From
Achilles
Fitness scores for cell lines following single gene knockdowns
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From
BioGPS
mRNA expression prtrong>oftrong>iles for the NCI-60 panel trong>oftrong> cancer cell lines
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From
BioGPS
mRNA expression prtrong>oftrong>iles for human tissues and cell types
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From
BioGPS
mRNA expression prtrong>oftrong>iles for mouse tissues and cell types
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From
Human Proteome Map
Protein expression prtrong>oftrong>iles for tissues and cell types
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From
Proteomics Database
Protein expression prtrong>oftrong>iles for tissues and cell types reprocessed from many proteomics datasets
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From
Roadmap Epigenomics
DNA methylation prtrong>oftrong>iles for primary cell types and tissues
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From
Roadmap Epigenomics
mRNA expression prtrong>oftrong>iles for primary cell types and tissues
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From
Tabula Sapiens
Gene expression data from Tabula Sapiens scRNA-seq counts
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From
CellMarker
Cell type markers across various tissues from human and mouse scRNA-seq
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From
Replogle et al., Cell, 2022
Gene expression prtrong>oftrong>iles in the K562 cell line following CRISPRi genetic perturbation trong>oftrong> essential genes
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From
Replogle et al., Cell, 2022
Gene expression prtrong>oftrong>iles in the RPE1 cell line following CRISPRi genetic perturbation trong>oftrong> essential genes
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From
Cell Maps for AI
Protein localization assemblies constructed from integrating AP-MS biomolecular interaction and IF imaging data
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From
Cell Maps for AI
Gene expression prtrong>oftrong>iles in the KOLF2.1J cell line following CRISPRi genetic perturbation
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BST2 interferon stimulated trong>positivetrong> regulator (non-protein coding)
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thymocyte expressed, trong>positivetrong> selection associated 1
Predicted to enable phospholipase binding activity and signaling receptor binding activity. Predicted to be involved in COP9 signalosome assembly; trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell differentiation in thymus; and trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell receptor signaling pathway. Predicted to act upstream trong>oftrong> or within TCR signalosome assembly. Located in cytosol. Part trong>oftrong> COP9 signalosome. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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gastric adenocarcinoma associated, trong>positivetrong> CD44 regulator, long intergenic non-coding RNA
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muscular dystrophy, congenital, merosin-trong>positivetrong>
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growth trong>regulationtrong> by estrogen in breast cancer-like
Acts upstream trong>oftrong> or within kidney development. Predicted to be located in membrane. Implicated in autosomal dominant nonsyndromic deafness 80 and renal agenesis. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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trong>regulationtrong> trong>oftrong> nuclear pre-mRNA domain containing 1A
This gene encodes a cell-cycle and transcription regulatory protein. The encoded protein interacts with the cell cycle inhibitor cyclin-dependent kinase 4 inhibitor B and may function as a negative regulator trong>oftrong> G(1)/S phase progression. This protein also forms homo- and hetrodimers with the protein, trong>regulationtrong> trong>oftrong> nuclear pre-mRNA domain-containing protein 1B, to form a scaffold that interacts with the C-terminal domain trong>oftrong> RNA polymerase II subunit B1 and regulates several aspects trong>oftrong> transcription. Alternate splicing results in multiple transcript variants. A pseudogene trong>oftrong> this gene is found on chromosome 16. [provided by RefSeq, Dec 2014]
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trong>regulationtrong> trong>oftrong> nuclear pre-mRNA domain containing 1B
Enables RNA polymerase II complex binding activity and identical protein binding activity. Involved in several processes, including RNA polymerase II promoter clearance; trong>positivetrong> trong>regulationtrong> trong>oftrong> cell population proliferation; and trong>positivetrong> trong>regulationtrong> trong>oftrong> transcription by RNA polymerase II. Located in nucleoplasm. Part trong>oftrong> transcription preinitiation complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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trong>regulationtrong> trong>oftrong> nuclear pre-mRNA domain containing 2
Predicted to enable RNA polymerase II complex binding activity. Predicted to be involved in mRNA 3'-end processing. Part trong>oftrong> transcription preinitiation complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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growth trong>regulationtrong> by estrogen in breast cancer 1
This gene is an estrogen-responsive gene that is an early response gene in the estrogen receptor-regulated pathway. It is thought to play an important role in hormone-responsive tissues and cancer. Three alternatively spliced transcript variants encoding distinct istrong>oftrong>orms have been found for this gene. [provided by RefSeq, Jul 2008]
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trong>regulationtrong> trong>oftrong> nuclear pre-mRNA domain containing 1A pseudogene
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plaque enriched lncRNA in atherosclerotic and inflammatory bowel macrophage trong>regulationtrong>
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p53 trong>regulationtrong> associated lncRNA
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cytotoxic and regulatory T cell molecule
The CRTAM gene is upregulated in CD4 (see MIM 186940)-trong>positivetrong> and CD8 (see CD8A; MIM 186910)-trong>positivetrong> T cells and encodes a type I transmembrane protein with V and C1-like Ig domains (Yeh et al., 2008 [PubMed 18329370]).[supplied by OMIM, Feb 2009]
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marginal zone B and B1 cell-specific protein
Involved in trong>positivetrong> trong>regulationtrong> trong>oftrong> cell population proliferation. Located in cytoplasm and extracellular region. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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speedy/RINGO cell cycle regulator family member E12, pseudogene
Predicted to enable protein kinase binding activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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cell cycle exit and neuronal differentiation protein 1-like
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cell division cycle 27 pseudogene 10
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cell division cycle 27 pseudogene 11
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cell division cycle associated 8 pseudogene
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B-cell translocation gene 4
The protein encoded by this gene is a member trong>oftrong> the BTG/Tob family. This family has structurally related proteins that appear to have antiproliferative properties. This encoded protein can induce G1 arrest in the cell cycle. [provided by RefSeq, Jul 2008]
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B-cell translocation gene 1, anti-proliferative
This gene is a member trong>oftrong> an anti-proliferative gene family that regulates cell growth and differentiation. Expression trong>oftrong> this gene is highest in the G0/G1 phases trong>oftrong> the cell cycle and downregulated when cells progressed through G1. The encoded protein interacts with several nuclear receptors, and functions as a coactivator trong>oftrong> cell differentiation. This locus has been shown to be involved in a t(8;12)(q24;q22) chromosomal translocation in a case trong>oftrong> B-cell chronic lymphocytic leukemia. [provided by RefSeq, Oct 2008]
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T cell receptor alpha variable 23/delta variable 6
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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putative glycine-rich cell wall structural protein 1
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mediator trong>oftrong> cell motility 1 pseudogene 4
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mediator trong>oftrong> cell motility 1 pseudogene 2
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mediator trong>oftrong> cell motility 1 pseudogene 3
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programmed cell death 6 pseudogene
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myeloid cell leukemia 1
This gene encodes an anti-apoptotic protein, which is a member trong>oftrong> the Bcl-2 family. Alternative splicing results in multiple transcript variants. The longest gene product (istrong>oftrong>orm 1) enhances cell survival by inhibiting apoptosis while the alternatively spliced shorter gene products (istrong>oftrong>orm 2 and istrong>oftrong>orm 3) promote apoptosis and are death-inducing. [provided by RefSeq, Oct 2010]
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T cell receptor beta joining 2-4
Predicted to be involved in adaptive immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta joining 2-5
Predicted to be involved in adaptive immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta joining 2-6
Predicted to be involved in adaptive immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta joining 2-7
Predicted to be involved in adaptive immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta joining 2-1
Predicted to be involved in adaptive immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta joining 2-2
Predicted to be involved in adaptive immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta joining 2-3
Predicted to be involved in adaptive immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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cell cycle exit and neuronal differentiation 1
The protein encoded by this gene is a neuron-specific protein. The similar protein in pig enhances neuroblastoma cell differentiation in vitro and may be involved in neuronal differentiation in vivo. Multiple pseudogenes have been reported for this gene. [provided by RefSeq, Jul 2008]
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proliferating cell nuclear antigen
The protein encoded by this gene is found in the nucleus and is a ctrong>oftrong>actor trong>oftrong> DNA polymerase delta. The encoded protein acts as a homotrimer and helps increase the processivity trong>oftrong> leading strand synthesis during DNA replication. In response to DNA damage, this protein is ubiquitinated and is involved in the RAD6-dependent DNA repair pathway. Two transcript variants encoding the same protein have been found for this gene. Pseudogenes trong>oftrong> this gene have been described on chromosome 4 and on the X chromosome. [provided by RefSeq, Jul 2008]
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BOC cell adhesion associated, oncogene regulated
The protein encoded by this gene is a member trong>oftrong> the immunoglobulin/fibronectin type III repeat family. It is a component trong>oftrong> a cell-surface receptor complex that mediates cell-cell interactions between muscle precursor cells, and promotes myogenic differentiation. Alternative splicing results in multiple transcript variants encoding different istrong>oftrong>orms. [provided by RefSeq, Sep 2014]
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T cell receptor beta variable 20-1
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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cell adhesion associated, oncogene regulated pseudogene
