrong>rid gene that results from the deletion of approximately 29.5 ktrong>btrong> of sequence trong>btrong>etween the APOtrong>Btrong>EC3A gene trong>andtrong> the adjacent gene APOtrong>Btrong>EC3trong>Btrong>. The trong>btrong>reakpoints of the deletion are within the two genes, so the deletion hytrong>btrong>rid is predicted to have the promoter trong>andtrong> coding region of APOtrong>Btrong>EC3A, trong>btrong>ut the 3' UTR of APOtrong>Btrong>EC3trong>Btrong>. [provided trong>btrong>y RefSeq, Jul 2012]

LOC100421372 Gene

zinc finger trong>andtrong> SCAN domain containing 29 pseudogene

Ftrong>Btrong>XW11P1 Gene

F-trong>btrong>ox trong>andtrong> WD repeat domain containing 11 pseudogene 1

LOC100996375 Gene

angiogenic factor with G patch trong>andtrong> FHA domains 1-like

LOC100862705 Gene

KN motif trong>andtrong> ankyrin repeat domains 1 pseudogene

ANKHD1 Gene

ankyrin repeat trong>andtrong> KH domain containing 1

This gene encodes a protein with multiple ankyrin repeat domains trong>andtrong> a single KH-domain. The protein is thought to function as a scaffolding protein, trong>andtrong> it may trong>btrong>e involved in the regulation of caspases trong>andtrong> theretrong>btrong>y play an antiapoptotic role in cell survival. Alternative splicing results in multiple transcript variants, one of which generates a fusion transcript (MASK-trong>Btrong>P3) with the downstream eIF4E-trong>btrong>inding protein 3 (EIF4Etrong>Btrong>P3) gene, resulting in a protein comprised of the ANKHD1 sequence for the majority of the protein trong>andtrong> a different C-terminus due to an alternate reading frame for the EIF4Etrong>Btrong>P3 segments. [provided trong>btrong>y RefSeq, Sep 2010]

TMCO1 Gene

transmemtrong>btrong>rane trong>andtrong> coiled-coil domains 1

This locus encodes a transmemtrong>btrong>rane protein. Mutations at this locus have trong>btrong>een associated with craniofacial dysmorphism, skeletal anomalies, trong>andtrong> cognitive disatrong>btrong>ility. Mutations at this locus have also trong>btrong>een associated with open angle glaucoma trong>btrong>lindness. Alternatively spliced transcript variants have trong>btrong>een descritrong>btrong>ed. [provided trong>btrong>y RefSeq, Jan 2012]

TMCO2 Gene

transmemtrong>btrong>rane trong>andtrong> coiled-coil domains 2

Located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

TMCO4 Gene

transmemtrong>btrong>rane trong>andtrong> coiled-coil domains 4

Predicted to trong>btrong>e located in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

TMCO6 Gene

transmemtrong>btrong>rane trong>andtrong> coiled-coil domains 6

Predicted to enatrong>btrong>le nuclear import signal receptor activity. Predicted to trong>btrong>e involved in protein import into nucleus. Predicted to trong>btrong>e located in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ANKItrong>Btrong>1 Gene

ankyrin repeat trong>andtrong> Itrong>Btrong>R domain containing 1

Predicted to enatrong>btrong>le utrong>btrong>iquitin conjugating enzyme trong>btrong>inding activity trong>andtrong> utrong>btrong>iquitin protein ligase activity. Predicted to trong>btrong>e involved in utrong>btrong>iquitin-dependent protein catatrong>btrong>olic process. Predicted to trong>btrong>e part of utrong>btrong>iquitin ligase complex. Predicted to trong>btrong>e active in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC100996813 Gene

multidrug trong>andtrong> toxin extrusion protein 2-like

LRIT2 Gene

leucine-rich repeat, immunoglotrong>btrong>ulin-like trong>andtrong> transmemtrong>btrong>rane domains 2

Predicted to trong>btrong>e located in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LRIT3 Gene

leucine-rich repeat, immunoglotrong>btrong>ulin-like trong>andtrong> transmemtrong>btrong>rane domains 3

This gene encodes a protein that has a fitrong>btrong>ronectin type III domain trong>andtrong> a C-terminal transmemtrong>btrong>rane domain, as well as a leucine-rich repeat domain trong>andtrong> immunoglotrong>btrong>ulin-like domain near the N-terminus. The encoded protein may regulate fitrong>btrong>rotrong>btrong>last growth factor receptors trong>andtrong> affect the modification of these receptors, which are glycosylated differently in the Golgi trong>andtrong> endoplasmic reticulum. Mutations in this gene are associated with congenital stationary night trong>btrong>lindness, type 1F. [provided trong>btrong>y RefSeq, May 2013]

LRIT1 Gene

leucine-rich repeat, immunoglotrong>btrong>ulin-like trong>andtrong> transmemtrong>btrong>rane domains 1

Predicted to trong>btrong>e involved in visual perception. Predicted to trong>btrong>e located in dendrite; endoplasmic reticulum; trong>andtrong> memtrong>btrong>rane. Predicted to trong>btrong>e active in endoplasmic reticulum memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

UACA Gene

uveal autoantigen with coiled-coil domains trong>andtrong> ankyrin repeats

This gene encodes a protein that contains ankyrin repeats trong>andtrong> coiled coil domains trong>andtrong> likely plays a role in apoptosis. Studies in rodents have implicated the encoded protein in the stimulation of apoptosis trong>andtrong> the regulation of mammary gltrong>andtrong> involution, in which the mammary gltrong>andtrong> returns to its pre-pregnant state. This protein has also trong>btrong>een proposed to negatively regulate apoptosis trong>btrong>ased on experiments in human cell lines in which the protein was shown to interact with PRKC apoptosis WT1 regulator protein, also known as PAR-4, trong>andtrong> inhitrong>btrong>it translocation of the PAR-4 receptor. Autoantitrong>btrong>odies to this protein have trong>btrong>een identified in human patients with panuveitis trong>andtrong> Graves' disease. Differential expression of this gene has trong>btrong>een otrong>btrong>served in various human cancers. [provided trong>btrong>y RefSeq, May 2017]

FARP2 Gene

FERM, RhoGEF trong>andtrong> pleckstrin domain protein 2

Enatrong>btrong>les guanyl-nucleotide exchange factor activity. Acts upstream of or within Rac protein signal transduction trong>andtrong> neuron remodeling. Located in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

FARP1 Gene

FERM, RhoGEF (ARHGEF) trong>andtrong> pleckstrin domain protein 1 (chondrocyte-derived)

This gene encodes a protein containing a FERM (4.2, exrin, radixin, moesin) domain, a Dtrong>btrong>l homology domain, trong>andtrong> two pleckstrin homology domains. These domains are found in guanine nucleotide exchange factors trong>andtrong> proteins that link the cytoskeleton to the cell memtrong>btrong>rane. The encoded protein functions in neurons to promote dendritic growth. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Nov 2013]

CCZ1 Gene

CCZ1 vacuolar protein trafficking trong>andtrong> trong>btrong>iogenesis associated homolog (S. cerevisiae)

Enatrong>btrong>les guanyl-nucleotide exchange factor activity. Predicted to trong>btrong>e involved in vesicle-mediated transport. Located in intracellular memtrong>btrong>rane-trong>btrong>ounded organelle. Part of Mon1-Ccz1 complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

HAPLN1 Gene

hyaluronan trong>andtrong> proteoglycan link protein 1

Predicted to enatrong>btrong>le hyaluronic acid trong>btrong>inding activity. Predicted to trong>btrong>e an extracellular matrix structural constituent conferring compression resistance. Predicted to trong>btrong>e involved in nervous system development; positive regulation of neurotrong>btrong>last proliferation; trong>andtrong> skeletal system development. Located in collagen-containing extracellular matrix. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

HAPLN3 Gene

hyaluronan trong>andtrong> proteoglycan link protein 3

This gene trong>btrong>elongs to the hyaluronan trong>andtrong> proteoglycan trong>btrong>inding link protein gene family. The protein encoded trong>btrong>y this gene may function in hyaluronic acid trong>btrong>inding trong>andtrong> cell adhesion. [provided trong>btrong>y RefSeq, Jul 2008]

HAPLN2 Gene

hyaluronan trong>andtrong> proteoglycan link protein 2

Predicted to enatrong>btrong>le hyaluronic acid trong>btrong>inding activity. Predicted to trong>btrong>e involved in nervous system development; positive regulation of neurotrong>btrong>last proliferation; trong>andtrong> skeletal system development. Predicted to act upstream of or within estatrong>btrong>lishment of trong>btrong>lood-nerve trong>btrong>arrier trong>andtrong> extracellular matrix assemtrong>btrong>ly. Predicted to trong>btrong>e located in extracellular matrix. Predicted to trong>btrong>e active in extracellular space; perineuronal net; trong>andtrong> synapse. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PHLPP2 Gene

PH domain trong>andtrong> leucine rich repeat protein phosphatase 2

Predicted to enatrong>btrong>le protein serine/threonine phosphatase activity. Predicted to trong>btrong>e involved in intracellular signal transduction. Located in several cellular components, including intercellular trong>btrong>ridge; mitotic spindle; trong>andtrong> nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

trong>Btrong>RWD1P2 Gene

trong>btrong>romodomain trong>andtrong> WD repeat domain containing 1 pseudogene 2

ODPF Gene

Osseous dysplasia, digital, with facial pigmentary defects trong>andtrong> multiple frenula

Ftrong>Btrong>XW12 Gene

F-trong>btrong>ox trong>andtrong> WD repeat domain containing 12

Memtrong>btrong>ers of the F-trong>btrong>ox protein family, such as Ftrong>Btrong>XW12, are characterized trong>btrong>y an approximately 40-amino acid F-trong>btrong>ox motif. SCF complexes, formed trong>btrong>y SKP1 (MIM 601434), cullin (see CUL1; MIM 603034), trong>andtrong> F-trong>btrong>ox proteins, act as protein-utrong>btrong>iquitin ligases. F-trong>btrong>ox proteins interact with SKP1 through the F trong>btrong>ox, trong>andtrong> they interact with utrong>btrong>iquitination targets through other protein interaction domains (Jin et al., 2004 [Putrong>btrong>Med 15520277]).[supplied trong>btrong>y OMIM, Mar 2008]

Ftrong>Btrong>XW10 Gene

F-trong>btrong>ox trong>andtrong> WD repeat domain containing 10

Memtrong>btrong>ers of the F-trong>btrong>ox protein family, such as Ftrong>Btrong>XW10, are characterized trong>btrong>y an approximately 40-amino acid F-trong>btrong>ox motif. SCF complexes, formed trong>btrong>y SKP1 (MIM 601434), cullin (see CUL1; MIM 603134), trong>andtrong> F-trong>btrong>ox proteins, act as protein-utrong>btrong>iquitin ligases. F-trong>btrong>ox proteins interact with SKP1 through the F trong>btrong>ox, trong>andtrong> they interact with utrong>btrong>iquitination targets through other protein interaction domains (Jin et al., 2004 [Putrong>btrong>Med 15520277]).[supplied trong>btrong>y OMIM, Mar 2008]

Ftrong>Btrong>XW11 Gene

F-trong>btrong>ox trong>andtrong> WD repeat domain containing 11

This gene encodes a memtrong>btrong>er of the F-trong>btrong>ox protein family which is characterized trong>btrong>y an approximately 40 amino acid motif, the F-trong>btrong>ox. The F-trong>btrong>ox proteins constitute one of the four sutrong>btrong>units of utrong>btrong>iquitin protein ligase complex called SCFs (SKP1-cullin-F-trong>btrong>ox), which function in phosphorylation-dependent utrong>btrong>iquitination. The F-trong>btrong>ox proteins are divided into 3 classes: Ftrong>btrong>ws containing WD-40 domains, Ftrong>btrong>ls containing leucine-rich repeats, trong>andtrong> Ftrong>btrong>xs containing either different protein-protein interaction modules or no recognizatrong>btrong>le motifs. The protein encoded trong>btrong>y this gene trong>btrong>elongs to the Ftrong>btrong>ws class trong>andtrong>, in addition to an F-trong>btrong>ox, contains multiple WD40 repeats. This gene contains at least 14 exons, trong>andtrong> its alternative splicing generates 3 transcript variants diverging at the presence/atrong>btrong>sence of two alternate exons. [provided trong>btrong>y RefSeq, Jul 2008]

LOC100421810 Gene

LON peptidase N-terminal domain trong>andtrong> ring finger 2 pseudogene

FIQTL1 Gene

fasting glucose trong>andtrong> specific insulin levels

MRST Gene

Mental retardation, severe, with spasticity trong>andtrong> tapetoretinal

SCIMP Gene

SLP adaptor trong>andtrong> CSK interacting memtrong>btrong>rane protein

This gene encodes a transmemtrong>btrong>rane adaptor protein that is expressed in antigen-presenting cells trong>andtrong> is localized in the immunologic synapse. The encoded protein is involved in major histocompatitrong>btrong>ility complex class II signal transduction trong>andtrong> immune synapse formation. Alternatively spliced transcript variants have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Dec 2012]

SH3TC2 Gene

SH3 domain trong>andtrong> tetratricopeptide repeats 2

This gene encodes a protein with two N-terminal Src homology 3 (SH3) domains trong>andtrong> 10 tetratricopeptide repeat (TPR) motifs, trong>andtrong> is a memtrong>btrong>er of a small gene family. The gene product has trong>btrong>een proposed to trong>btrong>e an adapter or docking molecule. Mutations in this gene result in autosomal recessive Charcot-Marie-Tooth disease type 4C, a childhood-onset neurodegenerative disease characterized trong>btrong>y demyelination of motor trong>andtrong> sensory neurons. [provided trong>btrong>y RefSeq, Jul 2008]

SH3TC1 Gene

SH3 domain trong>andtrong> tetratricopeptide repeats 1

CFAP46 Gene

cilia trong>andtrong> flagella associated protein 46

Predicted to trong>btrong>e involved in axoneme assemtrong>btrong>ly. Predicted to trong>btrong>e located in axoneme. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP45 Gene

cilia trong>andtrong> flagella associated protein 45

Enatrong>btrong>les AMP trong>btrong>inding activity. Involved in estatrong>btrong>lishment of left/right asymmetry trong>andtrong> flagellated sperm motility. Located in 9+2 motile cilium; axonemal microtutrong>btrong>ule; trong>andtrong> nucleoplasm. Implicated in visceral heterotaxy. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP43 Gene

cilia trong>andtrong> flagella associated protein 43

This gene encodes a memtrong>btrong>er of the cilia- trong>andtrong> flagella-associated protein family. [provided trong>btrong>y RefSeq, Sep 2016]

RFWD2 Gene

ring finger trong>andtrong> WD repeat domain 2, E3 utrong>btrong>iquitin protein ligase

Enatrong>btrong>les utrong>btrong>iquitin protein ligase activity. Involved in positive regulation of proteasomal utrong>btrong>iquitin-dependent protein catatrong>btrong>olic process; proteasome-mediated utrong>btrong>iquitin-dependent protein catatrong>btrong>olic process; trong>andtrong> response to ionizing radiation. Part of Cul4A-RING E3 utrong>btrong>iquitin ligase complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

RFWD3 Gene

ring finger trong>andtrong> WD repeat domain 3

Enatrong>btrong>les MDM2/MDM4 family protein trong>btrong>inding activity; p53 trong>btrong>inding activity; trong>andtrong> utrong>btrong>iquitin protein ligase activity. Involved in several processes, including DNA metatrong>btrong>olic process; regulation of cell cycle phase transition; trong>andtrong> response to ionizing radiation. Located in nucleoplasm trong>andtrong> site of doutrong>btrong>le-strtrong>andtrong> trong>btrong>reak. Implicated in Fanconi anemia complementation group W. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

C1QTNF8 Gene

C1q trong>andtrong> tumor necrosis factor related protein 8

Involved in positive regulation of cell motility. Predicted to trong>btrong>e located in extracellular region. Predicted to trong>btrong>e part of collagen trimer. Predicted to trong>btrong>e active in extracellular space. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

C1QTNF9 Gene

C1q trong>andtrong> tumor necrosis factor related protein 9

Enatrong>btrong>les identical protein trong>btrong>inding activity. Predicted to trong>btrong>e involved in signal transduction. Predicted to trong>btrong>e located in extracellular region. Predicted to trong>btrong>e part of collagen trimer. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

C1QTNF2 Gene

C1q trong>andtrong> tumor necrosis factor related protein 2

Predicted to enatrong>btrong>le identical protein trong>btrong>inding activity trong>andtrong> signaling receptor trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of lipid metatrong>btrong>olic process. Predicted to act upstream of or within positive regulation of D-glucose import; positive regulation of MAPK cascade; trong>andtrong> positive regulation of small molecule metatrong>btrong>olic process. Predicted to trong>btrong>e located in extracellular space. Predicted to trong>btrong>e part of protein-containing complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

C1QTNF3 Gene

C1q trong>andtrong> tumor necrosis factor related protein 3

Enatrong>btrong>les identical protein trong>btrong>inding activity. Involved in several processes, including intracellular triglyceride homeostasis; negative regulation of non-canonical NF-kappatrong>Btrong> signal transduction; trong>andtrong> regulation of cytokine production. Acts upstream of or within negative regulation of gluconeogenesis. Located in extracellular exosome trong>andtrong> memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

C1QTNF1 Gene

C1q trong>andtrong> tumor necrosis factor related protein 1

Enatrong>btrong>les collagen trong>btrong>inding activity. Involved in several processes, including negative regulation of platelet aggregation; positive regulation of aldosterone secretion; trong>andtrong> positive regulation of cytosolic calcium ion concentration. Located in extracellular space trong>andtrong> plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

C1QTNF6 Gene

C1q trong>andtrong> tumor necrosis factor related protein 6

Enatrong>btrong>les identical protein trong>btrong>inding activity. Predicted to trong>btrong>e located in extracellular region trong>andtrong> memtrong>btrong>rane. Predicted to trong>btrong>e part of collagen trimer. Predicted to trong>btrong>e active in extracellular space. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

C1QTNF7 Gene

C1q trong>andtrong> tumor necrosis factor related protein 7

Predicted to enatrong>btrong>le identical protein trong>btrong>inding activity. Predicted to trong>btrong>e located in extracellular space. Predicted to trong>btrong>e part of collagen trimer. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

C1QTNF4 Gene

C1q trong>andtrong> tumor necrosis factor related protein 4

Predicted to enatrong>btrong>le cytokine activity. Involved in positive regulation of cytokine production trong>andtrong> positive regulation of signal transduction. Located in extracellular space. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

C1QTNF5 Gene

C1q trong>andtrong> tumor necrosis factor related protein 5

This gene encodes a memtrong>btrong>er of a family of proteins that function as components of trong>btrong>asement memtrong>btrong>ranes trong>andtrong> may play a role in cell adhesion. Mutations in this gene have trong>btrong>een associated with late-onset retinal degeneration. The protein may trong>btrong>e encoded trong>btrong>y either a trong>btrong>icistronic transcript including sequence from the upstream memtrong>btrong>rane frizzled-related protein gene (MFRP), or trong>btrong>y a monocistronic transcript expressed from an internal promoter. [provided trong>btrong>y RefSeq, Jun 2013]

LOC642574 Gene

IQ motif trong>andtrong> ankyrin repeat domain-containing protein LOC642574

LRRCC1 Gene

leucine rich repeat trong>andtrong> coiled-coil centrosomal protein 1

This gene encodes a centrosomal protein that maintains the structural integrity of the centrosome trong>andtrong> plays a key role in mitotic spindle formation. The encoded protein contains an N-terminal leucine-rich repeat domain trong>andtrong> a C-terminal coiled-coil domain. It associates with the centrosome throughout the cell cycle trong>andtrong> accumulates on the mitotic centrosome. [provided trong>btrong>y RefSeq, Mar 2017]

NYNRIN Gene

NYN domain trong>andtrong> retroviral integrase containing

Predicted to enatrong>btrong>le RNA endonuclease activity trong>andtrong> mRNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in DNA integration; DNA synthesis involved in DNA repair; trong>andtrong> DNA-templated DNA replication. Predicted to trong>btrong>e located in memtrong>btrong>rane. Predicted to trong>btrong>e active in cytoplasmic ritrong>btrong>onucleoprotein granule trong>andtrong> nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

TKCR Gene

torticollis, keloids, cryptorchidism trong>andtrong> renal dysplasia

CPAMD8 Gene

C3 trong>andtrong> PZP-like, alpha-2-macroglotrong>btrong>ulin domain containing 8

This gene encodes a memtrong>btrong>er of the protease inhitrong>btrong>itor I39 (alpha-2-macroglotrong>btrong>ulin) family of proteins. These proteins are important in innate trong>andtrong> acquired immunity. The encoded protein is memtrong>btrong>rane-associated trong>andtrong> proteolytically processed to generate two chains. Mutations in this gene cause a form of anterior segment dysgenesis, a developmental disorder of the eye. [provided trong>btrong>y RefSeq, May 2017]

PIPSL Gene

PIP5K1A trong>andtrong> PSMD4-like, pseudogene

This locus is a transcritrong>btrong>ed pseudogene with similarity to two adjacent chromosome 1 loci: phosphatidylinositol-4-phosphate 5-kinase, type I, alpha (PIP5K1A, GeneID 8394) trong>andtrong> proteasome (prosome, macropain) 26S sutrong>btrong>unit, non-ATPase, 4 (PSMD4, GeneID 5710). The pseudogene is trong>btrong>elieved to have occurred from L1 retrotransposition into chromosome 10 of a read-through transcript trong>btrong>etween the two adjacent loci. Evidence of transcription has trong>btrong>een found (Putrong>btrong>Med IDs: 16344562 trong>andtrong> 17623810), trong>btrong>ut the latter putrong>btrong>lication found no evidence that the predicted protein is translated. The NCtrong>Btrong>I RefSeq Project therefore continues to treat this as a transcritrong>btrong>ed pseudogene. [provided trong>btrong>y RefSeq, Jan 2009]

LOC100133261 Gene

cysteine trong>andtrong> histidine-rich domain (CHORD) containing 1 pseudogene

SASH3 Gene

SAM trong>andtrong> SH3 domain containing 3

The protein encoded trong>btrong>y this gene contains a Src homology-3 (SH3) domain trong>andtrong> a sterile alpha motif (SAM), trong>btrong>oth of which are found in proteins involved in cell signaling. This protein may function as a signaling adapter protein in lymphocytes.[provided trong>btrong>y RefSeq, Sep 2009]

SASH1 Gene

SAM trong>andtrong> SH3 domain containing 1

This gene encodes a scaffold protein involved in the TLR4 signaling pathway that may stimulate cytokine production trong>andtrong> endothelial cell migration in response to invading pathogens. The encoded protein has also trong>btrong>een descritrong>btrong>ed as a potential tumor suppressor that may negatively regulate proliferation, apoptosis, trong>andtrong> invasion of cancer cells, trong>andtrong> reduced expression of this gene has trong>btrong>een otrong>btrong>served in multiple human cancers. Mutations in this gene may trong>btrong>e associated with atrong>btrong>normal skin pigmentation in human patients. [provided trong>btrong>y RefSeq, Oct 2016]

SENCR Gene

smooth muscle trong>andtrong> endothelial cell enriched migration/differentiation-associated long non-coding RNA

VSIG10 Gene

V-set trong>andtrong> immunoglotrong>btrong>ulin domain containing 10

Predicted to enatrong>btrong>le cell adhesion molecule trong>btrong>inding activity. Predicted to trong>btrong>e involved in cell-cell adhesion. Predicted to trong>btrong>e located in memtrong>btrong>rane. Predicted to trong>btrong>e active in cell-cell junction trong>andtrong> plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC642131 Gene

putative V-set trong>andtrong> immunoglotrong>btrong>ulin domain-containing-like protein IGHV4OR15-8

HMSNO Gene

Neuropathy, hereditary motor trong>andtrong> sensory, Okinawa type

TIMD4 Gene

T-cell immunoglotrong>btrong>ulin trong>andtrong> mucin domain containing 4

Predicted to enatrong>btrong>le phosphatidylserine trong>btrong>inding activity. Predicted to trong>btrong>e involved in apoptotic cell clearance trong>andtrong> cytoskeletal rearrangement involved in phagocytosis, engulfment. Predicted to trong>btrong>e located in extracellular region trong>andtrong> plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

VWCE Gene

von Willetrong>btrong>rtrong>andtrong> factor C trong>andtrong> EGF domains

Predicted to enatrong>btrong>le calcium ion trong>btrong>inding activity. Predicted to trong>btrong>e involved in cellular response to virus. Located in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC100379290 Gene

transmemtrong>btrong>rane trong>andtrong> coiled-coil domain family 1 pseudogene

TNAP Gene

TRAFs trong>andtrong> NIK-associated protein

PACSIN1 Gene

protein kinase C trong>andtrong> casein kinase sutrong>btrong>strate in neurons 1

Enatrong>btrong>les phospholipid trong>btrong>inding activity. Involved in plasma memtrong>btrong>rane tutrong>btrong>ulation. Located in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PACSIN3 Gene

protein kinase C trong>andtrong> casein kinase sutrong>btrong>strate in neurons 3

This gene is a memtrong>btrong>er of the protein kinase C trong>andtrong> casein kinase sutrong>btrong>strate in neurons family. The encoded protein is involved in linking the actin cytoskeleton with vesicle formation. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, May 2010]

PACSIN2 Gene

protein kinase C trong>andtrong> casein kinase sutrong>btrong>strate in neurons 2

This gene is a memtrong>btrong>er of the protein kinase C trong>andtrong> casein kinase sutrong>btrong>strate in neurons family. The encoded protein is involved in linking the actin cytoskeleton with vesicle formation trong>btrong>y regulating tutrong>btrong>ulin polymerization. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, May 2010]

PINLYP Gene

phospholipase A2 inhitrong>btrong>itor trong>andtrong> LY6/PLAUR domain containing

Predicted to enatrong>btrong>le phospholipase inhitrong>btrong>itor activity. Predicted to trong>btrong>e located in extracellular region. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP52 Gene

cilia trong>andtrong> flagella associated protein 52

WD repeat-containing proteins, such as WDR16, play crucial roles in a wide range of physiologic functions, including signal transduction, RNA processing, remodeling the cytoskeleton, regulation of vesicular traffic, trong>andtrong> cell division (Silva et al., 2005 [Putrong>btrong>Med 15967112]).[supplied trong>btrong>y OMIM, Mar 2008]

ASZ1 Gene

ankyrin repeat, SAM trong>andtrong> trong>btrong>asic leucine zipper domain containing 1

Predicted to trong>btrong>e involved in male meiotic nuclear division; spermatogenesis; trong>andtrong> transposatrong>btrong>le element silencing. Predicted to trong>btrong>e located in cytoplasm. Predicted to trong>btrong>e active in pi-trong>btrong>ody. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SNRPtrong>Btrong>P1 Gene

small nuclear ritrong>btrong>onucleoprotein polypeptides trong>Btrong> trong>andtrong> trong>Btrong>1 pseudogene 1

DFCTRPS Gene

Deafness, cataract, retinitis pigmentosa, trong>andtrong> sperm atrong>btrong>normalities

Ztrong>Btrong>Ttrong>Btrong>22 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 22

Enatrong>btrong>les sequence-specific doutrong>btrong>le-strtrong>andtrong>ed DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in chromatin. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>20 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 20

This gene, which was initially designated as dendritic cell-derived trong>Btrong>Ttrong>Btrong>/POZ zinc finger (DPZF), trong>btrong>elongs to a family of transcription factors with an N-terminal trong>Btrong>Ttrong>Btrong>/POZ domain trong>andtrong> a C-terminal DNA-trong>btrong>indng zinc finger domain. The trong>Btrong>Ttrong>Btrong>/POZ domain is a hydrophotrong>btrong>ic region of approximately 120 aa which mediates association with other trong>Btrong>Ttrong>Btrong>/POZ domain-containing proteins. This gene acts as a transcriptional repressor trong>andtrong> plays a role in many processes including neurogenesis, glucose homeostasis, trong>andtrong> postnatal growth. Mutations in this gene have trong>btrong>een associated with Primrose syndrome as well as the 3q13.31 microdeletion syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2017]

Ztrong>Btrong>Ttrong>Btrong>21 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 21

Enatrong>btrong>les several functions, including DNA-trong>btrong>inding transcription repressor activity, RNA polymerase II-specific; POZ domain trong>btrong>inding activity; trong>andtrong> methyl-CpG trong>btrong>inding activity. Involved in negative regulation of transcription trong>btrong>y RNA polymerase II. Located in cytosol trong>andtrong> nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ztrong>Btrong>Ttrong>Btrong>25 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 25

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription repressor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in negative regulation of transcription trong>btrong>y RNA polymerase II; regulation of cytokine production; trong>andtrong> regulation of immune system process. Located in nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LAMTOR4 Gene

late endosomal/lysosomal adaptor, MAPK trong>andtrong> MTOR activator 4

Contritrong>btrong>utes to guanyl-nucleotide exchange factor activity trong>andtrong> molecular adaptor activity. Involved in several processes, including cellular response to amino acid stimulus; positive regulation of TORC1 signaling; trong>andtrong> protein localization to lysosome. Located in lysosome. Part of FNIP-folliculin RagC/D GAP trong>andtrong> Ragulator complex. Is active in lysosomal memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LAMTOR5 Gene

late endosomal/lysosomal adaptor, MAPK trong>andtrong> MTOR activator 5

This gene encodes a protein that specifically complexes with the C-terminus of hepatitis trong>Btrong> virus X protein (Htrong>Btrong>x). The function of this protein is to negatively regulate Htrong>Btrong>x activity trong>andtrong> thus to alter the replication life cycle of the virus. [provided trong>btrong>y RefSeq, Jul 2008]

LAMTOR1 Gene

late endosomal/lysosomal adaptor, MAPK trong>andtrong> MTOR activator 1

Enatrong>btrong>les GTPase trong>btrong>inding activity trong>andtrong> protein-memtrong>btrong>rane adaptor activity. Contritrong>btrong>utes to guanyl-nucleotide exchange factor activity trong>andtrong> molecular adaptor activity. Involved in several processes, including cholesterol homeostasis; positive regulation of TORC1 signaling; trong>andtrong> regulation of cholesterol transport. Located in lysosome. Part of FNIP-folliculin RagC/D GAP. Is active in Ragulator complex trong>andtrong> lysosomal memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LAMTOR2 Gene

late endosomal/lysosomal adaptor, MAPK trong>andtrong> MTOR activator 2

The product of this gene is highly conserved with a mouse protein associated with the cytoplasmic face of late endosomes trong>andtrong> lysosomes. The mouse protein interacts with MAPK scaffold protein 1, a component of the mitogen-activated protein kinase pathway. In humans, a mutation in this gene has trong>btrong>een associated with a primary immunodeficiency syndrome, trong>andtrong> suggests a role for this protein in endosomal trong>btrong>iogenesis. Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2009]

LAMTOR3 Gene

late endosomal/lysosomal adaptor, MAPK trong>andtrong> MTOR activator 3

This gene encodes a scaffold protein that functions in the extracellular signal-regulated kinase (ERK) cascade. The protein is localized to late endosomes trong>btrong>y the mitogen-activated protein-trong>btrong>inding protein-interacting protein, trong>andtrong> trong>btrong>inds specifically to MAP kinase kinase MAP2K1/MEK1, MAP kinase MAPK3/ERK1, trong>andtrong> MAP kinase MAPK1/ERK2. Studies of the orthologous gene in mouse indicate that it regulates late endosomal traffic trong>andtrong> cell proliferation. Alternatively spliced transcript variants encoding multiple isoforms have trong>btrong>een otrong>btrong>served for this gene. A pseudogene of this gene is located on the long arm of chromosome 13. [provided trong>btrong>y RefSeq, Aug 2011]

STAC2 Gene

SH3 trong>andtrong> cysteine rich domain 2

This gene encodes a protein containing an SH3 domain trong>andtrong> a zinc finger domain. The encoded protein has trong>btrong>een shown to regulate calcium channel inactivation in a human cell line. Reduced expression of this gene has trong>btrong>een otrong>btrong>served in human heart failure. [provided trong>btrong>y RefSeq, May 2017]

STAC3 Gene

SH3 trong>andtrong> cysteine rich domain 3

The protein encoded trong>btrong>y this gene is a component of the excitation-contraction coupling machinery of muscles. This protein is a memtrong>btrong>er of the Stac gene family trong>andtrong> contains an N-terminal cysteine-rich domain trong>andtrong> two SH3 domains. Mutations in this gene are a cause of Native American myopathy. [provided trong>btrong>y RefSeq, Nov 2013]

UHRF2P1 Gene

utrong>btrong>iquitin-like with PHD trong>andtrong> ring finger domains 2 pseudogene 1

LEKR1 Gene

leucine, glutamate trong>andtrong> lysine rich 1

WDSUtrong>Btrong>1 Gene

WD repeat, sterile alpha motif trong>andtrong> U-trong>btrong>ox domain containing 1

Predicted to enatrong>btrong>le utrong>btrong>iquitin-protein transferase activity. Predicted to trong>btrong>e involved in protein utrong>btrong>iquitination. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

TRIOtrong>Btrong>P Gene

TRIO trong>andtrong> F-actin trong>btrong>inding protein

This gene encodes a protein with an N-terminal pleckstrin homology domain trong>andtrong> a C-terminal coiled-coil region. The protein interacts with trio, which is involved with neural tissue development trong>andtrong> controlling actin cytoskeleton organization, cell motility trong>andtrong> cell growth. The protein also associates with F-actin trong>andtrong> statrong>btrong>ilizes F-actin structures. Mutations in this gene have trong>btrong>een associated with a form of autosomal recessive nonsyndromic deafness. Multiple alternatively spliced transcript variants that would encode different isoforms have trong>btrong>een found for this gene, however some transcripts may trong>btrong>e sutrong>btrong>ject to nonsense-mediated decay (NMD). [provided trong>btrong>y RefSeq, Nov 2008]

trong>Btrong>AALC Gene

trong>btrong>rain trong>andtrong> acute leukemia, cytoplasmic

This gene was identified trong>btrong>y gene expression studies in patients with acute myeloid leukemia (AML). The gene is conserved among mammals trong>andtrong> is not found in lower organisms. Tissues that express this gene develop from the neuroectoderm. Multiple alternatively spliced transcript variants that encode different proteins have trong>btrong>een descritrong>btrong>ed for this gene; however, some of the transcript variants are found only in AML cell lines. [provided trong>btrong>y RefSeq, Jul 2008]

TEPP Gene

testis, prostate trong>andtrong> placenta expressed

Predicted to trong>btrong>e involved in flagellated sperm motility. Predicted to trong>btrong>e located in cytoplasm; cytoskeleton; trong>andtrong> motile cilium. Predicted to trong>btrong>e active in axonemal A tutrong>btrong>ule inner sheath trong>andtrong> sperm flagellum. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PKHD1 Gene

polycystic kidney trong>andtrong> hepatic disease 1 (autosomal recessive)

The protein encoded trong>btrong>y this gene is predicted to have a single transmemtrong>btrong>rane (TM)-spanning domain trong>andtrong> multiple copies of an immunoglotrong>btrong>ulin-like plexin-transcription-factor domain. Alternative splicing results in two transcript variants encoding different isoforms. Other alternatively spliced transcripts have trong>btrong>een descritrong>btrong>ed, trong>btrong>ut the full length sequences have not trong>btrong>een determined. Several of these transcripts are predicted to encode truncated products which lack the TM trong>andtrong> may trong>btrong>e secreted. Mutations in this gene cause autosomal recessive polycystic kidney disease, also known as polycystic kidney trong>andtrong> hepatic disease-1. [provided trong>btrong>y RefSeq, Jul 2008]

VSIG8 Gene

V-set trong>andtrong> immunoglotrong>btrong>ulin domain containing 8

Enatrong>btrong>les RNA trong>btrong>inding activity. Predicted to trong>btrong>e located in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

VSIG4 Gene

V-set trong>andtrong> immunoglotrong>btrong>ulin domain containing 4

This gene encodes a v-set trong>andtrong> immunoglotrong>btrong>ulin-domain containing protein that is structurally related to the trong>Btrong>7 family of immune regulatory proteins. The encoded protein may trong>btrong>e a negative regulator of T-cell responses. This protein is also a receptor for the complement component 3 fragments C3trong>btrong> trong>andtrong> iC3trong>btrong>. Alternate splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, May 2010]

VSIG2 Gene

V-set trong>andtrong> immunoglotrong>btrong>ulin domain containing 2

Predicted to trong>btrong>e involved in lipid metatrong>btrong>olic process. Predicted to trong>btrong>e located in plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

VSIG1 Gene

V-set trong>andtrong> immunoglotrong>btrong>ulin domain containing 1

This gene encodes a memtrong>btrong>er of the junctional adhesion molecule (JAM) family. The encoded protein contains multiple glycosylation sites at the N-terminal region, trong>andtrong> multiple phosphorylation sites trong>andtrong> glutamic acid/proline (EP) repeats at the C-terminal region. The gene is expressed in normal stomach trong>andtrong> testis, as well as in gastric, esophageal trong>andtrong> ovarian cancers. Alternatively spliced transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Dec 2009]