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cell division cycle 34
The protein encoded by this gene is a member trong>oftrong> the ubiquitin-conjugating enzyme family. Ubiquitin-conjugating enzyme catalyzes the covalent attachment trong>oftrong> ubiquitin to other proteins. This protein is a part trong>oftrong> the large multiprotein complex, which is required for ubiquitin-mediated degradation trong>oftrong> cell cycle G1 regulators, and for the initiation trong>oftrong> DNA replication. [provided by RefSeq, Jul 2008]
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cell division cycle 37
The protein encoded by this gene is highly similar to Cdc 37, a cell division cycle control protein trong>oftrong> Sacchromyces cerevisiae. This protein is a molecular chaperone with specific function in cell signal transduction. It has been shown to form complex with Hsp90 and a variety trong>oftrong> protein kinases including CDK4, CDK6, SRC, RAF-1, MOK, as well as eIF2 alpha kinases. It is thought to play a critical role in directing Hsp90 to its target kinases. [provided by RefSeq, Jul 2008]
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B-cell CLL/lymphoma 9
BCL9 is associated with B-cell acute lymphoblastic leukemia. It may be a target trong>oftrong> translocation in B-cell malignancies with abnormalities trong>oftrong> 1q21. Its function is unknown. The overexpression trong>oftrong> BCL9 may be trong>oftrong> pathogenic significance in B-cell malignancies. [provided by RefSeq, Jul 2008]
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B-cell CLL/lymphoma 6
The protein encoded by this gene is a zinc finger transcription factor and contains an N-terminal POZ domain. This protein acts as a sequence-specific repressor trong>oftrong> transcription, and has been shown to modulate the transcription trong>oftrong> STAT-dependent IL-4 responses trong>oftrong> B cells. This protein can interact with a variety trong>oftrong> POZ-containing proteins that function as transcription corepressors. This gene is found to be frequently translocated and hypermutated in diffuse large-cell lymphoma (DLCL), and may be involved in the pathogenesis trong>oftrong> DLCL. Alternatively spliced transcript variants encoding different protein istrong>oftrong>orms have been found for this gene. [provided by RefSeq, Aug 2015]
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B-cell CLL/lymphoma 3
This gene is a proto-oncogene candidate. It is identified by its translocation into the immunoglobulin alpha-locus in some cases trong>oftrong> B-cell leukemia. The protein encoded by this gene contains seven ankyrin repeats, which are most closely related to those found in I kappa B proteins. This protein functions as a transcriptional co-activator that activates through its association with NF-kappa B homodimers. The expression trong>oftrong> this gene can be induced by NF-kappa B, which forms a part trong>oftrong> the autoregulatory loop that controls the nuclear residence trong>oftrong> p50 NF-kappa B. [provided by RefSeq, Jul 2008]
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B-cell CLL/lymphoma 2
This gene encodes an integral outer mitochondrial membrane protein that blocks the apoptotic death trong>oftrong> some cells such as lymphocytes. Constitutive expression trong>oftrong> BCL2, such as in the case trong>oftrong> translocation trong>oftrong> BCL2 to Ig heavy chain locus, is thought to be the cause trong>oftrong> follicular lymphoma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]
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histone cell cycle regulator
This gene encodes a histone chaperone that preferentially places the variant histone H3.3 in nucleosomes. Orthologs trong>oftrong> this gene in yeast, flies, and plants are necessary for the formation trong>oftrong> transcriptionally silent heterochomatin. This gene plays an important role in the formation trong>oftrong> the senescence-associated heterochromatin foci. These foci likely mediate the irreversible cell cycle changes that occur in senescent cells. It is considered the primary candidate gene in some haploinsufficiency syndromes such as DiGeorge syndrome, and insufficient production trong>oftrong> the gene may disrupt normal embryonic development. [provided by RefSeq, Jul 2008]
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T cell receptor alpha joining 32
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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insulin-like 3 (Leydig cell)
This gene encodes a member trong>oftrong> the insulin-like hormone superfamily. The encoded protein is mainly produced in gonadal tissues. Studies trong>oftrong> the mouse counterpart suggest that this gene may be involved in the development trong>oftrong> urogenital tract and female fertility. This protein may also act as a hormone to regulate growth and differentiation trong>oftrong> gubernaculum, and thus mediating intra-abdominal testicular descent. Mutations in this gene may lead to cryptorchidism. Alternate splicing results in multiple transcript variants. [provided by RefSeq, May 2012]
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killer cell immunoglobulin-like receptor 3DL1
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killer cell immunoglobulin-like receptor, three domains, X1
Predicted to be involved in immune response-regulating signaling pathway. Predicted to be located in extracellular region. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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myeloid cell nuclear differentiation antigen
The myeloid cell nuclear differentiation antigen (MNDA) is detected only in nuclei trong>oftrong> cells trong>oftrong> the granulocyte-monocyte lineage. A 200-amino acid region trong>oftrong> human MNDA is strikingly similar to a region in the proteins encoded by a family trong>oftrong> interferon-inducible mouse genes, designated Ifi-201, Ifi-202, and Ifi-203, that are not regulated in a cell- or tissue-specific fashion. The 1.8-kb MNDA mRNA, which contains an interferon-stimulated response element in the 5-prime untranslated region, was significantly upregulated in human monocytes exposed to interferon alpha. MNDA is located within 2,200 kb trong>oftrong> FCER1A, APCS, CRP, and SPTA1. In its pattern trong>oftrong> expression and/or trong>regulationtrong>, MNDA resembles IFI16, suggesting that these genes participate in blood cell-specific responses to interferons. [provided by RefSeq, Jul 2008]
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T cell receptor gamma joining 2
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T cell receptor gamma joining 1
Predicted to be involved in adaptive immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor gamma joining P
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T cell receptor beta variable 6-8
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 6-9
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 6-5
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 6-6
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 6-7 (non-functional)
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 6-2 (gene/pseudogene)
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 6-3
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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proliferating cell nuclear antigen pseudogene 1
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proliferating cell nuclear antigen pseudogene 4
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T cell receptor beta constant 1
Predicted to be involved in T cell receptor signaling pathway; adaptive immune response; and alpha-beta T cell activation. Predicted to be located in membrane. Predicted to be part trong>oftrong> alpha-beta T cell receptor complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta constant 2
Predicted to be involved in T cell receptor signaling pathway; adaptive immune response; and alpha-beta T cell activation. Part trong>oftrong> alpha-beta T cell receptor complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 21-1 (pseudogene)
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cell death-inducing p53 target 1
Predicted to enable zinc ion binding activity. Acts upstream trong>oftrong> or within intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator. Located in cytoplasmic side trong>oftrong> late endosome membrane; cytoplasmic side trong>oftrong> lysosomal membrane; and nucleus. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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cell division cycle associated 8 pseudogene
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scribbled planar cell polarity protein
This gene encodes a protein that was identified as being similar to the Drosophila scribble protein. The mammalian protein is involved in tumor suppression pathways. As a scaffold protein involved in cell polarization processes, this protein binds to many other proteins. The encoded protein binds to papillomavirus E6 protein via its PDZ domain and the C-terminus trong>oftrong> E6. Two alternatively spliced transcript variants that encode different protein istrong>oftrong>orms have been found for this gene. [provided by RefSeq, Nov 2011]
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T-cell activation RhoGTPase activating protein
This gene encodes a member trong>oftrong> the Rho GTPase-activator protein superfamily. The encoded protein may function as a Rho GTPase-activating protein. Alterations in this gene may be associated with several diseases, including rheumatoid arthritis, celiac disease, and multiple sclerosis. Alternate splicing results in multiple transcript variants encoding distinct istrong>oftrong>orms. [provided by RefSeq, Jul 2013]
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neuronal cell adhesion molecule
Cell adhesion molecules (CAMs) are members trong>oftrong> the immunoglobulin superfamily. This gene encodes a neuronal cell adhesion molecule with multiple immunoglobulin-like C2-type domains and fibronectin type-III domains. This ankyrin-binding protein is involved in neuron-neuron adhesion and promotes directional signaling during axonal cone growth. This gene is also expressed in non-neural tissues and may play a general role in cell-cell communication via signaling from its intracellular domain to the actin cytoskeleton during directional cell migration. Allelic variants trong>oftrong> this gene have been associated with autism and addiction vulnerability. Alternative splicing results in multiple transcript variants encoding different istrong>oftrong>orms. [provided by RefSeq, Jul 2008]
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mediator trong>oftrong> cell motility 1 pseudogene 1
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defensin, alpha 6, Paneth cell-specific
Defensins are a family trong>oftrong> antimicrobial and cytotoxic peptides thought to be involved in host defense. They are abundant in the granules trong>oftrong> neutrophils and also found in the epithelia trong>oftrong> mucosal surfaces such as those trong>oftrong> the intestine, respiratory tract, urinary tract, and vagina. Members trong>oftrong> the defensin family are highly similar in protein sequence and distinguished by a conserved cysteine motif. Several alpha defensin genes appear to be clustered on chromosome 8. The protein encoded by this gene, defensin, alpha 6, is highly expressed in the secretory granules trong>oftrong> Paneth cells trong>oftrong> the small intestine, and likely plays a role in host defense trong>oftrong> human bowel. [provided by RefSeq, Oct 2014]
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defensin, alpha 5, Paneth cell-specific
Defensins are a family trong>oftrong> antimicrobial and cytotoxic peptides thought to be involved in host defense. They are abundant in the granules trong>oftrong> neutrophils and also found in the epithelia trong>oftrong> mucosal surfaces such as those trong>oftrong> the intestine, respiratory tract, urinary tract, and vagina. Members trong>oftrong> the defensin family are highly similar in protein sequence and distinguished by a conserved cysteine motif. Several trong>oftrong> the alpha defensin genes appear to be clustered on chromosome 8. The protein encoded by this gene, defensin, alpha 5, is highly expressed in the secretory granules trong>oftrong> Paneth cells trong>oftrong> the ileum. [provided by RefSeq, Oct 2014]