SPATC1 Gene

spermatogenesis trong>andtrong> centriole associated 1

Predicted to enatrong>btrong>le gamma-tutrong>btrong>ulin trong>btrong>inding activity. Located in centrosome. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

TAMM41 Gene

TAM41, mitochondrial translocator assemtrong>btrong>ly trong>andtrong> maintenance protein, homolog (S. cerevisiae)

Predicted to enatrong>btrong>le phosphatidate cytidylyltransferase activity. Predicted to trong>btrong>e involved in CDP-diacylglycerol trong>btrong>iosynthetic process trong>andtrong> cardiolipin trong>btrong>iosynthetic process. Is active in mitochondrion. Implicated in comtrong>btrong>ined oxidative phosphorylation deficiency 56. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

MAGI3 Gene

memtrong>btrong>rane associated guanylate kinase, WW trong>andtrong> PDZ domain containing 3

Predicted to enatrong>btrong>le frizzled trong>btrong>inding activity. Predicted to trong>btrong>e involved in signal transduction. Predicted to act upstream of or within positive regulation of JUN kinase activity. Located in cell junction. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

MAGI2 Gene

memtrong>btrong>rane associated guanylate kinase, WW trong>andtrong> PDZ domain containing 2

The protein encoded trong>btrong>y this gene interacts with atrophin-1. Atrophin-1 contains a polyglutamine repeat, expansion of which is responsitrong>btrong>le for dentatorutrong>btrong>ral trong>andtrong> pallidoluysian atrophy. This encoded protein is characterized trong>btrong>y two WW domains, a guanylate kinase-like domain, trong>andtrong> multiple PDZ domains. It has structural similarity to the memtrong>btrong>rane-associated guanylate kinase homologue (MAGUK) family. [provided trong>btrong>y RefSeq, Jul 2008]

MAGI1 Gene

memtrong>btrong>rane associated guanylate kinase, WW trong>andtrong> PDZ domain containing 1

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of the memtrong>btrong>rane-associated guanylate kinase homologue (MAGUK) family. MAGUK proteins participate in the assemtrong>btrong>ly of multiprotein complexes on the inner surface of the plasma memtrong>btrong>rane 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 trong>btrong>een identified. [provided trong>btrong>y RefSeq, Jul 2008]

TNIK Gene

TRAF2 trong>andtrong> NCK interacting kinase

Wnt signaling plays important roles in carcinogenesis trong>andtrong> emtrong>btrong>ryonic development. The protein encoded trong>btrong>y this gene is a serine/threonine kinase that functions as an activator of the Wnt signaling pathway. Mutations in this gene are associated with an autosomal recessive form of cognitive disatrong>btrong>ility. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided trong>btrong>y RefSeq, Jul 2017]

GCSAM Gene

germinal center-associated, signaling trong>andtrong> motility

This gene encodes a protein which may function in signal transduction pathways trong>andtrong> whose expression is elevated in germinal cell lymphomas. It contains a putative PDZ-interacting domain, an immunoreceptor tyrosine-trong>btrong>ased activation motif (ITAM), trong>andtrong> two putative SH2 trong>btrong>inding sites. In trong>Btrong> cells, its expression is specifically induced trong>btrong>y interleukin-4. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided trong>btrong>y RefSeq, Jul 2008]

EEC2 Gene

ectrodactyly, ectodermal dysplasia trong>andtrong> cleft lip/palate syndrome 2

EEC1 Gene

ectrodactyly, ectodermal dysplasia trong>andtrong> cleft lip/palate syndrome 1

LOC102723815 Gene

disintegrin trong>andtrong> metalloproteinase domain-containing protein 29-like

AStrong>Btrong>2 Gene

ankyrin repeat trong>andtrong> SOCS trong>btrong>ox containing 2

This gene encodes a memtrong>btrong>er of the ankyrin repeat trong>andtrong> SOCS trong>btrong>ox-containing (AStrong>Btrong>) protein family. These proteins play a role in protein degradation trong>btrong>y coupling suppressor of cytokine signalling (SOCS) proteins with the elongin trong>Btrong>C complex. The encoded protein is a sutrong>btrong>unit of a multimeric E3 utrong>btrong>iquitin ligase complex that mediates the degradation of actin-trong>btrong>inding proteins. This gene plays a role in retinoic acid-induced growth inhitrong>btrong>ition trong>andtrong> differentiation of myeloid leukemia cells. Alternatively spliced transcript variants encoding multiple isoforms have trong>btrong>een otrong>btrong>served for this gene. [provided trong>btrong>y RefSeq, Jan 2011]

AStrong>Btrong>3 Gene

ankyrin repeat trong>andtrong> SOCS trong>btrong>ox containing 3

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of the ankyrin repeat trong>andtrong> SOCS trong>btrong>ox-containing (AStrong>Btrong>) family of proteins. They contain ankyrin repeat sequence trong>andtrong> SOCS trong>btrong>ox domain. The SOCS trong>btrong>ox serves to couple suppressor of cytokine signalling (SOCS) proteins trong>andtrong> their trong>btrong>inding partners with the elongin trong>Btrong> trong>andtrong> C complex, possitrong>btrong>ly targeting them for degradation. Alternatively spliced transcript variants have trong>btrong>een descritrong>btrong>ed for this gene. [provided trong>btrong>y RefSeq, Jan 2011]

AStrong>Btrong>1 Gene

ankyrin repeat trong>andtrong> SOCS trong>btrong>ox containing 1

The protein encoded trong>btrong>y this gene contains an ankyrin repeat sequence trong>andtrong> SOCS trong>btrong>ox domain. The SOCS trong>btrong>ox serves to couple suppressor of cytokine signalling (SOCS) proteins trong>andtrong> their trong>btrong>inding partners with the elongin trong>Btrong> trong>andtrong> C complex, targeting them for utrong>btrong>iquitination trong>andtrong> degradation. [provided trong>btrong>y RefSeq, Aug 2016]

AStrong>Btrong>6 Gene

ankyrin repeat trong>andtrong> SOCS trong>btrong>ox containing 6

The protein encoded trong>btrong>y this gene trong>btrong>elongs to a family of ankyrin repeat proteins that, along with four other protein families, contain a C-terminal SOCS trong>btrong>ox motif. Growing evidence suggests that the SOCS trong>btrong>ox, similar to the F-trong>btrong>ox, acts as a trong>btrong>ridge trong>btrong>etween specific sutrong>btrong>strate-trong>btrong>inding domains trong>andtrong> the more generic proteins that comprise a large family of E3 utrong>btrong>iquitin protein ligases. Alternatively spliced transcript variants have trong>btrong>een identified for this gene. [provided trong>btrong>y RefSeq, Jan 2011]

AStrong>Btrong>7 Gene

ankyrin repeat trong>andtrong> SOCS trong>btrong>ox containing 7

The protein encoded trong>btrong>y this gene trong>btrong>elongs to a family of ankyrin repeat proteins that, along with four other protein families, contains a C-terminal SOCS trong>btrong>ox motif. Growing evidence suggests that the SOCS trong>btrong>ox acts as a trong>btrong>ridge trong>btrong>etween specific sutrong>btrong>strate-trong>btrong>inding domains trong>andtrong> the more generic proteins that comprise a large family of E3 utrong>btrong>iquitin protein ligases. In this way, SOCS trong>btrong>ox containing proteins may regulate protein turnover trong>btrong>y targeting proteins for polyutrong>btrong>iquination trong>andtrong>, therefore, for proteasome-mediated degradation. Two alternative transcripts encoding different isoforms have trong>btrong>een descritrong>btrong>ed. [provided trong>btrong>y RefSeq, Jul 2008]

AStrong>Btrong>4 Gene

ankyrin repeat trong>andtrong> SOCS trong>btrong>ox containing 4

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of the ankyrin repeat trong>andtrong> SOCS trong>btrong>ox-containing (AStrong>Btrong>) family of proteins. They contain ankyrin repeat sequence trong>andtrong> SOCS trong>btrong>ox domain. The SOCS trong>btrong>ox serves to couple suppressor of cytokine signalling (SOCS) proteins trong>andtrong> their trong>btrong>inding partners with the elongin trong>Btrong> trong>andtrong> C complex, possitrong>btrong>ly targeting them for degradation. Multiple alternatively spliced transcript variants have trong>btrong>een descritrong>btrong>ed for this gene trong>btrong>ut some of the full length sequences are not known. [provided trong>btrong>y RefSeq, Jul 2008]

AStrong>Btrong>5 Gene

ankyrin repeat trong>andtrong> SOCS trong>btrong>ox containing 5

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of the ankyrin repeat trong>andtrong> SOCS trong>btrong>ox-containing (AStrong>Btrong>) family of proteins. They contain ankyrin repeat sequence trong>andtrong> SOCS trong>btrong>ox domain. The SOCS trong>btrong>ox serves to couple suppressor of cytokine signalling (SOCS) proteins trong>andtrong> their trong>btrong>inding partners with the elongin trong>Btrong> trong>andtrong> C complex, possitrong>btrong>ly targeting them for degradation. Multiple alternatively spliced transcript variants have trong>btrong>een descritrong>btrong>ed for this gene trong>btrong>ut their full length sequences are not known. [provided trong>btrong>y RefSeq, Jul 2008]

AStrong>Btrong>8 Gene

ankyrin repeat trong>andtrong> SOCS trong>btrong>ox containing 8

Predicted to trong>btrong>e involved in intracellular signal transduction trong>andtrong> protein utrong>btrong>iquitination. Predicted to trong>btrong>e located in cytosol. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

AStrong>Btrong>9 Gene

ankyrin repeat trong>andtrong> SOCS trong>btrong>ox containing 9

This gene encodes a memtrong>btrong>er of the ankyrin repeat trong>andtrong> suppressor of cytokine signaling (SOCS) trong>btrong>ox protein family. Memtrong>btrong>ers of this family can interact with the elongin trong>Btrong>-C adapter complex via their SOCS trong>btrong>ox domain trong>andtrong> further complex with the cullin trong>andtrong> ring trong>btrong>ox proteins to form E3 utrong>btrong>iquitin ligase complexes. They may function to mediate the sutrong>btrong>strate-recognition of the E3 utrong>btrong>iquitin ligases. A transcritrong>btrong>ed pseudogene of this gene has trong>btrong>een identified on chromosome 15. Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Dec 2009]

SAG Gene

S-antigen; retina trong>andtrong> pineal gltrong>andtrong> (arrestin)

Memtrong>btrong>ers of arrestin/trong>btrong>eta-arrestin protein family are thought to participate in agonist-mediated desensitization of G-protein-coupled receptors trong>andtrong> cause specific dampening of cellular responses to stimuli such as hormones, neurotransmitters, or sensory signals. S-arrestin, also known as S-antigen, is a major solutrong>btrong>le photoreceptor protein that is involved in desensitization of the photoactivated transduction cascade. It is expressed in the retina trong>andtrong> the pineal gltrong>andtrong> trong>andtrong> inhitrong>btrong>its coupling of rhodopsin to transducin in vitro. Additionally, S-arrestin is highly antigenic, trong>andtrong> is capatrong>btrong>le of inducing experimental autoimmune uveoretinitis. Mutations in this gene have trong>btrong>een associated with Oguchi disease, a rare autosomal recessive form of night trong>btrong>lindness. [provided trong>btrong>y RefSeq, Jul 2008]

PROC Gene

protein C (inactivator of coagulation factors Va trong>andtrong> VIIIa)

This gene encodes a vitamin K-dependent plasma glycoprotein. The encoded protein is cleaved to its activated form trong>btrong>y the thromtrong>btrong>in-thromtrong>btrong>omodulin complex. This activated form contains a serine protease domain trong>andtrong> functions in degradation of the activated forms of coagulation factors V trong>andtrong> VIII. Mutations in this gene have trong>btrong>een associated with thromtrong>btrong>ophilia due to protein C deficiency, neonatal purpura fulminans, trong>andtrong> recurrent venous thromtrong>btrong>osis.[provided trong>btrong>y RefSeq, Dec 2009]

LOC100422285 Gene

cleavage trong>andtrong> polyadenylation specific factor 1, 160kDa pseudogene

ZSCAN32 Gene

zinc finger trong>andtrong> SCAN domain containing 32

Enatrong>btrong>les identical protein trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ZSCAN31 Gene

zinc finger trong>andtrong> SCAN domain containing 31

This gene encodes a protein containing multiple C2H2-type zinc finger motifs. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Jan 2016]

ZSCAN30 Gene

zinc finger trong>andtrong> SCAN domain containing 30

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

C1QTNF9trong>Btrong> Gene

C1q trong>andtrong> tumor necrosis factor related protein 9trong>Btrong>

Predicted to enatrong>btrong>le hormone activity trong>andtrong> identical protein trong>btrong>inding activity. Predicted to act upstream of or within several processes, including negative regulation of cell size; positive regulation of cellular response to insulin stimulus; trong>andtrong> positive regulation of protein serine/threonine kinase activity. Predicted to trong>btrong>e located in extracellular space. Predicted to trong>btrong>e part of collagen trimer. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC392268 Gene

neuropilin (NRP) trong>andtrong> tolloid (TLL)-like 2 pseudogene

MFI2 Gene

antigen p97 (melanoma associated) identified trong>btrong>y monoclonal antitrong>btrong>odies 133.2 trong>andtrong> 96.5

The protein encoded trong>btrong>y this gene is a cell-surface glycoprotein found on melanoma cells. The protein shares sequence similarity trong>andtrong> iron-trong>btrong>inding properties with memtrong>btrong>ers of the transferrin superfamily. The importance of the iron trong>btrong>inding function has not yet trong>btrong>een identified. This gene resides in the same region of chromosome 3 as memtrong>btrong>ers of the transferrin superfamily. Alternative splicing results in two transcript variants. [provided trong>btrong>y RefSeq, Jul 2008]

WHAMMP3 Gene

WAS protein homolog associated with actin, golgi memtrong>btrong>ranes trong>andtrong> microtutrong>btrong>ules pseudogene 3

WHAMMP2 Gene

WAS protein homolog associated with actin, golgi memtrong>btrong>ranes trong>andtrong> microtutrong>btrong>ules pseudogene 2

WHAMMP1 Gene

WAS protein homolog associated with actin, golgi memtrong>btrong>ranes trong>andtrong> microtutrong>btrong>ules pseudogene 1

IQUtrong>Btrong> Gene

IQ motif trong>andtrong> utrong>btrong>iquitin domain containing

Involved in flagellated sperm motility trong>andtrong> mating. Predicted to trong>btrong>e located in sperm flagellum. Predicted to trong>btrong>e part of radial spoke. Predicted to trong>btrong>e active in acrosomal vesicle trong>andtrong> motile cilium. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

TMIGD1 Gene

transmemtrong>btrong>rane trong>andtrong> immunoglotrong>btrong>ulin domain containing 1

Predicted to enatrong>btrong>le cell-cell adhesion mediator activity trong>andtrong> protein homodimerization activity. Involved in several processes, including negative regulation of apoptotic process; regulation of cell migration; trong>andtrong> regulation of memtrong>btrong>rane permeatrong>btrong>ility. Located in cytosol; mitochondrion; trong>andtrong> plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

MALRD1 Gene

MAM trong>andtrong> LDL receptor class A domain containing 1

This gene encodes a conserved protein that features multiple MAM (meprin-A5-protein tyrosine phosphatase mu) trong>andtrong> LDLR A2 (low density lipoprotein receptor A2) domains. Expression of this gene is enriched in the small intestine trong>andtrong> is upregulated during differentiation of a human cell line that exhitrong>btrong>its properties of intestinal epithelial cells. The encoded protein has trong>btrong>een shown to modulate production of FGF19 in a human intestinal cell line trong>andtrong> may regulate trong>btrong>ile acid metatrong>btrong>olism in the liver. A synergistic interaction trong>btrong>etween an allele of this gene trong>andtrong> the APOE E4 allele is associated with an elevated risk of Alzheimer's disease in human patients. [provided trong>btrong>y RefSeq, Jul 2017]

AStrong>Btrong>11 Gene

ankyrin repeat trong>andtrong> SOCS trong>btrong>ox containing 11, E3 utrong>btrong>iquitin protein ligase

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of the ankyrin repeat trong>andtrong> SOCS trong>btrong>ox-containing (AStrong>Btrong>) family of proteins. They contain ankyrin repeat sequence trong>andtrong> SOCS trong>btrong>ox domain. The SOCS trong>btrong>ox serves to couple suppressor of cytokine signalling (SOCS) proteins trong>andtrong> their trong>btrong>inding partners with the elongin trong>Btrong> trong>andtrong> C complex, possitrong>btrong>ly targeting them for degradation. Alternatively spliced transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jan 2011]

CFAP97 Gene

cilia trong>andtrong> flagella associated protein 97

Predicted to trong>btrong>e involved in spermatogenesis. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

TPTE2P2 Gene

transmemtrong>btrong>rane phosphoinositide 3-phosphatase trong>andtrong> tensin homolog 2 pseudogene 2

TPTE2P3 Gene

transmemtrong>btrong>rane phosphoinositide 3-phosphatase trong>andtrong> tensin homolog 2 pseudogene 3

TPTE2P1 Gene

transmemtrong>btrong>rane phosphoinositide 3-phosphatase trong>andtrong> tensin homolog 2 pseudogene 1

TPTE2P6 Gene

transmemtrong>btrong>rane phosphoinositide 3-phosphatase trong>andtrong> tensin homolog 2 pseudogene 6

TPTE2P4 Gene

transmemtrong>btrong>rane phosphoinositide 3-phosphatase trong>andtrong> tensin homolog 2 pseudogene 4

SEMA4A Gene

sema domain, immunoglotrong>btrong>ulin domain (Ig), transmemtrong>btrong>rane domain (TM) trong>andtrong> short cytoplasmic domain, (semaphorin) 4A

This gene encodes a memtrong>btrong>er of the semaphorin family of solutrong>btrong>le trong>andtrong> transmemtrong>btrong>rane proteins. Semaphorins are involved in numerous functions, including axon guidance, morphogenesis, carcinogenesis, trong>andtrong> immunomodulation. The encoded protein is a single-pass type I memtrong>btrong>rane protein containing an immunoglotrong>btrong>ulin-like C2-type domain, a PSI domain trong>andtrong> a sema domain. It inhitrong>btrong>its axonal extension trong>btrong>y providing local signals to specify territories inaccessitrong>btrong>le for growing axons. It is an activator of T-cell-mediated immunity trong>andtrong> suppresses vascular endothelial growth factor (VEGF)-mediated endothelial cell migration trong>andtrong> proliferation in vitro trong>andtrong> angiogenesis in vivo. Mutations in this gene are associated with retinal degenerative diseases including retinitis pigmentosa type 35 (RP35) trong>andtrong> cone-rod dystrophy type 10 (CORD10). Multiple alternatively spliced transcript variants encoding different isoforms have trong>btrong>een identified.[provided trong>btrong>y RefSeq, Sep 2010]

SEMA4trong>Btrong> Gene

sema domain, immunoglotrong>btrong>ulin domain (Ig), transmemtrong>btrong>rane domain (TM) trong>andtrong> short cytoplasmic domain, (semaphorin) 4trong>Btrong>

Predicted to enatrong>btrong>le chemorepellent activity; neuropilin trong>btrong>inding activity; trong>andtrong> semaphorin receptor trong>btrong>inding activity. Predicted to trong>btrong>e involved in several processes, including axon guidance; neural crest cell migration; trong>andtrong> semaphorin-plexin signaling pathway. Predicted to trong>btrong>e located in memtrong>btrong>rane trong>andtrong> synapse. Predicted to trong>btrong>e active in glutamatergic synapse trong>andtrong> postsynaptic density memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SEMA4C Gene

sema domain, immunoglotrong>btrong>ulin domain (Ig), transmemtrong>btrong>rane domain (TM) trong>andtrong> short cytoplasmic domain, (semaphorin) 4C

Predicted to enatrong>btrong>le chemorepellent activity; neuropilin trong>btrong>inding activity; trong>andtrong> semaphorin receptor trong>btrong>inding activity. Involved in muscle cell differentiation trong>andtrong> positive regulation of stress-activated MAPK cascade. Located in extracellular space. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SEMA4D Gene

sema domain, immunoglotrong>btrong>ulin domain (Ig), transmemtrong>btrong>rane domain (TM) trong>andtrong> short cytoplasmic domain, (semaphorin) 4D

Enatrong>btrong>les identical protein trong>btrong>inding activity; semaphorin receptor trong>btrong>inding activity; trong>andtrong> transmemtrong>btrong>rane signaling receptor activity. Involved in several processes, including ossification involved in trong>btrong>one maturation; positive regulation of phosphatidylinositol 3-kinase/protein kinase trong>Btrong> signal transduction; trong>andtrong> regulation of neuron projection development. Located in plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SEMA4F Gene

sema domain, immunoglotrong>btrong>ulin domain (Ig), transmemtrong>btrong>rane domain (TM) trong>andtrong> short cytoplasmic domain, (semaphorin) 4F

This gene encodes a transmemtrong>btrong>rane class IV semaphorin family protein, which plays a role in neural development. This gene may trong>btrong>e involved in neurogenesis in prostate cancer, the development of neurofitrong>btrong>romas, trong>andtrong> trong>btrong>reast cancer tumorigenesis. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Nov 2012]

SEMA4G Gene

sema domain, immunoglotrong>btrong>ulin domain (Ig), transmemtrong>btrong>rane domain (TM) trong>andtrong> short cytoplasmic domain, (semaphorin) 4G

Semaphorins are a large family of conserved secreted trong>andtrong> memtrong>btrong>rane associated proteins which possess a semaphorin (Sema) domain trong>andtrong> a PSI domain (found in plexins, semaphorins trong>andtrong> integrins) in the N-terminal extracellular portion. trong>Btrong>ased on sequence trong>andtrong> structural similarities, semaphorins are put into eight classes: invertetrong>btrong>rates contain classes 1 trong>andtrong> 2, viruses have class V, trong>andtrong> vertetrong>btrong>rates contain classes 3-7. Semaphorins serve as axon guidance ligtrong>andtrong>s via multimeric receptor complexes, some (if not all) containing plexin proteins. Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2011]

TMCO3 Gene

transmemtrong>btrong>rane trong>andtrong> coiled-coil domains 3

This gene encodes a memtrong>btrong>er of the monovalent cation:proton antiporter 2 (CPA2) family of transporter proteins. Memtrong>btrong>ers of this family typically couple the export of monovalent cations, such as potassium or sodium, to the import of protons across cellular memtrong>btrong>ranes. Mutations in this gene have trong>btrong>een identified in patients with a rare inherited vision defect, cornea guttata with anterior polar cataract. [provided trong>btrong>y RefSeq, Mar 2017]

DCAF13P3 Gene

DDtrong>Btrong>1 trong>andtrong> CUL4 associated factor 13 pseudogene 3

trong>Btrong>ZW1 Gene

trong>btrong>asic leucine zipper trong>andtrong> W2 domains 1

Enatrong>btrong>les RNA trong>btrong>inding activity trong>andtrong> cadherin trong>btrong>inding activity. Involved in regulation of translational initiation. Located in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

trong>Btrong>ZW2 Gene

trong>btrong>asic leucine zipper trong>andtrong> W2 domains 2

Enatrong>btrong>les cadherin trong>btrong>inding activity. Involved in regulation of translational initiation. Located in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CNNM1 Gene

cyclin trong>andtrong> Ctrong>Btrong>S domain divalent metal cation transport mediator 1

This gene encodes a memtrong>btrong>er of the ancient conserved domain protein family. The encoded protein may trong>btrong>ind copper. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Sep 2016]

CNNM3 Gene

cyclin trong>andtrong> Ctrong>Btrong>S domain divalent metal cation transport mediator 3

Predicted to enatrong>btrong>le transmemtrong>btrong>rane transporter activity. Predicted to trong>btrong>e involved in magnesium ion homeostasis. Located in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CNNM2 Gene

cyclin trong>andtrong> Ctrong>Btrong>S domain divalent metal cation transport mediator 2

This gene encodes a memtrong>btrong>er of the ancient conserved domain containing protein family. Memtrong>btrong>ers of this protein family contain a cyclin trong>btrong>ox motif trong>andtrong> have structural similarity to the cyclins. The encoded protein may play an important role in magnesium homeostasis trong>btrong>y mediating the epithelial transport trong>andtrong> renal reatrong>btrong>sorption of Mg2+. Mutations in this gene are associated with renal hypomagnesemia. Alternatively spliced transcript variants encoding multiple isoforms have trong>btrong>een otrong>btrong>served for this gene. [provided trong>btrong>y RefSeq, Dec 2011]

CNNM4 Gene

cyclin trong>andtrong> Ctrong>Btrong>S domain divalent metal cation transport mediator 4

This gene encodes a memtrong>btrong>er of the ancient conserved domain containing protein family. Memtrong>btrong>ers of this protein family contain a cyclin trong>btrong>ox motif trong>andtrong> have structural similarity to the cyclins. The encoded protein may play a role in metal ion transport. Mutations in this gene are associated with Jalili syndrome which consists of cone-rod dystrophy trong>andtrong> amelogenesis imperfecta. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2010]

CC2D1A Gene

coiled-coil trong>andtrong> C2 domain containing 1A

This gene encodes a transcriptional repressor that trong>btrong>inds to a conserved 14-trong>btrong>p 5'-repressor element trong>andtrong> regulates expression of the 5-hydroxytryptamine (serotonin) receptor 1A gene in neuronal cells. The DNA trong>btrong>inding trong>andtrong> transcriptional repressor activities of the protein are inhitrong>btrong>ited trong>btrong>y calcium. A mutation in this gene results in a nonsyndromic form of cognitive disatrong>btrong>ility (MRT3). [provided trong>btrong>y RefSeq, Jul 2017]

CC2D1trong>Btrong> Gene

coiled-coil trong>andtrong> C2 domain containing 1trong>Btrong>

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to act upstream of or within negative regulation of transcription trong>btrong>y RNA polymerase II. Located in nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LOC100131556 Gene

zinc finger CCHC-type trong>andtrong> RNA trong>btrong>inding motif 1 pseudogene

LOC100131553 Gene

disintegrin trong>andtrong> metalloproteinase domain-containing protein 21-like

trong>Btrong>CCIP Gene

trong>Btrong>RCA2 trong>andtrong> CDKN1A interacting protein

This gene product was isolated on the trong>btrong>asis of its interaction with trong>Btrong>RCA2 trong>andtrong> p21 proteins. It is an evolutionarily conserved nuclear protein with multiple interacting domains. The N-terminal half shares moderate homology with regions of calmodulin trong>andtrong> M-calpain, suggesting that it may also trong>btrong>ind calcium. Functional studies indicate that this protein may trong>btrong>e an important cofactor for trong>Btrong>RCA2 in tumor suppression, trong>andtrong> a modulator of CDK2 kinase activity via p21. This protein has also trong>btrong>een implicated in the regulation of trong>Btrong>RCA2 trong>andtrong> RAD51 nuclear focus formation, doutrong>btrong>le-strtrong>andtrong> trong>btrong>reak-induced homologous recomtrong>btrong>ination, trong>andtrong> cell cycle progression. Multiple transcript variants encoding different isoforms have trong>btrong>een descritrong>btrong>ed for this gene. [provided trong>btrong>y RefSeq, Jul 2008]

STUtrong>Btrong>1 Gene

STIP1 homology trong>andtrong> U-trong>btrong>ox containing protein 1, E3 utrong>btrong>iquitin protein ligase

This gene encodes a protein containing tetratricopeptide repeat trong>andtrong> a U-trong>btrong>ox that functions as a utrong>btrong>iquitin ligase/cochaperone. The encoded protein trong>btrong>inds to trong>andtrong> utrong>btrong>iquitinates shock cognate 71 kDa protein (Hspa8) trong>andtrong> DNA polymerase trong>btrong>eta (Poltrong>btrong>), among other targets. Mutations in this gene cause spinoceretrong>btrong>ellar ataxia, autosomal recessive 16. Alternative splicing results in multiple transcript variants. There is a pseudogene for this gene on chromosome 2. [provided trong>btrong>y RefSeq, Jun 2014]

SOHLH1 Gene

spermatogenesis trong>andtrong> oogenesis specific trong>btrong>asic helix-loop-helix 1

This gene encodes one of testis-specific transcription factors which are essential for spermatogenesis, oogenesis trong>andtrong> folliculogenesis. This gene is located on chromosome 9. Mutations in this gene are associated with nonotrong>btrong>structive azoospermia. Alternatively spliced transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Aug 2013]

SOHLH2 Gene

spermatogenesis trong>andtrong> oogenesis specific trong>btrong>asic helix-loop-helix 2

This gene encodes one of testis-specific transcription factors which are essential for spermatogenesis, oogenesis trong>andtrong> folliculogenesis. This gene is located on chromosome 13. The proteins encoded trong>btrong>y this gene trong>andtrong> another testis-specific transcription factor, SOHLH1, can form heterodimers, in addition to homodimers. There is a read-through locus (GeneID: 100526761) that shares sequence identity with this gene trong>andtrong> the upstream CCDC169 (GeneID: 728591). Alternatively spliced transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Aug 2013]

ZCRtrong>Btrong>1 Gene

zinc finger CCHC-type trong>andtrong> RNA trong>btrong>inding motif 1

Pre-mRNA splicing is catalyzed trong>btrong>y the spliceosome. U12-type spliceosome trong>btrong>inds U12-type pre-mRNAs trong>andtrong> recognizes the 5' splice site trong>andtrong> trong>btrong>ranch-point sequence. U11 trong>andtrong> U12 snRNPs are components of U12-type spliceosome trong>andtrong> function as a molecular trong>btrong>ridge connecting trong>btrong>oth ends of the intron. The protein encoded trong>btrong>y this gene contains a RNA recognition motif. It was identified as one of the protein components of U11/U12 snRNPs. This protein trong>andtrong> many other U11/U12 snRNP proteins are highly conserved in organisms known to contain U12-type introns. These proteins have trong>btrong>een shown to trong>btrong>e essential for cell viatrong>btrong>ility, suggesting the key roles in U12-type splicing. [provided trong>btrong>y RefSeq, Jul 2008]

RAX2 Gene

retina trong>andtrong> anterior neural fold homeotrong>btrong>ox 2

This gene encodes a homeodomain-containing protein that plays a role in eye development. Mutation of this gene causes age-related macular degeneration type 6, an eye disorder resulting in accumulations of protein trong>andtrong> lipid trong>btrong>eneath the retinal pigment epithelium trong>andtrong> within the trong>Btrong>ruch's memtrong>btrong>rane. Defects in this gene can also cause cone-rod dystrophy type 11, a disease characterized trong>btrong>y the initial degeneration of cone photoreceptor cells trong>andtrong> resulting in loss of color vision trong>andtrong> visual acuity, followed trong>btrong>y the degeneration of rod photoreceptor cells, which progresses to night trong>btrong>lindness trong>andtrong> the loss of peripheral vision. Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, Jan 2016]

UCMA Gene

upper zone of growth plate trong>andtrong> cartilage matrix associated

This gene encodes a chondrocyte-specific, highly charged protein that is atrong>btrong>undantly expressed in the upper immature zone of fetal trong>andtrong> juvenile epiphyseal cartilage. The encoded protein undergoes proteolytic processing to generate a mature protein that is secreted into the extracellular matrix. The glutamic acid residues in the encoded protein undergo gamma cartrong>btrong>oxylation in a vitamin K-dependent manner. Undercartrong>btrong>oxylation of the encoded protein is associated with osteoarthritis in humans. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided trong>btrong>y RefSeq, Jul 2015]

SND1 Gene

staphylococcal nuclease trong>andtrong> tudor domain containing 1

This gene encodes a transcriptional co-activator that interacts with the acidic domain of Epstein-trong>Btrong>arr virus nuclear antigen 2 (Etrong>Btrong>NA 2), a transcriptional activator that is required for trong>Btrong>-lymphocyte transformation. Other transcription factors that interact with this protein are signal transducers trong>andtrong> activators of transcription, STATs. This protein is also thought to trong>btrong>e essential for normal cell growth. A similar protein in mammals trong>andtrong> other organisms is a component of the RNA-induced silencing complex (RISC). [provided trong>btrong>y RefSeq, Jul 2016]

LOC100422402 Gene

RAS guanyl releasing protein 2 (calcium trong>andtrong> DAG-regulated) pseudogene

LOC100129957 Gene

PC4 trong>andtrong> SFRS1 interacting protein 1 pseudogene

LINGO4 Gene

leucine rich repeat trong>andtrong> Ig domain containing 4

Predicted to act upstream of or within positive regulation of synapse assemtrong>btrong>ly. Predicted to trong>btrong>e located in memtrong>btrong>rane. Predicted to trong>btrong>e active in extracellular matrix trong>andtrong> extracellular space. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LINGO3 Gene

leucine rich repeat trong>andtrong> Ig domain containing 3

Predicted to trong>btrong>e located in memtrong>btrong>rane. Predicted to trong>btrong>e active in extracellular matrix trong>andtrong> extracellular space. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LINGO2 Gene

leucine rich repeat trong>andtrong> Ig domain containing 2

Predicted to act upstream of or within positive regulation of synapse assemtrong>btrong>ly. Predicted to trong>btrong>e located in memtrong>btrong>rane. Predicted to trong>btrong>e active in several cellular components, including extracellular space; glutamatergic synapse; trong>andtrong> synaptic memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LINGO1 Gene

leucine rich repeat trong>andtrong> Ig domain containing 1

Predicted to enatrong>btrong>le epidermal growth factor receptor trong>btrong>inding activity. Predicted to act upstream of or within negative regulation of oligodendrocyte differentiation; negative regulation of phosphatidylinositol 3-kinase/protein kinase trong>Btrong> signal transduction; trong>andtrong> neuron development. Predicted to trong>btrong>e located in plasma memtrong>btrong>rane. Predicted to trong>btrong>e active in several cellular components, including extracellular space; glutamatergic synapse; trong>andtrong> presynapse. Implicated in autosomal recessive intellectual developmental disorder 64 trong>andtrong> glaucoma. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

STAT4 Gene

signal transducer trong>andtrong> activator of transcription 4

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of the STAT family of transcription factors. In response to cytokines trong>andtrong> growth factors, STAT family memtrong>btrong>ers are phosphorylated trong>btrong>y the receptor associated kinases, trong>andtrong> then form homo- or heterodimers that translocate to the cell nucleus where they act as transcription activators. This protein is essential for mediating responses to IL12 in lymphocytes, trong>andtrong> regulating the differentiation of T helper cells. Mutations in this gene may trong>btrong>e associated with systemic lupus erythematosus trong>andtrong> rheumatoid arthritis. Alternate splicing results in multiple transcript variants that encode the same protein. [provided trong>btrong>y RefSeq, Aug 2011]

STAT3 Gene

signal transducer trong>andtrong> activator of transcription 3 (acute-phase response factor)

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of the STAT protein family. In response to cytokines trong>andtrong> growth factors, STAT family memtrong>btrong>ers are phosphorylated trong>btrong>y the receptor associated kinases, trong>andtrong> then form homo- or heterodimers that translocate to the cell nucleus where they act as transcription activators. This protein is activated through phosphorylation in response to various cytokines trong>andtrong> growth factors including IFNs, EGF, IL5, IL6, HGF, LIF trong>andtrong> trong>Btrong>MP2. This protein mediates the expression of a variety of genes in response to cell stimuli, trong>andtrong> thus plays a key role in many cellular processes such as cell growth trong>andtrong> apoptosis. The small GTPase Rac1 has trong>btrong>een shown to trong>btrong>ind trong>andtrong> regulate the activity of this protein. PIAS3 protein is a specific inhitrong>btrong>itor of this protein. This gene also plays a role in regulating host response to viral trong>andtrong> trong>btrong>acterial infections. Mutations in this gene are associated with infantile-onset multisystem autoimmune disease trong>andtrong> hyper-immunoglotrong>btrong>ulin E syndrome. [provided trong>btrong>y RefSeq, Aug 2020]

STAT2 Gene

signal transducer trong>andtrong> activator of transcription 2, 113kDa

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of the STAT protein family. In response to cytokines trong>andtrong> growth factors, STAT family memtrong>btrong>ers are phosphorylated trong>btrong>y the receptor associated kinases, trong>andtrong> then form homo- or heterodimers that translocate to the cell nucleus where they act as transcription activators. In response to interferon (IFN), this protein forms a complex with STAT1 trong>andtrong> IFN regulatory factor family protein p48 (ISGF3G), in which this protein acts as a transactivator, trong>btrong>ut lacks the atrong>btrong>ility to trong>btrong>ind DNA directly. The protein mediates innate antiviral activity. Mutations in this gene result in Immunodeficiency 44. [provided trong>btrong>y RefSeq, Aug 2020]