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T cell receptor beta variable 23/OR9-2 (non-functional)
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programmed cell death 1 ligand 2
Involved in negative trong>regulationtrong> trong>oftrong> activated T cell proliferation; negative trong>regulationtrong> trong>oftrong> interleukin-10 production; and negative trong>regulationtrong> trong>oftrong> type II interferon production. Predicted to be located in plasma membrane. Predicted to be active in external side trong>oftrong> plasma membrane. Biomarker trong>oftrong> pulmonary tuberculosis. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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downregulated RNA in cancer, inhibitor trong>oftrong> cell invasion and migration
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T cell receptor beta variable 30 (gene/pseudogene)
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T-cell leukemia translocation altered
Involved in negative trong>regulationtrong> trong>oftrong> osteoclast differentiation and osteoclast fusion. Predicted to be located in membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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Sertoli cell-only syndrome, Y-linked
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carcinoembryonic antigen-related cell adhesion molecule 1 (biliary glycoprotein) pseudogene
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zyg-11 family member B, cell cycle regulator
Involved in trong>positivetrong> trong>regulationtrong> trong>oftrong> proteasomal ubiquitin-dependent protein catabolic process and protein quality control for misfolded or incompletely synthesized proteins. Part trong>oftrong> Cul2-RING ubiquitin ligase complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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zyg-11 family member A, cell cycle regulator
Predicted to be part trong>oftrong> Cul2-RING ubiquitin ligase complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 3-1
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 7-9
Predicted to enable MHC protein binding activity and peptide antigen binding activity. Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 7-8
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 7-1 (non-functional)
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 7-3
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 7-2
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 7-5 (pseudogene)
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T cell receptor beta variable 7-4 (gene/pseudogene)
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 7-7
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 7-6
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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hexokinase 3 (white cell)
Hexokinases phosphorylate glucose to produce glucose-6-phosphate, the first step in most glucose metabolism pathways. This gene encodes hexokinase 3. Similar to hexokinases 1 and 2, this allosteric enzyme is inhibited by its product glucose-6-phosphate. [provided by RefSeq, Apr 2009]
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cell wall biogenesis 43 C-terminal homolog (S. cerevisiae)
Predicted to be involved in GPI anchor biosynthetic process. Predicted to act upstream trong>oftrong> or within several processes, including cerebrospinal fluid circulation; establishment trong>oftrong> protein localization; and protein N-linked glycosylation. Predicted to be located in extracellular region and membrane. Predicted to be active in endoplasmic reticulum. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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mature T-cell proliferation 1
This gene was identified by involvement in some t(X;14) translocations associated with mature T-cell proliferations. This region has a complex gene structure, with a common promoter and 5' exon spliced to two different sets trong>oftrong> 3' exons that encode two different proteins. This gene represents the upstream 13 kDa protein that is a member trong>oftrong> the TCL1 family. This protein may be involved in leukemogenesis. [provided by RefSeq, Mar 2009]
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cell division cycle associated 2
This gene encodes a targeting subunit trong>oftrong> the cell-cycle associated protein, protein phosphatase 1, with a role in targeting this protein to chromatin during anaphase. These two proteins comprise a phosphatase complex that is involved in nuclear envelope reformation and trong>regulationtrong> trong>oftrong> the DNA damage response. The encoded protein may also play a role in cancer progression. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]
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cell division cycle associated 3
Predicted to be involved in cell division and protein ubiquitination. Located in adherens junction. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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cell division cycle associated 7
This gene was identified as a c-Myc responsive gene, and behaves as a direct c-Myc target gene. Overexpression trong>oftrong> this gene is found to enhance the transformation trong>oftrong> lymphoblastoid cells, and it complements a transformation-defective Myc Box II mutant, suggesting its involvement in c-Myc-mediated cell transformation. Two alternatively spliced transcript variants encoding distinct istrong>oftrong>orms have been reported. [provided by RefSeq, Jul 2008]
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cell division cycle associated 4
This gene encodes a protein that belongs to the E2F family trong>oftrong> transcription factors. This protein regulates E2F-dependent transcriptional activation and cell proliferation, mainly through the E2F/retinoblastoma protein pathway. It also functions in the trong>regulationtrong> trong>oftrong> JUN oncogene expression. This protein shows distinctive nuclear-mitotic apparatus distribution, it is involved in spindle organization from prometaphase, and may also play a role as a midzone factor involved in chromosome segregation or cytokinesis. Two alternatively spliced transcript variants encoding the same protein have been noted for this gene. Two pseudogenes have also been identified on chromosome 1. [provided by RefSeq, May 2014]
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cell division cycle associated 5
Predicted to enable chromatin binding activity. Involved in chromosome organization; double-strand break repair; and trong>positivetrong> trong>regulationtrong> trong>oftrong> exit from mitosis. Located in nucleoplasm. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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cell division cycle associated 8
This gene encodes a component trong>oftrong> the chromosomal passenger complex. This complex is an essential regulator trong>oftrong> mitosis and cell division. This protein is cell-cycle regulated and is required for chromatin-induced microtubule stabilization and spindle formation. Alternate splicing results in multiple transcript variants. Pseudgenes trong>oftrong> this gene are found on chromosomes 7, 8 and 16. [provided by RefSeq, Apr 2013]
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mucin 4, cell surface associated
The major constituents trong>oftrong> mucus, the viscous secretion that covers epithelial surfaces such as those in the trachea, colon, and cervix, are highly glycosylated proteins called mucins. These glycoproteins play important roles in the protection trong>oftrong> the epithelial cells and have been implicated in epithelial renewal and differentiation. This gene encodes an integral membrane glycoprotein found on the cell surface, although secreted istrong>oftrong>orms may exist. At least two dozen transcript variants trong>oftrong> this gene have been found, although for many trong>oftrong> them the full-length transcript has not been determined or they are found only in tumor tissues. This gene contains a region in the coding sequence which has a variable number (>100) trong>oftrong> 48 nt tandem repeats. [provided by RefSeq, Jul 2008]
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natural killer cell susceptibility 1
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cell migration inducing protein, hyaluronan binding
Enables several functions, including clathrin heavy chain binding activity; hyaluronic acid binding activity; and hyalurononglucosaminidase activity. Involved in several processes, including hyaluronan catabolic process; trong>positivetrong> trong>regulationtrong> trong>oftrong> protein phosphorylation; and trong>positivetrong> trong>regulationtrong> trong>oftrong> protein targeting to membrane. Located in several cellular components, including clathrin-coated endocytic vesicle; endoplasmic reticulum; and nucleus. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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epithelial cell adhesion molecule
This gene encodes a carcinoma-associated antigen and is a member trong>oftrong> a family that includes at least two type I membrane proteins. This antigen is expressed on most normal epithelial cells and gastrointestinal carcinomas and functions as a homotypic calcium-independent cell adhesion molecule. The antigen is being used as a target for immunotherapy treatment trong>oftrong> human carcinomas. Mutations in this gene result in congenital tufting enteropathy. [provided by RefSeq, Dec 2008]
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T cell receptor alpha joining 29
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 28
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 27
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 26
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 25 (non-functional)
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 24
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 23
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 22
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 21
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 20
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 5
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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regulator trong>oftrong> cell cycle
This gene is thought to regulate cell cycle progression. It is induced by p53 in response to DNA damage, or by sublytic levels trong>oftrong> complement system proteins that result in activation trong>oftrong> the cell cycle. The encoded protein localizes to the cytoplasm during interphase and to centrosomes during mitosis. The protein forms a complex with polo-like kinase 1. The protein also translocates to the nucleus in response to treatment with complement system proteins, and can associate with and increase the kinase activity trong>oftrong> cell division cycle 2 protein. In different assays and cell types, overexpression trong>oftrong> this protein has been shown to activate or suppress cell cycle progression. [provided by RefSeq, Jul 2008]
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T-cell leukemia/lymphoma 6 (non-protein coding)
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T-cell leukemia/lymphoma 4
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5-hydroxymethylcytosine (hmC) binding, ES cell-specific
Enables DNA-(abasic site) binding activity; protein-DNA covalent cross-linking activity; and single-stranded DNA binding activity. Involved in interstrand cross-link repair; protein-DNA covalent cross-linking repair; and somatic hypermutation trong>oftrong> immunoglobulin genes. Is active in replication fork. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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host cell factor C1 regulator 1 (XPO1 dependent)
Located in nucleoplasm. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor alpha variable 29/delta variable 5 (gene/pseudogene)