STAT1 Gene

signal transducer trong>andtrong> activator of transcription 1, 91kDa

The protein encoded trong>btrong>y this gene is a memtrong>btrong>er of the STAT protein family. In response to cytokines trong>andtrong> growth factors, STAT family memtrong>btrong>ers are phosphorylated trong>btrong>y the receptor associated kinases, trong>andtrong> then form homo- or heterodimers that translocate to the cell nucleus where they act as transcription activators. The protein encoded trong>btrong>y this gene can trong>btrong>e activated trong>btrong>y various ligtrong>andtrong>s including interferon-alpha, interferon-gamma, EGF, PDGF trong>andtrong> IL6. This protein mediates the expression of a variety of genes, which is thought to trong>btrong>e important for cell viatrong>btrong>ility in response to different cell stimuli trong>andtrong> pathogens. The protein plays an important role in immune responses to viral, fungal trong>andtrong> mycotrong>btrong>acterial pathogens. Mutations in this gene are associated with Immunodeficiency 31trong>Btrong>, 31A, trong>andtrong> 31C. [provided trong>btrong>y RefSeq, Jun 2020]

ELFN1 Gene

extracellular leucine-rich repeat trong>andtrong> fitrong>btrong>ronectin type III domain containing 1

Predicted to enatrong>btrong>le protein phosphatase inhitrong>btrong>itor activity. Predicted to trong>btrong>e involved in synapse organization. Predicted to act upstream of or within several processes, including chemical synaptic transmission; synapse assemtrong>btrong>ly; trong>andtrong> visual perception. Predicted to trong>btrong>e located in dendrite trong>andtrong> excitatory synapse. Predicted to trong>btrong>e active in several cellular components, including axon terminus; glutamatergic synapse; trong>andtrong> postsynaptic density memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ELFN2 Gene

extracellular leucine-rich repeat trong>andtrong> fitrong>btrong>ronectin type III domain containing 2

Predicted to enatrong>btrong>le protein phosphatase inhitrong>btrong>itor activity. Predicted to trong>btrong>e involved in synaptic memtrong>btrong>rane adhesion. Predicted to act upstream of or within chemical synaptic transmission; estatrong>btrong>lishment of protein localization; trong>andtrong> gene expression. Located in extracellular space. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ACAP1 Gene

ArfGAP with coiled-coil, ankyrin repeat trong>andtrong> PH domains 1

Predicted to enatrong>btrong>le GTPase activator activity trong>andtrong> metal ion trong>btrong>inding activity. Predicted to trong>btrong>e involved in protein transport. Located in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ACAP3 Gene

ArfGAP with coiled-coil, ankyrin repeat trong>andtrong> PH domains 3

Predicted to enatrong>btrong>le GTPase activator activity trong>andtrong> metal ion trong>btrong>inding activity. Predicted to act upstream of or within neuron migration trong>andtrong> regulation of neuron projection development. Predicted to trong>btrong>e located in endosome memtrong>btrong>rane trong>andtrong> growth cone. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ZNRF2P1 Gene

zinc trong>andtrong> ring finger 2 pseudogene 1

ZNRF2P3 Gene

zinc trong>andtrong> ring finger 2 pseudogene 3

ZNRF2P2 Gene

zinc trong>andtrong> ring finger 2 pseudogene 2

PTRF Gene

polymerase I trong>andtrong> transcript release factor

This gene encodes a protein that enatrong>btrong>les the dissociation of paused ternary polymerase I transcription complexes from the 3' end of pre-rRNA transcripts. This protein regulates rRNA transcription trong>btrong>y promoting the dissociation of transcription complexes trong>andtrong> the reinitiation of polymerase I on nascent rRNA transcripts. This protein also localizes to caveolae at the plasma memtrong>btrong>rane trong>andtrong> is thought to play a critical role in the formation of caveolae trong>andtrong> the statrong>btrong>ilization of caveolins. This protein translocates from caveolae to the cytoplasm after insulin stimulation. Caveolae contain truncated forms of this protein trong>andtrong> may trong>btrong>e the site of phosphorylation-dependent proteolysis. This protein is also thought to modify lipid metatrong>btrong>olism trong>andtrong> insulin-regulated gene expression. Mutations in this gene result in a disorder characterized trong>btrong>y generalized lipodystrophy trong>andtrong> muscular dystrophy. [provided trong>btrong>y RefSeq, Nov 2009]

CARMIL1 Gene

capping protein regulator trong>andtrong> myosin 1 linker 1

Involved in several processes, including actin filament network formation; plasma memtrong>btrong>rane trong>btrong>ounded cell projection organization; trong>andtrong> positive regulation of cellular component organization. Located in several cellular components, including lamellipodium; macropinosome; trong>andtrong> nuclear speck. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

trong>Btrong>UD23 Gene

trong>Btrong>UD23 rRNA methyltransferase trong>andtrong> ritrong>btrong>osome maturation factor

This gene encodes a protein containing a nuclear localization signal trong>andtrong> an S-adenosyl-L-methionine trong>btrong>inding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused trong>btrong>y the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have trong>btrong>een found. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2011]

PAtrong>Btrong>IR1 Gene

PP2A Aalpha (PPP2R1A) trong>andtrong> trong>Btrong>55A (PPP2R2A) interacting phosphatase regulator 1

Enatrong>btrong>les protein phosphatase 2A trong>btrong>inding activity trong>andtrong> protein serine/threonine phosphatase inhitrong>btrong>itor activity. Involved in mitotic G2/M transition checkpoint; positive regulation of cell growth; trong>andtrong> positive regulation of proteasomal utrong>btrong>iquitin-dependent protein catatrong>btrong>olic process. Located in cytoplasm trong>andtrong> nuclear trong>btrong>ody. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

EIPR1 Gene

EARP complex trong>andtrong> GARP complex interacting protein 1

This gene has trong>btrong>een reported in PMID 9403053 as one of several tumor-suppressing sutrong>btrong>transferatrong>btrong>le fragments located in the imprinted gene domain of 11p15.5, an important tumor-suppressor gene region. Alterations in this region have trong>btrong>een associated with the trong>Btrong>eckwith-Wiedemann syndrome, Wilms tumor, rhatrong>btrong>domyosarcoma, adrenocortical carcinoma, trong>andtrong> lung, ovarian, trong>andtrong> trong>btrong>reast cancer. Alignment of this gene to genomic sequence data suggests that this gene resides on chromosome 2 rather than chromosome 11. [provided trong>btrong>y RefSeq, Dec 2008]

CFAP251 Gene

cilia trong>andtrong> flagella associated protein 251

This protein encoded trong>btrong>y this gene trong>btrong>elongs to the WD repeat-containing family of proteins, which function in the formation of protein-protein complexes in a variety of trong>btrong>iological pathways. This family memtrong>btrong>er appears to function in the determination of mean platelet volume (MPV), trong>andtrong> polymorphisms in this gene have trong>btrong>een associated with variance in MPV. Alternative splicing of this gene results in multiple transcript variants. [provided trong>btrong>y RefSeq, Sep 2011]

SPINDOC Gene

spindlin interactor trong>andtrong> repressor of chromatin trong>btrong>inding

Involved in DNA damage response trong>andtrong> negative regulation of DNA-templated transcription. Is active in nucleus trong>andtrong> site of DNA damage. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ELAPOR1 Gene

endosome-lysosome associated apoptosis trong>andtrong> autophagy regulator 1

Expression of this gene is induced trong>btrong>y estrogen trong>andtrong> the encoded protein has trong>btrong>een characterized as a transmemtrong>btrong>rane protein. The encoded protein has trong>btrong>een found in to correlate with survival in certain carcinomas (PMID: 21102415) trong>andtrong> may trong>btrong>e important for cellular response to stress (PMID: 21072319). Alternative splicing results in multiple transcript variants. [provided trong>btrong>y RefSeq, May 2012]

DCAF1 Gene

DDtrong>Btrong>1 trong>andtrong> CUL4 associated factor 1

Enatrong>btrong>les histone H2AT120 kinase activity; nuclear estrogen receptor trong>btrong>inding activity; trong>andtrong> utrong>btrong>iquitin-like ligase-sutrong>btrong>strate adaptor activity. Involved in several processes, including cell competition in a multicellular organism; proteasome-mediated utrong>btrong>iquitin-dependent protein catatrong>btrong>olic process; trong>andtrong> regulation of primary metatrong>btrong>olic process. Located in COP9 signalosome; fitrong>btrong>rillar center; trong>andtrong> nucleoplasm. Part of Cul4-RING E3 utrong>btrong>iquitin ligase complex. Is active in centrosome. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ECPAS Gene

Ecm29 proteasome adaptor trong>andtrong> scaffold

Enatrong>btrong>les proteasome trong>btrong>inding activity. Involved in ERAD pathway. Located in several cellular components, including centrosome; cytoplasmic vesicle; trong>andtrong> nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CARMIL2 Gene

capping protein regulator trong>andtrong> myosin 1 linker 2

This gene encodes a memtrong>btrong>er of the CARMIL (capping protein, Arp2/3, myosin-I linker) family of proteins. The encoded protein interacts with trong>andtrong> negatively regulates the heterodimeric capping protein trong>andtrong> promotes cell migration. Reduced expression of this gene has trong>btrong>een otrong>btrong>served in human psoriasis patients. Mutations in this gene cause a human immunodeficiency syndrome characterized trong>btrong>y smooth muscle tumors trong>andtrong> impaired T-cell function. [provided trong>btrong>y RefSeq, May 2017]

RTRAF Gene

RNA transcription, translation trong>andtrong> transport factor

Enatrong>btrong>les RNA trong>btrong>inding activity; RNA polymerase II complex trong>btrong>inding activity; trong>andtrong> identical protein trong>btrong>inding activity. Involved in negative regulation of protein kinase activity; positive regulation of transcription trong>btrong>y RNA polymerase II; trong>andtrong> tRNA splicing, via endonucleolytic cleavage trong>andtrong> ligation. Located in microtutrong>btrong>ule cytoskeleton; nucleoplasm; trong>andtrong> perinuclear region of cytoplasm. Part of tRNA-splicing ligase complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

trong>Btrong>Atrong>Btrong>AM2 Gene

trong>Btrong>RISC trong>andtrong> trong>Btrong>RCA1 A complex memtrong>btrong>er 2

This gene encodes an anti-apoptotic, death receptor-associated protein that interacts with tumor necrosis factor-receptor-1. The encoded protein acts as an adapter in several protein complexes, including the trong>Btrong>RCA1-A complex trong>andtrong> the trong>Btrong>RISC complex. The trong>Btrong>RCA1-A complex possesses utrong>btrong>iquitinase activity trong>andtrong> targets sites of doutrong>btrong>le strtrong>andtrong> DNA trong>btrong>reaks, while the trong>Btrong>RISC complex exhitrong>btrong>its deutrong>btrong>iquitinase activity trong>andtrong> is involved in mitotic spindle assemtrong>btrong>ly. This gene is upregulated in several types of cancer. [provided trong>btrong>y RefSeq, Jun 2016]

CFAP298 Gene

cilia trong>andtrong> flagella associated protein 298

This gene encodes a protein that plays a critical role in dynein arm assemtrong>btrong>ly trong>andtrong> motile cilia function. Mutations in this gene result in primary ciliary dyskinesia. Naturally occuring readthrough transcription occurs from this locus to the downstream t-complex 10 like (TCP10L) gene. [provided trong>btrong>y RefSeq, Apr 2017]

CFAP65 Gene

cilia trong>andtrong> flagella associated protein 65

The protein encoded trong>btrong>y this gene has putative coiled-coil domains trong>andtrong> may trong>btrong>e a transmemtrong>btrong>rane protein. The chicken ortholog of this gene is involved in the Rose-comtrong>btrong> mutation, which is a large chromosome inversion, resulting in altered comtrong>btrong> morphology trong>andtrong> defects in sperm motility. [provided trong>btrong>y RefSeq, Aug 2016]

DERPC Gene

DERPC proline trong>andtrong> glycine rich nuclear protein

Located in nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CPLANE1 Gene

ciliogenesis trong>andtrong> planar polarity effector complex sutrong>btrong>unit 1

The protein encoded trong>btrong>y this gene has putative coiled-coil domains trong>andtrong> may trong>btrong>e a transmemtrong>btrong>rane protein. Defects in this gene are a cause of Joutrong>btrong>ert syndrome (Jtrong>Btrong>TS). [provided trong>btrong>y RefSeq, May 2012]

LARGE2 Gene

LARGE xylosyl- trong>andtrong> glucuronyltransferase 2

Predicted to enatrong>btrong>le dystroglycan trong>btrong>inding activity; glucuronosyltransferase activity; trong>andtrong> xylosyltransferase activity. Involved in protein O-linked mannosylation. Predicted to trong>btrong>e located in intracellular memtrong>btrong>rane-trong>btrong>ounded organelle. Predicted to trong>btrong>e active in Golgi apparatus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP410 Gene

cilia trong>andtrong> flagella associated protein 410

Four alternatively spliced transcript variants encoding four different isoforms have trong>btrong>een found for this nuclear gene. All isoforms contain leucine-rich repeats. Three of these isoforms are mitochondrial proteins trong>andtrong> one of them lacks the target peptide, so is not located in mitochondrion. This gene is down-regulated in Down syndrome (DS) trong>btrong>rain, which may represent mitochondrial dysfunction in DS patients. [provided trong>btrong>y RefSeq, Sep 2012]

MARF1 Gene

meiosis regulator trong>andtrong> mRNA statrong>btrong>ility factor 1

This gene encodes a putative peroxisomal protein that appears to trong>btrong>e conserved across Euteleostomi. In humans, it may trong>btrong>e autoantigenic. [provided trong>btrong>y RefSeq, Jul 2010]

MICOS10 Gene

mitochondrial contact site trong>andtrong> cristae organizing system sutrong>btrong>unit 10

Involved in cristae formation. Located in mitochondrion. Part of MItrong>Btrong> complex; MICOS complex; trong>andtrong> SAM complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

trong>Btrong>CLAF3 Gene

trong>Btrong>CLAF1 trong>andtrong> THRAP3 family memtrong>btrong>er 3

Predicted to enatrong>btrong>le DNA trong>btrong>inding activity trong>andtrong> transcription coregulator activity. Predicted to trong>btrong>e involved in positive regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in mitochondrion. Predicted to trong>btrong>e part of mediator complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PLAAT3 Gene

phospholipase A trong>andtrong> acyltransferase 3

Enatrong>btrong>les N-acyltransferase activity; lipid trong>btrong>inding activity; trong>andtrong> phospholipase activity. Involved in N-acylphosphatidylethanolamine metatrong>btrong>olic process. Predicted to trong>btrong>e located in several cellular components, including lysosome; nuclear envelope; trong>andtrong> peroxisome. Predicted to trong>btrong>e active in cytoplasm. trong>Btrong>iomarker of seminoma. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ATP23 Gene

ATP23 metallopeptidase trong>andtrong> ATP synthase assemtrong>btrong>ly factor homolog

The protein encoded trong>btrong>y this gene is amplified in gliotrong>btrong>lastomas trong>andtrong> interacts with the DNA trong>btrong>inding sutrong>btrong>unit of DNA-dependent protein kinase. This kinase is involved in doutrong>btrong>le-strtrong>andtrong> trong>btrong>reak repair (DStrong>Btrong>), trong>andtrong> higher expression of the encoded protein increases the efficiency of DStrong>Btrong>. In addition, comparison to orthologous proteins strongly suggests that this protein is a metalloprotease important in the trong>btrong>iosynthesis of mitochondrial ATPase. Several transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Fetrong>btrong> 2016]

EPOP Gene

elongin trong>Btrong>C trong>andtrong> polycomtrong>btrong> repressive complex 2 associated protein

Predicted to enatrong>btrong>le chromatin trong>btrong>inding activity. Predicted to trong>btrong>e involved in neuron fate commitment; regulation of transcription trong>btrong>y RNA polymerase II; trong>andtrong> stem cell differentiation. Predicted to trong>btrong>e located in chromosome trong>andtrong> nucleus. Predicted to trong>btrong>e part of ESC/E(Z) complex trong>andtrong> elongin complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

TEDC1 Gene

tutrong>btrong>ulin epsilon trong>andtrong> delta complex 1

Predicted to trong>btrong>e involved in positive regulation of smoothened signaling pathway. Predicted to trong>btrong>e located in centriole trong>andtrong> cilium. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

TEDC2 Gene

tutrong>btrong>ulin epsilon trong>andtrong> delta complex 2

Predicted to trong>btrong>e involved in positive regulation of smoothened signaling pathway. Predicted to trong>btrong>e located in centriole trong>andtrong> cilium. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

MICOS13 Gene

mitochondrial contact site trong>andtrong> cristae organizing system sutrong>btrong>unit 13

Involved in cristae formation. Located in mitochondrial crista junction trong>andtrong> nucleoplasm. Part of MICOS complex. Implicated in comtrong>btrong>ined oxidative phosphorylation deficiency 37. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

WDCP Gene

WD repeat trong>andtrong> coiled coil containing

Enatrong>btrong>les kinase trong>btrong>inding activity. Involved in protein complex oligomerization. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SCYGR4 Gene

small cysteine trong>andtrong> glycine repeat containing 4

Predicted to trong>btrong>e located in intermediate filament. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

TCIM Gene

transcriptional trong>andtrong> immune response regulator

This gene encodes a small, monomeric, predominantly unstructured protein that functions as a positive regulator of the Wnt/trong>btrong>eta-catenin signaling pathway. This protein interacts with a repressor of trong>btrong>eta-catenin mediated transcription at nuclear speckles. It is thought to competitively trong>btrong>lock interactions of the repressor with trong>btrong>eta-catenin, resulting in up-regulation of trong>btrong>eta-catenin target genes. The encoded protein may also play a role in the NF-kappatrong>Btrong> trong>andtrong> ERK1/2 signaling pathways. Expression of this gene may play a role in the proliferation of several types of cancer including thyroid cancer, trong>btrong>reast cancer trong>andtrong> hematological malignancies. [provided trong>btrong>y RefSeq, Nov 2011]

GARRE1 Gene

granule associated Rac trong>andtrong> RHOG effector 1

Enatrong>btrong>les CCR4-NOT complex trong>btrong>inding activity trong>andtrong> small GTPase trong>btrong>inding activity. Involved in Rac protein signal transduction. Located in P-trong>btrong>ody. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PLAAT4 Gene

phospholipase A trong>andtrong> acyltransferase 4

Retinoids exert trong>btrong>iologic effects such as potent growth inhitrong>btrong>itory trong>andtrong> cell differentiation activities trong>andtrong> are used in the treatment of hyperproliferative dermatological diseases. These effects are mediated trong>btrong>y specific nuclear receptor proteins that are memtrong>btrong>ers of the steroid trong>andtrong> thyroid hormone receptor superfamily of transcriptional regulators. RARRES1, RARRES2, trong>andtrong> RARRES3 are genes whose expression is upregulated trong>btrong>y the synthetic retinoid tazarotene. RARRES3 is thought act as a tumor suppressor or growth regulator. [provided trong>btrong>y RefSeq, Jul 2008]

PLAAT1 Gene

phospholipase A trong>andtrong> acyltransferase 1

Enatrong>btrong>les acyltransferase activity, transferring groups other than amino-acyl groups trong>andtrong> phospholipase activity. Involved in N-acylphosphatidylethanolamine metatrong>btrong>olic process trong>andtrong> phosphatidylcholine metatrong>btrong>olic process. Located in cytoplasm trong>andtrong> nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LARGE1 Gene

LARGE xylosyl- trong>andtrong> glucuronyltransferase 1

This gene encodes a memtrong>btrong>er of the N-acetylglucosaminyltransferase gene family. It encodes a glycosyltransferase which participates in glycosylation of alpha-dystroglycan, trong>andtrong> may carry out the synthesis of glycoprotein trong>andtrong> glycosphingolipid sugar chains. It may also trong>btrong>e involved in the addition of a repeated disaccharide unit. The protein encoded trong>btrong>y this gene is the glycotransferase that adds the final xylose trong>andtrong> glucuronic acid to alpha-dystroglycan trong>andtrong> theretrong>btrong>y allows alpha-dystroglycan to trong>btrong>ind ligtrong>andtrong>s including laminin 211 trong>andtrong> neurexin. Mutations in this gene cause several forms of congenital muscular dystrophy characterized trong>btrong>y cognitive disatrong>btrong>ility trong>andtrong> atrong>btrong>normal glycosylation of alpha-dystroglycan. Alternative splicing of this gene results in multiple transcript variants that encode the same protein. [provided trong>btrong>y RefSeq, May 2018]

PLAAT2 Gene

phospholipase A trong>andtrong> acyltransferase 2

The protein encoded trong>btrong>y this gene has trong>btrong>oth phospholipase trong>andtrong> acyltransferase activities trong>andtrong> acts as a tumor suppressor. The encoded protein can hydrolyze dipalmitoylated phosphatidylcholine (PC) to palmitic acid trong>andtrong> lyso-PC. In addition, this protein can catalyze the N-acylation of phosphatidylethanolamine trong>andtrong> can catalyze the O-acylation of lyso-PC to form PC. [provided trong>btrong>y RefSeq, Jul 2016]

CFAP418 Gene

cilia trong>andtrong> flagella associated protein 418

This gene encodes a utrong>btrong>iquitously expressed protein of unknown function. It has high levels of mRNA expression in the trong>btrong>rain, heart, trong>andtrong> retina trong>andtrong> the protein co-localizes with polyglutamylated tutrong>btrong>ulin at the trong>btrong>ase of the primary cilium in human retinal pigment epithelial cells. Mutations in this gene have trong>btrong>een associated with autosomal recessive cone-rod dystrophy (arCRD) trong>andtrong> retinitis pigmentosa (arRP). [provided trong>btrong>y RefSeq, Mar 2012]

CFAP77 Gene

cilia trong>andtrong> flagella associated protein 77

Predicted to trong>btrong>e involved in flagellated sperm motility. Located in axonemal microtutrong>btrong>ule. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CARMIL3 Gene

capping protein regulator trong>andtrong> myosin 1 linker 3

Predicted to trong>btrong>e involved in cell migration trong>andtrong> regulation of Arp2/3 complex-mediated actin nucleation. Located in cytoplasm trong>andtrong> plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP119 Gene

cilia trong>andtrong> flagella associated protein 119

Predicted to act upstream of or within gene expression; single fertilization; trong>andtrong> sperm flagellum assemtrong>btrong>ly. Predicted to trong>btrong>e located in acrosomal vesicle trong>andtrong> sperm principal piece. Predicted to trong>btrong>e part of radial spoke. Predicted to trong>btrong>e active in axoneme. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

TAMALIN Gene

trafficking regulator trong>andtrong> scaffold protein tamalin

This gene encodes a protein that functions as a molecular scaffold, linking receptors, including group 1 metatrong>btrong>otropic glutamate receptors, to neuronal proteins. The encoded protein contains conserved domains, including a leucine zipper sequence, PDZ domain trong>andtrong> a C-terminal PDZ-trong>btrong>inding motif. Alternately spliced transcript variants have trong>btrong>een otrong>btrong>served for this gene.[provided trong>btrong>y RefSeq, Dec 2012]

Atrong>Btrong>Ttrong>Btrong>3 Gene

ankyrin repeat trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 3

Predicted to enatrong>btrong>le PDZ domain trong>btrong>inding activity trong>andtrong> protein heterodimerization activity. Predicted to act upstream of or within exploration trong>btrong>ehavior; glutamatergic synaptic transmission; trong>andtrong> protein statrong>btrong>ilization. Predicted to trong>btrong>e located in glutamatergic synapse trong>andtrong> memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP210 Gene

cilia trong>andtrong> flagella associated protein 210

Predicted to trong>btrong>e involved in flagellated sperm motility. Located in axonemal microtutrong>btrong>ule. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PALM2AKAP2 Gene

PALM2 trong>andtrong> AKAP2 fusion

This gene trong>btrong>elongs to the paralemmin downstream gene (PDG) family defined in PMID:22855693. Paralemmin downstream genes may have evolved contiguously with the paralemmin genes trong>andtrong> are associated with other paralemmin paralogs in humans trong>andtrong> several other taxa. The gene encodes three distinct protein isoforms, the PALM2 isoform, the AKAP2 isoform trong>andtrong> the PALM2-AKAP2 isoform. The trong>btrong>iological significance of the PALM2-AKAP2 isoforms is yet unknown. Earlier, PALM2 trong>andtrong> AKAP2 were annotated as separate genes trong>andtrong> PALM2-AKAP2 was annotated as a readthrough gene. [provided trong>btrong>y RefSeq, May 2019]

CFAP300 Gene

cilia trong>andtrong> flagella associated protein 300

Predicted to trong>btrong>e located in cytoplasm trong>andtrong> motile cilium. Implicated in primary ciliary dyskinesia 38. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

C1QTNF12 Gene

C1q trong>andtrong> TNF related 12

Predicted to enatrong>btrong>le hormone activity. Predicted to trong>btrong>e involved in negative regulation of gluconeogenesis; positive regulation of D-glucose import; trong>andtrong> positive regulation of insulin receptor signaling pathway. Predicted to act upstream of or within negative regulation of inflammatory response; positive regulation of cell communication; trong>andtrong> regulation of glucose metatrong>btrong>olic process. Predicted to trong>btrong>e located in extracellular region. Predicted to trong>btrong>e active in extracellular space. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

NEPRO Gene

nucleolus trong>andtrong> neural progenitor protein

Predicted to trong>btrong>e involved in negative regulation of neuron differentiation trong>andtrong> positive regulation of Notch signaling pathway. Predicted to trong>btrong>e located in nucleolus. Predicted to trong>btrong>e active in nucleus. Implicated in anauxetic dysplasia 3. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PLAAT5 Gene

phospholipase A trong>andtrong> acyltransferase 5

Enatrong>btrong>les N-acyltransferase activity; phospholipase A1 activity; trong>andtrong> phospholipase A2 activity. Acts upstream of or within N-acylphosphatidylethanolamine metatrong>btrong>olic process. Predicted to trong>btrong>e located in cytosol. Predicted to trong>btrong>e active in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CPLANE2 Gene

ciliogenesis trong>andtrong> planar polarity effector complex sutrong>btrong>unit 2

Predicted to enatrong>btrong>le GTP trong>btrong>inding activity. Predicted to trong>btrong>e involved in cilium assemtrong>btrong>ly; protein localization; trong>andtrong> regulation of vesicle-mediated transport. Predicted to act upstream of or within several processes, including axoneme assemtrong>btrong>ly; endocardial cushion fusion; trong>andtrong> regulation of smoothened signaling pathway. Located in centriole; ciliary trong>btrong>asal trong>btrong>ody; trong>andtrong> ciliary transition zone. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP100 Gene

cilia trong>andtrong> flagella associated protein 100

Predicted to enatrong>btrong>le dynein complex trong>btrong>inding activity. Predicted to trong>btrong>e involved in cilium movement trong>andtrong> inner dynein arm assemtrong>btrong>ly. Located in ciliary trong>btrong>asal trong>btrong>ody. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

NEXMIF Gene

neurite extension trong>andtrong> migration factor

An inversion on the X chromosome which disrupts this gene trong>andtrong> a G-protein coupled purinergic receptor gene located in the pseudoautosomal region of the X chromosome has trong>btrong>een linked to X linked cognitive disatrong>btrong>ility.[provided trong>btrong>y RefSeq, Mar 2009]

CFAP157 Gene

cilia trong>andtrong> flagella associated protein 157

Predicted to enatrong>btrong>le microtutrong>btrong>ule trong>btrong>inding activity. Predicted to trong>btrong>e involved in sperm axoneme assemtrong>btrong>ly. Located in cytosol; intracellular memtrong>btrong>rane-trong>btrong>ounded organelle; trong>andtrong> plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP141 Gene

cilia trong>andtrong> flagella associated protein 141

Predicted to trong>btrong>e involved in flagellated sperm motility. Located in axonemal microtutrong>btrong>ule. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SANtrong>Btrong>R Gene

SANT trong>andtrong> trong>Btrong>Ttrong>Btrong> domain regulator of CSR

Predicted to enatrong>btrong>le identical protein trong>btrong>inding activity. Predicted to trong>btrong>e involved in isotype switching. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ELAPOR2 Gene

endosome-lysosome associated apoptosis trong>andtrong> autophagy regulator family memtrong>btrong>er 2

Predicted to enatrong>btrong>le trong>Btrong>MP receptor trong>btrong>inding activity. Predicted to trong>btrong>e involved in negative regulation of nervous system development; positive regulation of trong>Btrong>MP signaling pathway; trong>andtrong> positive regulation of epidermis development. Predicted to trong>btrong>e located in plasma memtrong>btrong>rane. Predicted to trong>btrong>e active in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ALKAL1 Gene

ALK trong>andtrong> LTK ligtrong>andtrong> 1

Enatrong>btrong>les protein tyrosine kinase activator activity trong>andtrong> signaling receptor trong>btrong>inding activity. Involved in cell surface receptor protein tyrosine kinase signaling pathway; positive regulation of MAPK cascade; trong>andtrong> positive regulation of neuron projection development. Is active in extracellular space. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

MPIG6trong>Btrong> Gene

megakaryocyte trong>andtrong> platelet inhitrong>btrong>itory receptor G6trong>btrong>

This gene is a memtrong>btrong>er of the immunoglotrong>btrong>ulin (Ig) superfamily trong>andtrong> is located in the major histocompatitrong>btrong>ility complex (MHC) class III region. The protein encoded trong>btrong>y this gene is a glycosylated, plasma memtrong>btrong>rane-trong>btrong>ound cell surface receptor, trong>btrong>ut solutrong>btrong>le isoforms encoded trong>btrong>y some transcript variants have trong>btrong>een found in the endoplasmic reticulum trong>andtrong> Golgi trong>btrong>efore trong>btrong>eing secreted. Multiple transcript variants encoding different isoforms have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Jul 2008]

Ftrong>Btrong>XL9P Gene

F-trong>btrong>ox trong>andtrong> leucine rich repeat protein, pseudogene

This gene encodes a memtrong>btrong>er of the F-trong>btrong>ox protein family which is characterized trong>btrong>y an approximately 40 amino acid motif, the F-trong>btrong>ox. The F-trong>btrong>ox proteins constitute one of the four sutrong>btrong>units of utrong>btrong>iquitin protein ligase complex called SCFs (SKP1-cullin-F-trong>btrong>ox), which function in phosphorylation-dependent utrong>btrong>iquitination. The F-trong>btrong>ox proteins are divided into 3 classes: Ftrong>btrong>ws containing WD-40 domains, Ftrong>btrong>ls containing leucine-rich repeats, trong>andtrong> Ftrong>btrong>xs containing either different protein-protein interaction modules or no recognizatrong>btrong>le motifs. The protein encoded trong>btrong>y this gene trong>btrong>elongs to the Ftrong>btrong>ls class trong>andtrong>, in addition to an F-trong>btrong>ox, contains 9 ttrong>andtrong>em leucine-rich repeats. Two transcript variants encoding the same protein have trong>btrong>een found for this gene. Other variants may occur, trong>btrong>ut their full-length natures have not trong>btrong>een characterized. [provided trong>btrong>y RefSeq, Jul 2008]

ZSCAN5DP Gene

zinc finger trong>andtrong> SCAN domain containing 5D pseudogene

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ftrong>Btrong>XL21P Gene

F-trong>btrong>ox trong>andtrong> leucine rich repeat protein 21, pseudogene

This locus represents a transcritrong>btrong>ed pseudogene that is related to genes encoding memtrong>btrong>ers of the F-trong>btrong>ox family of proteins. [provided trong>btrong>y RefSeq, Nov 2017]

CFAP68 Gene

cilia trong>andtrong> flagella associated protein 68

Predicted to trong>btrong>e involved in flagellated sperm motility. Located in axoneme trong>andtrong> nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP91 Gene

cilia trong>andtrong> flagella associated protein 91

Involved in axonemal central apparatus assemtrong>btrong>ly trong>andtrong> spermatogenesis. Predicted to trong>btrong>e located in motile cilium trong>andtrong> radial spoke stalk. Implicated in spermatogenic failure 51. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP161 Gene

cilia trong>andtrong> flagella associated protein 161

Predicted to trong>btrong>e involved in cilium assemtrong>btrong>ly trong>andtrong> flagellated sperm motility. Located in axonemal microtutrong>btrong>ule. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP206 Gene

cilia trong>andtrong> flagella associated protein 206

Predicted to trong>btrong>e involved in regulation of cilium trong>btrong>eat frequency; regulation of flagellated sperm motility; trong>andtrong> sperm axoneme assemtrong>btrong>ly. Predicted to trong>btrong>e located in A axonemal microtutrong>btrong>ule trong>andtrong> motile cilium. Predicted to trong>btrong>e part of radial spoke. Predicted to trong>btrong>e active in axoneme trong>andtrong> ciliary trong>btrong>asal trong>btrong>ody. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

Ftrong>Btrong>XW10trong>Btrong> Gene

F-trong>btrong>ox trong>andtrong> WD repeat domain containing 10trong>Btrong>

Memtrong>btrong>ers of the F-trong>btrong>ox protein family, such as Ftrong>Btrong>XW10, are characterized trong>btrong>y an approximately 40-amino acid F-trong>btrong>ox motif. SCF complexes, formed trong>btrong>y SKP1 (MIM 601434), cullin (see CUL1; MIM 603034), trong>andtrong> F-trong>btrong>ox proteins, act as protein-utrong>btrong>iquitin ligases. F-trong>btrong>ox proteins interact with SKP1 through the F trong>btrong>ox, trong>andtrong> they interact with utrong>btrong>iquitination targets through other protein interaction domains (Jin et al., 2004 [Putrong>btrong>Med 15520277]).[supplied trong>btrong>y OMIM, Mar 2008]

PPDPFL Gene

pancreatic progenitor cell differentiation trong>andtrong> proliferation factor like

Predicted to trong>btrong>e involved in cell differentiation. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP107 Gene

cilia trong>andtrong> flagella associated protein 107

Predicted to trong>btrong>e involved in flagellated sperm motility. Located in axonemal microtutrong>btrong>ule. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP299 Gene

cilia trong>andtrong> flagella associated protein 299

Predicted to trong>btrong>e located in cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP276 Gene

cilia trong>andtrong> flagella associated protein 276

Predicted to trong>btrong>e involved in flagellated sperm motility. Located in axonemal microtutrong>btrong>ule. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP92 Gene

cilia trong>andtrong> flagella associated protein 92 (putative)

HOATZ Gene

HOATZ cilia trong>andtrong> flagella associated protein

Predicted to trong>btrong>e involved in axoneme assemtrong>btrong>ly; flagellated sperm motility; trong>andtrong> spermatogenesis. Predicted to trong>btrong>e located in cilium trong>andtrong> cytoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ZSCAN5C Gene

zinc finger trong>andtrong> SCAN domain containing 5C

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription factor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in regulation of transcription trong>btrong>y RNA polymerase II. Predicted to trong>btrong>e located in nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP73 Gene

cilia trong>andtrong> flagella associated protein 73

Predicted to enatrong>btrong>le dynein complex trong>btrong>inding activity. Predicted to trong>btrong>e involved in cilium movement; inner dynein arm assemtrong>btrong>ly; trong>andtrong> spermatid development. Predicted to trong>btrong>e located in axonemal doutrong>btrong>let microtutrong>btrong>ule trong>andtrong> motile cilium. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP90 Gene

cilia trong>andtrong> flagella associated protein 90

Predicted to trong>btrong>e involved in flagellated sperm motility. Located in axoneme trong>andtrong> ciliary trong>btrong>asal trong>btrong>ody. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

ALKAL2 Gene

ALK trong>andtrong> LTK ligtrong>andtrong> 2

Enatrong>btrong>les protein tyrosine kinase activator activity trong>andtrong> signaling receptor trong>btrong>inding activity. Involved in cell surface receptor protein tyrosine kinase signaling pathway; positive regulation of MAPK cascade; trong>andtrong> positive regulation of neuron projection development. Is active in extracellular space. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SERTM2 Gene

serine rich trong>andtrong> transmemtrong>btrong>rane domain containing 2

Predicted to trong>btrong>e located in memtrong>btrong>rane. Predicted to trong>btrong>e active in intracellular memtrong>btrong>rane-trong>btrong>ounded organelle. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP95 Gene

cilia trong>andtrong> flagella associated protein 95

Predicted to trong>btrong>e involved in flagellated sperm motility. Located in axonemal microtutrong>btrong>ule trong>andtrong> plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

RHEX Gene

regulator of hemoglotrong>btrong>inization trong>andtrong> erythroid cell expansion

Enatrong>btrong>les erythropoietin receptor trong>btrong>inding activity. Involved in erythropoietin-mediated signaling pathway trong>andtrong> positive regulation of erythrocyte differentiation. Located in plasma memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

IQANK1 Gene

IQ motif trong>andtrong> ankyrin repeat containing 1

SRARP Gene

steroid receptor associated trong>andtrong> regulated protein

Enatrong>btrong>les nuclear estrogen receptor trong>btrong>inding activity. Involved in positive regulation of intracellular estrogen receptor signaling pathway. Located in cytoplasm trong>andtrong> nucleus. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

LIX1-AS1 Gene

LIX1 trong>andtrong> RIOK2 antisense RNA 1

TSPOAP1-AS1 Gene

TSPOAP1, SUPT4H1 trong>andtrong> RNF43 antisense RNA 1

PIRAT1 Gene

PU.1 (SP1) induced regulator of S100A8 trong>andtrong> S100A9 alarmin transcription 1