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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mucin 17, cell surface associated
The protein encoded by this gene is a membrane-bound mucin that provides protection to gut epithelial cells. The encoded protein contains about 60 tandem repeats, with each repeat being around 60 aa. N-glycosylation enables the encoded protein to localize on the cell surface, while the C-terminus interacts with the scaffold protein PDZ domain containing 1 (PDZK1). Two transcript variants, one protein-coding and the other non-protein coding, have been found for this gene. [provided by RefSeq, Nov 2015]
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mucin 16, cell surface associated
This gene encodes a protein that is a member trong>oftrong> the mucin family. Mucins are high molecular weight, O-glycosylated proteins that play an important role in forming a protective mucous barrier, and are found on the apical surfaces trong>oftrong> the epithelia. The encoded protein is a membrane-tethered mucin that contains an extracellular domain at its amino terminus, a large tandem repeat domain, and a transmembrane domain with a short cytoplasmic domain. The amino terminus is highly glycosylated, while the repeat region contains 156 amino acid repeats unit that are rich in serines, threonines, and prolines. Interspersed within the repeats are Sea urchin sperm protein Enterokinase and Agrin (SEA) modules, leucine-rich repeats and ankyrin (ANK) repeats. These regions together form the ectodomain, and there is a potential cleavage site found near an SEA module close to the transmembrane domain. This protein is thought to play a role in forming a barrier, protecting epithelial cells from pathogens. Products trong>oftrong> this gene have been used as a marker for different cancers, with higher expression levels associated with poorer outcomes. [provided by RefSeq, May 2017]
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mucin 15, cell surface associated
Predicted to be located in Golgi lumen and plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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mucin 13, cell surface associated
Epithelial mucins, such as MUC13, are a family trong>oftrong> secreted and cell surface glycoproteins expressed by ductal and glandular epithelial tissues (Williams et al., 2001 [PubMed 11278439]).[supplied by OMIM, Jul 2008]
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mucin 12, cell surface associated
This gene encodes an integral membrane glycoprotein that is a member trong>oftrong> the mucin family. Mucins are O-glycosylated proteins that play an essential role in forming protective mucous barriers on epithelial surfaces and have been implicated in epithelial renewal and differentiation. These glycoproteins also play a role in intracellular signaling. This protein is expressed on the apical membrane surface trong>oftrong> epithelial cells that line the mucosal surfaces trong>oftrong> many different tissues including the colon, pancreas, prostate, and uterus. The expression trong>oftrong> this gene is downregulated in colorectal cancer tissue. [provided by RefSeq, Apr 2017]
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thyroid carcinoma, Hurthle cell
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neural precursor cell expressed, developmentally down-regulated 8
Enables ubiquitin protein ligase binding activity. Acts upstream trong>oftrong> or within protein neddylation. Located in cytosol and nucleoplasm. Biomarker trong>oftrong> Parkinson's disease and malignant astrocytoma. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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neural precursor cell expressed, developmentally down-regulated 9
The protein encoded by this gene is a member trong>oftrong> the CRK-associated substrates family. Members trong>oftrong> this family are adhesion docking molecules that mediate protein-protein interactions for signal transduction pathways. This protein is a focal adhesion protein that acts as a scaffold to regulate signaling complexes important in cell attachment, migration and invasion as well as apoptosis and the cell cycle. This protein has also been reported to have a role in cancer metastasis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2012]
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neural precursor cell expressed, developmentally down-regulated 1
Predicted to enable gamma-tubulin binding activity. Predicted to be involved in microtubule nucleation and mitotic cell cycle. Located in centrosome; cytosol; and nuclear lumen. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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hematopoietic cell-specific Lyn substrate 1
Enables RNA polymerase II-specific DNA-binding transcription factor binding activity; protein kinase binding activity; and signaling adaptor activity. Involved in several processes, including granulocyte colony-stimulating factor signaling pathway; trong>positivetrong> trong>regulationtrong> trong>oftrong> macromolecule metabolic process; and trong>positivetrong> trong>regulationtrong> trong>oftrong> phosphatidylinositol 3-kinase/protein kinase B signal transduction. Located in cytosol; nucleus; and plasma membrane. Part trong>oftrong> transcription regulator complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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E2F1-regulated inhibitor trong>oftrong> cell death (non-protein coding)
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T cell receptor gamma variable 5P (pseudogene)
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par-3 family cell polarity regulator
This gene encodes a member trong>oftrong> the PARD protein family. PARD family members interact with other PARD family members and other proteins; they affect asymmetrical cell division and direct polarized cell growth. Multiple alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Oct 2011]
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mal, T-cell differentiation protein-like pseudogene
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CD244 molecule, natural killer cell receptor 2B4
This gene encodes a cell surface receptor expressed on natural killer (NK) cells (and some T cells) that mediate non-major histocompatibility complex (MHC) restricted killing. The interaction between NK-cell and target cells via this receptor is thought to modulate NK-cell cytolytic activity. Alternatively spliced transcript variants encoding different istrong>oftrong>orms have been found for this gene.[provided by RefSeq, Oct 2009]
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carboxypeptidase A3 (mast cell)
This gene encodes a member trong>oftrong> the carboxypeptidase A family trong>oftrong> zinc metalloproteases. The encoded preproprotein is proteolytically processed to generate a mature protease that is released by mast cells and may be involved in the degradation trong>oftrong> endogenous proteins and the inactivation trong>oftrong> venom-associated peptides. Expression trong>oftrong> this gene may be elevated in human asthma patients. [provided by RefSeq, Nov 2015]
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LIM and senescent cell antigen-like domains 3-like
Predicted to enable metal ion binding activity. Predicted to be located in cytoplasm; focal adhesion; and plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor gamma variable 10 (non-functional)
Predicted to be involved in adaptive immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3
This gene encodes a subunit trong>oftrong> a large protein complex known as a vacuolar H+-ATPase (V-ATPase). The protein complex acts as a pump to move protons across the membrane. This movement trong>oftrong> protons helps regulate the pH trong>oftrong> cells and their surrounding environment. V-ATPase dependent organelle acidification is necessary for such intracellular processes as protein sorting, zymogen activation, and receptor-mediated endocytosis. V-ATPase is comprised trong>oftrong> a cytosolic V1 domain and a transmembrane V0 domain. Alternative splicing results in multiple transcript variants. Mutations in this gene are associated with infantile malignant osteopetrosis. [provided by RefSeq, May 2017]
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frequently rearranged in advanced T-cell lymphomas 1
The protein encoded by this gene belongs to the GSK-3-binding protein family. The protein inhibits GSK-3-mediated phosphorylation trong>oftrong> beta-catenin and trong>positivetrong>ly regulates the Wnt signaling pathway. It may function in tumor progression and in lymphomagenesis. [provided by RefSeq, Oct 2008]
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frequently rearranged in advanced T-cell lymphomas 2
The protein encoded by this intronless gene belongs to the GSK-3-binding protein family. Studies show that this protein plays a role as a trong>positivetrong> regulator trong>oftrong> the WNT signaling pathway. It may be upregulated in tumor progression. [provided by RefSeq, Jul 2008]
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killer cell immunoglobulin-like receptor 2DL2
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stromal cell-derived factor 2-like 1
Enables misfolded protein binding activity. Involved in chaperone ctrong>oftrong>actor-dependent protein refolding. Located in endoplasmic reticulum. Part trong>oftrong> protein folding chaperone complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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vegetative cell wall protein gp1-like
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Basal cell carcinoma, susceptibility to, 5
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T cell receptor beta variable 21/OR9-2 (pseudogene)
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vegetative cell wall protein gp1-like
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melanoma cell adhesion molecule
Involved in glomerular filtration and vascular wound healing. Acts upstream trong>oftrong> or within angiogenesis. Located in external side trong>oftrong> plasma membrane. Biomarker trong>oftrong> chronic obstructive pulmonary disease and uveal melanoma. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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killer cell lectin-like receptor subfamily G, member 1
Natural killer (NK) cells are lymphocytes that can mediate lysis trong>oftrong> certain tumor cells and virus-infected cells without previous activation. They can also regulate specific humoral and cell-mediated immunity. The protein encoded by this gene belongs to the killer cell lectin-like receptor (KLR) family, which is a group trong>oftrong> transmembrane proteins preferentially expressed in NK cells. Studies in mice suggested that the expression trong>oftrong> this gene may be regulated by MHC class I molecules. [provided by RefSeq, Jun 2016]
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malignant T cell amplified sequence 1
Enables RNA cap binding activity; ribosomal small subunit binding activity; and translation factor activity, non-nucleic acid binding. Involved in IRES-dependent viral translational initiation; cytoplasmic translational initiation; and ribosome disassembly. Is active in cytoplasm. Implicated in primary immunodeficiency disease. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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cell division cycle and apoptosis regulator 1
Enables RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; nuclear receptor coactivator activity; and transcription corepressor activity. Involved in trong>positivetrong> trong>regulationtrong> trong>oftrong> cell migration and trong>positivetrong> trong>regulationtrong> trong>oftrong> cell population proliferation. Acts upstream trong>oftrong> or within trong>positivetrong> trong>regulationtrong> trong>oftrong> apoptotic process. Located in nuclear envelope lumen. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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cell cycle and apoptosis regulator 2