CERNA1 Gene

competing endogenous lncRNA 1 for miR-4707-5p trong>andtrong> miR-4767

MROCKI Gene

MARCKS cis regulating lncRNA promoter of cytokines trong>andtrong> inflammation

KCNK15-AS1 Gene

KCNK15 trong>andtrong> WISP2 antisense RNA 1

Ztrong>Btrong>Ttrong>Btrong>12trong>Btrong>P Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 12trong>Btrong>, pseudogene

PLEKHM1P1 Gene

pleckstrin homology trong>andtrong> RUN domain containing M1 pseudogene 1

PELATON Gene

plaque enriched lncRNA in atherosclerotic trong>andtrong> inflammatory trong>btrong>owel macrophage regulation

AGAP12P Gene

ArfGAP with GTPase domain, ankyrin repeat trong>andtrong> PH domain 12, pseudogene

MIR200CHG Gene

MIR200C trong>andtrong> MIR141 host gene

MIR29trong>Btrong>2CHG Gene

MIR29trong>Btrong>2 trong>andtrong> MIR29C host gene

Predicted to trong>btrong>e involved in miRNA-mediated post-transcriptional gene silencing. Predicted to trong>btrong>e part of RISC complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

RLIG1 Gene

RNA 5'-phosphate trong>andtrong> 3'-OH ligase 1

Enatrong>btrong>les RNA ligase (ATP) activity. Involved in response to reactive oxygen species. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

TMDD1 Gene

transmemtrong>btrong>rane trong>andtrong> death domain 1

Predicted to trong>btrong>e involved in signal transduction. Predicted to trong>btrong>e located in memtrong>btrong>rane. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

FIRRM Gene

FIGNL1 interacting regulator of recomtrong>btrong>ination trong>andtrong> mitosis

Enatrong>btrong>les protein kinase trong>btrong>inding activity. Involved in several processes, including chromosome segregation; interstrtrong>andtrong> cross-link repair; trong>andtrong> regulation of protein kinase activity. Located in several cellular components, including kinetochore; midtrong>btrong>ody; trong>andtrong> spindle midzone. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CFAP96 Gene

cilia trong>andtrong> flagella associated protein 96

Located in 9+0 non-motile cilium; centrosome; trong>andtrong> cytoplasmic microtutrong>btrong>ule. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PRADX Gene

PRC2 trong>andtrong> DDX5 associated lncRNA

KIF23-AS1 Gene

KIF23 trong>andtrong> PAQR5 antisense RNA 1

CHMP3-AS1 Gene

CHMP3 trong>andtrong> RNF103 antisense RNA 1

MHENCR Gene

melanoma highly expressed competing endogenous lncRNA for miR-425 trong>andtrong> miR-489

MIR3677HG Gene

MIR3677 trong>andtrong> MIR940 host gene

Predicted to trong>btrong>e involved in miRNA-mediated post-transcriptional gene silencing. Predicted to trong>btrong>e part of RISC complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

HRG-AS1 Gene

HRG trong>andtrong> FETUtrong>Btrong> antisense RNA 1

ZNF225-AS1 Gene

ZNF225 trong>andtrong> ZNF224 antisense RNA 1

LITATS1 Gene

lncRNA induced trong>btrong>y TGF-trong>btrong>eta trong>andtrong> antagonizes TGF-trong>btrong>eta signaling 1

ARHGAP44-AS1 Gene

ARHGAP44 trong>andtrong> MYOCD antisense RNA 1

LNC-Ltrong>Btrong>CS Gene

lncRNA trong>btrong>ladder trong>andtrong> prostate cancer suppressor, hnRNPK interacting

SCYGR6 Gene

small cysteine trong>andtrong> glycine repeat containing 6

Predicted to trong>btrong>e located in intermediate filament. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SCYGR10 Gene

small cysteine trong>andtrong> glycine repeat containing 10 (gene/pseudogene)

This gene is a memtrong>btrong>er of a large gene family that encodes keratin associated proteins (KRTAP) that play a role in hair formation. This gene trong>btrong>elongs to a sutrong>btrong>family of the KRTAP family termed small cysteine trong>andtrong> glycine repeat containing (SCYGR) genes trong>andtrong> it resides in a cluster of SCYGR genes on chromosome 2q36.3. Allelic polymorphisms in this gene result in trong>btrong>oth coding trong>andtrong> non-coding transcripts; the reference genome represents the non-coding allele. [provided trong>btrong>y RefSeq, Jan 2024]

KPLCE Gene

KPRP N-terminal trong>andtrong> LCE C-terminal like protein

Predicted to trong>btrong>e involved in epidermis development. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

CPAP Gene

centrosome assemtrong>btrong>ly trong>andtrong> centriole elongation protein

This gene encodes a protein that trong>btrong>elongs to the centromere protein family. During cell division, this protein plays a structural role in the maintenance of centrosome integrity trong>andtrong> normal spindle morphology, trong>andtrong> it is involved in microtutrong>btrong>ule disassemtrong>btrong>ly at the centrosome. This protein can function as a transcriptional coactivator in the Stat5 signaling pathway, trong>andtrong> also as a coactivator of NF-kappatrong>Btrong>-mediated transcription, likely via its interaction with the coactivator p300/CREtrong>Btrong>-trong>btrong>inding protein. Mutations in this gene are associated with primary autosomal recessive microcephaly, a disorder characterized trong>btrong>y severely reduced trong>btrong>rain size trong>andtrong> cognitive disatrong>btrong>ility. Alternatively spliced transcript variants have trong>btrong>een found for this gene. [provided trong>btrong>y RefSeq, Apr 2012]

HEMK2 Gene

HemK methyltransferase 2, ETF1 glutamine trong>andtrong> histone H4 lysine

This gene encodes an N(6)-adenine-specific DNA methyltransferase. The encoded enzyme may trong>btrong>e involved in the methylation of release factor I during translation termination. This enzyme is also involved in converting the arsenic metatrong>btrong>olite monomethylarsonous acid to the less toxic dimethylarsonic acid. Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has trong>btrong>een identified on chromosome 11. [provided trong>btrong>y RefSeq, Mar 2023]

CFAP144 Gene

cilia trong>andtrong> flagella associated protein 144

Enatrong>btrong>les microtutrong>btrong>ule trong>btrong>inding activity. Predicted to trong>btrong>e involved in flagellated sperm motility. Located in axonemal microtutrong>btrong>ule. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

SCYGR1 Gene

small cysteine trong>andtrong> glycine repeat containing 1

SCYGR7 Gene

small cysteine trong>andtrong> glycine repeat containing 7

SCYGR8 Gene

small cysteine trong>andtrong> glycine repeat containing 8

SCYGR3 Gene

small cysteine trong>andtrong> glycine repeat containing 3

SCYGR2 Gene

small cysteine trong>andtrong> glycine repeat containing 2

SCYGR5 Gene

small cysteine trong>andtrong> glycine repeat containing 5

CIRSR Gene

corepressor of Rtrong>Btrong>PJ trong>andtrong> splicing regulator

Enatrong>btrong>les histone deacetylase trong>btrong>inding activity; protein kinase trong>btrong>inding activity; trong>andtrong> transcription corepressor activity. Acts upstream of or within negative regulation of transcription trong>btrong>y RNA polymerase II. Located in centrosome trong>andtrong> nuclear speck. Part of protein-containing complex. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PGCKA1 Gene

PDCD10 trong>andtrong> GCKIII kinases associated 1

RUMY1 Gene

regulator of UNG2 trong>andtrong> MKLN1 interacting yippee protein 1

Predicted to act upstream of or within positive regulation of apoptotic process. Located in cytosol trong>andtrong> intracellular memtrong>btrong>rane-trong>btrong>ounded organelle. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

HDIP1 Gene

HDAC trong>andtrong> MIER1 interacting protein 1

Ztrong>Btrong>Ttrong>Btrong>35 Gene

zinc finger trong>andtrong> trong>Btrong>Ttrong>Btrong> domain containing 35

Predicted to enatrong>btrong>le DNA-trong>btrong>inding transcription repressor activity, RNA polymerase II-specific trong>andtrong> RNA polymerase II cis-regulatory region sequence-specific DNA trong>btrong>inding activity. Predicted to trong>btrong>e involved in negative regulation of transcription trong>btrong>y RNA polymerase II; regulation of cytokine production; trong>andtrong> regulation of immune system process. Located in intermediate filament cytoskeleton trong>andtrong> nucleoplasm. [provided trong>btrong>y Alliance of Genome Resources, Mar 2025]

PGtrong>Btrong>DF Gene

plakoglotrong>btrong>in trong>btrong>inding trong>andtrong> degradation factor

trong>Btrong> AND T LYMPHOCYTE ATTENUATOR Gene Set

From DGIdb Drug Targets 2026

interacting proteins for the trong>Btrong> AND T LYMPHOCYTE ATTENUATOR drug from theDGIdtrong>btrong> Drug Targets 2026 dataset.

attenuator Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the trong>btrong>iological term attenuator in literature-supported statements descritrong>btrong>ing functions of genes from the GeneRIF trong>Btrong>iological Term Annotations dataset.

Dendritic cell, monocyte, trong>Btrong> lymphocyte, trong>andtrong> natural killer lymphocyte deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dendritic cell, monocyte, trong>Btrong> lymphocyte, trong>andtrong> natural killer lymphocyte deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteolysis_Leukocyte - Lymphocyte - trong>Btrong>-Lymphocyte - Plasma Cell (MMHCC)_GSE755 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Osteolysis_Leukocyte - Lymphocyte - trong>Btrong>-Lymphocyte - Plasma Cell (MMHCC)_GSE755 disease perturtrong>btrong>ation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Myelin trong>andtrong> lymphocyte (MAL) protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Myelin trong>andtrong> lymphocyte (MAL) protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transport of glucose trong>andtrong> other sugars, trong>btrong>ile salts trong>andtrong> organic acids, metal ions trong>andtrong> amine compounds Gene Set

From Reactome Pathways 2014

proteins participating in the Transport of glucose trong>andtrong> other sugars, trong>btrong>ile salts trong>andtrong> organic acids, metal ions trong>andtrong> amine compounds pathway from the Reactome Pathways dataset.

Myeloid trong>andtrong> lymphoid neoplasms with eosinophilia trong>andtrong> atrong>btrong>normalities of PDGFRA, PDGFRtrong>Btrong>, trong>andtrong> FGFR1 Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Myeloid trong>andtrong> lymphoid neoplasms with eosinophilia trong>andtrong> atrong>btrong>normalities of PDGFRA, PDGFRtrong>Btrong>, trong>andtrong> FGFR1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Myeloid trong>andtrong> lymphoid neoplasms with eosinophilia trong>andtrong> atrong>btrong>normalities of PDGFRA, PDGFRtrong>Btrong>, trong>andtrong> FGFR1 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Myeloid trong>andtrong> lymphoid neoplasms with eosinophilia trong>andtrong> atrong>btrong>normalities of PDGFRA, PDGFRtrong>Btrong>, trong>andtrong> FGFR1 in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

trong>Btrong>are Lymphocyte Syndrome, Type II, Complementation Group D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Btrong>are Lymphocyte Syndrome, Type II, Complementation Group D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Btrong>are lymphocyte syndrome type 2, complementation group E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Btrong>are lymphocyte syndrome type 2, complementation group E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Btrong>are lymphocyte syndrome type 2, complementation group A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Btrong>are lymphocyte syndrome type 2, complementation group A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Btrong>ARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP trong>Btrong> Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Btrong>ARE LYMPHOCYTE SYNDROME, TYPE II, COMPLEMENTATION GROUP trong>Btrong> phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Btrong>are Lymphocyte Syndrome, Type I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease trong>Btrong>are Lymphocyte Syndrome, Type I from the curated CTD Gene-Disease Associations dataset.

trong>Btrong>are lymphocyte syndrome 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease trong>Btrong>are lymphocyte syndrome 2 from the curated CTD Gene-Disease Associations dataset.

Lymphocyte Count Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Lymphocyte Count in GWAS trong>andtrong> other genetic association datasets from the dtrong>btrong>GAP Gene-Trait Associations dataset.

t lymphocyte deficiency Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease t lymphocyte deficiency in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

t-cell large granular lymphocyte leukemia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease t-cell large granular lymphocyte leukemia in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

lymphocyte count Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphocyte count in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

systemic lupus erythematosus; prolactin, lymphocyte Gene Set

From GAD Gene-Disease Associations

genes associated with the disease systemic lupus erythematosus; prolactin, lymphocyte in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphocyte sutrong>btrong>set counts in neonates Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphocyte sutrong>btrong>set counts in neonates in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

clonal t-cell large granular lymphocyte disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease clonal t-cell large granular lymphocyte disease in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis; felty's syndrome; large granular lymphocyte syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis; felty's syndrome; large granular lymphocyte syndrome in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

solutrong>btrong>le cytotoxic t lymphocyte-associated antigen-4 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease solutrong>btrong>le cytotoxic t lymphocyte-associated antigen-4 in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

autologous mixed lymphocyte reaction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autologous mixed lymphocyte reaction in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphocyte Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the trong>btrong>iological term lymphocyte in literature-supported statements descritrong>btrong>ing functions of genes from the GeneRIF trong>Btrong>iological Term Annotations dataset.

lymphocyte migration into lymph node Gene Set

From GO Biological Process Annotations 2015

genes participating in the lymphocyte migration into lymph node trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

regulation of lymphocyte chemotaxis Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of lymphocyte chemotaxis trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

regulation of lymphocyte differentiation Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of lymphocyte differentiation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

lymphocyte aggregation Gene Set

From GO Biological Process Annotations 2015

genes participating in the lymphocyte aggregation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

negative regulation of lymphocyte apoptotic process Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of lymphocyte apoptotic process trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

lymphocyte differentiation Gene Set

From GO Biological Process Annotations 2015

genes participating in the lymphocyte differentiation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

negative regulation of lymphocyte migration Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of lymphocyte migration trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

negative regulation of lymphocyte anergy Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of lymphocyte anergy trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

regulation of lymphocyte apoptotic process Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of lymphocyte apoptotic process trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

lymphocyte migration into lymphoid organs Gene Set

From GO Biological Process Annotations 2015

genes participating in the lymphocyte migration into lymphoid organs trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

positive regulation of lymphocyte mediated immunity Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of lymphocyte mediated immunity trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

negative regulation of lymphocyte chemotaxis Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of lymphocyte chemotaxis trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

positive regulation of lymphocyte migration Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of lymphocyte migration trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

positive regulation of lymphocyte differentiation Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of lymphocyte differentiation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

regulation of lymphocyte mediated immunity Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of lymphocyte mediated immunity trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

positive regulation of lymphocyte apoptotic process Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of lymphocyte apoptotic process trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

negative regulation of lymphocyte differentiation Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of lymphocyte differentiation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

estatrong>btrong>lishment of lymphocyte polarity Gene Set

From GO Biological Process Annotations 2015

genes participating in the estatrong>btrong>lishment of lymphocyte polarity trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

regulation of lymphocyte activation Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of lymphocyte activation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

lymphocyte costimulation Gene Set

From GO Biological Process Annotations 2015

genes participating in the lymphocyte costimulation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

positive regulation of lymphocyte activation Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of lymphocyte activation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

positive regulation of lymphocyte anergy Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of lymphocyte anergy trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

regulation of lymphocyte migration Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of lymphocyte migration trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

lymphocyte chemotaxis across high endothelial venule Gene Set

From GO Biological Process Annotations 2015

genes participating in the lymphocyte chemotaxis across high endothelial venule trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

lymphocyte mediated immunity Gene Set

From GO Biological Process Annotations 2015

genes participating in the lymphocyte mediated immunity trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

lymphocyte apoptotic process Gene Set

From GO Biological Process Annotations 2015

genes participating in the lymphocyte apoptotic process trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

regulation of lymphocyte anergy Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of lymphocyte anergy trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

regulation of lymphocyte proliferation Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of lymphocyte proliferation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

positive regulation of lymphocyte proliferation Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of lymphocyte proliferation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

negative regulation of lymphocyte proliferation Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of lymphocyte proliferation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

lymphocyte proliferation Gene Set

From GO Biological Process Annotations 2015

genes participating in the lymphocyte proliferation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

lymphocyte homeostasis Gene Set

From GO Biological Process Annotations 2015

genes participating in the lymphocyte homeostasis trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

lymphocyte chemotaxis Gene Set

From GO Biological Process Annotations 2015

genes participating in the lymphocyte chemotaxis trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

negative regulation of lymphocyte activation Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of lymphocyte activation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

lymphocyte activation involved in immune response Gene Set

From GO Biological Process Annotations 2015

genes participating in the lymphocyte activation involved in immune response trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

lymphocyte migration Gene Set

From GO Biological Process Annotations 2015

genes participating in the lymphocyte migration trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

negative regulation of lymphocyte mediated immunity Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of lymphocyte mediated immunity trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

lymphocyte activation Gene Set

From GO Biological Process Annotations 2015

genes participating in the lymphocyte activation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2015 dataset.

Lymphocyte counts Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Lymphocyte counts phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

defective lymphocyte apoptosis Gene Set

From HPO Gene-Disease Associations

genes associated with the defective lymphocyte apoptosis phenotype trong>btrong>y mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired lymphocyte transformation with phytohemagglutinin Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired lymphocyte transformation with phytohemagglutinin phenotype trong>btrong>y mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

reduced lymphocyte surface expression of cd43 (sialophorin) Gene Set

From HPO Gene-Disease Associations

genes associated with the reduced lymphocyte surface expression of cd43 (sialophorin) phenotype trong>btrong>y mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

atrong>btrong>normal lymphocyte count Gene Set

From HPO Gene-Disease Associations

genes associated with the atrong>btrong>normal lymphocyte count phenotype trong>btrong>y mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Lymphocyte antigen 6 complex locus protein G6d/G6f Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lymphocyte antigen 6 complex locus protein G6d/G6f protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Caldesmon/lymphocyte specific protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Caldesmon/lymphocyte specific protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Lymphocyte-specific protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lymphocyte-specific protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytotoxic T-lymphocyte antigen 4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytotoxic T-lymphocyte antigen 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Lymphocyte antigen 6 complex locus protein G5c Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lymphocyte antigen 6 complex locus protein G5c protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Signalling lymphocyte activation molecule family receptors Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Signalling lymphocyte activation molecule family receptors protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Lymphocyte function associated antigen 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lymphocyte function associated antigen 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

atrong>btrong>normal lymphocyte cell numtrong>btrong>er Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the atrong>btrong>normal lymphocyte cell numtrong>btrong>er phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

atrong>btrong>normal trong>btrong> lymphocyte antigen presentation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the atrong>btrong>normal trong>btrong> lymphocyte antigen presentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

atrong>btrong>normal lymphocyte physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the atrong>btrong>normal lymphocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

atrong>btrong>sent lymphocyte Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the atrong>btrong>sent lymphocyte phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

atrong>btrong>normal common lymphocyte progenitor cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the atrong>btrong>normal common lymphocyte progenitor cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased lymphocyte cell numtrong>btrong>er Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased lymphocyte cell numtrong>btrong>er phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased lymphocyte chemotaxis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased lymphocyte chemotaxis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

atrong>btrong>normal lymphocyte anergy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the atrong>btrong>normal lymphocyte anergy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

atrong>btrong>normal lymphocyte morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the atrong>btrong>normal lymphocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased lymphocyte cell numtrong>btrong>er Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased lymphocyte cell numtrong>btrong>er phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

trong>btrong>are lymphocyte syndrome, type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the trong>btrong>are lymphocyte syndrome, type i phenotype from the curated OMIM Gene-Disease Associations dataset.

trong>btrong>are lymphocyte syndrome, type ii, complementation group c Gene Set

From OMIM Gene-Disease Associations

genes associated with the trong>btrong>are lymphocyte syndrome, type ii, complementation group c phenotype from the curated OMIM Gene-Disease Associations dataset.

trong>btrong>are lymphocyte syndrome, type ii, complementation group a Gene Set

From OMIM Gene-Disease Associations

genes associated with the trong>btrong>are lymphocyte syndrome, type ii, complementation group a phenotype from the curated OMIM Gene-Disease Associations dataset.

trong>btrong>are lymphocyte syndrome, type ii, complementation group d Gene Set

From OMIM Gene-Disease Associations

genes associated with the trong>btrong>are lymphocyte syndrome, type ii, complementation group d phenotype from the curated OMIM Gene-Disease Associations dataset.

trong>btrong>are lymphocyte syndrome, type i, due to tap2 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the trong>btrong>are lymphocyte syndrome, type i, due to tap2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

trong>btrong>are lymphocyte syndrome, type ii, complementation group e Gene Set

From OMIM Gene-Disease Associations

genes associated with the trong>btrong>are lymphocyte syndrome, type ii, complementation group e phenotype from the curated OMIM Gene-Disease Associations dataset.

helper T-lymphocyte Gene Set

From ProteomicsDB Cell Type and Tissue Protein Expression Profiles

proteins with high or low expression in helper T-lymphocyte relative to other cell types trong>andtrong> tissues from the ProteomicsDtrong>Btrong> Cell Type trong>andtrong> Tissue Protein Expression Profiles dataset.

cytotoxic T-lymphocyte Gene Set

From ProteomicsDB Cell Type and Tissue Protein Expression Profiles

proteins with high or low expression in cytotoxic T-lymphocyte relative to other cell types trong>andtrong> tissues from the ProteomicsDtrong>Btrong> Cell Type trong>andtrong> Tissue Protein Expression Profiles dataset.

trong>Btrong>-lymphocyte Gene Set

From ProteomicsDB Cell Type and Tissue Protein Expression Profiles

proteins with high or low expression in trong>Btrong>-lymphocyte relative to other cell types trong>andtrong> tissues from the ProteomicsDtrong>Btrong> Cell Type trong>andtrong> Tissue Protein Expression Profiles dataset.

trong>btrong>-lymphocyte cell line Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue trong>btrong>-lymphocyte cell line from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

pro-trong>btrong>-lymphocyte Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue pro-trong>btrong>-lymphocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

pre-trong>btrong>-lymphocyte Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue pre-trong>btrong>-lymphocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

large granular lymphocyte Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue large granular lymphocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

pre-t-lymphocyte Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue pre-t-lymphocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

t-lymphocyte Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue t-lymphocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

lymphocyte Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue lymphocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

peripheral trong>btrong>lood lymphocyte Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue peripheral trong>btrong>lood lymphocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

cytotoxic t-lymphocyte Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue cytotoxic t-lymphocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

trong>btrong>-lymphocyte Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue trong>btrong>-lymphocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

t-lymphocyte Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue t-lymphocyte in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

helper t-lymphocyte Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue helper t-lymphocyte in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

large granular lymphocyte Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue large granular lymphocyte in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

lymphocyte Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue lymphocyte in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

trong>btrong>-lymphocyte Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue trong>btrong>-lymphocyte in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

cytotoxic t-lymphocyte Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue cytotoxic t-lymphocyte in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores dataset.

trong>btrong>-lymphocyte cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue trong>btrong>-lymphocyte cell line in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

pro-trong>btrong>-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue pro-trong>btrong>-lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

pro-trong>btrong>-lymphocyte cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue pro-trong>btrong>-lymphocyte cell line in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

memory t-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue memory t-lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

plasmacytoid t-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue plasmacytoid t-lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

pre-t-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue pre-t-lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

regulatory t-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue regulatory t-lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

t-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue t-lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

pre-trong>btrong>-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue pre-trong>btrong>-lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

cytotoxic t-lymphocyte cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue cytotoxic t-lymphocyte cell line in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

helper t-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue helper t-lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

t-lymphocyte cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue t-lymphocyte cell line in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

large granular lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue large granular lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

peripheral trong>btrong>lood lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue peripheral trong>btrong>lood lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

cytotoxic t-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue cytotoxic t-lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

trong>btrong>-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue trong>btrong>-lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

pre-trong>btrong>-lymphocyte cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue pre-trong>btrong>-lymphocyte cell line in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

Passenger Lymphocyte Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Passenger Lymphocyte Syndrome in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

T-Lymphocyte Immunodeficiency Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease T-Lymphocyte Immunodeficiency in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Adult Nodular Lymphocyte Predominant Hodgkin Lymphoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Adult Nodular Lymphocyte Predominant Hodgkin Lymphoma in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Childhood Nodular Lymphocyte Predominant Hodgkin Lymphoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Childhood Nodular Lymphocyte Predominant Hodgkin Lymphoma in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Nodular Lymphocyte Predominant Hodgkin Lymphoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Nodular Lymphocyte Predominant Hodgkin Lymphoma in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

trong>Btrong>are Lymphocyte Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease trong>Btrong>are Lymphocyte Syndrome in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Hodgkin Lymphoma, Nodular Lymphocyte Predominance Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Hodgkin Lymphoma, Nodular Lymphocyte Predominance in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

T-Cell Large Granular Lymphocyte Leukemia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease T-Cell Large Granular Lymphocyte Leukemia in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

T-Lymphocyte Deficiency Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease T-Lymphocyte Deficiency in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Hodgkin Lymphoma, Lymphocyte Depletion Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Hodgkin Lymphoma, Lymphocyte Depletion in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Lymphocyte Rich Classical Hodgkin Lymphoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Lymphocyte Rich Classical Hodgkin Lymphoma in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Adult Lymphocyte-Rich Classical Hodgkin Lymphoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Adult Lymphocyte-Rich Classical Hodgkin Lymphoma in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Childhood Lymphocyte-Rich Classic Hodgkin Lymphoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Childhood Lymphocyte-Rich Classic Hodgkin Lymphoma in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

T Lymphocyte Disorder Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease T Lymphocyte Disorder in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Lymphocyte Count Measurement Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Lymphocyte Count Measurement in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Atypical Lymphocyte Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Atypical Lymphocyte in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Vacuolated Lymphocyte Count Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Vacuolated Lymphocyte Count in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Decreased Lymphocyte Apoptosis Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Decreased Lymphocyte Apoptosis in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Decreased Lymphocyte Proliferation In Response To Mitogen Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Decreased Lymphocyte Proliferation In Response To Mitogen in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Impaired Lymphocyte Transformation With Phytohemagglutinin Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Impaired Lymphocyte Transformation With Phytohemagglutinin in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Atrong>btrong>normal Lymphocyte Physiology Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Atrong>btrong>normal Lymphocyte Physiology in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Lymphocyte Count Atrong>btrong>normal Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Lymphocyte Count Atrong>btrong>normal in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Reduced Lymphocyte Surface Expression Of Cd43 Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Reduced Lymphocyte Surface Expression Of Cd43 in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

negative regulation of lymphocyte migration Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of lymphocyte migration trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

negative regulation of lymphocyte proliferation Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of lymphocyte proliferation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

positive regulation of lymphocyte proliferation Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of lymphocyte proliferation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

lymphocyte chemotaxis across high endothelial venule Gene Set

From GO Biological Process Annotations 2023

genes participating in the lymphocyte chemotaxis across high endothelial venule trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

regulation of lymphocyte migration Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of lymphocyte migration trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

lymphocyte migration into lymphoid organs Gene Set

From GO Biological Process Annotations 2023

genes participating in the lymphocyte migration into lymphoid organs trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

regulation of lymphocyte activation Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of lymphocyte activation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

regulation of lymphocyte apoptotic process Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of lymphocyte apoptotic process trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

lymphocyte chemotaxis Gene Set

From GO Biological Process Annotations 2023

genes participating in the lymphocyte chemotaxis trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

positive regulation of lymphocyte differentiation Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of lymphocyte differentiation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

lymphocyte aggregation Gene Set

From GO Biological Process Annotations 2023

genes participating in the lymphocyte aggregation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

lymphocyte migration into lymph node Gene Set

From GO Biological Process Annotations 2023

genes participating in the lymphocyte migration into lymph node trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

lymphocyte migration Gene Set

From GO Biological Process Annotations 2023

genes participating in the lymphocyte migration trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

lymphocyte proliferation Gene Set

From GO Biological Process Annotations 2023

genes participating in the lymphocyte proliferation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

lymphocyte apoptotic process Gene Set

From GO Biological Process Annotations 2023

genes participating in the lymphocyte apoptotic process trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

positive regulation of lymphocyte migration Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of lymphocyte migration trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

lymphocyte differentiation Gene Set

From GO Biological Process Annotations 2023

genes participating in the lymphocyte differentiation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

positive regulation of lymphocyte chemotaxis Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of lymphocyte chemotaxis trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

regulation of lymphocyte chemotaxis Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of lymphocyte chemotaxis trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

positive regulation of lymphocyte activation Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of lymphocyte activation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

regulation of lymphocyte differentiation Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of lymphocyte differentiation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

negative regulation of lymphocyte chemotaxis Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of lymphocyte chemotaxis trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

positive regulation of lymphocyte apoptotic process Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of lymphocyte apoptotic process trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

lymphocyte mediated immunity Gene Set

From GO Biological Process Annotations 2023

genes participating in the lymphocyte mediated immunity trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

regulation of lymphocyte proliferation Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of lymphocyte proliferation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

negative regulation of lymphocyte activation Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of lymphocyte activation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

estatrong>btrong>lishment of lymphocyte polarity Gene Set

From GO Biological Process Annotations 2023

genes participating in the estatrong>btrong>lishment of lymphocyte polarity trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

positive regulation of lymphocyte mediated immunity Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of lymphocyte mediated immunity trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

negative regulation of lymphocyte differentiation Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of lymphocyte differentiation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

lymphocyte activation involved in immune response Gene Set

From GO Biological Process Annotations 2023

genes participating in the lymphocyte activation involved in immune response trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

regulation of lymphocyte anergy Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of lymphocyte anergy trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

negative regulation of lymphocyte apoptotic process Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of lymphocyte apoptotic process trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

regulation of lymphocyte mediated immunity Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of lymphocyte mediated immunity trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

negative regulation of lymphocyte mediated immunity Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of lymphocyte mediated immunity trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

positive regulation of lymphocyte anergy Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of lymphocyte anergy trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2023 dataset.

FOXO1-25302145-T-LYMPHOCYTE-MOUSE Gene Set

From ChEA Transcription Factor Targets 2022

target genes of the FOXO1-25302145-T-LYMPHOCYTE-MOUSE transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.

decreased lymphocyte cell numtrong>btrong>er Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased lymphocyte cell numtrong>btrong>er phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

atrong>btrong>normal lymphocyte physiology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the atrong>btrong>normal lymphocyte physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased lymphocyte cell numtrong>btrong>er Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased lymphocyte cell numtrong>btrong>er phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

atrong>btrong>normal lymphocyte morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the atrong>btrong>normal lymphocyte morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

atrong>btrong>normal common lymphocyte progenitor cell morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the atrong>btrong>normal common lymphocyte progenitor cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

atrong>btrong>normal lymphocyte cell numtrong>btrong>er Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the atrong>btrong>normal lymphocyte cell numtrong>btrong>er phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

atrong>btrong>sent lymphocyte Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the atrong>btrong>sent lymphocyte phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

atrong>btrong>normal lymphocyte chemotaxis Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the atrong>btrong>normal lymphocyte chemotaxis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

atrong>btrong>normal lymphocyte anergy Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the atrong>btrong>normal lymphocyte anergy phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

atrong>btrong>normal trong>Btrong> lymphocyte antigen presentation Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the atrong>btrong>normal trong>Btrong> lymphocyte antigen presentation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased common lymphocyte progenitor cell numtrong>btrong>er Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased common lymphocyte progenitor cell numtrong>btrong>er phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

increased common lymphocyte progenitor cell numtrong>btrong>er Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the increased common lymphocyte progenitor cell numtrong>btrong>er phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased lymphocyte chemotaxis Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the decreased lymphocyte chemotaxis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

decreased lymphocyte cell numtrong>btrong>er Gene Set

From IMPC Knockout Mouse Phenotypes

gene knockouts causing the decreased lymphocyte cell numtrong>btrong>er phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.

increased lymphocyte cell numtrong>btrong>er Gene Set

From IMPC Knockout Mouse Phenotypes

gene knockouts causing the increased lymphocyte cell numtrong>btrong>er phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.

Tumor-infiltrating lymphocyte(TIL)_trong>Btrong>ladder_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Tumor-infiltrating lymphocyte(TIL)_trong>Btrong>ladder_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Intraepithelial lymphocyte cell_Epithelium_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intraepithelial lymphocyte cell_Epithelium_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Intraepithelial lymphocyte cell_Intestine_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Intraepithelial lymphocyte cell_Intestine_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Lymphocyte lineage_Lung_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Lymphocyte lineage_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Large intestine_CT1_surface intraepithelial CD8+ alph alpha positive alpha/trong>btrong>eta lymphocyte Gene Set

From HuBMAP ASCT+B Annotations

trong>btrong>iomarker genes for the Large intestine_CT1_surface intraepithelial CD8+ alph alpha positive alpha/trong>btrong>eta lymphocyte cell type from the Hutrong>Btrong>MAP ASCT+trong>Btrong> dataset.

Large intestine_CT1_surface intraepithelial CD8+ lymphocyte gamma/delta Gene Set

From HuBMAP ASCT+B Annotations

trong>btrong>iomarker genes for the Large intestine_CT1_surface intraepithelial CD8+ lymphocyte gamma/delta cell type from the Hutrong>Btrong>MAP ASCT+trong>Btrong> dataset.

Large intestine_CT1_surface intraepithelial CD8+ alph trong>btrong>eta positive alpha/trong>btrong>eta lymphocyte Gene Set

From HuBMAP ASCT+B Annotations

trong>btrong>iomarker genes for the Large intestine_CT1_surface intraepithelial CD8+ alph trong>btrong>eta positive alpha/trong>btrong>eta lymphocyte cell type from the Hutrong>Btrong>MAP ASCT+trong>Btrong> dataset.

Large intestine_CT1_surface intraepithelial CD4+ lymphocyte Gene Set

From HuBMAP ASCT+B Annotations

trong>btrong>iomarker genes for the Large intestine_CT1_surface intraepithelial CD4+ lymphocyte cell type from the Hutrong>Btrong>MAP ASCT+trong>Btrong> dataset.

Large intestine_CT1_surface intraepithelial CD4-CD8- lymphocyte alpha/trong>btrong>eta Gene Set

From HuBMAP ASCT+B Annotations

trong>btrong>iomarker genes for the Large intestine_CT1_surface intraepithelial CD4-CD8- lymphocyte alpha/trong>btrong>eta cell type from the Hutrong>Btrong>MAP ASCT+trong>Btrong> dataset.

Large intestine_CT1_surface intraepithelial CD8+ alpha alpha positive alpha/trong>btrong>eta lymphocyte Gene Set

From HuBMAP ASCT+B Annotations

trong>btrong>iomarker genes for the Large intestine_CT1_surface intraepithelial CD8+ alpha alpha positive alpha/trong>btrong>eta lymphocyte cell type from the Hutrong>Btrong>MAP ASCT+trong>Btrong> dataset.

Large intestine_CT1_surface intraepithelial CD8+ alpha trong>btrong>eta positive alpha/trong>btrong>eta lymphocyte Gene Set

From HuBMAP ASCT+B Annotations

trong>btrong>iomarker genes for the Large intestine_CT1_surface intraepithelial CD8+ alpha trong>btrong>eta positive alpha/trong>btrong>eta lymphocyte cell type from the Hutrong>Btrong>MAP ASCT+trong>Btrong> dataset.

Pancreas_CT2_trong>Btrong> lymphocyte Gene Set

From HuBMAP ASCT+B Annotations

trong>btrong>iomarker genes for the Pancreas_CT2_trong>Btrong> lymphocyte cell type from the Hutrong>Btrong>MAP ASCT+trong>Btrong> dataset.

Pancreas_CT2_T lymphocyte Gene Set

From HuBMAP ASCT+B Annotations

trong>btrong>iomarker genes for the Pancreas_CT2_T lymphocyte cell type from the Hutrong>Btrong>MAP ASCT+trong>Btrong> dataset.

Large intestine_CT1_surface intraepithelial CD4+ lymphocyte Gene Set

From HuBMAP ASCT+B Augmented with RNA-seq Coexpression

trong>btrong>iomarker genes for the Large intestine_CT1_surface intraepithelial CD4+ lymphocyte cell type from the Hutrong>Btrong>MAP ASCT+trong>Btrong> Augmented with RNA-seq Coexpression dataset.

Large intestine_CT1_surface intraepithelial CD4-CD8- lymphocyte alpha/trong>btrong>eta Gene Set

From HuBMAP ASCT+B Augmented with RNA-seq Coexpression

trong>btrong>iomarker genes for the Large intestine_CT1_surface intraepithelial CD4-CD8- lymphocyte alpha/trong>btrong>eta cell type from the Hutrong>Btrong>MAP ASCT+trong>Btrong> Augmented with RNA-seq Coexpression dataset.

Large intestine_CT1_surface intraepithelial CD8+ alph alpha positive alpha/trong>btrong>eta lymphocyte Gene Set

From HuBMAP ASCT+B Augmented with RNA-seq Coexpression

trong>btrong>iomarker genes for the Large intestine_CT1_surface intraepithelial CD8+ alph alpha positive alpha/trong>btrong>eta lymphocyte cell type from the Hutrong>Btrong>MAP ASCT+trong>Btrong> Augmented with RNA-seq Coexpression dataset.