Enables RNA polymerase II complex binding activity and enzyme inhibitor activity. Involved in several processes, including mitochondrial fragmentation involved in apoptotic process; trong>regulationtrong> trong>oftrong> primary metabolic process; and trong>regulationtrong> trong>oftrong> signal transduction. Located in several cellular components, including mitochondrial matrix; nucleoplasm; and spindle. Part trong>oftrong> DBIRD complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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programmed cell death 2 pseudogene
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meteorin, glial cell differentiation regulator
Meteorin regulates glial cell differentiation and promotes the formation trong>oftrong> axonal networks during neurogenesis (Nishino et al., 2004 [PubMed 15085178]).[supplied by OMIM, Mar 2008]
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Purkinje cell protein 4
Enables calcium ion binding activity and calmodulin binding activity. Involved in trong>positivetrong> trong>regulationtrong> trong>oftrong> CAMKK-AMPK signaling cascade and trong>positivetrong> trong>regulationtrong> trong>oftrong> neuron differentiation. Located in cytosol and nucleus. Part trong>oftrong> protein-containing complex. Biomarker trong>oftrong> Huntington's disease and leiomyoma. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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Purkinje cell protein 2
Predicted to enable guanyl-nucleotide exchange factor activity. Predicted to act upstream trong>oftrong> or within G protein-coupled opsin signaling pathway. Predicted to be located in neuronal cell body. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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cutaneous T-cell lymphoma-associated antigen 1
Predicted to be involved in endoplasmic reticulum to Golgi vesicle-mediated transport; protein secretion; and vesicle cargo loading. Predicted to be located in membrane. Predicted to be active in endoplasmic reticulum exit site and endoplasmic reticulum membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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germ cell-less, spermatogenesis associated 1 pseudogene 1
This locus shares a high degree trong>oftrong> identity with the multi-exon germ cell-less gene on chromosome 2. Despite its single-exon nature, this chromosome 5 locus contains an open reading frame that could putatively encode a full-length germ cell-less related protein. [provided by RefSeq, Jul 2008]
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germ cell-less, spermatogenesis associated 1 pseudogene 2
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T cell receptor alpha variable 14/delta variable 4
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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killer cell lectin-like receptor subfamily G, member 2
Predicted to enable carbohydrate binding activity. Predicted to be located in membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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small cell cancer trong>oftrong> the lung
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killer cell lectin-like receptor subfamily B, member 1
Natural killer (NK) cells are lymphocytes that mediate cytotoxicity and secrete cytokines after immune stimulation. Several genes trong>oftrong> the C-type lectin superfamily, including the rodent NKRP1 family trong>oftrong> glycoproteins, are expressed by NK cells and may be involved in the trong>regulationtrong> trong>oftrong> NK cell function. The KLRB1 protein contains an extracellular domain with several motifs characteristic trong>oftrong> C-type lectins, a transmembrane domain, and a cytoplasmic domain. The KLRB1 protein is classified as a type II membrane protein because it has an external C terminus. [provided by RefSeq, Jul 2008]
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Disrupted in B-cell neoplasia
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T cell receptor beta diversity 1
Predicted to be involved in adaptive immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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killer cell immunoglobulin-like receptor 2DS1
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vegetative cell wall protein gp1-like
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cell death-inducing DFFA-like effector c pseudogene
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cell division cycle 20B
Predicted to enable anaphase-promoting complex binding activity and ubiquitin ligase activator activity. Involved in de novo centriole assembly. Located in deuterosome. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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Basal cell carcinoma, susceptibility to, 6
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VANGL planar cell polarity protein 1
This gene encodes a member trong>oftrong> the tretraspanin family. The encoded protein may be involved in mediating intestinal trefoil factor induced wound healing in the intestinal mucosa. Mutations in this gene are associated with neural tube defects. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]
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T cell receptor alpha joining 16
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 17
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 14
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 15
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 12
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 13
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 10
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 11
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 18
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 19 (non-functional)
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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B-cell CLL/lymphoma 6, member B
Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in negative trong>regulationtrong> trong>oftrong> transcription by RNA polymerase II; trong>regulationtrong> trong>oftrong> cytokine production; and trong>regulationtrong> trong>oftrong> immune system process. Predicted to be located in nucleus. Predicted to be active in nucleoplasm. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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SWAP switching B-cell complex 70kDa subunit
Enables cadherin binding activity. Predicted to be involved in trong>regulationtrong> trong>oftrong> small GTPase mediated signal transduction. Predicted to act upstream trong>oftrong> or within isotype switching. Located in actin cytoskeleton; cytoplasm; and plasma membrane. Is active in postsynapse. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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cell division cycle 5-like
The protein encoded by this gene shares a significant similarity with Schizosaccharomyces pombe cdc5 gene product, which is a cell cycle regulator important for G2/M transition. This protein has been demonstrated to act as a trong>positivetrong> regulator trong>oftrong> cell cycle G2/M progression. It was also found to be an essential component trong>oftrong> a non-snRNA spliceosome, which contains at least five additional protein factors and is required for the second catalytic step trong>oftrong> pre-mRNA splicing. [provided by RefSeq, Jul 2008]
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killer cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 5
Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets trong>oftrong> T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content trong>oftrong> the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number trong>oftrong> extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets trong>oftrong> HLA class I molecules; thus, KIR proteins are thought to play an important role in trong>regulationtrong> trong>oftrong> the immune response. [provided by RefSeq, Jul 2008]
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killer cell immunoglobulin-like receptor, three domains, pseudogene
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killer cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 2
Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets trong>oftrong> T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content trong>oftrong> the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number trong>oftrong> extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets trong>oftrong> HLA class I molecules; thus, KIR proteins are thought to play an important role in trong>regulationtrong> trong>oftrong> the immune response. This gene represents a haplotype-specific family member that encodes a protein with a short cytoplasmic tail. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]
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cell death regulator Aven-like
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speedy/RINGO cell cycle regulator family member E10, pseudogene
Enables acetylcholine receptor regulator activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta joining 2-2P (non-functional)
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follicular dendritic cell secreted protein
This gene encodes a small secreted protein that is expressed in follicular dendritic cells. This protein specifically binds to activated B cells, and functions as a regulator trong>oftrong> antibody responses. It is also thought to contribute to tumor metastases by promoting cancer cell migration and invasion. [provided by RefSeq, Dec 2011]
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T cell receptor beta variable 11-3
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 11-1
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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early B-cell factor 4
EBF4 belongs to the conserved Olf/EBF family trong>oftrong> helix-loop-helix transcription factors, members trong>oftrong> which play important roles in neural development and B-cell maturation (Wang et al., 2002 [PubMed 12139918]).[supplied by OMIM, Mar 2008]
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early B-cell factor 3
This gene encodes a member trong>oftrong> the early B-cell factor (EBF) family trong>oftrong> DNA binding transcription factors. EBF proteins are involved in B-cell differentiation, bone development and neurogenesis, and may also function as tumor suppressors. The encoded protein inhibits cell survival through the trong>regulationtrong> trong>oftrong> genes involved in cell cycle arrest and apoptosis, and aberrant methylation or deletion trong>oftrong> this gene may play a role in multiple malignancies including glioblastoma multiforme and gastric carcinoma. [provided by RefSeq, Sep 2011]
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early B-cell factor 2
The protein encoded by this gene belongs to the COE (Collier/Olf/EBF) family trong>oftrong> non-basic, helix-loop-helix transcription factors that have a well conserved DNA binding domain. The COE family proteins play an important role in variety trong>oftrong> developmental processes. Studies in mouse suggest that this gene may be involved in the differentiation trong>oftrong> osteoblasts. [provided by RefSeq, Oct 2011]
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early B-cell factor 1
Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in trong>positivetrong> trong>regulationtrong> trong>oftrong> transcription by RNA polymerase II. Predicted to act upstream trong>oftrong> or within trong>positivetrong> trong>regulationtrong> trong>oftrong> DNA-templated transcription. Predicted to be located in chromatin. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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cell growth regulator with ring finger domain 1
Predicted to enable metal ion binding activity. Predicted to be involved in negative trong>regulationtrong> trong>oftrong> cell growth. Located in endoplasmic reticulum and nucleoplasm. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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glycosylation dependent cell adhesion molecule 1 (pseudogene)
Predicted to enable cell adhesion molecule binding activity and sulfate binding activity. Predicted to act upstream trong>oftrong> or within response to bacterium. Predicted to be located in extracellular region. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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vegetative cell wall protein gp1
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T cell receptor alpha variable 20
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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cell division cycle associated 7-like
Acts upstream trong>oftrong> or within trong>positivetrong> trong>regulationtrong> trong>oftrong> cell population proliferation. Located in cytosol; fibrillar center; and nucleoplasm. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell immunoreceptor with Ig and ITIM domains
This gene encodes a member trong>oftrong> the PVR (poliovirus receptor) family trong>oftrong> immunoglobin proteins. The product trong>oftrong> this gene is expressed on several classes trong>oftrong> T cells including follicular B helper T cells (TFH). The protein has been shown to bind PVR with high affinity; this binding is thought to assist interactions between TFH and dendritic cells to regulate T cell dependent B cell responses.[provided by RefSeq, Sep 2009]
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multiciliate differentiation and DNA synthesis associated cell cycle protein
This gene encodes a member trong>oftrong> the geminin family trong>oftrong> proteins. The encoded nuclear protein is required for the generation trong>oftrong> 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 trong>oftrong> multiple motile cilia (RGMC). [provided by RefSeq, Sep 2016]
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natural killer cell cytotoxicity receptor 3 ligand 1
B7H6 belongs to the B7 family (see MIM 605402) and is selectively expressed on tumor cells. Interaction trong>oftrong> B7H6 with NKp30 (NCR3; MIM 611550) results in natural killer (NK) cell activation and cytotoxicity (Brandt et al., 2009 [PubMed 19528259]).[supplied by OMIM, Jan 2011]
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killer cell immunoglobulin-like receptor, three domains, long cytoplasmic tail, 1
Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets trong>oftrong> T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content trong>oftrong> the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number trong>oftrong> extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets trong>oftrong> HLA class I molecules; thus, KIR proteins are thought to play an important role in trong>regulationtrong> trong>oftrong> the immune response. [provided by RefSeq, Jul 2008]
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killer cell immunoglobulin-like receptor, three domains, long cytoplasmic tail, 2
Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets trong>oftrong> T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content trong>oftrong> the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number trong>oftrong> extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets trong>oftrong> HLA class I molecules; thus, KIR proteins are thought to play an important role in trong>regulationtrong> trong>oftrong> the immune response. This gene is one trong>oftrong> the `framework` loci that is present on all haplotypes. Alternatively spliced transcript variants encoding multiple istrong>oftrong>orms have been observed for this gene. [provided by RefSeq, Jun 2011]
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killer cell immunoglobulin-like receptor, three domains, long cytoplasmic tail, 3
Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets trong>oftrong> T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content trong>oftrong> the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number trong>oftrong> extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets trong>oftrong> HLA class I molecules; thus, KIR proteins are thought to play an important role in trong>regulationtrong> trong>oftrong> the immune response. This gene is one trong>oftrong> the `framework` loci that is present on all haplotypes. [provided by RefSeq, Jul 2008]
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mediator trong>oftrong> cell motility 1
Involved in trong>regulationtrong> trong>oftrong> microtubule-based process. Located in cytosol and nucleus. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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BH3-like motif containing, cell death inducer
This gene encodes a BH3-like motif containing protein involved in cell death. The encoded protein may induce apoptosis in a caspase-dependent manner. The protein is localized in both the cytoplasm and the mitochondrion. [provided by RefSeq, Aug 2011]
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endothelial cell adhesion molecule
Enables cell-cell adhesion mediator activity. Involved in several processes, including bicellular tight junction assembly; cell-cell adhesion; and trong>regulationtrong> trong>oftrong> actin filament polymerization. Located in cell-cell junction and plasma membrane. Part trong>oftrong> protein-containing complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 24-1
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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B-cell scaffold protein with ankyrin repeats 1
The protein encoded by this gene is a B-cell-specific scaffold protein that functions in B-cell receptor-induced calcium mobilization from intracellular stores. This protein can also promote Lyn-mediated tyrosine phosphorylation trong>oftrong> inositol 1,4,5-trisphosphate receptors. Polymorphisms in this gene are associated with susceptibility to systemic lupus erythematosus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]
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fuzzy planar cell polarity protein
This gene encodes a planar cell polarity protein that is involved in ciliogenesis and directional cell movement. Knockout studies in mice exhibit neural tube defects and defective cilia, and mutations in this gene are associated with neural tube defects in humans. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2012]
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carcinoembryonic antigen-related cell adhesion molecule 19
Predicted to be involved in heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules. Predicted to be located in membrane. Predicted to be active in cell surface. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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carcinoembryonic antigen-related cell adhesion molecule 18
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carcinoembryonic antigen-related cell adhesion molecule 16
The protein encoded by this gene is a secreted glycoprotein that in mouse interacts with tectorial membrane proteins in the inner ear. The encoded adhesion protein is found in cochlear outer hair cells and appears to be important for proper hearing over an extended frequency range. Defects in this gene likely are a cause trong>oftrong> non-syndromic autosomal dominant hearing loss. [provided by RefSeq, May 2012]
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cell death-inducing DFFA-like effector c
This gene encodes a member trong>oftrong> the cell death-inducing DNA fragmentation factor-like effector family. Members trong>oftrong> this family play important roles in apoptosis. The encoded protein promotes lipid droplet formation in adipocytes and may mediate adipocyte apoptosis. This gene is regulated by insulin and its expression is trong>positivetrong>ly correlated with insulin sensitivity. Mutations in this gene may contribute to insulin resistant diabetes. A pseudogene trong>oftrong> this gene is located on the short arm trong>oftrong> chromosome 3. Alternatively spliced transcript variants that encode different istrong>oftrong>orms have been observed for this gene. [provided by RefSeq, Dec 2010]
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cell death-inducing DFFA-like effector a
This gene encodes the homolog trong>oftrong> the mouse protein Cidea that has been shown to activate apoptosis. This activation trong>oftrong> apoptosis is inhibited by the DNA fragmentation factor DFF45 but not by caspase inhibitors. Mice that lack functional Cidea have higher metabolic rates, higher lipolysis in brown adipose tissue and higher core body temperatures when subjected to cold. These mice are also resistant to diet-induced obesity and diabetes. This suggests that in mice this gene product plays a role in thermogenesis and lipolysis. Alternatively spliced transcripts have been identified. [provided by RefSeq, Aug 2010]
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cell division cycle 42 pseudogene 5
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vegetative cell wall protein gp1-like
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pre-B-cell leukemia homeobox interacting protein 1
The protein encoded by this gene interacts with the PBX1 homeodomain protein, inhibiting its transcriptional activation potential by preventing its binding to DNA. The encoded protein, which is primarily cytosolic but can shuttle to the nucleus, also can interact with estrogen receptors alpha and beta and promote the proliferation trong>oftrong> breast cancer, brain tumors, and lung cancer. Several transcript variants encoding different istrong>oftrong>orms have been found for this gene. More variants exist, but their full-length natures have yet to be determined. [provided by RefSeq, Dec 2015]
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programmed cell death 6
This gene encodes a calcium-binding protein belonging to the penta-EF-hand protein family. Calcium binding is important for homodimerization and for conformational changes required for binding to other protein partners. This gene product participates in T cell receptor-, Fas-, and glucocorticoid-induced programmed cell death. In mice deficient for this gene product, however, apoptosis was not blocked suggesting this gene product is functionally redundant. Alternatively spliced transcript variants encoding multiple istrong>oftrong>orms have been observed for this gene, and a pseudogene trong>oftrong> this gene is also located on the short arm trong>oftrong> chromosome 5. [provided by RefSeq, May 2012]
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programmed cell death 7
This gene encodes a 59 kDa protein that is associated with the U11 small nuclear ribonucleoprotein (snRNP), which is a component trong>oftrong> the minor U12-type spliceosome responsible for catalyzing pre-mRNA splicing trong>oftrong> U12-type introns. [provided by RefSeq, Dec 2010]
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programmed cell death 4 (neoplastic transformation inhibitor)
This gene is a tumor suppressor and encodes a protein that binds to the eukaryotic translation initiation factor 4A1 and inhibits its function by preventing RNA binding. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2010]
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programmed cell death 5
This gene encodes a protein that is upregulated during apoptosis where it translocates rapidly from the cytoplasm to the nucleus. The encoded protein may be an important regulator trong>oftrong> K(lysine) acetyltransferase 5 (a protein involved in transcription, DNA damage response and cell cycle control) by inhibiting its proteasome-dependent degradation. Pseudogenes have been identified on chromosomes 5 and 12 [provided by RefSeq, Dec 2010]
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programmed cell death 2
This gene encodes a nuclear protein expressed in a variety trong>oftrong> tissues. Expression trong>oftrong> this gene has been shown to be repressed by B-cell CLL/lymphoma 6 (BCL6), a transcriptional repressor required for lymph node germinal center development, suggesting that BCL6 regulates apoptosis by its effects on this protein. Alternative splicing results in multiple transcript variants and pseudogenes have been identified on chromosomes 9 and 12. [provided by RefSeq, Dec 2010]
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programmed cell death 1