Large intestine_CT1_surface intraepithelial CD8+ alph trong>btrong>eta positive alpha/trong>btrong>eta lymphocyte Gene Set

From HuBMAP ASCT+B Augmented with RNA-seq Coexpression

trong>btrong>iomarker genes for the Large intestine_CT1_surface intraepithelial CD8+ alph trong>btrong>eta positive alpha/trong>btrong>eta lymphocyte cell type from the Hutrong>Btrong>MAP ASCT+trong>Btrong> Augmented with RNA-seq Coexpression dataset.

Large intestine_CT1_surface intraepithelial CD8+ alpha alpha positive alpha/trong>btrong>eta lymphocyte Gene Set

From HuBMAP ASCT+B Augmented with RNA-seq Coexpression

trong>btrong>iomarker genes for the Large intestine_CT1_surface intraepithelial CD8+ alpha alpha positive alpha/trong>btrong>eta lymphocyte cell type from the Hutrong>Btrong>MAP ASCT+trong>Btrong> Augmented with RNA-seq Coexpression dataset.

Large intestine_CT1_surface intraepithelial CD8+ alpha trong>btrong>eta positive alpha/trong>btrong>eta lymphocyte Gene Set

From HuBMAP ASCT+B Augmented with RNA-seq Coexpression

trong>btrong>iomarker genes for the Large intestine_CT1_surface intraepithelial CD8+ alpha trong>btrong>eta positive alpha/trong>btrong>eta lymphocyte cell type from the Hutrong>Btrong>MAP ASCT+trong>Btrong> Augmented with RNA-seq Coexpression dataset.

Large intestine_CT1_surface intraepithelial CD8+ lymphocyte gamma/delta Gene Set

From HuBMAP ASCT+B Augmented with RNA-seq Coexpression

trong>btrong>iomarker genes for the Large intestine_CT1_surface intraepithelial CD8+ lymphocyte gamma/delta cell type from the Hutrong>Btrong>MAP ASCT+trong>Btrong> Augmented with RNA-seq Coexpression dataset.

Pancreas_CT2_trong>Btrong> lymphocyte Gene Set

From HuBMAP ASCT+B Augmented with RNA-seq Coexpression

trong>btrong>iomarker genes for the Pancreas_CT2_trong>Btrong> lymphocyte cell type from the Hutrong>Btrong>MAP ASCT+trong>Btrong> Augmented with RNA-seq Coexpression dataset.

Pancreas_CT2_T lymphocyte Gene Set

From HuBMAP ASCT+B Augmented with RNA-seq Coexpression

trong>btrong>iomarker genes for the Pancreas_CT2_T lymphocyte cell type from the Hutrong>Btrong>MAP ASCT+trong>Btrong> Augmented with RNA-seq Coexpression dataset.

negative regulation of lymphocyte migration Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of lymphocyte migration trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

negative regulation of lymphocyte proliferation Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of lymphocyte proliferation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

positive regulation of lymphocyte proliferation Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of lymphocyte proliferation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

lymphocyte chemotaxis across high endothelial venule Gene Set

From GO Biological Process Annotations 2025

genes participating in the lymphocyte chemotaxis across high endothelial venule trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

regulation of lymphocyte migration Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of lymphocyte migration trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

lymphocyte migration into lymphoid organs Gene Set

From GO Biological Process Annotations 2025

genes participating in the lymphocyte migration into lymphoid organs trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

regulation of lymphocyte activation Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of lymphocyte activation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

regulation of lymphocyte apoptotic process Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of lymphocyte apoptotic process trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

lymphocyte chemotaxis Gene Set

From GO Biological Process Annotations 2025

genes participating in the lymphocyte chemotaxis trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

positive regulation of lymphocyte differentiation Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of lymphocyte differentiation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

lymphocyte aggregation Gene Set

From GO Biological Process Annotations 2025

genes participating in the lymphocyte aggregation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

lymphocyte migration into lymph node Gene Set

From GO Biological Process Annotations 2025

genes participating in the lymphocyte migration into lymph node trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

lymphocyte migration Gene Set

From GO Biological Process Annotations 2025

genes participating in the lymphocyte migration trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

lymphocyte proliferation Gene Set

From GO Biological Process Annotations 2025

genes participating in the lymphocyte proliferation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

lymphocyte apoptotic process Gene Set

From GO Biological Process Annotations 2025

genes participating in the lymphocyte apoptotic process trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

positive regulation of lymphocyte migration Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of lymphocyte migration trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

lymphocyte differentiation Gene Set

From GO Biological Process Annotations 2025

genes participating in the lymphocyte differentiation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

positive regulation of lymphocyte chemotaxis Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of lymphocyte chemotaxis trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

regulation of lymphocyte chemotaxis Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of lymphocyte chemotaxis trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

positive regulation of lymphocyte activation Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of lymphocyte activation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

regulation of lymphocyte differentiation Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of lymphocyte differentiation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

negative regulation of lymphocyte chemotaxis Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of lymphocyte chemotaxis trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

positive regulation of lymphocyte apoptotic process Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of lymphocyte apoptotic process trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

lymphocyte mediated immunity Gene Set

From GO Biological Process Annotations 2025

genes participating in the lymphocyte mediated immunity trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

regulation of lymphocyte proliferation Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of lymphocyte proliferation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

negative regulation of lymphocyte activation Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of lymphocyte activation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

positive regulation of lymphocyte anergy Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of lymphocyte anergy trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

estatrong>btrong>lishment of lymphocyte polarity Gene Set

From GO Biological Process Annotations 2025

genes participating in the estatrong>btrong>lishment of lymphocyte polarity trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

positive regulation of lymphocyte mediated immunity Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of lymphocyte mediated immunity trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

negative regulation of lymphocyte differentiation Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of lymphocyte differentiation trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

lymphocyte activation involved in immune response Gene Set

From GO Biological Process Annotations 2025

genes participating in the lymphocyte activation involved in immune response trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

regulation of lymphocyte anergy Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of lymphocyte anergy trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

negative regulation of lymphocyte apoptotic process Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of lymphocyte apoptotic process trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

regulation of lymphocyte mediated immunity Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of lymphocyte mediated immunity trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

negative regulation of lymphocyte mediated immunity Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of lymphocyte mediated immunity trong>btrong>iological process from the curated GO trong>Btrong>iological Process Annotations 2025 dataset.

T-cell large granular lymphocyte leukemia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease T-cell large granular lymphocyte leukemia in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Lymphocyte Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue Lymphocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.

T-lymphocyte Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue T-lymphocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.

trong>Btrong>-lymphocyte cell line Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue trong>Btrong>-lymphocyte cell line from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.

Peripheral trong>btrong>lood lymphocyte Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue Peripheral trong>btrong>lood lymphocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.

Large granular lymphocyte Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue Large granular lymphocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.

pre-T-lymphocyte Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue pre-T-lymphocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.

trong>Btrong>-lymphocyte Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue trong>Btrong>-lymphocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.

pre-trong>Btrong>-lymphocyte Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue pre-trong>Btrong>-lymphocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.

pro-trong>Btrong>-lymphocyte Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue pro-trong>Btrong>-lymphocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.

Cytotoxic T-lymphocyte Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue Cytotoxic T-lymphocyte from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.

trong>Btrong>-lymphocyte Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue trong>Btrong>-lymphocyte in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.

Lymphocyte Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue Lymphocyte in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.

Large granular lymphocyte Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue Large granular lymphocyte in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.

Cytotoxic T-lymphocyte Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue Cytotoxic T-lymphocyte in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.

T-lymphocyte Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue T-lymphocyte in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.

Helper T-lymphocyte Gene Set

From TISSUES Experimental Tissue Protein Expression Evidence Scores 2025

proteins highly expressed in the tissue Helper T-lymphocyte in proteomics datasets from the TISSUES Experimental Tissue Protein Expression Evidence Scores 2025 dataset.

Lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Memory T-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Memory T-lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

trong>Btrong>-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue trong>Btrong>-lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

T-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue T-lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Large granular lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Large granular lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Cytotoxic T-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Cytotoxic T-lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Regulatory T-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Regulatory T-lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Helper T-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Helper T-lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Naive T-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Naive T-lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

pre-T-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue pre-T-lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Gamma delta T-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Gamma delta T-lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

T-lymphocyte cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue T-lymphocyte cell line in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

pro-trong>Btrong>-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue pro-trong>Btrong>-lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Peripheral trong>btrong>lood lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Peripheral trong>btrong>lood lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

pre-trong>Btrong>-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue pre-trong>Btrong>-lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

pro-trong>Btrong>-lymphocyte cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue pro-trong>Btrong>-lymphocyte cell line in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

pre-trong>Btrong>-lymphocyte cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue pre-trong>Btrong>-lymphocyte cell line in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

trong>Btrong>-lymphocyte cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue trong>Btrong>-lymphocyte cell line in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Plasmacytoid T-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Plasmacytoid T-lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Cytotoxic T-lymphocyte cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Cytotoxic T-lymphocyte cell line in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Vgamma9Vdelta2 T-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Vgamma9Vdelta2 T-lymphocyte in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Decreased total lymphocyte count Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Decreased total lymphocyte count phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

T-lymphocyte deficiency Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the T-lymphocyte deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lymphocyte percentage of white cells Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Lymphocyte percentage of white cells phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Lymphocyte count Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Lymphocyte count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Monocyte-lymphocyte ratio Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Monocyte-lymphocyte ratio phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

CD4:CD8 lymphocyte ratio Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the CD4:CD8 lymphocyte ratio phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

CD8-positive T-lymphocyte count Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the CD8-positive T-lymphocyte count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

White trong>btrong>lood cell count (lymphocyte) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the White trong>btrong>lood cell count (lymphocyte) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

CD19CAR-CD3ZETA-4-1trong>Btrong>trong>Btrong>-EXPRESSING ALLOGENEIC T-LYMPHOCYTE CELLS Gene Set

From DGIdb Drug Targets 2026

interacting proteins for the CD19CAR-CD3ZETA-4-1trong>Btrong>trong>Btrong>-EXPRESSING ALLOGENEIC T-LYMPHOCYTE CELLS drug from theDGIdtrong>btrong> Drug Targets 2026 dataset.

HORSE ANTI-MOUSE ANTI-LYMPHOCYTE SERUM Gene Set

From DGIdb Drug Targets 2026

interacting proteins for the HORSE ANTI-MOUSE ANTI-LYMPHOCYTE SERUM drug from theDGIdtrong>btrong> Drug Targets 2026 dataset.

trong>btrong>asic mechanism of action of ppara ppartrong>btrong>(d) trong>andtrong> pparg trong>andtrong> effects on gene expression Gene Set

From Biocarta Pathways

proteins participating in the trong>btrong>asic mechanism of action of ppara ppartrong>btrong>(d) trong>andtrong> pparg trong>andtrong> effects on gene expression pathway from the trong>Btrong>iocarta Pathways dataset.

trong>Btrong>RCA1 trong>andtrong> trong>Btrong>RCA2 Hereditary trong>Btrong>reast trong>andtrong> Ovarian Cancer Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Btrong>RCA1 trong>andtrong> trong>Btrong>RCA2 Hereditary trong>Btrong>reast trong>andtrong> Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Centromeric instatrong>btrong>ility of chromosomes 1,9 trong>andtrong> 16 trong>andtrong> immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Centromeric instatrong>btrong>ility of chromosomes 1,9 trong>andtrong> 16 trong>andtrong> immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Colotrong>btrong>oma, uveal, with cleft lip trong>andtrong> palate trong>andtrong> mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Colotrong>btrong>oma, uveal, with cleft lip trong>andtrong> palate trong>andtrong> mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomyelination with trong>btrong>rainstem trong>andtrong> spinal cord involvement trong>andtrong> leg spasticity Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination with trong>btrong>rainstem trong>andtrong> spinal cord involvement trong>andtrong> leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leukoencephalopathy with trong>Btrong>rainstem trong>andtrong> Spinal Cord Involvement trong>andtrong> Lactate Elevation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leukoencephalopathy with trong>Btrong>rainstem trong>andtrong> Spinal Cord Involvement trong>andtrong> Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth trong>andtrong> mental retardation, mtrong>andtrong>itrong>btrong>ulofacial dysostosis, microcephaly, trong>andtrong> cleft palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth trong>andtrong> mental retardation, mtrong>andtrong>itrong>btrong>ulofacial dysostosis, microcephaly, trong>andtrong> cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, progressive, with seizures trong>andtrong> ceretrong>btrong>ral trong>andtrong> ceretrong>btrong>ellar atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, progressive, with seizures trong>andtrong> ceretrong>btrong>ral trong>andtrong> ceretrong>btrong>ellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation trong>andtrong> microcephaly with pontine trong>andtrong> ceretrong>btrong>ellar hypoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation trong>andtrong> microcephaly with pontine trong>andtrong> ceretrong>btrong>ellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diatrong>btrong>etes mellitus AND insipidus with optic atrophy AND deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diatrong>btrong>etes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR Atrong>Btrong>NORMALITY AND MENTAL AND GROWTH Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR Atrong>Btrong>NORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset.

Leukoencephalopathy with trong>Btrong>rainstem trong>andtrong> Spinal Cord Involvement trong>andtrong> Lactate Elevation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukoencephalopathy with trong>Btrong>rainstem trong>andtrong> Spinal Cord Involvement trong>andtrong> Lactate Elevation from the curated CTD Gene-Disease Associations dataset.

Congenital, Hereditary, trong>andtrong> Neonatal Diseases trong>andtrong> Atrong>btrong>normalities Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital, Hereditary, trong>andtrong> Neonatal Diseases trong>andtrong> Atrong>btrong>normalities from the curated CTD Gene-Disease Associations dataset.

Mental Retardation trong>Andtrong> Microcephaly With Pontine trong>Andtrong> Ceretrong>btrong>ellar Hypoplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation trong>Andtrong> Microcephaly With Pontine trong>Andtrong> Ceretrong>btrong>ellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.

Neuropathy, Hereditary Sensory trong>Andtrong> Autonomic, Type I, With Cough trong>Andtrong> Gastroesophageal Reflux Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, Hereditary Sensory trong>Andtrong> Autonomic, Type I, With Cough trong>Andtrong> Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset.

Toe Syndactyly, Telecanthus, trong>andtrong> Anogenital trong>andtrong> Renal Malformations Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Toe Syndactyly, Telecanthus, trong>andtrong> Anogenital trong>andtrong> Renal Malformations from the curated CTD Gene-Disease Associations dataset.

postheparin plasma lipase activities trong>btrong>ody fat trong>andtrong> plasma lipid trong>andtrong> lipoprotein concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease postheparin plasma lipase activities trong>btrong>ody fat trong>andtrong> plasma lipid trong>andtrong> lipoprotein concentrations in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

anxiety trong>andtrong> hostility trong>andtrong> depression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anxiety trong>andtrong> hostility trong>andtrong> depression in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

charcot-marie-tooth disease; hereditary motor trong>andtrong> sensory neuropathies; hereditary sensory trong>andtrong> motor neuropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth disease; hereditary motor trong>andtrong> sensory neuropathies; hereditary sensory trong>andtrong> motor neuropathy in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

frontotemporal dementia trong>andtrong> pick-like 3r trong>andtrong> 4r tauopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease frontotemporal dementia trong>andtrong> pick-like 3r trong>andtrong> 4r tauopathy in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

adipose tissue lipoprotein lipase activity trong>andtrong> lipoprotein lipid trong>andtrong> glucose concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adipose tissue lipoprotein lipase activity trong>andtrong> lipoprotein lipid trong>andtrong> glucose concentrations in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

squamous cell carcinomas of the head trong>andtrong> neck (scchn) trong>andtrong> trong>btrong>reast cancer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease squamous cell carcinomas of the head trong>andtrong> neck (scchn) trong>andtrong> trong>btrong>reast cancer in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

vitamins trong>andtrong> metatrong>btrong>olites in pregnant women trong>andtrong> neonates Gene Set

From GAD Gene-Disease Associations

genes associated with the disease vitamins trong>andtrong> metatrong>btrong>olites in pregnant women trong>andtrong> neonates in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

racemase trong>andtrong> epimerase activity, acting on amino acids trong>andtrong> derivatives Gene Set

From GO Molecular Function Annotations 2015

genes performing the racemase trong>andtrong> epimerase activity, acting on amino acids trong>andtrong> derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.

racemase trong>andtrong> epimerase activity, acting on cartrong>btrong>ohydrates trong>andtrong> derivatives Gene Set

From GO Molecular Function Annotations 2015

genes performing the racemase trong>andtrong> epimerase activity, acting on cartrong>btrong>ohydrates trong>andtrong> derivatives molecular function from the curated GO Molecular Function Annotations 2015 dataset.

leukoencephalopathy with trong>btrong>rain stem trong>andtrong> spinal cord involvement trong>andtrong> lactate elevation Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukoencephalopathy with trong>btrong>rain stem trong>andtrong> spinal cord involvement trong>andtrong> lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset.

microspherophakia trong>andtrong>/or megalocornea, with ectopia lentis trong>andtrong> with or without secondary glaucoma Gene Set

From OMIM Gene-Disease Associations

genes associated with the microspherophakia trong>andtrong>/or megalocornea, with ectopia lentis trong>andtrong> with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.

hypomyelination with trong>btrong>rainstem trong>andtrong> spinal cord involvement trong>andtrong> leg spasticity Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypomyelination with trong>btrong>rainstem trong>andtrong> spinal cord involvement trong>andtrong> leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, mental retardation, trong>andtrong> distinctive facies, with cardiac trong>andtrong> genitourinary malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, mental retardation, trong>andtrong> distinctive facies, with cardiac trong>andtrong> genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation trong>andtrong> microcephaly with pontine trong>andtrong> ceretrong>btrong>ellar hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation trong>andtrong> microcephaly with pontine trong>andtrong> ceretrong>btrong>ellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, progressive, seizures, trong>andtrong> ceretrong>btrong>ral trong>andtrong> ceretrong>btrong>ellar atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, progressive, seizures, trong>andtrong> ceretrong>btrong>ral trong>andtrong> ceretrong>btrong>ellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

craniosynostosis with radiohumeral fusions trong>andtrong> other skeletal trong>andtrong> craniofacial anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniosynostosis with radiohumeral fusions trong>andtrong> other skeletal trong>andtrong> craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

Activation of the mRNA upon trong>btrong>inding of the cap-trong>btrong>inding complex trong>andtrong> eIFs, trong>andtrong> sutrong>btrong>sequent trong>btrong>inding to 43S Gene Set

From Reactome Pathways 2014

proteins participating in the Activation of the mRNA upon trong>btrong>inding of the cap-trong>btrong>inding complex trong>andtrong> eIFs, trong>andtrong> sutrong>btrong>sequent trong>btrong>inding to 43S pathway from the Reactome Pathways dataset.

Cooperation of Prefoldin trong>andtrong> TriC/CCT in actin trong>andtrong> tutrong>btrong>ulin folding Gene Set

From Reactome Pathways 2014

proteins participating in the Cooperation of Prefoldin trong>andtrong> TriC/CCT in actin trong>andtrong> tutrong>btrong>ulin folding pathway from the Reactome Pathways dataset.

PI trong>andtrong> PC transport trong>btrong>etween ER trong>andtrong> Golgi memtrong>btrong>ranes Gene Set

From Reactome Pathways 2014

proteins participating in the PI trong>andtrong> PC transport trong>btrong>etween ER trong>andtrong> Golgi memtrong>btrong>ranes pathway from the Reactome Pathways dataset.

Orexin trong>andtrong> neuropeptides FF trong>andtrong> QRFP trong>btrong>ind to their respective receptors Gene Set

From Reactome Pathways 2014

proteins participating in the Orexin trong>andtrong> neuropeptides FF trong>andtrong> QRFP trong>btrong>ind to their respective receptors pathway from the Reactome Pathways dataset.

FGFR1c trong>andtrong> Klotho ligtrong>andtrong> trong>btrong>inding trong>andtrong> activation Gene Set

From Reactome Pathways 2014

proteins participating in the FGFR1c trong>andtrong> Klotho ligtrong>andtrong> trong>btrong>inding trong>andtrong> activation pathway from the Reactome Pathways dataset.

Transport of nucleosides trong>andtrong> free purine trong>andtrong> pyrimidine trong>btrong>ases across the plasma memtrong>btrong>rane Gene Set

From Reactome Pathways 2014

proteins participating in the Transport of nucleosides trong>andtrong> free purine trong>andtrong> pyrimidine trong>btrong>ases across the plasma memtrong>btrong>rane pathway from the Reactome Pathways dataset.

Synthesis trong>andtrong> processing of ENV trong>andtrong> VPU Gene Set

From Reactome Pathways 2014

proteins participating in the Synthesis trong>andtrong> processing of ENV trong>andtrong> VPU pathway from the Reactome Pathways dataset.

Synthesis trong>andtrong> interconversion of nucleotide di- trong>andtrong> triphosphates Gene Set

From Reactome Pathways 2014

proteins participating in the Synthesis trong>andtrong> interconversion of nucleotide di- trong>andtrong> triphosphates pathway from the Reactome Pathways dataset.

SREtrong>Btrong>F trong>andtrong> miR33 in cholesterol trong>andtrong> lipid homeostasis(Homo sapiens) Gene Set

From WikiPathways Pathways 2014

proteins participating in the SREtrong>Btrong>F trong>andtrong> miR33 in cholesterol trong>andtrong> lipid homeostasis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.

SREtrong>Btrong>F trong>andtrong> miR33 in cholesterol trong>andtrong> lipid homeostasis(Mus musculus) Gene Set

From WikiPathways Pathways 2014

proteins participating in the SREtrong>Btrong>F trong>andtrong> miR33 in cholesterol trong>andtrong> lipid homeostasis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset.

SRF trong>andtrong> miRs in Smooth Muscle Differentiation trong>andtrong> Proliferation(Homo sapiens) Gene Set

From WikiPathways Pathways 2014

proteins participating in the SRF trong>andtrong> miRs in Smooth Muscle Differentiation trong>andtrong> Proliferation(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset.

High-Grade trong>Btrong>-Cell Lymphoma, With Myc trong>Andtrong> trong>Btrong>cl2 trong>Andtrong>/Or trong>Btrong>cl6 Rearrangements Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease High-Grade trong>Btrong>-Cell Lymphoma, With Myc trong>Andtrong> trong>Btrong>cl2 trong>Andtrong>/Or trong>Btrong>cl6 Rearrangements in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Toe Syndactyly, Telecanthus, trong>Andtrong> Anogenital trong>Andtrong> Renal Malformations Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Toe Syndactyly, Telecanthus, trong>Andtrong> Anogenital trong>Andtrong> Renal Malformations in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Hypomyelination With trong>Btrong>rain Stem trong>Andtrong> Spinal Cord Involvement trong>Andtrong> Leg Spasticity Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Hypomyelination With trong>Btrong>rain Stem trong>Andtrong> Spinal Cord Involvement trong>Andtrong> Leg Spasticity in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Growth trong>Andtrong> Mental Retardation, Mtrong>andtrong>itrong>btrong>ulofacial Dysostosis, Microcephaly, trong>Andtrong> Cleft Palate Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Growth trong>Andtrong> Mental Retardation, Mtrong>andtrong>itrong>btrong>ulofacial Dysostosis, Microcephaly, trong>Andtrong> Cleft Palate in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Contractures Of The Limtrong>btrong>s trong>Andtrong> Face, Hypotonia, trong>Andtrong> Developmental Delay Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Contractures Of The Limtrong>btrong>s trong>Andtrong> Face, Hypotonia, trong>Andtrong> Developmental Delay in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Microspherophakia trong>Andtrong>/Or Megalocornea, With Ectopia Lentis trong>Andtrong> With Or Without Secondary Glaucoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Microspherophakia trong>Andtrong>/Or Megalocornea, With Ectopia Lentis trong>Andtrong> With Or Without Secondary Glaucoma in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Anal Intraepithelial Neoplasia I trong>Andtrong> Ii (Ain I trong>Andtrong> Ii) (Histologically Confirmed) Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Anal Intraepithelial Neoplasia I trong>Andtrong> Ii (Ain I trong>Andtrong> Ii) (Histologically Confirmed) in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Pierre Rotrong>btrong>in Sequence With Pectus Excavatum trong>Andtrong> Ritrong>btrong> trong>Andtrong> Scapular Anomalies Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Pierre Rotrong>btrong>in Sequence With Pectus Excavatum trong>Andtrong> Ritrong>btrong> trong>Andtrong> Scapular Anomalies in GWAS trong>andtrong> other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

racemase trong>andtrong> epimerase activity, acting on cartrong>btrong>ohydrates trong>andtrong> derivatives Gene Set

From GO Molecular Function Annotations 2023

genes performing the racemase trong>andtrong> epimerase activity, acting on cartrong>btrong>ohydrates trong>andtrong> derivatives molecular function from the curated GO Molecular Function Annotations 2023 dataset.

SRF trong>andtrong> miRs in smooth muscle differentiation trong>andtrong> proliferation Gene Set

From WikiPathways Pathways 2024

proteins participating in the SRF trong>andtrong> miRs in smooth muscle differentiation trong>andtrong> proliferation pathway from the WikiPathways Pathways 2024 dataset.

SREtrong>Btrong>F trong>andtrong> miR33 in cholesterol trong>andtrong> lipid homeostasis Gene Set

From WikiPathways Pathways 2024

proteins participating in the SREtrong>Btrong>F trong>andtrong> miR33 in cholesterol trong>andtrong> lipid homeostasis pathway from the WikiPathways Pathways 2024 dataset.

RIOK1 trong>andtrong> RIOK2 in EGFR trong>andtrong> PI3K mediated tumorigenesis Gene Set

From WikiPathways Pathways 2024

proteins participating in the RIOK1 trong>andtrong> RIOK2 in EGFR trong>andtrong> PI3K mediated tumorigenesis pathway from the WikiPathways Pathways 2024 dataset.

ApoE trong>andtrong> miR 146 in inflammation trong>andtrong> atherosclerosis Gene Set

From WikiPathways Pathways 2024

proteins participating in the ApoE trong>andtrong> miR 146 in inflammation trong>andtrong> atherosclerosis pathway from the WikiPathways Pathways 2024 dataset.

trong>Btrong>iosynthesis trong>andtrong> regeneration of tetrahydrotrong>btrong>iopterin trong>andtrong> catatrong>btrong>olism of phenylalanine Gene Set

From WikiPathways Pathways 2024

proteins participating in the trong>Btrong>iosynthesis trong>andtrong> regeneration of tetrahydrotrong>btrong>iopterin trong>andtrong> catatrong>btrong>olism of phenylalanine pathway from the WikiPathways Pathways 2024 dataset.

Somatroph axis GH trong>andtrong> its relationship to dietary restriction trong>andtrong> aging Gene Set

From WikiPathways Pathways 2024

proteins participating in the Somatroph axis GH trong>andtrong> its relationship to dietary restriction trong>andtrong> aging pathway from the WikiPathways Pathways 2024 dataset.

Mechanoregulation trong>andtrong> pathology of YAP TAZ via Hippo trong>andtrong> non Hippo mechanisms Gene Set

From WikiPathways Pathways 2024

proteins participating in the Mechanoregulation trong>andtrong> pathology of YAP TAZ via Hippo trong>andtrong> non Hippo mechanisms pathway from the WikiPathways Pathways 2024 dataset.

GLP 1 from intestine trong>andtrong> pancreas trong>andtrong> role in glucose homeostasis Gene Set

From WikiPathways Pathways 2024

proteins participating in the GLP 1 from intestine trong>andtrong> pancreas trong>andtrong> role in glucose homeostasis pathway from the WikiPathways Pathways 2024 dataset.

Activation of the mRNA upon trong>btrong>inding of the cap-trong>btrong>inding complex trong>andtrong> eIFs, trong>andtrong> sutrong>btrong>sequent trong>btrong>inding to 43S Gene Set

From Reactome Pathways 2024

proteins participating in the Activation of the mRNA upon trong>btrong>inding of the cap-trong>btrong>inding complex trong>andtrong> eIFs, trong>andtrong> sutrong>btrong>sequent trong>btrong>inding to 43S pathway from the Reactome Pathways 2024 dataset.

trong>Btrong>iosynthesis of protectin trong>andtrong> resolvin conjugates in tissue regeneration (PCTR trong>andtrong> RCTR) Gene Set

From Reactome Pathways 2024

proteins participating in the trong>Btrong>iosynthesis of protectin trong>andtrong> resolvin conjugates in tissue regeneration (PCTR trong>andtrong> RCTR) pathway from the Reactome Pathways 2024 dataset.

Cooperation of Prefoldin trong>andtrong> TriC/CCT in actin trong>andtrong> tutrong>btrong>ulin folding Gene Set

From Reactome Pathways 2024

proteins participating in the Cooperation of Prefoldin trong>andtrong> TriC/CCT in actin trong>andtrong> tutrong>btrong>ulin folding pathway from the Reactome Pathways 2024 dataset.

FGFR1c trong>andtrong> Klotho ligtrong>andtrong> trong>btrong>inding trong>andtrong> activation Gene Set

From Reactome Pathways 2024

proteins participating in the FGFR1c trong>andtrong> Klotho ligtrong>andtrong> trong>btrong>inding trong>andtrong> activation pathway from the Reactome Pathways 2024 dataset.

MLL4 trong>andtrong> MLL3 complexes regulate expression of PPARG target genes in adipogenesis trong>andtrong> hepatic steatosis Gene Set

From Reactome Pathways 2024

proteins participating in the MLL4 trong>andtrong> MLL3 complexes regulate expression of PPARG target genes in adipogenesis trong>andtrong> hepatic steatosis pathway from the Reactome Pathways 2024 dataset.

Orexin trong>andtrong> neuropeptides FF trong>andtrong> QRFP trong>btrong>ind to their respective receptors Gene Set

From Reactome Pathways 2024

proteins participating in the Orexin trong>andtrong> neuropeptides FF trong>andtrong> QRFP trong>btrong>ind to their respective receptors pathway from the Reactome Pathways 2024 dataset.

PI trong>andtrong> PC transport trong>btrong>etween ER trong>andtrong> Golgi memtrong>btrong>ranes Gene Set

From Reactome Pathways 2024

proteins participating in the PI trong>andtrong> PC transport trong>btrong>etween ER trong>andtrong> Golgi memtrong>btrong>ranes pathway from the Reactome Pathways 2024 dataset.

PTK6 Regulates RTKs trong>andtrong> Their Effectors AKT1 trong>andtrong> DOK1 Gene Set

From Reactome Pathways 2024

proteins participating in the PTK6 Regulates RTKs trong>andtrong> Their Effectors AKT1 trong>andtrong> DOK1 pathway from the Reactome Pathways 2024 dataset.

Recruitment trong>andtrong> ATM-mediated phosphorylation of repair trong>andtrong> signaling proteins at DNA doutrong>btrong>le strtrong>andtrong> trong>btrong>reaks Gene Set

From Reactome Pathways 2024

proteins participating in the Recruitment trong>andtrong> ATM-mediated phosphorylation of repair trong>andtrong> signaling proteins at DNA doutrong>btrong>le strtrong>andtrong> trong>btrong>reaks pathway from the Reactome Pathways 2024 dataset.

Synthesis trong>andtrong> processing of ENV trong>andtrong> VPU Gene Set

From Reactome Pathways 2024

proteins participating in the Synthesis trong>andtrong> processing of ENV trong>andtrong> VPU pathway from the Reactome Pathways 2024 dataset.

Transcriptional trong>andtrong> post-translational regulation of MITF-M expression trong>andtrong> activity Gene Set

From Reactome Pathways 2024

proteins participating in the Transcriptional trong>andtrong> post-translational regulation of MITF-M expression trong>andtrong> activity pathway from the Reactome Pathways 2024 dataset.

Transport of trong>btrong>ile salts trong>andtrong> organic acids, metal ions trong>andtrong> amine compounds Gene Set

From Reactome Pathways 2024

proteins participating in the Transport of trong>btrong>ile salts trong>andtrong> organic acids, metal ions trong>andtrong> amine compounds pathway from the Reactome Pathways 2024 dataset.

Transport of nucleosides trong>andtrong> free purine trong>andtrong> pyrimidine trong>btrong>ases across the plasma memtrong>btrong>rane Gene Set

From Reactome Pathways 2024

proteins participating in the Transport of nucleosides trong>andtrong> free purine trong>andtrong> pyrimidine trong>btrong>ases across the plasma memtrong>btrong>rane pathway from the Reactome Pathways 2024 dataset.

racemase trong>andtrong> epimerase activity, acting on cartrong>btrong>ohydrates trong>andtrong> derivatives Gene Set

From GO Molecular Function Annotations 2025

genes performing the racemase trong>andtrong> epimerase activity, acting on cartrong>btrong>ohydrates trong>andtrong> derivatives molecular function from the curated GO Molecular Function Annotations 2025 dataset.

Vertetrong>btrong>ral anomalies trong>andtrong> variatrong>btrong>le endocrine trong>andtrong> T-cell dysfunction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Vertetrong>btrong>ral anomalies trong>andtrong> variatrong>btrong>le endocrine trong>andtrong> T-cell dysfunction in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Vertetrong>btrong>ral anomalies trong>andtrong> variatrong>btrong>le endocrine trong>andtrong> T-cell dysfunction Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Vertetrong>btrong>ral anomalies trong>andtrong> variatrong>btrong>le endocrine trong>andtrong> T-cell dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Regulation of gene expression trong>andtrong> signal transduction in immune trong>andtrong> stress responses Gene Set

From CM4AI U2OS Cell Map Protein Localization Assemblies

proteins comprising Regulation of gene expression trong>andtrong> signal transduction in immune trong>andtrong> stress responses assemtrong>btrong>ly using integrated AP-MS trong>andtrong> IF data from the CM4AI U2OS Cell Map Protein Localization Assemtrong>btrong>lies dataset.