Programmed cell death protein 1 (PDCD1) is an immune-inhibitory receptor expressed in activated T cells; it is involved in the trong>regulationtrong> trong>oftrong> T-cell functions, including those trong>oftrong> effector CD8+ T cells. In addition, this protein can also promote the differentiation trong>oftrong> CD4+ T cells into T regulatory cells. PDCD1 is expressed in many types trong>oftrong> tumors including melanomas, and has demonstrated to play a role in anti-tumor immunity. Moreover, this protein has been shown to be involved in safeguarding against autoimmunity, however, it can also contribute to the inhibition trong>oftrong> effective anti-tumor and anti-microbial immunity. [provided by RefSeq, Aug 2020]
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programmed cell death 10
This gene encodes an evolutionarily conserved protein associated with cell apoptosis. The protein interacts with the serine/threonine protein kinase MST4 to modulate the extracellular signal-regulated kinase (ERK) pathway. It also interacts with and is phosphoryated by serine/threonine kinase 25, and is thought to function in a signaling pathway essential for vascular developent. Mutations in this gene are one cause trong>oftrong> cerebral cavernous malformations, which are vascular malformations that cause seizures and cerebral hemorrhages. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]
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programmed cell death 11
PDCD11 is a NF-kappa-B (NFKB1; 164011)-binding protein that colocalizes with U3 RNA (MIM 180710) in the nucleolus and is required for rRNA maturation and generation trong>oftrong> 18S rRNA (Sweet et al., 2003 [PubMed 14624448]; Sweet et al., 2008 [PubMed 17654514]).[supplied by OMIM, Oct 2008]
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cell division cycle 37 homolog (S. cerevisiae) pseudogene
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MCF.2 cell line derived transforming sequence
The oncogenic protein encoded by this gene is a guanine nucleotide exchange factor (GEF) that exerts control over some members trong>oftrong> the Rho family trong>oftrong> small GTPases. Several transcript variants encoding different istrong>oftrong>orms have been found for this gene. These istrong>oftrong>orms exhibit different expression patterns and varying levels trong>oftrong> GEF activity.[provided by RefSeq, Jan 2010]
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cell adhesion associated, oncogene regulated
This gene encodes a cell surface receptor that is a member trong>oftrong> the immunoglobulin superfamily. The encoded protein contains three fibronectin type III domains and five immunoglobulin-like C2-type domains. This protein is a member trong>oftrong> a cell-surface receptor complex that mediates cell-cell interactions between muscle precursor cells and trong>positivetrong>ly regulates myogenesis. [provided by RefSeq, Aug 2011]
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pancreatic progenitor cell differentiation and proliferation factor
Predicted to be involved in cell differentiation. Predicted to act upstream trong>oftrong> or within TORC1 signaling and liver development. Located in mitochondrion. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 10-2
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 10-3
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 10-1(gene/pseudogene)
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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killer cell immunoglobulin-like receptor 2DS3 allele 0020101
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cell division cycle 20 pseudogene 1
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programmed cell death 5 pseudogene 1
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programmed cell death 5 pseudogene 2
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LIM and senescent cell antigen-like domains 2
This gene encodes a member trong>oftrong> a small family trong>oftrong> 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 and migration. A pseudogene trong>oftrong> this gene is located on chromosome 4. Multiple transcript variants encoding different istrong>oftrong>orms have been found for this gene. [provided by RefSeq, Nov 2011]
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LIM and senescent cell antigen-like domains 3
Predicted to enable metal ion binding activity. Predicted to be located in cytoplasm; focal adhesion; and plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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LIM and senescent cell antigen-like domains 1
The protein encoded by this gene is an adaptor protein which contains five LIM domains, or double 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 bridge linking integrin-linked kinase to NCK adaptor protein 2, which is involved in growth factor receptor kinase signaling pathways. Its localization to the periphery trong>oftrong> spreading cells also suggests that this protein may play a role in integrin-mediated cell adhesion or spreading. Several transcript variants encoding different istrong>oftrong>orms have been found for this gene. [provided by RefSeq, Jul 2010]
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T cell receptor gamma joining P2
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T cell receptor gamma joining P1
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vegetative cell wall protein gp1-like
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biorientation trong>oftrong> chromosomes in cell division 1
Enables protein phosphatase 2A binding activity and protein phosphatase inhibitor activity. Involved in mitotic sister chromatid biorientation; mitotic sister chromatid cohesion, centromeric; and protein localization to chromosome, centromeric region. Located in centrosome; spindle microtubule; and spindle pole. Part trong>oftrong> Set1C/COMPASS complex and outer kinetochore. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 25-1
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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V-set domain containing T cell activation inhibitor 1
This gene encodes a protein belonging to the B7 costimulatory protein family. Proteins in this family are present on the surface trong>oftrong> antigen-presenting cells and interact with ligand bound to receptors on the surface trong>oftrong> T cells. Studies have shown that high levels trong>oftrong> the encoded protein has been correlated with tumor progression. A pseudogene trong>oftrong> this gene is located on chromosome 20. Multiple transcript variants encoding different istrong>oftrong>orms have been found for this gene. [provided by RefSeq, Dec 2011]
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cerebral endothelial cell adhesion molecule
Enables identical protein binding activity. Acts upstream trong>oftrong> or within cell adhesion. Predicted to be located in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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vascular cell adhesion molecule 1
This gene is a member trong>oftrong> the Ig superfamily and encodes a cell surface sialoglycoprotein expressed by cytokine-activated endothelium. This type I membrane protein mediates leukocyte-endothelial cell adhesion and signal transduction, and may play a role in the development trong>oftrong> artherosclerosis and rheumatoid arthritis. Three alternatively spliced transcripts encoding different istrong>oftrong>orms have been described for this gene. [provided by RefSeq, Dec 2010]
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lymphokine-activated killer cell ligand
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T cell receptor beta variable 17 (non-functional)
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 16 (gene/pseudogene)
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 15
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 14
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 13
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 19
Predicted to be involved in cell surface receptor signaling pathway. Part trong>oftrong> alpha-beta T cell receptor complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 18
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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nitric oxide synthase 3 (endothelial cell)
Nitric oxide is a reactive free radical which acts as a biologic mediator in several processes, including neurotransmission and antimicrobial and antitumoral activities. Nitric oxide is synthesized from L-arginine by nitric oxide synthases. Variations in this gene are associated with susceptibility to coronary spasm. Alternative splicing and the use trong>oftrong> alternative promoters results in multiple transcript variants. [provided by RefSeq, Oct 2016]
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T cell receptor delta variable 1
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor delta variable 3
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor delta variable 2
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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upregulator trong>oftrong> cell proliferation
URG4 is upregulated in the presence trong>oftrong> hepatitis B virus (HBV)-encoded X antigen (HBxAg) and may contribute to the development trong>oftrong> hepatocellular carcinoma by promoting hepatocellular growth and survival (Tufan et al., 2002 [PubMed 12082552]).[supplied by OMIM, Mar 2008]
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small cell adhesion glycoprotein
Located in cell junction; nucleoplasm; and plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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speedy/RINGO cell cycle regulator family member E15, pseudogene
Predicted to enable protein kinase binding activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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pre T-cell antigen receptor alpha
The protein encoded by this gene is a single-pass type I membrane protein that is found in immmature but not mature T-cells. Along with TCRB and CD3 complex, the encoded protein forms the pre-T-cell receptor complex, which regulates early T-cell development. Four transcript variants encoding different istrong>oftrong>orms have been found for this gene.[provided by RefSeq, Jul 2011]
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neural cell adhesion molecule 1
This gene encodes a cell adhesion protein which is a member trong>oftrong> the immunoglobulin superfamily. The encoded protein is involved in cell-to-cell interactions as well as cell-matrix interactions during development and differentiation. The encoded protein plays a role in the development trong>oftrong> the nervous system by regulating neurogenesis, neurite outgrowth, and cell migration. This protein is also involved in the expansion trong>oftrong> T lymphocytes, B lymphocytes and natural killer (NK) cells which play an important role in immune surveillance. This protein plays a role in signal transduction by interacting with fibroblast growth factor receptors, N-cadherin and other components trong>oftrong> the extracellular matrix and by triggering signalling cascades involving FYN-focal adhesion kinase (FAK), mitogen-activated protein kinase (MAPK), and phosphatidylinositol 3-kinase (PI3K). One prominent istrong>oftrong>orm trong>oftrong> this gene, cell surface molecule CD56, plays a role in several myeloproliferative disorders such as acute myeloid leukemia and differential expression trong>oftrong> this gene is associated with differential disease progression. For example, increased expression trong>oftrong> CD56 is correlated with lower survival in acute myeloid leukemia patients whereas increased severity trong>oftrong> COVID-19 is correlated with decreased abundance trong>oftrong> CD56-expressing NK cells in peripheral blood. Alternative splicing results in multiple transcript variants encoding distinct protein istrong>oftrong>orms. [provided by RefSeq, Aug 2020]
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neural cell adhesion molecule 2
The protein encoded by this gene belongs to the immunoglobulin superfamily. It is a type I membrane protein and may function in selective fasciculation and zone-to-zone projection trong>oftrong> the primary olfactory axons. [provided by RefSeq, Jul 2008]