Gastroesophageal reflux disease, peptic ulcer disease trong>andtrong>/or corresponding medications trong>andtrong> treatment Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Gastroesophageal reflux disease, peptic ulcer disease trong>andtrong>/or corresponding medications trong>andtrong> treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

trong>Btrong>asic cell groups trong>andtrong> regions Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in trong>Btrong>asic cell groups trong>andtrong> regions relative to other tissues from the Allen trong>Btrong>rain Atlas Adult Mouse trong>Btrong>rain Tissue Gene Expression Profiles dataset.

head trong>andtrong> face region of M1 Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in head trong>andtrong> face region of M1 relative to other tissues from the Allen trong>Btrong>rain Atlas Prenatal Human trong>Btrong>rain Tissue Gene Expression Profiles dataset.

telomeres telomerase cellular aging trong>andtrong> immortality Gene Set

From Biocarta Pathways

proteins participating in the telomeres telomerase cellular aging trong>andtrong> immortality pathway from the trong>Btrong>iocarta Pathways dataset.

mcalpain trong>andtrong> friends in cell motility Gene Set

From Biocarta Pathways

proteins participating in the mcalpain trong>andtrong> friends in cell motility pathway from the trong>Btrong>iocarta Pathways dataset.

role of ppar-gamma coactivators in otrong>btrong>esity trong>andtrong> thermogenesis Gene Set

From Biocarta Pathways

proteins participating in the role of ppar-gamma coactivators in otrong>btrong>esity trong>andtrong> thermogenesis pathway from the trong>Btrong>iocarta Pathways dataset.

il12 trong>andtrong> stat4 dependent signaling pathway in th1 development Gene Set

From Biocarta Pathways

proteins participating in the il12 trong>andtrong> stat4 dependent signaling pathway in th1 development pathway from the trong>Btrong>iocarta Pathways dataset.

hypoxia trong>andtrong> p53 in the cardiovascular system Gene Set

From Biocarta Pathways

proteins participating in the hypoxia trong>andtrong> p53 in the cardiovascular system pathway from the trong>Btrong>iocarta Pathways dataset.

lissencephaly gene (lis1) in neuronal migration trong>andtrong> development Gene Set

From Biocarta Pathways

proteins participating in the lissencephaly gene (lis1) in neuronal migration trong>andtrong> development pathway from the trong>Btrong>iocarta Pathways dataset.

role of ertrong>btrong>trong>btrong>2 in signal transduction trong>andtrong> oncology Gene Set

From Biocarta Pathways

proteins participating in the role of ertrong>btrong>trong>btrong>2 in signal transduction trong>andtrong> oncology pathway from the trong>Btrong>iocarta Pathways dataset.

corticosteroids trong>andtrong> cardioprotection Gene Set

From Biocarta Pathways

proteins participating in the corticosteroids trong>andtrong> cardioprotection pathway from the trong>Btrong>iocarta Pathways dataset.

cyclins trong>andtrong> cell cycle regulation Gene Set

From Biocarta Pathways

proteins participating in the cyclins trong>andtrong> cell cycle regulation pathway from the trong>Btrong>iocarta Pathways dataset.

mechanism of acetaminophen activity trong>andtrong> toxicity Gene Set

From Biocarta Pathways

proteins participating in the mechanism of acetaminophen activity trong>andtrong> toxicity pathway from the trong>Btrong>iocarta Pathways dataset.

nfat trong>andtrong> hypertrophy of the heart Gene Set

From Biocarta Pathways

proteins participating in the nfat trong>andtrong> hypertrophy of the heart pathway from the trong>Btrong>iocarta Pathways dataset.

acetylation trong>andtrong> deacetylation of rela in nucleus Gene Set

From Biocarta Pathways

proteins participating in the acetylation trong>andtrong> deacetylation of rela in nucleus pathway from the trong>Btrong>iocarta Pathways dataset.

thromtrong>btrong>in signaling trong>andtrong> protease-activated receptors Gene Set

From Biocarta Pathways

proteins participating in the thromtrong>btrong>in signaling trong>andtrong> protease-activated receptors pathway from the trong>Btrong>iocarta Pathways dataset.

antigen processing trong>andtrong> presentation Gene Set

From Biocarta Pathways

proteins participating in the antigen processing trong>andtrong> presentation pathway from the trong>Btrong>iocarta Pathways dataset.

stathmin trong>andtrong> trong>btrong>reast cancer resistance to antimicrotutrong>btrong>ule agents Gene Set

From Biocarta Pathways

proteins participating in the stathmin trong>andtrong> trong>btrong>reast cancer resistance to antimicrotutrong>btrong>ule agents pathway from the trong>Btrong>iocarta Pathways dataset.

role of ß-arrestins in the activation trong>andtrong> targeting of map kinases Gene Set

From Biocarta Pathways

proteins participating in the role of ß-arrestins in the activation trong>andtrong> targeting of map kinases pathway from the trong>Btrong>iocarta Pathways dataset.

cystic fitrong>btrong>rosis transmemtrong>btrong>rane conductance regulator (cftr) trong>andtrong> trong>btrong>eta 2 adrenergic receptor (trong>btrong>2ar) pathway Gene Set

From Biocarta Pathways

proteins participating in the cystic fitrong>btrong>rosis transmemtrong>btrong>rane conductance regulator (cftr) trong>andtrong> trong>btrong>eta 2 adrenergic receptor (trong>btrong>2ar) pathway pathway from the trong>Btrong>iocarta Pathways dataset.

role of pi3k sutrong>btrong>unit p85 in regulation of actin organization trong>andtrong> cell migration Gene Set

From Biocarta Pathways

proteins participating in the role of pi3k sutrong>btrong>unit p85 in regulation of actin organization trong>andtrong> cell migration pathway from the trong>Btrong>iocarta Pathways dataset.

trong>btrong>tg family proteins trong>andtrong> cell cycle regulation Gene Set

From Biocarta Pathways

proteins participating in the trong>btrong>tg family proteins trong>andtrong> cell cycle regulation pathway from the trong>Btrong>iocarta Pathways dataset.

control of skeletal myogenesis trong>btrong>y hdac trong>andtrong> calcium/calmodulin-dependent kinase (camk) Gene Set

From Biocarta Pathways

proteins participating in the control of skeletal myogenesis trong>btrong>y hdac trong>andtrong> calcium/calmodulin-dependent kinase (camk) pathway from the trong>Btrong>iocarta Pathways dataset.

endocytotic role of ndk phosphins trong>andtrong> dynamin Gene Set

From Biocarta Pathways

proteins participating in the endocytotic role of ndk phosphins trong>andtrong> dynamin pathway from the trong>Btrong>iocarta Pathways dataset.

regulation of eif-4e trong>andtrong> p70s6 kinase Gene Set

From Biocarta Pathways

proteins participating in the regulation of eif-4e trong>andtrong> p70s6 kinase pathway from the trong>Btrong>iocarta Pathways dataset.

estrogen responsive protein efp controls cell cycle trong>andtrong> trong>btrong>reast tumors growth Gene Set

From Biocarta Pathways

proteins participating in the estrogen responsive protein efp controls cell cycle trong>andtrong> trong>btrong>reast tumors growth pathway from the trong>Btrong>iocarta Pathways dataset.

vegf hypoxia trong>andtrong> angiogenesis Gene Set

From Biocarta Pathways

proteins participating in the vegf hypoxia trong>andtrong> angiogenesis pathway from the trong>Btrong>iocarta Pathways dataset.

yaci trong>andtrong> trong>btrong>cma stimulation of trong>btrong> cell immune responses Gene Set

From Biocarta Pathways

proteins participating in the yaci trong>andtrong> trong>btrong>cma stimulation of trong>btrong> cell immune responses pathway from the trong>Btrong>iocarta Pathways dataset.

lck trong>andtrong> fyn tyrosine kinases in initiation of tcr activation Gene Set

From Biocarta Pathways

proteins participating in the lck trong>andtrong> fyn tyrosine kinases in initiation of tcr activation pathway from the trong>Btrong>iocarta Pathways dataset.

hiv-1 nef: negative effector of fas trong>andtrong> tnf Gene Set

From Biocarta Pathways

proteins participating in the hiv-1 nef: negative effector of fas trong>andtrong> tnf pathway from the trong>Btrong>iocarta Pathways dataset.

nuclear receptors coordinate the activities of chromatin remodeling complexes trong>andtrong> coactivators to facilitate initiation of transcription in carcinoma cells Gene Set

From Biocarta Pathways

proteins participating in the nuclear receptors coordinate the activities of chromatin remodeling complexes trong>andtrong> coactivators to facilitate initiation of transcription in carcinoma cells pathway from the trong>Btrong>iocarta Pathways dataset.

ucalpain trong>andtrong> friends in cell spread Gene Set

From Biocarta Pathways

proteins participating in the ucalpain trong>andtrong> friends in cell spread pathway from the trong>Btrong>iocarta Pathways dataset.

ionomycin trong>andtrong> phortrong>btrong>al ester signaling pathway Gene Set

From Biocarta Pathways

proteins participating in the ionomycin trong>andtrong> phortrong>btrong>al ester signaling pathway pathway from the trong>Btrong>iocarta Pathways dataset.

carm1 trong>andtrong> regulation of the estrogen receptor Gene Set

From Biocarta Pathways

proteins participating in the carm1 trong>andtrong> regulation of the estrogen receptor pathway from the trong>Btrong>iocarta Pathways dataset.

phosphoinositides trong>andtrong> their downstream targets Gene Set

From Biocarta Pathways

proteins participating in the phosphoinositides trong>andtrong> their downstream targets pathway from the trong>Btrong>iocarta Pathways dataset.

melanocyte development trong>andtrong> pigmentation pathway Gene Set

From Biocarta Pathways

proteins participating in the melanocyte development trong>andtrong> pigmentation pathway pathway from the trong>Btrong>iocarta Pathways dataset.

akap95 role in mitosis trong>andtrong> chromosome dynamics Gene Set

From Biocarta Pathways

proteins participating in the akap95 role in mitosis trong>andtrong> chromosome dynamics pathway from the trong>Btrong>iocarta Pathways dataset.

transcription factor cretrong>btrong> trong>andtrong> its extracellular signals Gene Set

From Biocarta Pathways

proteins participating in the transcription factor cretrong>btrong> trong>andtrong> its extracellular signals pathway from the trong>Btrong>iocarta Pathways dataset.

visceral fat deposits trong>andtrong> the metatrong>btrong>olic syndrome Gene Set

From Biocarta Pathways

proteins participating in the visceral fat deposits trong>andtrong> the metatrong>btrong>olic syndrome pathway from the trong>Btrong>iocarta Pathways dataset.

the igf-1 receptor trong>andtrong> longevity Gene Set

From Biocarta Pathways

proteins participating in the the igf-1 receptor trong>andtrong> longevity pathway from the trong>Btrong>iocarta Pathways dataset.

cdc25 trong>andtrong> chk1 regulatory pathway in response to dna damage Gene Set

From Biocarta Pathways

proteins participating in the cdc25 trong>andtrong> chk1 regulatory pathway in response to dna damage pathway from the trong>Btrong>iocarta Pathways dataset.

human cytomegalovirus trong>andtrong> map kinase pathways Gene Set

From Biocarta Pathways

proteins participating in the human cytomegalovirus trong>andtrong> map kinase pathways pathway from the trong>Btrong>iocarta Pathways dataset.

influence of ras trong>andtrong> rho proteins on g1 to s transition Gene Set

From Biocarta Pathways

proteins participating in the influence of ras trong>andtrong> rho proteins on g1 to s transition pathway from the trong>Btrong>iocarta Pathways dataset.

proteolysis trong>andtrong> signaling pathway of notch Gene Set

From Biocarta Pathways

proteins participating in the proteolysis trong>andtrong> signaling pathway of notch pathway from the trong>Btrong>iocarta Pathways dataset.

apoptotic dna-fragmentation trong>andtrong> tissue homeostasis Gene Set

From Biocarta Pathways

proteins participating in the apoptotic dna-fragmentation trong>andtrong> tissue homeostasis pathway from the trong>Btrong>iocarta Pathways dataset.

ion channels trong>andtrong> their functional role in vascular endothelium Gene Set

From Biocarta Pathways

proteins participating in the ion channels trong>andtrong> their functional role in vascular endothelium pathway from the trong>Btrong>iocarta Pathways dataset.

alpha-synuclein trong>andtrong> parkin-mediated proteolysis in parkinson`s disease Gene Set

From Biocarta Pathways

proteins participating in the alpha-synuclein trong>andtrong> parkin-mediated proteolysis in parkinson`s disease pathway from the trong>Btrong>iocarta Pathways dataset.

fostrong>btrong> gene expression trong>andtrong> drug atrong>btrong>use Gene Set

From Biocarta Pathways

proteins participating in the fostrong>btrong> gene expression trong>andtrong> drug atrong>btrong>use pathway from the trong>Btrong>iocarta Pathways dataset.

links trong>btrong>etween pyk2 trong>andtrong> map kinases Gene Set

From Biocarta Pathways

proteins participating in the links trong>btrong>etween pyk2 trong>andtrong> map kinases pathway from the trong>Btrong>iocarta Pathways dataset.

opposing roles of aif in apoptosis trong>andtrong> cell survival Gene Set

From Biocarta Pathways

proteins participating in the opposing roles of aif in apoptosis trong>andtrong> cell survival pathway from the trong>Btrong>iocarta Pathways dataset.

degradation of the rar trong>andtrong> rxr trong>btrong>y the proteasome Gene Set

From Biocarta Pathways

proteins participating in the degradation of the rar trong>andtrong> rxr trong>btrong>y the proteasome pathway from the trong>Btrong>iocarta Pathways dataset.

cadmium induces dna synthesis trong>andtrong> proliferation in macrophages Gene Set

From Biocarta Pathways

proteins participating in the cadmium induces dna synthesis trong>andtrong> proliferation in macrophages pathway from the trong>Btrong>iocarta Pathways dataset.

erk trong>andtrong> pi-3 kinase are necessary for collagen trong>btrong>inding in corneal epithelia Gene Set

From Biocarta Pathways

proteins participating in the erk trong>andtrong> pi-3 kinase are necessary for collagen trong>btrong>inding in corneal epithelia pathway from the trong>Btrong>iocarta Pathways dataset.

role of trong>btrong>rca1 trong>btrong>rca2 trong>andtrong> atr in cancer susceptitrong>btrong>ility Gene Set

From Biocarta Pathways

proteins participating in the role of trong>btrong>rca1 trong>btrong>rca2 trong>andtrong> atr in cancer susceptitrong>btrong>ility pathway from the trong>Btrong>iocarta Pathways dataset.

chretrong>btrong>p regulation trong>btrong>y cartrong>btrong>ohydrates trong>andtrong> camp Gene Set

From Biocarta Pathways

proteins participating in the chretrong>btrong>p regulation trong>btrong>y cartrong>btrong>ohydrates trong>andtrong> camp pathway from the trong>Btrong>iocarta Pathways dataset.

pten dependent cell cycle arrest trong>andtrong> apoptosis Gene Set

From Biocarta Pathways

proteins participating in the pten dependent cell cycle arrest trong>andtrong> apoptosis pathway from the trong>Btrong>iocarta Pathways dataset.

induction of apoptosis through dr3 trong>andtrong> dr4/5 death receptors Gene Set

From Biocarta Pathways

proteins participating in the induction of apoptosis through dr3 trong>andtrong> dr4/5 death receptors pathway from the trong>Btrong>iocarta Pathways dataset.

CIITA-18437201-Raji trong>Btrong> cells trong>andtrong> iDC-human Gene Set

From ChEA Transcription Factor Binding Site Profiles

genes with transcription factor trong>btrong>inding evidence in the CIITA-18437201-Raji trong>Btrong> cells trong>andtrong> iDC-human transcription factor trong>btrong>inding site profile from the CHEA Transcription Factor trong>Btrong>inding Site Profiles dataset.

FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN Gene Set

From ChEA Transcription Factor Binding Site Profiles

genes with transcription factor trong>btrong>inding evidence in the FOXP2-23625967-PFSK-1 AND SK-N-MC-HUMAN transcription factor trong>btrong>inding site profile from the CHEA Transcription Factor trong>Btrong>inding Site Profiles dataset.

VDR-23401126-LCL-AND-THP1-HUMAN Gene Set

From ChEA Transcription Factor Binding Site Profiles

genes with transcription factor trong>btrong>inding evidence in the VDR-23401126-LCL-AND-THP1-HUMAN transcription factor trong>btrong>inding site profile from the CHEA Transcription Factor trong>Btrong>inding Site Profiles dataset.

YY1-23942234-MYOtrong>Btrong>LASTS AND MYOTUtrong>Btrong>ES-MOUSE Gene Set

From ChEA Transcription Factor Binding Site Profiles

genes with transcription factor trong>btrong>inding evidence in the YY1-23942234-MYOtrong>Btrong>LASTS AND MYOTUtrong>Btrong>ES-MOUSE transcription factor trong>btrong>inding site profile from the CHEA Transcription Factor trong>Btrong>inding Site Profiles dataset.

trong>Btrong>ACH1-22875853-HELA-AND-SCP4-HUMAN Gene Set

From ChEA Transcription Factor Binding Site Profiles

genes with transcription factor trong>btrong>inding evidence in the trong>Btrong>ACH1-22875853-HELA-AND-SCP4-HUMAN transcription factor trong>btrong>inding site profile from the CHEA Transcription Factor trong>Btrong>inding Site Profiles dataset.

EZH2-23942234-MYOtrong>Btrong>LASTS AND MYOTUtrong>Btrong>ES-MOUSE Gene Set

From ChEA Transcription Factor Binding Site Profiles

genes with transcription factor trong>btrong>inding evidence in the EZH2-23942234-MYOtrong>Btrong>LASTS AND MYOTUtrong>Btrong>ES-MOUSE transcription factor trong>btrong>inding site profile from the CHEA Transcription Factor trong>Btrong>inding Site Profiles dataset.

Hypothyroidism, central, trong>andtrong> testicular enlargement Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypothyroidism, central, trong>andtrong> testicular enlargement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Trifunctional protein deficiency with myopathy trong>andtrong> neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Trifunctional protein deficiency with myopathy trong>andtrong> neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy, juvenile cataracts, trong>andtrong> short stature syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, juvenile cataracts, trong>andtrong> short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Holoprosencephaly, ectrodactyly, trong>andtrong> trong>btrong>ilateral cleft lip/palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Holoprosencephaly, ectrodactyly, trong>andtrong> trong>btrong>ilateral cleft lip/palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Foveal hypoplasia trong>andtrong> presenile cataract syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Foveal hypoplasia trong>andtrong> presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arthrogryposis, mental retardation, trong>andtrong> seizures Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arthrogryposis, mental retardation, trong>andtrong> seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Vater association with macrocephaly trong>andtrong> ventriculomegaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Vater association with macrocephaly trong>andtrong> ventriculomegaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal hamartomas nephrotrong>btrong>lastomatosis trong>andtrong> fetal gigantism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal hamartomas nephrotrong>btrong>lastomatosis trong>andtrong> fetal gigantism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, trong>andtrong> genital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, trong>andtrong> genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Exocrine pancreatic insufficiency, dyserythropoietic anemia, trong>andtrong> calvarial hyperostosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Exocrine pancreatic insufficiency, dyserythropoietic anemia, trong>andtrong> calvarial hyperostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, lactic acidosis, trong>andtrong> siderotrong>btrong>lastic anemia 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, lactic acidosis, trong>andtrong> siderotrong>btrong>lastic anemia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microtia, hearing impairment, trong>andtrong> cleft palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microtia, hearing impairment, trong>andtrong> cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, trong>andtrong> hyper-ige Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, trong>andtrong> hyper-ige phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ichthyosis, spastic quadriplegia, trong>andtrong> mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ichthyosis, spastic quadriplegia, trong>andtrong> mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypermanganesemia with dystonia, polycythemia trong>andtrong> cirrhosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypermanganesemia with dystonia, polycythemia trong>andtrong> cirrhosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Comtrong>btrong>ined cellular trong>andtrong> humoral immune defects with granulomas Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Comtrong>btrong>ined cellular trong>andtrong> humoral immune defects with granulomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple joint dislocations, short stature, craniofacial dysmorphism, trong>andtrong> congenital heart defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, trong>andtrong> congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Comtrong>btrong>ined d-2- trong>andtrong> l-2-hydroxyglutaric aciduria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Comtrong>btrong>ined d-2- trong>andtrong> l-2-hydroxyglutaric aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sinoatrial node dysfunction trong>andtrong> deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sinoatrial node dysfunction trong>andtrong> deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, trong>andtrong> lymphedema Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, trong>andtrong> lymphedema phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

T-cell immunodeficiency, recurrent infections, trong>andtrong> autoimmunity with or without cardiac malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the T-cell immunodeficiency, recurrent infections, trong>andtrong> autoimmunity with or without cardiac malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ceretrong>btrong>ral dysgenesis, neuropathy, ichthyosis, trong>andtrong> palmoplantar keratoderma syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ceretrong>btrong>ral dysgenesis, neuropathy, ichthyosis, trong>andtrong> palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation with language impairment trong>andtrong> autistic features Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation with language impairment trong>andtrong> autistic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Warts, hypogammaglotrong>btrong>ulinemia, infections, trong>andtrong> myelokathexis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Warts, hypogammaglotrong>btrong>ulinemia, infections, trong>andtrong> myelokathexis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fitrong>btrong>ular hypoplasia trong>andtrong> complex trong>btrong>rachydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fitrong>btrong>ular hypoplasia trong>andtrong> complex trong>btrong>rachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoinflammation, antitrong>btrong>ody deficiency, trong>andtrong> immune dysregulation, plcg2-associated Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoinflammation, antitrong>btrong>ody deficiency, trong>andtrong> immune dysregulation, plcg2-associated phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, anterior maxillary protrusion, trong>andtrong> stratrong>btrong>ismus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, anterior maxillary protrusion, trong>andtrong> stratrong>btrong>ismus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile convulsions trong>andtrong> paroxysmal choreoathetosis, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile convulsions trong>andtrong> paroxysmal choreoathetosis, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, optic nerve atrophy, trong>andtrong> pelger-huet anomaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, optic nerve atrophy, trong>andtrong> pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alzheimer disease, familial, 3, with spastic paraparesis trong>andtrong> apraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alzheimer disease, familial, 3, with spastic paraparesis trong>andtrong> apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Proliferative vasculopathy trong>andtrong> hydranencephaly-hydrocephaly syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Proliferative vasculopathy trong>andtrong> hydranencephaly-hydrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Insulin-resistant diatrong>btrong>etes mellitus AND acanthosis nigricans Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Insulin-resistant diatrong>btrong>etes mellitus AND acanthosis nigricans phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypertelorism, severe, with midface prominence, myopia, mental retardation, trong>andtrong> trong>btrong>one fragility Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, trong>andtrong> trong>btrong>one fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenic syndrome, congenital, with pre- trong>andtrong> postsynaptic defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, congenital, with pre- trong>andtrong> postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sensory ataxic neuropathy, dysarthria, trong>andtrong> ophthalmoparesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sensory ataxic neuropathy, dysarthria, trong>andtrong> ophthalmoparesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniofacial anomalies trong>andtrong> anterior segment dysgenesis syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniofacial anomalies trong>andtrong> anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness with latrong>btrong>yrinthine aplasia microtia trong>andtrong> microdontia (LAMM) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness with latrong>btrong>yrinthine aplasia microtia trong>andtrong> microdontia (LAMM) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple Cutaneous trong>andtrong> Mucosal Venous Malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple Cutaneous trong>andtrong> Mucosal Venous Malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neuropathy hereditary sensory trong>andtrong> autonomic type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy hereditary sensory trong>andtrong> autonomic type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly with mental retardation trong>andtrong> digital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly with mental retardation trong>andtrong> digital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Poikiloderma, hereditary fitrong>btrong>rosing, with tendon contractures, myopathy, trong>andtrong> pulmonary fitrong>btrong>rosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Poikiloderma, hereditary fitrong>btrong>rosing, with tendon contractures, myopathy, trong>andtrong> pulmonary fitrong>btrong>rosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peripheral neuropathy, myopathy, hoarseness, trong>andtrong> hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peripheral neuropathy, myopathy, hoarseness, trong>andtrong> hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency, X-Linked, with magnesium defect, Epstein-trong>Btrong>arr virus infection, trong>andtrong> neoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency, X-Linked, with magnesium defect, Epstein-trong>Btrong>arr virus infection, trong>andtrong> neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth retardation, developmental delay, coarse facies, trong>andtrong> early death Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth retardation, developmental delay, coarse facies, trong>andtrong> early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inflammatory skin trong>andtrong> trong>btrong>owel disease, neonatal, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inflammatory skin trong>andtrong> trong>btrong>owel disease, neonatal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

3-methylglutaconic aciduria with deafness, encephalopathy, trong>andtrong> Leigh-like syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, trong>andtrong> Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anemia siderotrong>btrong>lastic trong>andtrong> spinoceretrong>btrong>ellar ataxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anemia siderotrong>btrong>lastic trong>andtrong> spinoceretrong>btrong>ellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Facial dysmorphism, immunodeficiency, livedo, trong>andtrong> short stature Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Facial dysmorphism, immunodeficiency, livedo, trong>andtrong> short stature phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, congenital heart defects, trong>andtrong> posterior emtrong>btrong>ryotoxon Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, congenital heart defects, trong>andtrong> posterior emtrong>btrong>ryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with trong>btrong>rain trong>andtrong> eye anomalies, type A10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with trong>btrong>rain trong>andtrong> eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with trong>btrong>rain trong>andtrong> eye anomalies, type A12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with trong>btrong>rain trong>andtrong> eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ceretrong>btrong>ellar ataxia, areflexia, pes cavus, optic atrophy trong>andtrong> sensorinural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ceretrong>btrong>ellar ataxia, areflexia, pes cavus, optic atrophy trong>andtrong> sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infertility associated with multi-tailed spermatozoa trong>andtrong> excessive DNA Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infertility associated with multi-tailed spermatozoa trong>andtrong> excessive DNA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Iris colotrong>btrong>oma with ptosis, hypertelorism, trong>andtrong> mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Iris colotrong>btrong>oma with ptosis, hypertelorism, trong>andtrong> mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ceretrong>btrong>ral autosomal recessive arteriopathy with sutrong>btrong>cortical infarcts trong>andtrong> leukoencephalopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ceretrong>btrong>ral autosomal recessive arteriopathy with sutrong>btrong>cortical infarcts trong>andtrong> leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Rigidity trong>andtrong> multifocal seizure syndrome, lethal neonatal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Rigidity trong>andtrong> multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alopecia, neurologic defects, trong>andtrong> endocrinopathy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alopecia, neurologic defects, trong>andtrong> endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mullerian aplasia trong>andtrong> hypertrong>andtrong>rogenism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mullerian aplasia trong>andtrong> hypertrong>andtrong>rogenism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Knuckle pads, deafness AND leukonychia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Knuckle pads, deafness AND leukonychia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, trong>andtrong> cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, trong>andtrong> cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mtrong>andtrong>itrong>btrong>ular hypoplasia, deafness, progeroid features, trong>andtrong> lipodystrophy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mtrong>andtrong>itrong>btrong>ular hypoplasia, deafness, progeroid features, trong>andtrong> lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, ctrong>btrong>lJ TYPE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, ctrong>btrong>lJ TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Angiopathy, hereditary, with nephropathy, aneurysms, trong>andtrong> muscle cramps Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Angiopathy, hereditary, with nephropathy, aneurysms, trong>andtrong> muscle cramps phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inclusion trong>btrong>ody myopathy with early-onset paget disease trong>andtrong> frontotemporal dementia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inclusion trong>btrong>ody myopathy with early-onset paget disease trong>andtrong> frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multicentric osteolysis, nodulosis trong>andtrong> arthropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multicentric osteolysis, nodulosis trong>andtrong> arthropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Stapes ankylosis with trong>btrong>road thumtrong>btrong> trong>andtrong> toes Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Stapes ankylosis with trong>btrong>road thumtrong>btrong> trong>andtrong> toes phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal dystrophy trong>andtrong> perceptive deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal dystrophy trong>andtrong> perceptive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, trong>andtrong> developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, trong>andtrong> developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma trong>andtrong> woolly hair Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma trong>andtrong> woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Megalotrong>btrong>lastic anemia, thiamine-responsive, with diatrong>btrong>etes mellitus trong>andtrong> sensorineural deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Megalotrong>btrong>lastic anemia, thiamine-responsive, with diatrong>btrong>etes mellitus trong>andtrong> sensorineural deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Proteinuria, low molecular weight, with hypercalciuria trong>andtrong> nephrocalcinosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Proteinuria, low molecular weight, with hypercalciuria trong>andtrong> nephrocalcinosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Noonan syndrome trong>andtrong> Noonan-related syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Noonan syndrome trong>andtrong> Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, lactic acidosis, trong>andtrong> siderotrong>btrong>lastic anemia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, lactic acidosis, trong>andtrong> siderotrong>btrong>lastic anemia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neuropathy, hereditary motor trong>andtrong> sensory, Okinawa type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy, hereditary motor trong>andtrong> sensory, Okinawa type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, onychodysplasia, facial dysmorphism, trong>andtrong> hypotrichosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, onychodysplasia, facial dysmorphism, trong>andtrong> hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, short stature, trong>andtrong> impaired glucose metatrong>btrong>olism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, short stature, trong>andtrong> impaired glucose metatrong>btrong>olism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemorrhagic destruction of the trong>btrong>rain, sutrong>btrong>ependymal calcification, trong>andtrong> cataracts Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemorrhagic destruction of the trong>btrong>rain, sutrong>btrong>ependymal calcification, trong>andtrong> cataracts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Jervell trong>andtrong> Lange-Nielsen syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Jervell trong>andtrong> Lange-Nielsen syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Macrocephaly, alopecia, cutis laxa, trong>andtrong> scoliosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Macrocephaly, alopecia, cutis laxa, trong>andtrong> scoliosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomyelination trong>andtrong> Congenital Cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination trong>andtrong> Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniofacial dysmorphism, skeletal anomalies, trong>andtrong> mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniofacial dysmorphism, skeletal anomalies, trong>andtrong> mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hirschsprung disease, cardiac defects, trong>andtrong> autonomic dysfunction Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hirschsprung disease, cardiac defects, trong>andtrong> autonomic dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiomyopathy dilated with woolly hair trong>andtrong> keratoderma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy dilated with woolly hair trong>andtrong> keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arthrogryposis, renal dysfunction, trong>andtrong> cholestasis 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arthrogryposis, renal dysfunction, trong>andtrong> cholestasis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract trong>andtrong> cardiomyopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract trong>andtrong> cardiomyopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inflammatory skin trong>andtrong> trong>btrong>owel disease, neonatal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inflammatory skin trong>andtrong> trong>btrong>owel disease, neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation X-linked with ceretrong>btrong>ellar hypoplasia trong>andtrong> distinctive facial appearance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation X-linked with ceretrong>btrong>ellar hypoplasia trong>andtrong> distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, microphthalmia trong>andtrong> nystagmus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, microphthalmia trong>andtrong> nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Foveal hypoplasia trong>andtrong> anterior segment dysgenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Foveal hypoplasia trong>andtrong> anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperuricemia, pulmonary hypertension, renal failure, trong>andtrong> alkalosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperuricemia, pulmonary hypertension, renal failure, trong>andtrong> alkalosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with trong>btrong>rain trong>andtrong> eye anomalies, type A2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with trong>btrong>rain trong>andtrong> eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with trong>btrong>rain trong>andtrong> eye anomalies, type A7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with trong>btrong>rain trong>andtrong> eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with trong>btrong>rain trong>andtrong> eye anomalies, type A6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with trong>btrong>rain trong>andtrong> eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with trong>btrong>rain trong>andtrong> eye anomalies, type A8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with trong>btrong>rain trong>andtrong> eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Btrong>one fragility with contractures, arterial rupture, trong>andtrong> deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Btrong>one fragility with contractures, arterial rupture, trong>andtrong> deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectrodactyly, ectodermal dysplasia, trong>andtrong> cleft lip/palate syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectrodactyly, ectodermal dysplasia, trong>andtrong> cleft lip/palate syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy with inner retinal dysfunction trong>andtrong> ganglion cell atrong>btrong>normalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy with inner retinal dysfunction trong>andtrong> ganglion cell atrong>btrong>normalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gyrate atrophy of choroid trong>andtrong> retina with pyridoxine-responsive ornithinemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gyrate atrophy of choroid trong>andtrong> retina with pyridoxine-responsive ornithinemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ulna trong>andtrong> fitrong>btrong>ula atrong>btrong>sence of with severe limtrong>btrong> deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ulna trong>andtrong> fitrong>btrong>ula atrong>btrong>sence of with severe limtrong>btrong> deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Factor v trong>andtrong> factor viii, comtrong>btrong>ined deficiency of, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Factor v trong>andtrong> factor viii, comtrong>btrong>ined deficiency of, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, areflexia, respiratory distress, trong>andtrong> dysphagia, early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, areflexia, respiratory distress, trong>andtrong> dysphagia, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alpha/trong>btrong>eta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, trong>andtrong> autoimmunity Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alpha/trong>btrong>eta T-cell lymphopenia with gamma/delta T-cell expansion, severe cytomegalovirus infection, trong>andtrong> autoimmunity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary Paragangliomas trong>andtrong> Pheochromocytomas Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary Paragangliomas trong>andtrong> Pheochromocytomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked roltrong>andtrong>ic epilepsy with mental retardation trong>andtrong> speech dyspraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked roltrong>andtrong>ic epilepsy with mental retardation trong>andtrong> speech dyspraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Btrong>trong>andtrong>-like calcification with simplified gyration trong>andtrong> polymicrogyria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Btrong>trong>andtrong>-like calcification with simplified gyration trong>andtrong> polymicrogyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypercarotenemia trong>andtrong> vitamin a deficiency, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypercarotenemia trong>andtrong> vitamin a deficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with trong>btrong>rain trong>andtrong> eye anomalies, type A14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with trong>btrong>rain trong>andtrong> eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, epilepsy, trong>andtrong> diatrong>btrong>etes syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, epilepsy, trong>andtrong> diatrong>btrong>etes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ceretrong>btrong>ellar ataxia trong>andtrong> hypogonadotropic hypogonadism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ceretrong>btrong>ellar ataxia trong>andtrong> hypogonadotropic hypogonadism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with trong>btrong>rain trong>andtrong> eye anomalies type A5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with trong>btrong>rain trong>andtrong> eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

PULMONARY FItrong>Btrong>ROSIS AND/OR trong>Btrong>ONE MARROW FAILURE, TELOMERE-RELATED, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the PULMONARY FItrong>Btrong>ROSIS AND/OR trong>Btrong>ONE MARROW FAILURE, TELOMERE-RELATED, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epilepsy, X-linked, with variatrong>btrong>le learning disatrong>btrong>ilities trong>andtrong> trong>btrong>ehavior disorders Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epilepsy, X-linked, with variatrong>btrong>le learning disatrong>btrong>ilities trong>andtrong> trong>btrong>ehavior disorders phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Optic atrophy trong>andtrong> cataract, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Optic atrophy trong>andtrong> cataract, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, juvenile, with microcornea trong>andtrong> glucosuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, juvenile, with microcornea trong>andtrong> glucosuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peripheral demyelinating neuropathy, central dysmyelination, Waardentrong>btrong>urg syndrome, trong>andtrong> Hirschsprung disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardentrong>btrong>urg syndrome, trong>andtrong> Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VII phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe comtrong>btrong>ined immunodeficiency with microcephaly, growth retardation, trong>andtrong> sensitivity to ionizing radiation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe comtrong>btrong>ined immunodeficiency with microcephaly, growth retardation, trong>andtrong> sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ceretrong>btrong>ellar ataxia, deafness, trong>andtrong> narcolepsy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ceretrong>btrong>ellar ataxia, deafness, trong>andtrong> narcolepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cutis laxa with severe pulmonary, gastrointestinal, trong>andtrong> urinary atrong>btrong>normalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cutis laxa with severe pulmonary, gastrointestinal, trong>andtrong> urinary atrong>btrong>normalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ceretrong>btrong>ral autosomal dominant arteriopathy with sutrong>btrong>cortical infarcts trong>andtrong> leukoencephalopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ceretrong>btrong>ral autosomal dominant arteriopathy with sutrong>btrong>cortical infarcts trong>andtrong> leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Juvenile macular degeneration trong>andtrong> hypotrichosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Juvenile macular degeneration trong>andtrong> hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary motor trong>andtrong> sensory neuropathy with optic atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary motor trong>andtrong> sensory neuropathy with optic atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary leiomyomatosis trong>andtrong> renal cell cancer Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary leiomyomatosis trong>andtrong> renal cell cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Monocyte trong>andtrong> dendritic cell deficiency, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Monocyte trong>andtrong> dendritic cell deficiency, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Interstitial lung disease, nephrotic syndrome, trong>andtrong> epidermolysis trong>btrong>ullosa, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Interstitial lung disease, nephrotic syndrome, trong>andtrong> epidermolysis trong>btrong>ullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, hiatal hernia trong>andtrong> nephrotic syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, hiatal hernia trong>andtrong> nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

T-cell immunodeficiency, congenital alopecia trong>andtrong> nail dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the T-cell immunodeficiency, congenital alopecia trong>andtrong> nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pancreatic agenesis trong>andtrong> congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pancreatic agenesis trong>andtrong> congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypopretrong>btrong>etalipoproteinemia, acanthocytosis, retinitis pigmentosa, trong>andtrong> pallidal degeneration Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypopretrong>btrong>etalipoproteinemia, acanthocytosis, retinitis pigmentosa, trong>andtrong> pallidal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcornea, rod-cone dystrophy, cataract, trong>andtrong> posterior staphyloma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcornea, rod-cone dystrophy, cataract, trong>andtrong> posterior staphyloma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Jervell trong>andtrong> Lange-Nielsen syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Jervell trong>andtrong> Lange-Nielsen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Comtrong>btrong>ined malonic trong>andtrong> methylmalonic aciduria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Comtrong>btrong>ined malonic trong>andtrong> methylmalonic aciduria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcornea, myopic chorioretinal atrophy, trong>andtrong> telecanthus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcornea, myopic chorioretinal atrophy, trong>andtrong> telecanthus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, stereotypic movements, epilepsy, trong>andtrong>/or ceretrong>btrong>ral malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, stereotypic movements, epilepsy, trong>andtrong>/or ceretrong>btrong>ral malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glomerulocystic kidney disease with hyperuricemia trong>andtrong> isosthenuria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glomerulocystic kidney disease with hyperuricemia trong>andtrong> isosthenuria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thromtrong>btrong>ocytopenia, platelet dysfunction, hemolysis, trong>andtrong> imtrong>btrong>alanced glotrong>btrong>in synthesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thromtrong>btrong>ocytopenia, platelet dysfunction, hemolysis, trong>andtrong> imtrong>btrong>alanced glotrong>btrong>in synthesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cutis Gyrata syndrome of trong>Btrong>eare trong>andtrong> Stevenson Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cutis Gyrata syndrome of trong>Btrong>eare trong>andtrong> Stevenson phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly trong>andtrong> chorioretinopathy, autosomal recessive, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly trong>andtrong> chorioretinopathy, autosomal recessive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal intraepithelial dyskeratosis trong>andtrong> ectodermal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal intraepithelial dyskeratosis trong>andtrong> ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aniridia, ceretrong>btrong>ellar ataxia, trong>andtrong> mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aniridia, ceretrong>btrong>ellar ataxia, trong>andtrong> mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked hereditary motor trong>andtrong> sensory neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked hereditary motor trong>andtrong> sensory neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal tutrong>btrong>ular acidosis, proximal, with ocular atrong>btrong>normalities trong>andtrong> mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tutrong>btrong>ular acidosis, proximal, with ocular atrong>btrong>normalities trong>andtrong> mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniosynostosis trong>andtrong> dental anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniosynostosis trong>andtrong> dental anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mycotrong>btrong>acterial trong>andtrong> viral infections, susceptitrong>btrong>ility to, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mycotrong>btrong>acterial trong>andtrong> viral infections, susceptitrong>btrong>ility to, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Otrong>btrong>esity, hyperphagia, trong>andtrong> developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Otrong>btrong>esity, hyperphagia, trong>andtrong> developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ceretrong>btrong>roretinal microangiopathy with calcifications trong>andtrong> cysts Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ceretrong>btrong>roretinal microangiopathy with calcifications trong>andtrong> cysts phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Generalized epilepsy trong>andtrong> paroxysmal dyskinesia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Generalized epilepsy trong>andtrong> paroxysmal dyskinesia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VI phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alacrima, achalasia, trong>andtrong> mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alacrima, achalasia, trong>andtrong> mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, normal intelligence trong>andtrong> immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, normal intelligence trong>andtrong> immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Calcification of joints trong>andtrong> arteries Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Calcification of joints trong>andtrong> arteries phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypotrichosis trong>andtrong> recurrent skin vesicles Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypotrichosis trong>andtrong> recurrent skin vesicles phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epidermolysa trong>btrong>ullosa simplex trong>andtrong> limtrong>btrong> girdle muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epidermolysa trong>btrong>ullosa simplex trong>andtrong> limtrong>btrong> girdle muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ceretrong>btrong>ellar ataxia, mental retardation, trong>andtrong> dysequilitrong>btrong>rium syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ceretrong>btrong>ellar ataxia, mental retardation, trong>andtrong> dysequilitrong>btrong>rium syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ceretrong>btrong>ellar ataxia, mental retardation, trong>andtrong> dysequilitrong>btrong>rium syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ceretrong>btrong>ellar ataxia, mental retardation, trong>andtrong> dysequilitrong>btrong>rium syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ceretrong>btrong>ellar ataxia, mental retardation, trong>andtrong> dysequilitrong>btrong>rium syndrome 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ceretrong>btrong>ellar ataxia, mental retardation, trong>andtrong> dysequilitrong>btrong>rium syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Antley-trong>Btrong>ixler syndrome with genital anomalies trong>andtrong> disordered steroidogenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Antley-trong>Btrong>ixler syndrome with genital anomalies trong>andtrong> disordered steroidogenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Psychomotor retardation, epilepsy, trong>andtrong> craniofacial dysmorphism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Psychomotor retardation, epilepsy, trong>andtrong> craniofacial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epiphyseal dysplasia, multiple, with myopia trong>andtrong> conductive deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epiphyseal dysplasia, multiple, with myopia trong>andtrong> conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Frontotemporal dementia trong>andtrong>/or amyotrophic lateral sclerosis 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Frontotemporal dementia trong>andtrong>/or amyotrophic lateral sclerosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cutaneous telangiectasia trong>andtrong> cancer syndrome, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cutaneous telangiectasia trong>andtrong> cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC, SEVERE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pineal hyperplasia AND diatrong>btrong>etes mellitus syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pineal hyperplasia AND diatrong>btrong>etes mellitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mortrong>btrong>id otrong>btrong>esity trong>andtrong> spermatogenic failure Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mortrong>btrong>id otrong>btrong>esity trong>andtrong> spermatogenic failure phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skeletal defects, genital hypoplasia, trong>andtrong> mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skeletal defects, genital hypoplasia, trong>andtrong> mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Siderotrong>btrong>lastic anemia with trong>btrong>-cell immunodeficiency, periodic fevers, trong>andtrong> developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Siderotrong>btrong>lastic anemia with trong>btrong>-cell immunodeficiency, periodic fevers, trong>andtrong> developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Striatal necrosis, trong>btrong>ilateral, trong>andtrong> progressive polyneuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Striatal necrosis, trong>btrong>ilateral, trong>andtrong> progressive polyneuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary sensory trong>andtrong> autonomic neuropathy type IIA Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary sensory trong>andtrong> autonomic neuropathy type IIA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopia, high, with cataract trong>andtrong> vitreoretinal degeneration Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopia, high, with cataract trong>andtrong> vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Comtrong>btrong>ined deficiency of factor V trong>andtrong> factor VIII, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Comtrong>btrong>ined deficiency of factor V trong>andtrong> factor VIII, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Camptodactyly, tall stature, trong>andtrong> hearing loss syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Camptodactyly, tall stature, trong>andtrong> hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal fragility keratoglotrong>btrong>us, trong>btrong>lue sclerae AND joint hypermotrong>btrong>ility Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal fragility keratoglotrong>btrong>us, trong>btrong>lue sclerae AND joint hypermotrong>btrong>ility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pyogenic arthritis, pyoderma gangrenosum trong>andtrong> acne Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pyogenic arthritis, pyoderma gangrenosum trong>andtrong> acne phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, areflexia, respiratory distress, trong>andtrong> dysphagia, early-onset, mild variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, areflexia, respiratory distress, trong>andtrong> dysphagia, early-onset, mild variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth deficiency trong>andtrong> mental retardation with facial dysmorphism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth deficiency trong>andtrong> mental retardation with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital Cataracts, Facial Dysmorphism, trong>andtrong> Neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital Cataracts, Facial Dysmorphism, trong>andtrong> Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, cochlear, with myopia trong>andtrong> intellectual impairment Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, cochlear, with myopia trong>andtrong> intellectual impairment phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Comtrong>btrong>ined deficiency of sialidase AND trong>btrong>eta galactosidase Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Comtrong>btrong>ined deficiency of sialidase AND trong>btrong>eta galactosidase phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation with short stature, hypogonadism trong>andtrong> atrong>btrong>normal gait Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation with short stature, hypogonadism trong>andtrong> atrong>btrong>normal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, postnatal progressive, with seizures trong>andtrong> trong>btrong>rain atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, postnatal progressive, with seizures trong>andtrong> trong>btrong>rain atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiomyopathy, dilated, with woolly hair, keratoderma, trong>andtrong> tooth agenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiomyopathy, dilated, with woolly hair, keratoderma, trong>andtrong> tooth agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy, iris colotrong>btrong>oma, trong>andtrong> comedogenic acne syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, iris colotrong>btrong>oma, trong>andtrong> comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal dysplasia, retinal pigmentary dystrophy, ceretrong>btrong>ellar ataxia trong>andtrong> skeletal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal dysplasia, retinal pigmentary dystrophy, ceretrong>btrong>ellar ataxia trong>andtrong> skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, trong>andtrong> other congenital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, trong>andtrong> other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ichthyosis, follicular atrophoderma, hypotrichosis, trong>andtrong> hypohidrosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ichthyosis, follicular atrophoderma, hypotrichosis, trong>andtrong> hypohidrosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

calcium- trong>andtrong> calmodulin-dependent protein kinase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the calcium- trong>andtrong> calmodulin-dependent protein kinase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mrna cleavage trong>andtrong> polyadenylation specificity factor complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mrna cleavage trong>andtrong> polyadenylation specificity factor complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

mitochondrial sorting trong>andtrong> assemtrong>btrong>ly machinery complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the mitochondrial sorting trong>andtrong> assemtrong>btrong>ly machinery complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

calcium- trong>andtrong> calmodulin-dependent protein kinase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the calcium- trong>andtrong> calmodulin-dependent protein kinase complex cellular component in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

cortical layer of collagen trong>andtrong> cuticulin-trong>btrong>ased cuticle extracellular matrix Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the cortical layer of collagen trong>andtrong> cuticulin-trong>btrong>ased cuticle extracellular matrix cellular component in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen trong>andtrong> cuticulin-trong>btrong>ased cuticle extracellular matrix Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen trong>andtrong> cuticulin-trong>btrong>ased cuticle extracellular matrix cellular component in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mrna cleavage trong>andtrong> polyadenylation specificity factor complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mrna cleavage trong>andtrong> polyadenylation specificity factor complex cellular component in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

collagen trong>andtrong> cuticulin-trong>btrong>ased cuticle extracellular matrix part Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the collagen trong>andtrong> cuticulin-trong>btrong>ased cuticle extracellular matrix part cellular component in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial sorting trong>andtrong> assemtrong>btrong>ly machinery complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial sorting trong>andtrong> assemtrong>btrong>ly machinery complex cellular component in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

TRtrong>Btrong>P containing complex (DICER, RPL7A, EIF6, MOV10 trong>andtrong> sutrong>btrong>units of the 60S ritrong>btrong>osomal particle) Gene Set

From CORUM Protein Complexes

proteins in the TRtrong>Btrong>P containing complex (DICER, RPL7A, EIF6, MOV10 trong>andtrong> sutrong>btrong>units of the 60S ritrong>btrong>osomal particle) protein complex from the CORUM Protein Complexes dataset.

NRD complex (Nucleosome remodeling trong>andtrong> deacetylation complex) Gene Set

From CORUM Protein Complexes

proteins in the NRD complex (Nucleosome remodeling trong>andtrong> deacetylation complex) protein complex from the CORUM Protein Complexes dataset.

6S methyltransferase trong>andtrong> RG-containing Sm proteins complex Gene Set

From CORUM Protein Complexes

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

Remodeling trong>andtrong> spacing factor (RSF) complex Gene Set

From CORUM Protein Complexes

proteins in the Remodeling trong>andtrong> spacing factor (RSF) complex protein complex from the CORUM Protein Complexes dataset.

Ptrong>Btrong>AF complex (Polytrong>btrong>romo- trong>andtrong> trong>Btrong>AF containing complex) Gene Set

From CORUM Protein Complexes

proteins in the Ptrong>Btrong>AF complex (Polytrong>btrong>romo- trong>andtrong> trong>Btrong>AF containing complex) protein complex from the CORUM Protein Complexes dataset.

Cleavage trong>andtrong> polyadenylation factor (CPSF) Gene Set

From CORUM Protein Complexes

proteins in the Cleavage trong>andtrong> polyadenylation factor (CPSF) protein complex from the CORUM Protein Complexes dataset.

Apoptosis- trong>andtrong> splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L Gene Set

From CORUM Protein Complexes

proteins in the Apoptosis- trong>andtrong> splicing-associated protein complex (ASAP-L), SAP18-RNPS1-Acinus-L protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (intermediate I/200kD trong>andtrong> III/250kD), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (intermediate I/200kD trong>andtrong> III/250kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Nucleic trong>andtrong> chromatin Fanconi complex Gene Set

From CORUM Protein Complexes

proteins in the Nucleic trong>andtrong> chromatin Fanconi complex protein complex from the CORUM Protein Complexes dataset.

Respiratory chain complex I (intermediate V/380kD trong>andtrong> VI/480kD), mitochondrial Gene Set

From CORUM Protein Complexes

proteins in the Respiratory chain complex I (intermediate V/380kD trong>andtrong> VI/480kD), mitochondrial protein complex from the CORUM Protein Complexes dataset.

Apoptosis- trong>andtrong> splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S Gene Set

From CORUM Protein Complexes

proteins in the Apoptosis- trong>andtrong> splicing-associated protein complex (ASAP-S), SAP18-RNPS1-Acinus-S protein complex from the CORUM Protein Complexes dataset.

ATP-utilizing chromatin assemtrong>btrong>ly trong>andtrong> remodeling factor (hACF) complex Gene Set

From CORUM Protein Complexes

proteins in the ATP-utilizing chromatin assemtrong>btrong>ly trong>andtrong> remodeling factor (hACF) complex protein complex from the CORUM Protein Complexes dataset.

20S methylosome trong>andtrong> RG-containing Sm protein complex Gene Set

From CORUM Protein Complexes

proteins in the 20S methylosome trong>andtrong> RG-containing Sm protein complex protein complex from the CORUM Protein Complexes dataset.

Amino Acids, Peptides, trong>andtrong> Proteins Gene Set

From CTD Gene-Chemical Interactions

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

trong>Btrong>ile Acids trong>andtrong> Salts Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical trong>Btrong>ile Acids trong>andtrong> Salts from the curated CTD Gene-Chemical Interactions dataset.

Prime trong>andtrong> trong>Btrong>ond NT Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Prime trong>andtrong> trong>Btrong>ond NT from the curated CTD Gene-Chemical Interactions dataset.

drospirenone trong>andtrong> ethinyl estradiol comtrong>btrong>ination Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical drospirenone trong>andtrong> ethinyl estradiol comtrong>btrong>ination from the curated CTD Gene-Chemical Interactions dataset.

Hypophosphatemic Rickets trong>Andtrong> Hyperparathyroidism Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypophosphatemic Rickets trong>Andtrong> Hyperparathyroidism from the curated CTD Gene-Disease Associations dataset.

Severe Comtrong>btrong>ined Immunodeficiency with Microcephaly, Growth Retardation, trong>andtrong> Sensitivity to Ionizing Radiation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Severe Comtrong>btrong>ined Immunodeficiency with Microcephaly, Growth Retardation, trong>andtrong> Sensitivity to Ionizing Radiation from the curated CTD Gene-Disease Associations dataset.

Fitrong>btrong>ular hypoplasia trong>andtrong> complex trong>btrong>rachydactyly Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fitrong>btrong>ular hypoplasia trong>andtrong> complex trong>btrong>rachydactyly from the curated CTD Gene-Disease Associations dataset.

Synovitis granulomatous with uveitis trong>andtrong> cranial neuropathies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Synovitis granulomatous with uveitis trong>andtrong> cranial neuropathies from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRAtrong>Btrong>ISMUS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRAtrong>Btrong>ISMUS from the curated CTD Gene-Disease Associations dataset.

Hereditary Sensory trong>andtrong> Motor Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary Sensory trong>andtrong> Motor Neuropathy from the curated CTD Gene-Disease Associations dataset.

Preaxial deficiency, postaxial polydactyly trong>andtrong> hypospadias Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Preaxial deficiency, postaxial polydactyly trong>andtrong> hypospadias from the curated CTD Gene-Disease Associations dataset.

Comtrong>btrong>ined Cellular trong>Andtrong> Humoral Immune Defects With Granulomas Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Comtrong>btrong>ined Cellular trong>Andtrong> Humoral Immune Defects With Granulomas from the curated CTD Gene-Disease Associations dataset.

OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease OSTEOMYELITIS, STERILE MULTIFOCAL, WITH PERIOSTITIS AND PUSTULOSIS from the curated CTD Gene-Disease Associations dataset.

Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Colotrong>btrong>oma, trong>andtrong> Micrognathia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Colotrong>btrong>oma, trong>andtrong> Micrognathia from the curated CTD Gene-Disease Associations dataset.

Deafness, Congenital, with Inner Ear Agenesis, Microtia, trong>andtrong> Microdontia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, Congenital, with Inner Ear Agenesis, Microtia, trong>andtrong> Microdontia from the curated CTD Gene-Disease Associations dataset.

Epilepsy, roltrong>andtrong>ic with paroxysmal exercise-induced dystonia trong>andtrong> writer's cramp Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, roltrong>andtrong>ic with paroxysmal exercise-induced dystonia trong>andtrong> writer's cramp from the curated CTD Gene-Disease Associations dataset.

Low Molecular Weight Proteinuria with Hypercalciuria trong>andtrong> Nephrocalcinosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Low Molecular Weight Proteinuria with Hypercalciuria trong>andtrong> Nephrocalcinosis from the curated CTD Gene-Disease Associations dataset.

Keratosis Linearis with Ichthyosis Congenita trong>andtrong> Sclerosing Keratoderma Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Keratosis Linearis with Ichthyosis Congenita trong>andtrong> Sclerosing Keratoderma from the curated CTD Gene-Disease Associations dataset.

Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, trong>andtrong> Lymphedema Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, trong>andtrong> Lymphedema from the curated CTD Gene-Disease Associations dataset.

Microtia, Hearing Impairment, trong>Andtrong> Cleft Palate Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microtia, Hearing Impairment, trong>Andtrong> Cleft Palate from the curated CTD Gene-Disease Associations dataset.

OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS from the curated CTD Gene-Disease Associations dataset.

Neuropathy, Hereditary Sensory trong>Andtrong> Autonomic, Type IItrong>Btrong> Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, Hereditary Sensory trong>Andtrong> Autonomic, Type IItrong>Btrong> from the curated CTD Gene-Disease Associations dataset.

Acromegaloid features, overgrowth, cleft palate, trong>andtrong> hernia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Acromegaloid features, overgrowth, cleft palate, trong>andtrong> hernia from the curated CTD Gene-Disease Associations dataset.

Ceretrong>btrong>ral dysgenesis, neuropathy, ichthyosis, trong>andtrong> palmoplantar keratoderma syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ceretrong>btrong>ral dysgenesis, neuropathy, ichthyosis, trong>andtrong> palmoplantar keratoderma syndrome from the curated CTD Gene-Disease Associations dataset.

46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease 46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS from the curated CTD Gene-Disease Associations dataset.

Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardentrong>btrong>urg Syndrome, trong>andtrong> Hirschsprung Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardentrong>btrong>urg Syndrome, trong>andtrong> Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset.

Choreoathetosis, Hypothyroidism, trong>Andtrong> Neonatal Respiratory Distress Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Choreoathetosis, Hypothyroidism, trong>Andtrong> Neonatal Respiratory Distress from the curated CTD Gene-Disease Associations dataset.

Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, trong>andtrong> Calvarial Hyperostosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, trong>andtrong> Calvarial Hyperostosis from the curated CTD Gene-Disease Associations dataset.

Craniosynostosis, anal anomalies, trong>andtrong> porokeratosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Craniosynostosis, anal anomalies, trong>andtrong> porokeratosis from the curated CTD Gene-Disease Associations dataset.

Sacral defect trong>andtrong> anterior sacral meningocele Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sacral defect trong>andtrong> anterior sacral meningocele from the curated CTD Gene-Disease Associations dataset.

Classical Lissencephalies trong>andtrong> Sutrong>btrong>cortical trong>Btrong>trong>andtrong> Heterotopias Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Classical Lissencephalies trong>andtrong> Sutrong>btrong>cortical trong>Btrong>trong>andtrong> Heterotopias from the curated CTD Gene-Disease Associations dataset.

Epiphyseal Dysplasia, Multiple, with Myopia trong>andtrong> Conductive Deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal Dysplasia, Multiple, with Myopia trong>andtrong> Conductive Deafness from the curated CTD Gene-Disease Associations dataset.

Optic atrophy 1 trong>andtrong> deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic atrophy 1 trong>andtrong> deafness from the curated CTD Gene-Disease Associations dataset.

Neuropathy, hereditary motor trong>andtrong> sensory, Russe type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, hereditary motor trong>andtrong> sensory, Russe type from the curated CTD Gene-Disease Associations dataset.

trong>Btrong>lepharophimosis, Ptosis, trong>andtrong> Epicanthus Inversus Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease trong>Btrong>lepharophimosis, Ptosis, trong>andtrong> Epicanthus Inversus from the curated CTD Gene-Disease Associations dataset.

Hypotrichosis trong>Andtrong> Recurrent Skin Vesicles Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypotrichosis trong>Andtrong> Recurrent Skin Vesicles from the curated CTD Gene-Disease Associations dataset.

Signs trong>andtrong> Symptoms, Digestive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Signs trong>andtrong> Symptoms, Digestive from the curated CTD Gene-Disease Associations dataset.

Inclusion trong>Btrong>ody Myopathy With Early-Onset Paget Disease trong>Andtrong> Frontotemporal Dementia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inclusion trong>Btrong>ody Myopathy With Early-Onset Paget Disease trong>Andtrong> Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset.

Methylmalonic Aciduria trong>andtrong> Homocystinuria, Ctrong>btrong>lD Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Methylmalonic Aciduria trong>andtrong> Homocystinuria, Ctrong>btrong>lD Type from the curated CTD Gene-Disease Associations dataset.

Head trong>andtrong> Neck Neoplasms Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Head trong>andtrong> Neck Neoplasms from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES from the curated CTD Gene-Disease Associations dataset.

Congenital Hemidysplasia with Ichthyosiform Erythroderma trong>andtrong> Limtrong>btrong> Defects Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Hemidysplasia with Ichthyosiform Erythroderma trong>andtrong> Limtrong>btrong> Defects from the curated CTD Gene-Disease Associations dataset.

Cataract, Juvenile, With Microcornea trong>Andtrong> Glucosuria Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Juvenile, With Microcornea trong>Andtrong> Glucosuria from the curated CTD Gene-Disease Associations dataset.

HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CANCER from the curated CTD Gene-Disease Associations dataset.

Venous Malformations, Multiple Cutaneous trong>andtrong> Mucosal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Venous Malformations, Multiple Cutaneous trong>andtrong> Mucosal from the curated CTD Gene-Disease Associations dataset.

trong>Btrong>AND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease trong>Btrong>AND-LIKE CALCIFICATION WITH SIMPLIFIED GYRATION AND POLYMICROGYRIA from the curated CTD Gene-Disease Associations dataset.

Postoperative Nausea trong>andtrong> Vomiting Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Postoperative Nausea trong>andtrong> Vomiting from the curated CTD Gene-Disease Associations dataset.

Myopathy with lactic acidosis trong>andtrong> siderotrong>btrong>lastic anemia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy with lactic acidosis trong>andtrong> siderotrong>btrong>lastic anemia from the curated CTD Gene-Disease Associations dataset.

Altrong>btrong>inism with hemorrhagic diathesis trong>andtrong> pigmented reticuloendothelial cells Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Altrong>btrong>inism with hemorrhagic diathesis trong>andtrong> pigmented reticuloendothelial cells from the curated CTD Gene-Disease Associations dataset.

Trifunctional Protein Deficiency With Myopathy trong>Andtrong> Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Trifunctional Protein Deficiency With Myopathy trong>Andtrong> Neuropathy from the curated CTD Gene-Disease Associations dataset.

MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND trong>Btrong>RAIN ATROPHY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND trong>Btrong>RAIN ATROPHY from the curated CTD Gene-Disease Associations dataset.

Keratitis, Ichthyosis, trong>andtrong> Deafness (KID) Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Keratitis, Ichthyosis, trong>andtrong> Deafness (KID) Syndrome from the curated CTD Gene-Disease Associations dataset.

trong>Btrong>ifid Nose With Or Without Anorectal trong>Andtrong> Renal Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease trong>Btrong>ifid Nose With Or Without Anorectal trong>Andtrong> Renal Anomalies from the curated CTD Gene-Disease Associations dataset.

Congenital Cataracts, Facial Dysmorphism, trong>Andtrong> Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Cataracts, Facial Dysmorphism, trong>Andtrong> Neuropathy from the curated CTD Gene-Disease Associations dataset.

Corneal dystrophy trong>andtrong> perceptive deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal dystrophy trong>andtrong> perceptive deafness from the curated CTD Gene-Disease Associations dataset.

VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY from the curated CTD Gene-Disease Associations dataset.

Ceretrong>btrong>ellar Ataxia, Mental Retardation, trong>Andtrong> Dysequilitrong>btrong>rium Syndrome 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ceretrong>btrong>ellar Ataxia, Mental Retardation, trong>Andtrong> Dysequilitrong>btrong>rium Syndrome 3 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Skeletal Dysplasia, trong>andtrong> Atrong>btrong>ducens Palsy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Skeletal Dysplasia, trong>andtrong> Atrong>btrong>ducens Palsy from the curated CTD Gene-Disease Associations dataset.

Hypopituitarism trong>andtrong> septooptic 'dysplasia' Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypopituitarism trong>andtrong> septooptic 'dysplasia' from the curated CTD Gene-Disease Associations dataset.

PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PALMOPLANTAR HYPERKERATOSIS WITH SQUAMOUS CELL CARCINOMA OF SKIN AND 46,XX SEX REVERSAL from the curated CTD Gene-Disease Associations dataset.

Angiopathy, Hereditary, With Nephropathy, Aneurysms, trong>Andtrong> Muscle Cramps Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Angiopathy, Hereditary, With Nephropathy, Aneurysms, trong>Andtrong> Muscle Cramps from the curated CTD Gene-Disease Associations dataset.

Aplasia of Lacrimal trong>andtrong> Salivary Gltrong>andtrong>s Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aplasia of Lacrimal trong>andtrong> Salivary Gltrong>andtrong>s from the curated CTD Gene-Disease Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA from the curated CTD Gene-Disease Associations dataset.

Deafness, Cataract, Retinitis Pigmentosa, trong>Andtrong> Sperm Atrong>btrong>normalities Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, Cataract, Retinitis Pigmentosa, trong>Andtrong> Sperm Atrong>btrong>normalities from the curated CTD Gene-Disease Associations dataset.

MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY from the curated CTD Gene-Disease Associations dataset.

Glomerulocystic Kidney Disease with Hyperuricemia trong>andtrong> Isosthenuria Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glomerulocystic Kidney Disease with Hyperuricemia trong>andtrong> Isosthenuria from the curated CTD Gene-Disease Associations dataset.

Calcification of Joints trong>andtrong> Arteries Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Calcification of Joints trong>andtrong> Arteries from the curated CTD Gene-Disease Associations dataset.

CHOANAL ATRESIA AND LYMPHEDEMA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CHOANAL ATRESIA AND LYMPHEDEMA from the curated CTD Gene-Disease Associations dataset.

Macrocephaly, Alopecia, Cutis Laxa, trong>andtrong> Scoliosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macrocephaly, Alopecia, Cutis Laxa, trong>andtrong> Scoliosis from the curated CTD Gene-Disease Associations dataset.

Hereditary Motor trong>Andtrong> Sensory Neuropathy, Type IIC Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary Motor trong>Andtrong> Sensory Neuropathy, Type IIC from the curated CTD Gene-Disease Associations dataset.

Asthma, Nasal Polyps, trong>Andtrong> Aspirin Intolerance Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Asthma, Nasal Polyps, trong>Andtrong> Aspirin Intolerance from the curated CTD Gene-Disease Associations dataset.

Neoplasms, Germ Cell trong>andtrong> Emtrong>btrong>ryonal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neoplasms, Germ Cell trong>andtrong> Emtrong>btrong>ryonal from the curated CTD Gene-Disease Associations dataset.

Hereditary Motor trong>Andtrong> Sensory Neuropathy VI Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary Motor trong>Andtrong> Sensory Neuropathy VI from the curated CTD Gene-Disease Associations dataset.

Cutis Gyrata Syndrome of trong>Btrong>eare trong>Andtrong> Stevenson Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cutis Gyrata Syndrome of trong>Btrong>eare trong>Andtrong> Stevenson from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH trong>Btrong>RAIN AND EYE ANOMALIES), TYPE A, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH trong>Btrong>RAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH trong>Btrong>RAIN AND EYE ANOMALIES), TYPE A, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH trong>Btrong>RAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH trong>Btrong>RAIN AND EYE ANOMALIES), TYPE A, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH trong>Btrong>RAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset.

Wounds trong>andtrong> Injuries Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Wounds trong>andtrong> Injuries from the curated CTD Gene-Disease Associations dataset.

Schizophrenia trong>andtrong> Disorders with Psychotic Features Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Schizophrenia trong>andtrong> Disorders with Psychotic Features from the curated CTD Gene-Disease Associations dataset.

Hypopretrong>btrong>etalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, trong>Andtrong> Pallidal Degeneration Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypopretrong>btrong>etalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, trong>Andtrong> Pallidal Degeneration from the curated CTD Gene-Disease Associations dataset.

Sleep Initiation trong>andtrong> Maintenance Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sleep Initiation trong>andtrong> Maintenance Disorders from the curated CTD Gene-Disease Associations dataset.

Methylmalonic Aciduria trong>andtrong> Homocystinuria, Ctrong>btrong>lF Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Methylmalonic Aciduria trong>andtrong> Homocystinuria, Ctrong>btrong>lF Type from the curated CTD Gene-Disease Associations dataset.

Scaphocephaly, Maxillary Retrusion, trong>Andtrong> Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Scaphocephaly, Maxillary Retrusion, trong>Andtrong> Mental Retardation from the curated CTD Gene-Disease Associations dataset.

Cataract trong>andtrong> cardiomyopathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract trong>andtrong> cardiomyopathy from the curated CTD Gene-Disease Associations dataset.

Ectrodactyly, Ectodermal Dysplasia, trong>Andtrong> Cleft Lip/Palate Syndrome 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, trong>Andtrong> Cleft Lip/Palate Syndrome 1 from the curated CTD Gene-Disease Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA from the curated CTD Gene-Disease Associations dataset.

FACTOR V AND FACTOR VIII, COMtrong>Btrong>INED DEFICIENCY OF, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FACTOR V AND FACTOR VIII, COMtrong>Btrong>INED DEFICIENCY OF, 1 from the curated CTD Gene-Disease Associations dataset.

Neuropathy, hereditary motor trong>andtrong> sensory, Okinawa type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, hereditary motor trong>andtrong> sensory, Okinawa type from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia, Optic Atrophy, trong>andtrong> Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia, Optic Atrophy, trong>andtrong> Neuropathy from the curated CTD Gene-Disease Associations dataset.

Generalized Epilepsy trong>andtrong> Paroxysmal Dyskinesia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Generalized Epilepsy trong>andtrong> Paroxysmal Dyskinesia from the curated CTD Gene-Disease Associations dataset.

Hereditary trong>Btrong>reast trong>andtrong> Ovarian Cancer Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary trong>Btrong>reast trong>andtrong> Ovarian Cancer Syndrome from the curated CTD Gene-Disease Associations dataset.

Keratosis palmoplantaris with periodontopathia trong>andtrong> onychogryposis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Keratosis palmoplantaris with periodontopathia trong>andtrong> onychogryposis from the curated CTD Gene-Disease Associations dataset.

Intracranial Emtrong>btrong>olism trong>andtrong> Thromtrong>btrong>osis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Intracranial Emtrong>btrong>olism trong>andtrong> Thromtrong>btrong>osis from the curated CTD Gene-Disease Associations dataset.

LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease LEUKOENCEPHALOPATHY WITH DYSTONIA AND MOTOR NEUROPATHY from the curated CTD Gene-Disease Associations dataset.

Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, trong>Andtrong> Cataract Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, trong>Andtrong> Cataract from the curated CTD Gene-Disease Associations dataset.

FACTOR V AND FACTOR VIII, COMtrong>Btrong>INED DEFICIENCY OF, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FACTOR V AND FACTOR VIII, COMtrong>Btrong>INED DEFICIENCY OF, 2 from the curated CTD Gene-Disease Associations dataset.

Microtia With Nasolacrimal Duct Imperforation trong>Andtrong> Eye Colotrong>btrong>oma Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microtia With Nasolacrimal Duct Imperforation trong>Andtrong> Eye Colotrong>btrong>oma from the curated CTD Gene-Disease Associations dataset.

Nevi trong>andtrong> Melanomas Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nevi trong>andtrong> Melanomas from the curated CTD Gene-Disease Associations dataset.

Epilepsy, X-Linked, with Variatrong>btrong>le Learning Disatrong>btrong>ilities trong>andtrong> trong>Btrong>ehavior Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, X-Linked, with Variatrong>btrong>le Learning Disatrong>btrong>ilities trong>andtrong> trong>Btrong>ehavior Disorders from the curated CTD Gene-Disease Associations dataset.

Attention Deficit trong>andtrong> Disruptive trong>Btrong>ehavior Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Attention Deficit trong>andtrong> Disruptive trong>Btrong>ehavior Disorders from the curated CTD Gene-Disease Associations dataset.

Cardiomyopathy dilated with Woolly hair trong>andtrong> keratoderma Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiomyopathy dilated with Woolly hair trong>andtrong> keratoderma from the curated CTD Gene-Disease Associations dataset.

Microcephaly, microphthalmia, ectrodactyly of lower limtrong>btrong>s, trong>andtrong> prognathism Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microcephaly, microphthalmia, ectrodactyly of lower limtrong>btrong>s, trong>andtrong> prognathism from the curated CTD Gene-Disease Associations dataset.

Optic atrophy trong>andtrong> cataract, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Optic atrophy trong>andtrong> cataract, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH trong>Btrong>RAIN AND EYE ANOMALIES), TYPE A, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH trong>Btrong>RAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset.

Skeletal Defects, Genital Hypoplasia, trong>Andtrong> Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Skeletal Defects, Genital Hypoplasia, trong>Andtrong> Mental Retardation from the curated CTD Gene-Disease Associations dataset.

Hypermanganesemia with Dystonia Polycythemia trong>andtrong> Cirrhosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypermanganesemia with Dystonia Polycythemia trong>andtrong> Cirrhosis from the curated CTD Gene-Disease Associations dataset.

Juvenile macular degeneration trong>andtrong> hypotrichosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Juvenile macular degeneration trong>andtrong> hypotrichosis from the curated CTD Gene-Disease Associations dataset.

ANTLEY-trong>Btrong>IXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ANTLEY-trong>Btrong>IXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS from the curated CTD Gene-Disease Associations dataset.

Mullerian Aplasia trong>andtrong> Hypertrong>andtrong>rogenism Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mullerian Aplasia trong>andtrong> Hypertrong>andtrong>rogenism from the curated CTD Gene-Disease Associations dataset.

Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, trong>Andtrong> Developmental Delay Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, trong>Andtrong> Developmental Delay from the curated CTD Gene-Disease Associations dataset.

Esophageal trong>andtrong> Gastric Varices Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Esophageal trong>andtrong> Gastric Varices from the curated CTD Gene-Disease Associations dataset.

NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC from the curated CTD Gene-Disease Associations dataset.

Hypogammaglotrong>btrong>ulinemia trong>andtrong> Isolated growth hormone deficiency, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypogammaglotrong>btrong>ulinemia trong>andtrong> Isolated growth hormone deficiency, X-linked from the curated CTD Gene-Disease Associations dataset.

Carcinoma, squamous cell of head trong>andtrong> neck Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Carcinoma, squamous cell of head trong>andtrong> neck from the curated CTD Gene-Disease Associations dataset.

Polycythemia, primary familial trong>andtrong> congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polycythemia, primary familial trong>andtrong> congenital from the curated CTD Gene-Disease Associations dataset.

Extravasation of Diagnostic trong>andtrong> Therapeutic Materials Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Extravasation of Diagnostic trong>andtrong> Therapeutic Materials from the curated CTD Gene-Disease Associations dataset.

Ichthyosis, Leukocyte Vacuoles, Alopecia, trong>Andtrong> Sclerosing Cholangitis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ichthyosis, Leukocyte Vacuoles, Alopecia, trong>Andtrong> Sclerosing Cholangitis from the curated CTD Gene-Disease Associations dataset.

Ceretrong>btrong>ellar Ataxia, Mental Retardation, trong>Andtrong> Dysequilitrong>btrong>rium Syndrome 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ceretrong>btrong>ellar Ataxia, Mental Retardation, trong>Andtrong> Dysequilitrong>btrong>rium Syndrome 2 from the curated CTD Gene-Disease Associations dataset.

Knuckle pads, leuconychia trong>andtrong> sensorineural deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Knuckle pads, leuconychia trong>andtrong> sensorineural deafness from the curated CTD Gene-Disease Associations dataset.

Renal Tutrong>btrong>ular Acidosis, Proximal, With Ocular Atrong>btrong>normalities trong>Andtrong> Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal Tutrong>btrong>ular Acidosis, Proximal, With Ocular Atrong>btrong>normalities trong>Andtrong> Mental Retardation from the curated CTD Gene-Disease Associations dataset.

Immunodysregulation, Polyendocrinopathy, trong>andtrong> Enteropathy, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immunodysregulation, Polyendocrinopathy, trong>andtrong> Enteropathy, X-Linked from the curated CTD Gene-Disease Associations dataset.

Hyperekplexia trong>andtrong> Epilepsy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperekplexia trong>andtrong> Epilepsy from the curated CTD Gene-Disease Associations dataset.

Alzheimer Disease, Familial, 3, with Spastic Paraparesis trong>andtrong> Apraxia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alzheimer Disease, Familial, 3, with Spastic Paraparesis trong>andtrong> Apraxia from the curated CTD Gene-Disease Associations dataset.

Epidermolysis trong>Btrong>ullosa With Congenital Localized Atrong>btrong>sence Of Skin trong>Andtrong> Deformity Of Nails Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epidermolysis trong>Btrong>ullosa With Congenital Localized Atrong>btrong>sence Of Skin trong>Andtrong> Deformity Of Nails from the curated CTD Gene-Disease Associations dataset.

Iris hypoplasia trong>andtrong> glaucoma Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Iris hypoplasia trong>andtrong> glaucoma from the curated CTD Gene-Disease Associations dataset.

NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NATURAL KILLER CELL AND GLUCOCORTICOID DEFICIENCY WITH DNA REPAIR DEFECT from the curated CTD Gene-Disease Associations dataset.

Sarcoma family syndrome of Li trong>andtrong> Fraumeni Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sarcoma family syndrome of Li trong>andtrong> Fraumeni from the curated CTD Gene-Disease Associations dataset.

PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS from the curated CTD Gene-Disease Associations dataset.

Nephropathy with Pretitrong>btrong>ial Epidermolysis trong>Btrong>ullosa trong>andtrong> Deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nephropathy with Pretitrong>btrong>ial Epidermolysis trong>Btrong>ullosa trong>andtrong> Deafness from the curated CTD Gene-Disease Associations dataset.

Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, trong>andtrong> Otrong>btrong>esity Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, trong>andtrong> Otrong>btrong>esity Syndrome from the curated CTD Gene-Disease Associations dataset.

Lipoid Proteinosis of Urtrong>btrong>ach trong>andtrong> Wiethe Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lipoid Proteinosis of Urtrong>btrong>ach trong>andtrong> Wiethe from the curated CTD Gene-Disease Associations dataset.

Hypertelorism with esophageal atrong>btrong>normality trong>andtrong> hypospadias Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertelorism with esophageal atrong>btrong>normality trong>andtrong> hypospadias from the curated CTD Gene-Disease Associations dataset.

Alport Syndrome, Mental Retardation, Midface Hypoplasia, trong>andtrong> Elliptocytosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alport Syndrome, Mental Retardation, Midface Hypoplasia, trong>andtrong> Elliptocytosis from the curated CTD Gene-Disease Associations dataset.

Ectrodactyly, Ectodermal Dysplasia, trong>andtrong> Cleft Lip/Palate Syndrome 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, trong>andtrong> Cleft Lip/Palate Syndrome 3 from the curated CTD Gene-Disease Associations dataset.

trong>Btrong>one Fragility with Contractures, Arterial Rupture, trong>andtrong> Deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease trong>Btrong>one Fragility with Contractures, Arterial Rupture, trong>andtrong> Deafness from the curated CTD Gene-Disease Associations dataset.

Thromtrong>btrong>ocytopenia, Platelet Dysfunction, Hemolysis, trong>andtrong> Imtrong>btrong>alanced Glotrong>btrong>in Synthesis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thromtrong>btrong>ocytopenia, Platelet Dysfunction, Hemolysis, trong>andtrong> Imtrong>btrong>alanced Glotrong>btrong>in Synthesis from the curated CTD Gene-Disease Associations dataset.

Jervell trong>Andtrong> Lange-Nielsen Syndrome 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Jervell trong>Andtrong> Lange-Nielsen Syndrome 2 from the curated CTD Gene-Disease Associations dataset.

Neoplasms, Gltrong>andtrong>ular trong>andtrong> Epithelial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neoplasms, Gltrong>andtrong>ular trong>andtrong> Epithelial from the curated CTD Gene-Disease Associations dataset.

Ectodermal dysplasia, ectrodactyly, trong>andtrong> macular dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal dysplasia, ectrodactyly, trong>andtrong> macular dystrophy from the curated CTD Gene-Disease Associations dataset.

Alopecia, Neurologic Defects, trong>andtrong> Endocrinopathy Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alopecia, Neurologic Defects, trong>andtrong> Endocrinopathy Syndrome from the curated CTD Gene-Disease Associations dataset.

Retinitis Pigmentosa, X-Linked, trong>Andtrong> Sinorespiratory Infections, With Or Without Deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinitis Pigmentosa, X-Linked, trong>Andtrong> Sinorespiratory Infections, With Or Without Deafness from the curated CTD Gene-Disease Associations dataset.

Early-onset ataxia with oculomotor apraxia trong>andtrong> hypoaltrong>btrong>uminemia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Early-onset ataxia with oculomotor apraxia trong>andtrong> hypoaltrong>btrong>uminemia from the curated CTD Gene-Disease Associations dataset.

Pyogenic arthritis, pyoderma gangrenosum, trong>andtrong> acne Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pyogenic arthritis, pyoderma gangrenosum, trong>andtrong> acne from the curated CTD Gene-Disease Associations dataset.

Epidermolysa trong>btrong>ullosa simplex trong>andtrong> limtrong>btrong> girdle muscular dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epidermolysa trong>btrong>ullosa simplex trong>andtrong> limtrong>btrong> girdle muscular dystrophy from the curated CTD Gene-Disease Associations dataset.

Cleft Palate, Isolated, trong>Andtrong> Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cleft Palate, Isolated, trong>Andtrong> Mental Retardation from the curated CTD Gene-Disease Associations dataset.

Atrong>btrong>sent radii trong>andtrong> thromtrong>btrong>ocytopenia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Atrong>btrong>sent radii trong>andtrong> thromtrong>btrong>ocytopenia from the curated CTD Gene-Disease Associations dataset.

Hypercarotenemia trong>Andtrong> Vitamin A Deficiency, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypercarotenemia trong>Andtrong> Vitamin A Deficiency, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

HEMORRHAGIC DESTRUCTION OF THE trong>Btrong>RAIN, SUtrong>Btrong>EPENDYMAL CALCIFICATION, AND CATARACTS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEMORRHAGIC DESTRUCTION OF THE trong>Btrong>RAIN, SUtrong>Btrong>EPENDYMAL CALCIFICATION, AND CATARACTS from the curated CTD Gene-Disease Associations dataset.

Microcephaly with Mental Retardation trong>andtrong> Digital Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microcephaly with Mental Retardation trong>andtrong> Digital Anomalies from the curated CTD Gene-Disease Associations dataset.

Macrocephaly with Multiple Epiphyseal Dysplasia trong>andtrong> Distinctive Facies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macrocephaly with Multiple Epiphyseal Dysplasia trong>andtrong> Distinctive Facies from the curated CTD Gene-Disease Associations dataset.

STAPES ANKYLOSIS WITH trong>Btrong>ROAD THUMtrong>Btrong> AND TOES Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease STAPES ANKYLOSIS WITH trong>Btrong>ROAD THUMtrong>Btrong> AND TOES from the curated CTD Gene-Disease Associations dataset.

Cutis Laxa With Severe Pulmonary, Gastrointestinal, trong>Andtrong> Urinary Atrong>btrong>normalities Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cutis Laxa With Severe Pulmonary, Gastrointestinal, trong>Andtrong> Urinary Atrong>btrong>normalities from the curated CTD Gene-Disease Associations dataset.

Polyhydramnios, Megalencephaly, trong>Andtrong> Symptomatic Epilepsy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polyhydramnios, Megalencephaly, trong>Andtrong> Symptomatic Epilepsy from the curated CTD Gene-Disease Associations dataset.

Mental retardation, X-linked, with ceretrong>btrong>ellar hypoplasia trong>andtrong> distinctive facial appearance Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental retardation, X-linked, with ceretrong>btrong>ellar hypoplasia trong>andtrong> distinctive facial appearance from the curated CTD Gene-Disease Associations dataset.

Alpha/trong>Btrong>eta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, trong>andtrong> Autoimmunity Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alpha/trong>Btrong>eta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, trong>andtrong> Autoimmunity from the curated CTD Gene-Disease Associations dataset.

Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, trong>andtrong> Perinatal Edema Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dehydrated Hereditary Stomatocytosis, Pseudohyperkalemia, trong>andtrong> Perinatal Edema from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Severe, With Spasticity trong>Andtrong> Pigmentary Tapetoretinal Degeneration Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Severe, With Spasticity trong>Andtrong> Pigmentary Tapetoretinal Degeneration from the curated CTD Gene-Disease Associations dataset.

Signs trong>andtrong> Symptoms, Respiratory Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Signs trong>andtrong> Symptoms, Respiratory from the curated CTD Gene-Disease Associations dataset.

Renal cysts trong>andtrong> diatrong>btrong>etes syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal cysts trong>andtrong> diatrong>btrong>etes syndrome from the curated CTD Gene-Disease Associations dataset.

Neuropathy, hereditary motor trong>andtrong> sensory, LOM type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, hereditary motor trong>andtrong> sensory, LOM type from the curated CTD Gene-Disease Associations dataset.

Nephrotrong>btrong>lastomatosis, fetal ascites, macrosomia trong>andtrong> Wilms tumor Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nephrotrong>btrong>lastomatosis, fetal ascites, macrosomia trong>andtrong> Wilms tumor from the curated CTD Gene-Disease Associations dataset.

Hereditary Angioedema Types I trong>andtrong> II Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary Angioedema Types I trong>andtrong> II from the curated CTD Gene-Disease Associations dataset.

Drug-Related Side Effects trong>andtrong> Adverse Reactions Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Drug-Related Side Effects trong>andtrong> Adverse Reactions from the curated CTD Gene-Disease Associations dataset.

Insect trong>Btrong>ites trong>andtrong> Stings Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Insect trong>Btrong>ites trong>andtrong> Stings from the curated CTD Gene-Disease Associations dataset.

T-cell immunodeficiency, congenital alopecia trong>andtrong> nail dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease T-cell immunodeficiency, congenital alopecia trong>andtrong> nail dystrophy from the curated CTD Gene-Disease Associations dataset.

Foveal Hypoplasia trong>andtrong> Anterior Segment Dysgenesis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Foveal Hypoplasia trong>andtrong> Anterior Segment Dysgenesis from the curated CTD Gene-Disease Associations dataset.

Cutrong>btrong>itus Valgus with Mental Retardation trong>andtrong> Unusual Facies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cutrong>btrong>itus Valgus with Mental Retardation trong>andtrong> Unusual Facies from the curated CTD Gene-Disease Associations dataset.

Ophthalmoplegia, External, trong>andtrong> Myopia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ophthalmoplegia, External, trong>andtrong> Myopia from the curated CTD Gene-Disease Associations dataset.

Deafness, Sensorineural, trong>Andtrong> Male Infertility Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, Sensorineural, trong>Andtrong> Male Infertility from the curated CTD Gene-Disease Associations dataset.

Hereditary Sensory trong>andtrong> Autonomic Neuropathies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary Sensory trong>andtrong> Autonomic Neuropathies from the curated CTD Gene-Disease Associations dataset.

Histiocytosis with joint contractures trong>andtrong> sensorineural deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Histiocytosis with joint contractures trong>andtrong> sensorineural deafness from the curated CTD Gene-Disease Associations dataset.

Roltrong>andtrong>ic Epilepsy, Mental Retardation, trong>andtrong> Speech Dyspraxia, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Roltrong>andtrong>ic Epilepsy, Mental Retardation, trong>andtrong> Speech Dyspraxia, X-Linked from the curated CTD Gene-Disease Associations dataset.

Leiomyomatosis, esophageal trong>andtrong> vulval, with nephropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leiomyomatosis, esophageal trong>andtrong> vulval, with nephropathy from the curated CTD Gene-Disease Associations dataset.

Growth Retardation, Developmental Delay, Coarse Facies, trong>Andtrong> Early Death Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Growth Retardation, Developmental Delay, Coarse Facies, trong>Andtrong> Early Death from the curated CTD Gene-Disease Associations dataset.

Sensory ataxic neuropathy, dysarthria, trong>andtrong> ophthalmoparesis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sensory ataxic neuropathy, dysarthria, trong>andtrong> ophthalmoparesis from the curated CTD Gene-Disease Associations dataset.

Emtrong>btrong>olism trong>andtrong> Thromtrong>btrong>osis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Emtrong>btrong>olism trong>andtrong> Thromtrong>btrong>osis from the curated CTD Gene-Disease Associations dataset.

Religion trong>andtrong> Psychology Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Religion trong>andtrong> Psychology in GWAS trong>andtrong> other genetic association datasets from the dtrong>btrong>GAP Gene-Trait Associations dataset.

Attention Deficit trong>andtrong> Disruptive trong>Btrong>ehavior Disorders Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Attention Deficit trong>andtrong> Disruptive trong>Btrong>ehavior Disorders in GWAS trong>andtrong> other genetic association datasets from the dtrong>btrong>GAP Gene-Trait Associations dataset.

trong>Btrong>ody Weights trong>andtrong> Measures Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait trong>Btrong>ody Weights trong>andtrong> Measures in GWAS trong>andtrong> other genetic association datasets from the dtrong>btrong>GAP Gene-Trait Associations dataset.

Nevi trong>andtrong> Melanomas Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Nevi trong>andtrong> Melanomas in GWAS trong>andtrong> other genetic association datasets from the dtrong>btrong>GAP Gene-Trait Associations dataset.

Head trong>andtrong> Neck Neoplasms Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Head trong>andtrong> Neck Neoplasms in GWAS trong>andtrong> other genetic association datasets from the dtrong>btrong>GAP Gene-Trait Associations dataset.

trong>btrong>lepharophimosis, ptosis, trong>andtrong> epicanthus inversus syndrome Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease trong>btrong>lepharophimosis, ptosis, trong>andtrong> epicanthus inversus syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

degeneration of macula trong>andtrong> posterior pole Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease degeneration of macula trong>andtrong> posterior pole from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

eye trong>andtrong> adnexa disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease eye trong>andtrong> adnexa disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

comtrong>btrong>ined t cell trong>andtrong> trong>btrong> cell immunodeficiency Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease comtrong>btrong>ined t cell trong>andtrong> trong>btrong> cell immunodeficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

eye trong>andtrong> adnexa disease Gene Set

From DISEASES Experimental Gene-Disease Association Evidence Scores

genes associated with the disease eye trong>andtrong> adnexa disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

inflammatory trong>andtrong> toxic neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease inflammatory trong>andtrong> toxic neuropathy in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

mucinous tutrong>btrong>ular trong>andtrong> spindle renal cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease mucinous tutrong>btrong>ular trong>andtrong> spindle renal cell carcinoma in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

pustulosis of palm trong>andtrong> sole Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease pustulosis of palm trong>andtrong> sole in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

htrong>andtrong>, foot trong>andtrong> mouth disease Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease htrong>andtrong>, foot trong>andtrong> mouth disease in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

tooth trong>andtrong> nail syndrome Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease tooth trong>andtrong> nail syndrome in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

extrapyramidal trong>andtrong> movement disease Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease extrapyramidal trong>andtrong> movement disease in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

mononeuritis of upper limtrong>btrong> trong>andtrong> mononeuritis multiplex Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease mononeuritis of upper limtrong>btrong> trong>andtrong> mononeuritis multiplex in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

lung mixed small cell trong>andtrong> squamous cell carcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease lung mixed small cell trong>andtrong> squamous cell carcinoma in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

autoimmune disease of skin trong>andtrong> connective tissue Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease autoimmune disease of skin trong>andtrong> connective tissue in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

histiocytic trong>andtrong> dendritic cell cancer Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease histiocytic trong>andtrong> dendritic cell cancer in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

methylmalonic aciduria trong>andtrong> homocystinuria type ctrong>btrong>lc Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease methylmalonic aciduria trong>andtrong> homocystinuria type ctrong>btrong>lc in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

trong>btrong>lepharophimosis, ptosis, trong>andtrong> epicanthus inversus syndrome Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease trong>btrong>lepharophimosis, ptosis, trong>andtrong> epicanthus inversus syndrome in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

germ cell trong>andtrong> emtrong>btrong>ryonal cancer Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease germ cell trong>andtrong> emtrong>btrong>ryonal cancer in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

mixed endometrial stromal trong>andtrong> smooth muscle tumor Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease mixed endometrial stromal trong>andtrong> smooth muscle tumor in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

spinal canal trong>andtrong> spinal cord meningioma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease spinal canal trong>andtrong> spinal cord meningioma in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

ovarian germ cell monodermal trong>andtrong> highly specialized teratoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease ovarian germ cell monodermal trong>andtrong> highly specialized teratoma in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

degeneration of macula trong>andtrong> posterior pole Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease degeneration of macula trong>andtrong> posterior pole in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

comtrong>btrong>ined t cell trong>andtrong> trong>btrong> cell immunodeficiency Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease comtrong>btrong>ined t cell trong>andtrong> trong>btrong> cell immunodeficiency in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

mature t-cell trong>andtrong> nk-cell lymphoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease mature t-cell trong>andtrong> nk-cell lymphoma in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

eye trong>andtrong> adnexa disease Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease eye trong>andtrong> adnexa disease in atrong>btrong>stracts of trong>btrong>iomedical putrong>btrong>lications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

trong>btrong>reast trong>andtrong> lung cancer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease trong>btrong>reast trong>andtrong> lung cancer in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

increased chromosome atrong>btrong>errations trong>andtrong> higher lung cancer risk Gene Set

From GAD Gene-Disease Associations

genes associated with the disease increased chromosome atrong>btrong>errations trong>andtrong> higher lung cancer risk in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyper-ige syndrome trong>andtrong> severe eczema. atopy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyper-ige syndrome trong>andtrong> severe eczema. atopy in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

factor viii trong>andtrong> factor ix genes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease factor viii trong>andtrong> factor ix genes in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

flecainide trong>andtrong> paroxetine Gene Set

From GAD Gene-Disease Associations

genes associated with the disease flecainide trong>andtrong> paroxetine in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

pre-term delivery infant mortality trong>andtrong> malaria mortrong>btrong>idity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pre-term delivery infant mortality trong>andtrong> malaria mortrong>btrong>idity in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

alopecia trong>andtrong> lumtrong>btrong>ar herniated disk Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alopecia trong>andtrong> lumtrong>btrong>ar herniated disk in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

trong>btrong>aroreflex trong>andtrong> trong>btrong>lood pressure regulation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease trong>btrong>aroreflex trong>andtrong> trong>btrong>lood pressure regulation in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

neuropathy, hereditary motor trong>andtrong> sensory Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neuropathy, hereditary motor trong>andtrong> sensory in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

psoriasis, psoriatic arthritis, trong>andtrong> sapho syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease psoriasis, psoriatic arthritis, trong>andtrong> sapho syndrome in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

platelet reactivity trong>andtrong> clopidogrel resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease platelet reactivity trong>andtrong> clopidogrel resistance in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome atrong>btrong>errations; chromosome atrong>btrong>normality; neoplasms, germ cell trong>andtrong> emtrong>btrong>ryonal; neoplasms, testis; testicular neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome atrong>btrong>errations; chromosome atrong>btrong>normality; neoplasms, germ cell trong>andtrong> emtrong>btrong>ryonal; neoplasms, testis; testicular neoplasms in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

low mpa exposure trong>andtrong> acute rejection in mmf/tacrolimus-treated kidney transplant patients Gene Set

From GAD Gene-Disease Associations

genes associated with the disease low mpa exposure trong>andtrong> acute rejection in mmf/tacrolimus-treated kidney transplant patients in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

multisystem atrophy, progressive supranuclear palsy trong>andtrong> corticotrong>btrong>asal degeneration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multisystem atrophy, progressive supranuclear palsy trong>andtrong> corticotrong>btrong>asal degeneration in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

jervell trong>andtrong> lange-nielsen syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease jervell trong>andtrong> lange-nielsen syndrome in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

anovulation trong>andtrong> fecundity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anovulation trong>andtrong> fecundity in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

proteinuria trong>andtrong> cardiovascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease proteinuria trong>andtrong> cardiovascular disease in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

thyroid trong>andtrong> neurological atrong>btrong>normalities Gene Set

From GAD Gene-Disease Associations

genes associated with the disease thyroid trong>andtrong> neurological atrong>btrong>normalities in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

homocysteine, folate trong>andtrong> vitamin trong>btrong>12 levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease homocysteine, folate trong>andtrong> vitamin trong>btrong>12 levels in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension trong>andtrong> otrong>btrong>esity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension trong>andtrong> otrong>btrong>esity in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

child hyperactivity-impulsivity trong>andtrong> oppositional trong>btrong>ehaviors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease child hyperactivity-impulsivity trong>andtrong> oppositional trong>btrong>ehaviors in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

head trong>andtrong> neck squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease head trong>andtrong> neck squamous cell carcinoma in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma trong>andtrong> atopy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma trong>andtrong> atopy in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

hiv-rna trong>andtrong> cellular hiv-dna levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hiv-rna trong>andtrong> cellular hiv-dna levels in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin release trong>andtrong> insulin sensitivity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin release trong>andtrong> insulin sensitivity in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

hip trong>btrong>one loss trong>andtrong> fracture Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hip trong>btrong>one loss trong>andtrong> fracture in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

risperidone trong>andtrong> perospirone Gene Set

From GAD Gene-Disease Associations

genes associated with the disease risperidone trong>andtrong> perospirone in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

infectious risk trong>andtrong> outcome in surgical intensive care patients Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infectious risk trong>andtrong> outcome in surgical intensive care patients in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip trong>andtrong> palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip trong>andtrong> palate in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

reduced muscle mrna levels trong>andtrong> insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced muscle mrna levels trong>andtrong> insulin resistance in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

hemostatic factors trong>andtrong> hematological phenotypes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hemostatic factors trong>andtrong> hematological phenotypes in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

reduced gene expression trong>andtrong> lower plasma levels of trong>btrong>eta2-glycoprotein i Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced gene expression trong>andtrong> lower plasma levels of trong>btrong>eta2-glycoprotein i in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

menarche trong>andtrong> menopause (age at onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease menarche trong>andtrong> menopause (age at onset) in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple organ failure; sepsis; shock, septic; wounds trong>andtrong> injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; sepsis; shock, septic; wounds trong>andtrong> injuries in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

dna damage; head trong>andtrong> neck neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dna damage; head trong>andtrong> neck neoplasms in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; head trong>andtrong> neck neoplasms; neoplasms, second primary; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; head trong>andtrong> neck neoplasms; neoplasms, second primary; squamous cell carcinoma in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds trong>andtrong> injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds trong>andtrong> injuries in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

adiposity trong>andtrong> atrong>btrong>dominal otrong>btrong>esity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adiposity trong>andtrong> atrong>btrong>dominal otrong>btrong>esity in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

trong>btrong>reast trong>andtrong> carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease trong>btrong>reast trong>andtrong> carcinoma in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

tropical pancreatitis trong>andtrong> type ii diatrong>btrong>etes mellitus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease tropical pancreatitis trong>andtrong> type ii diatrong>btrong>etes mellitus in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

polymyositis trong>andtrong> dermatomyositis. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polymyositis trong>andtrong> dermatomyositis. in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

head trong>andtrong> neck neoplasms; neoplasms, squamous cell Gene Set

From GAD Gene-Disease Associations

genes associated with the disease head trong>andtrong> neck neoplasms; neoplasms, squamous cell in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; atopy; dermatitis trong>andtrong> eczema Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; atopy; dermatitis trong>andtrong> eczema in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple organ failure; sepsis; wounds trong>andtrong> injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; sepsis; wounds trong>andtrong> injuries in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

head trong>andtrong> neck neoplasms; inflammation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease head trong>andtrong> neck neoplasms; inflammation in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

non-syndromic cleft lip trong>andtrong> palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease non-syndromic cleft lip trong>andtrong> palate in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

postoperative nausea trong>andtrong> vomiting Gene Set

From GAD Gene-Disease Associations

genes associated with the disease postoperative nausea trong>andtrong> vomiting in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

calcium homeostasis trong>andtrong> peripheral trong>btrong>one density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease calcium homeostasis trong>andtrong> peripheral trong>btrong>one density in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal adenomatous polyps trong>andtrong> adenocarcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal adenomatous polyps trong>andtrong> adenocarcinoma in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin trong>andtrong> homa levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin trong>andtrong> homa levels in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

financial trong>andtrong> psychological risk attitudes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease financial trong>andtrong> psychological risk attitudes in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

mother trong>andtrong> child trong>btrong>ehavior Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mother trong>andtrong> child trong>btrong>ehavior in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

rna expression of cartrong>btrong>oxylesterases 1 trong>andtrong> 2. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease rna expression of cartrong>btrong>oxylesterases 1 trong>andtrong> 2. in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

cigarette smoking trong>btrong>ehavior trong>andtrong> reward Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cigarette smoking trong>btrong>ehavior trong>andtrong> reward in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; chromosome deletion; head trong>andtrong> neck neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; chromosome deletion; head trong>andtrong> neck neoplasms; squamous cell carcinoma in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds trong>andtrong> injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds trong>andtrong> injuries in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

serum estrogen trong>andtrong> progesterone concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease serum estrogen trong>andtrong> progesterone concentrations in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

quantitative variation in lipid trong>andtrong> lipoprotein traits Gene Set

From GAD Gene-Disease Associations

genes associated with the disease quantitative variation in lipid trong>andtrong> lipoprotein traits in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; head trong>andtrong> neck neoplasms; squamous cell carcinoma; totrong>btrong>acco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; head trong>andtrong> neck neoplasms; squamous cell carcinoma; totrong>btrong>acco use disorder in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

chiari type i malformation trong>andtrong> syringomyelia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chiari type i malformation trong>andtrong> syringomyelia in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; head trong>andtrong> neck neoplasms; lung neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; head trong>andtrong> neck neoplasms; lung neoplasms in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

hunger trong>andtrong> satiety Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hunger trong>andtrong> satiety in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft palate trong>andtrong> calvaria defects. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft palate trong>andtrong> calvaria defects. in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

lung cancer susceptitrong>btrong>ility trong>andtrong> prognosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lung cancer susceptitrong>btrong>ility trong>andtrong> prognosis in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertrophic cardiomyopathy trong>andtrong> cytochrome c oxidase deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertrophic cardiomyopathy trong>andtrong> cytochrome c oxidase deficiency in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

endometriosis; neoplasms, gltrong>andtrong>ular trong>andtrong> epithelial; ovarian neoplasm; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease endometriosis; neoplasms, gltrong>andtrong>ular trong>andtrong> epithelial; ovarian neoplasm; ovarian neoplasms in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

lung cancer; colorectal cancer; esophageal cancer; head trong>andtrong> neck cancer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lung cancer; colorectal cancer; esophageal cancer; head trong>andtrong> neck cancer in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

proximal chromosome 9p to q trong>andtrong> distal chromosome 9q Gene Set

From GAD Gene-Disease Associations

genes associated with the disease proximal chromosome 9p to q trong>andtrong> distal chromosome 9q in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

loperamide disposition trong>andtrong> central nervous system effects. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease loperamide disposition trong>andtrong> central nervous system effects. in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

cutaneous trong>andtrong> uterine leiomyomata Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cutaneous trong>andtrong> uterine leiomyomata in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyper-igm syndrome can form oligomers trong>andtrong> trigger cd40-mediated signals Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyper-igm syndrome can form oligomers trong>andtrong> trigger cd40-mediated signals in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

major trong>andtrong> trong>btrong>ipolar depressives Gene Set

From GAD Gene-Disease Associations

genes associated with the disease major trong>andtrong> trong>btrong>ipolar depressives in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma glucose, trong>btrong>asal hepatic glucose trong>andtrong> increased insulin release Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma glucose, trong>btrong>asal hepatic glucose trong>andtrong> increased insulin release in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

leigh syndrome trong>andtrong> cytochrome c oxidase deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leigh syndrome trong>andtrong> cytochrome c oxidase deficiency in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

recurrence trong>andtrong> early onset of venous thromtrong>btrong>osis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease recurrence trong>andtrong> early onset of venous thromtrong>btrong>osis in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

normal trong>andtrong> arrhythmia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease normal trong>andtrong> arrhythmia in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

fasting total cholesterol trong>andtrong> ldl-cholesterol concentrations only Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fasting total cholesterol trong>andtrong> ldl-cholesterol concentrations only in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

genetically deficient metatrong>btrong>olism of detrong>btrong>risoquine trong>andtrong> other drugs Gene Set

From GAD Gene-Disease Associations

genes associated with the disease genetically deficient metatrong>btrong>olism of detrong>btrong>risoquine trong>andtrong> other drugs in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

sepsis; wounds trong>andtrong> injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sepsis; wounds trong>andtrong> injuries in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

nevi trong>andtrong> melanomas Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nevi trong>andtrong> melanomas in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrong>btrong>errant promoter methylation of p16(ink4a) trong>andtrong> o(6)-methylguanine-dna methyltransferase Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrong>btrong>errant promoter methylation of p16(ink4a) trong>andtrong> o(6)-methylguanine-dna methyltransferase in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

neoplasms, germ cell trong>andtrong> emtrong>btrong>ryonal; seminoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neoplasms, germ cell trong>andtrong> emtrong>btrong>ryonal; seminoma in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

trong>btrong>ile lipid composition trong>andtrong> cholesterol gallstone Gene Set

From GAD Gene-Disease Associations

genes associated with the disease trong>btrong>ile lipid composition trong>andtrong> cholesterol gallstone in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

ptx3 production trong>andtrong> fertility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ptx3 production trong>andtrong> fertility in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

low insulin trong>andtrong> cholesterol levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease low insulin trong>andtrong> cholesterol levels in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

amygdalar trong>andtrong> hippocampal volumes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amygdalar trong>andtrong> hippocampal volumes in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

medical history histopathology trong>andtrong> environmental exposures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease medical history histopathology trong>andtrong> environmental exposures in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

age trong>andtrong> adiposity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease age trong>andtrong> adiposity in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

depression, psychosis trong>andtrong> antipsychotic response Gene Set

From GAD Gene-Disease Associations

genes associated with the disease depression, psychosis trong>andtrong> antipsychotic response in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute trong>andtrong> chronic kidney transplant outcome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute trong>andtrong> chronic kidney transplant outcome in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; head trong>andtrong> neck neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; head trong>andtrong> neck neoplasms in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

neoplasms, germ cell trong>andtrong> emtrong>btrong>ryonal; pulmonary fitrong>btrong>rosis; testicular neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neoplasms, germ cell trong>andtrong> emtrong>btrong>ryonal; pulmonary fitrong>btrong>rosis; testicular neoplasms in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma high density lipoprotein cholesterol trong>andtrong> apolipoprotein ai Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma high density lipoprotein cholesterol trong>andtrong> apolipoprotein ai in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenoma; carcinoma, papillary; carcinoma, papillary, follicular; papillary trong>andtrong> follicular adenocarcinoma; thyroid neoplasm; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenoma; carcinoma, papillary; carcinoma, papillary, follicular; papillary trong>andtrong> follicular adenocarcinoma; thyroid neoplasm; thyroid neoplasms in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

type ii diatrong>btrong>etes trong>andtrong> hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease type ii diatrong>btrong>etes trong>andtrong> hypertension in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

vertrong>btrong>al trong>andtrong> figural creative achievement Gene Set

From GAD Gene-Disease Associations

genes associated with the disease vertrong>btrong>al trong>andtrong> figural creative achievement in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

cross infection; pneumonia, ventilator-associated; wounds trong>andtrong> injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cross infection; pneumonia, ventilator-associated; wounds trong>andtrong> injuries in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

infection; leg dermatoses; nail diseases; psoriasis; scalp dermatoses; wounds trong>andtrong> injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infection; leg dermatoses; nail diseases; psoriasis; scalp dermatoses; wounds trong>andtrong> injuries in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

trong>btrong>ipolar trong>andtrong> unipolar disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease trong>btrong>ipolar trong>andtrong> unipolar disorder in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

trong>btrong>ody weights trong>andtrong> measures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease trong>btrong>ody weights trong>andtrong> measures in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

adolescent nephronophthisis, tapeto-retinal degeneration trong>andtrong> hepatic fitrong>btrong>rosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adolescent nephronophthisis, tapeto-retinal degeneration trong>andtrong> hepatic fitrong>btrong>rosis in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

wounds trong>andtrong> injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease wounds trong>andtrong> injuries in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

decreases transcriptional activity trong>andtrong> responsiveness to interleukin-6 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease decreases transcriptional activity trong>andtrong> responsiveness to interleukin-6 in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarction trong>andtrong> stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarction trong>andtrong> stroke in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

estrogen trong>andtrong> estrogen/testosterone ratio Gene Set

From GAD Gene-Disease Associations

genes associated with the disease estrogen trong>andtrong> estrogen/testosterone ratio in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; head trong>andtrong> neck neoplasms; totrong>btrong>acco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; head trong>andtrong> neck neoplasms; totrong>btrong>acco use disorder in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

lead trong>andtrong> mercury metatrong>btrong>olism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lead trong>andtrong> mercury metatrong>btrong>olism in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

tumour kinetics trong>andtrong> chromosomal instatrong>btrong>ility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease tumour kinetics trong>andtrong> chromosomal instatrong>btrong>ility in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma total homocysteine trong>andtrong> folate concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma total homocysteine trong>andtrong> folate concentrations in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

growth hormone secretion trong>andtrong> height Gene Set

From GAD Gene-Disease Associations

genes associated with the disease growth hormone secretion trong>andtrong> height in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

free thyroxine trong>andtrong> triiodothyronine Gene Set

From GAD Gene-Disease Associations

genes associated with the disease free thyroxine trong>andtrong> triiodothyronine in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

attention deficit trong>andtrong> disruptive trong>btrong>ehavior disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease attention deficit trong>andtrong> disruptive trong>btrong>ehavior disorders in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

hereditary trong>andtrong> sporadic prostate cancer risk. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hereditary trong>andtrong> sporadic prostate cancer risk. in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; head trong>andtrong> neck neoplasms; neoplasm metastasis; neoplasm recurrence, local; neoplasms, second primary; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; head trong>andtrong> neck neoplasms; neoplasm metastasis; neoplasm recurrence, local; neoplasms, second primary; squamous cell carcinoma in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

increased serum iron transferrin saturation trong>andtrong> hemoglotrong>btrong>in Gene Set

From GAD Gene-Disease Associations

genes associated with the disease increased serum iron transferrin saturation trong>andtrong> hemoglotrong>btrong>in in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

serum lipoprotein lipid trong>andtrong> apolipoprotein levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease serum lipoprotein lipid trong>andtrong> apolipoprotein levels in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

attention deficit hyperactivity disorder trong>andtrong> conduct disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease attention deficit hyperactivity disorder trong>andtrong> conduct disorder in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

colorectal neoplasms; esophageal neoplasms; head trong>andtrong> neck neoplasms; lung neoplasms; neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal neoplasms; esophageal neoplasms; head trong>andtrong> neck neoplasms; lung neoplasms; neoplasms in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

acid lipase deficiency trong>andtrong> cholesterol ester storage disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acid lipase deficiency trong>andtrong> cholesterol ester storage disease in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; head trong>andtrong> neck neoplasms; laryngeal neoplasm; laryngeal neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; head trong>andtrong> neck neoplasms; laryngeal neoplasm; laryngeal neoplasms; squamous cell carcinoma in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

complete trong>andtrong>rogen insensitivity syndrome trong>andtrong> sertoli cell adenoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complete trong>andtrong>rogen insensitivity syndrome trong>andtrong> sertoli cell adenoma in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

chorioamnionitis; infection of amniotic sac trong>andtrong> memtrong>btrong>ranes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chorioamnionitis; infection of amniotic sac trong>andtrong> memtrong>btrong>ranes in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

two major non-ritrong>btrong>osomal nucleolar proteins trong>andtrong> its implication Gene Set

From GAD Gene-Disease Associations

genes associated with the disease two major non-ritrong>btrong>osomal nucleolar proteins trong>andtrong> its implication in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

chorioamnionitis; fetal memtrong>btrong>ranes, premature rupture; infection of amniotic sac trong>andtrong> memtrong>btrong>ranes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chorioamnionitis; fetal memtrong>btrong>ranes, premature rupture; infection of amniotic sac trong>andtrong> memtrong>btrong>ranes in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

head trong>andtrong> neck cancer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease head trong>andtrong> neck cancer in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

cores trong>andtrong> rods is associated Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cores trong>andtrong> rods is associated in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

head trong>andtrong> neck neoplasms; neoplasm recurrence, local; neoplasms, second primary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease head trong>andtrong> neck neoplasms; neoplasm recurrence, local; neoplasms, second primary in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn's disease trong>andtrong> itrong>btrong>d Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn's disease trong>andtrong> itrong>btrong>d in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

circulating protein c levels trong>andtrong> thromtrong>btrong>otic risk Gene Set

From GAD Gene-Disease Associations

genes associated with the disease circulating protein c levels trong>andtrong> thromtrong>btrong>otic risk in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

reduced serum c-peptide trong>andtrong> insulin responses to an oral glucose challenge Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced serum c-peptide trong>andtrong> insulin responses to an oral glucose challenge in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; head trong>andtrong> neck neoplasms; neoplasm recurrence, local; neoplasms, second primary; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; head trong>andtrong> neck neoplasms; neoplasm recurrence, local; neoplasms, second primary; squamous cell carcinoma in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

critical illness; sepsis; systemic infection; wounds trong>andtrong> injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease critical illness; sepsis; systemic infection; wounds trong>andtrong> injuries in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

ceretrong>btrong>ellar medullotrong>btrong>lastomas trong>andtrong> cutaneous trong>btrong>asal cell carcinomas. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ceretrong>btrong>ellar medullotrong>btrong>lastomas trong>andtrong> cutaneous trong>btrong>asal cell carcinomas. in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholic intoxication; wounds trong>andtrong> injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholic intoxication; wounds trong>andtrong> injuries in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

head trong>andtrong> neck squamous cell cancer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease head trong>andtrong> neck squamous cell cancer in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatic iron trong>andtrong> fitrong>btrong>rosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatic iron trong>andtrong> fitrong>btrong>rosis in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

cancer progression trong>andtrong> tumor cell motility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cancer progression trong>andtrong> tumor cell motility in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

doutrong>btrong>le homozygosity for receptor polymorphisms of platelet gpia trong>andtrong> gpiiia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease doutrong>btrong>le homozygosity for receptor polymorphisms of platelet gpia trong>andtrong> gpiiia in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

endogenous hypertriglyceridemia trong>andtrong> familial hypercholesterolemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease endogenous hypertriglyceridemia trong>andtrong> familial hypercholesterolemia in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; head trong>andtrong> neck neoplasms; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; pharyngeal neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; head trong>andtrong> neck neoplasms; laryngeal neoplasm; laryngeal neoplasms; mouth neoplasms; pharyngeal neoplasms; squamous cell carcinoma in GWAS trong>andtrong> other genetic association datasets from the GAD Gene-Disease Associations dataset.