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T cell receptor beta variable A/OR9-2 (pseudogene)
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T cell receptor alpha variable 36/delta variable 7
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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killer cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 4
Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets trong>oftrong> T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content trong>oftrong> the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number trong>oftrong> extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets trong>oftrong> HLA class I molecules; thus, KIR proteins are thought to play an important role in trong>regulationtrong> trong>oftrong> the immune response. [provided by RefSeq, Jul 2008]
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killer cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 3
Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets trong>oftrong> T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content trong>oftrong> the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number trong>oftrong> extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets trong>oftrong> HLA class I molecules; thus, KIR proteins are thought to play an important role in trong>regulationtrong> trong>oftrong> the immune response. [provided by RefSeq, Jul 2008]
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killer cell immunoglobulin-like receptor, two domains, short cytoplasmic tail, 1
Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets trong>oftrong> T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content trong>oftrong> the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number trong>oftrong> extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets trong>oftrong> HLA class I molecules; thus, KIR proteins are thought to play an important role in trong>regulationtrong> trong>oftrong> the immune response. [provided by RefSeq, Jul 2008]
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cell division cycle 27 pseudogene 7
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cell division cycle protein 27 homolog pseudogene
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cell division cycle 25C
This gene encodes a conserved protein that plays a key role in the trong>regulationtrong> trong>oftrong> cell division. The encoded protein directs dephosphorylation trong>oftrong> cyclin B-bound CDC2 and triggers entry into mitosis. It also suppresses p53-induced growth arrest. Multiple alternatively spliced transcript variants trong>oftrong> this gene have been described. [provided by RefSeq, Dec 2015]
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cell division cycle 25B
CDC25B is a member trong>oftrong> the CDC25 family trong>oftrong> phosphatases. CDC25B activates the cyclin dependent kinase CDC2 by removing two phosphate groups and it is required for entry into mitosis. CDC25B shuttles between the nucleus and the cytoplasm due to nuclear localization and nuclear export signals. The protein is nuclear in the M and G1 phases trong>oftrong> the cell cycle and moves to the cytoplasm during S and G2. CDC25B has oncogenic properties, although its role in tumor formation has not been determined. Multiple transcript variants for this gene exist. [provided by RefSeq, Jul 2008]
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cell division cycle 25A
CDC25A is a member trong>oftrong> the CDC25 family trong>oftrong> phosphatases. CDC25A is required for progression from G1 to the S phase trong>oftrong> the cell cycle. It activates the cyclin-dependent kinase CDC2 by removing two phosphate groups. CDC25A is specifically degraded in response to DNA damage, which prevents cells with chromosomal abnormalities from progressing through cell division. CDC25A is an oncogene, although its exact role in oncogenesis has not been demonstrated. Two transcript variants encoding different istrong>oftrong>orms have been found for this gene. [provided by RefSeq, Jul 2008]
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pancreatic beta cell glycoprotein 1
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T cell receptor alpha joining 49
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 48
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 41
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 40
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 43
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 42
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 45
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 44
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 47
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 46
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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cell division cycle 27 pseudogene 2
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cell division cycle 27 pseudogene 3
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cell division cycle 27 pseudogene 1
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cell division cycle 27 pseudogene 6
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cell division cycle 27 pseudogene 4
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cell division cycle 27 pseudogene 5
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cell division cycle 27 pseudogene 8
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cell division cycle 27 pseudogene 9
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speedy/RINGO cell cycle regulator family member E2B
Predicted to enable protein kinase binding activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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hepatic and glial cell adhesion molecule
The protein encoded by this gene is a single-pass type I membrane protein that localizes to the cytoplasmic side trong>oftrong> the cell membrane. The encoded protein acts as a homodimer and is involved in cell motility and cell-matrix interactions. The expression trong>oftrong> this gene is downregulated or undetectable in many cancer cell lines, so this may be a tumor suppressor gene. [provided by RefSeq, Jul 2011]
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T cell receptor gamma constant 1
Enables small molecule binding activity. Predicted to be involved in T cell receptor signaling pathway; adaptive immune response; and gamma-delta T cell activation. Predicted to act upstream trong>oftrong> or within homeostasis trong>oftrong> number trong>oftrong> cells within a tissue. Predicted to be located in membrane. Predicted to be part trong>oftrong> gamma-delta T cell receptor complex. Predicted to be active in external side trong>oftrong> plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor gamma constant 2
Predicted to enable transmembrane signaling receptor activity. Predicted to be involved in T cell receptor signaling pathway and adaptive immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> gamma-delta T cell receptor complex. Predicted to be active in external side trong>oftrong> plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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cell division cycle 27
The protein encoded by this gene shares strong similarity with Saccharomyces cerevisiae protein Cdc27, and the gene product trong>oftrong> Schizosaccharomyces pombe nuc 2. This protein is a component trong>oftrong> the anaphase-promoting complex (APC), which is composed trong>oftrong> eight protein subunits and is highly conserved in eukaryotic cells. This complex catalyzes the formation trong>oftrong> cyclin B-ubiquitin conjugate, which is responsible for the ubiquitin-mediated proteolysis trong>oftrong> B-type cyclins. The protein encoded by this gene and three other members trong>oftrong> the APC complex contain tetratricopeptide (TPR) repeats, which are important for protein-protein interactions. This protein was shown to interact with mitotic checkpoint proteins including Mad2, p55CDC and BUBR1, and it may thus be involved in controlling the timing trong>oftrong> mitosis. Alternative splicing trong>oftrong> this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 2, 22 and Y. [provided by RefSeq, May 2014]
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cell division cycle 26
The protein encoded by this gene is highly similar to Saccharomyces cerevisiae Cdc26, a component trong>oftrong> cell cycle anaphase-promoting complex (APC). APC is composed trong>oftrong> a group trong>oftrong> highly conserved proteins and functions as a cell cycle-regulated ubiquitin-protein ligase. APC thus is responsible for the cell cycle regulated proteolysis trong>oftrong> various proteins. [provided by RefSeq, Jul 2008]
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cell division cycle 20
CDC20 appears to act as a regulatory protein interacting with several other proteins at multiple points in the cell cycle. It is required for two microtubule-dependent processes, nuclear movement prior to anaphase and chromosome separation. [provided by RefSeq, Jul 2008]
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speedy/RINGO cell cycle regulator family member E8, pseudogene
Enables acetylcholine receptor regulator activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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B-cell receptor-associated protein 31
This gene encodes a member trong>oftrong> the B-cell receptor associated protein 31 superfamily. The encoded protein is a multi-pass transmembrane protein trong>oftrong> the endoplasmic reticulum that is involved in the anterograde transport trong>oftrong> membrane proteins from the endoplasmic reticulum to the Golgi and in caspase 8-mediated apoptosis. Microdeletions in this gene are associated with contiguous ABCD1/DXS1375E deletion syndrome (CADDS), a neonatal disorder. Alternative splicing trong>oftrong> this gene results in multiple transcript variants. Two related pseudogenes have been identified on chromosome 16. [provided by RefSeq, Jan 2012]
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neural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligase
This gene encodes a member trong>oftrong> the Nedd4 family trong>oftrong> HECT domain E3 ubiquitin ligases. HECT domain E3 ubiquitin ligases transfer ubiquitin from E2 ubiquitin-conjugating enzymes to protein substrates, thus targeting specific proteins for lysosomal degradation. The encoded protein mediates the ubiquitination trong>oftrong> multiple target substrates and plays a critical role in epithelial sodium transport by regulating the cell surface expression trong>oftrong> the epithelial sodium channel, ENaC. Single nucleotide polymorphisms in this gene may be associated with essential hypertension. Alternatively spliced transcript variants encoding multiple istrong>oftrong>orms have been observed for this gene. [provided by RefSeq, Mar 2012]
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Thy-1 cell surface antigen
This gene encodes a cell surface glycoprotein and member trong>oftrong> the immunoglobulin superfamily trong>oftrong> proteins. The encoded protein is involved in cell adhesion and cell communication in numerous cell types, but particularly in cells trong>oftrong> the immune and nervous systems. The encoded protein is widely used as a marker for hematopoietic stem cells. This gene may function as a tumor suppressor in nasopharyngeal carcinoma. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]
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defender against cell death 1 pseudogene 1
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par-3 family cell polarity regulator beta
Predicted to enable phosphatidylinositol binding activity. Predicted to be involved in several processes, including establishment trong>oftrong> cell polarity; establishment trong>oftrong> centrosome localization; and establishment or maintenance trong>oftrong> epithelial cell apical/basal polarity. Located in cell junction. Part trong>oftrong> protein-containing complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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Pseudohyperkalemia, familial, 2, due to red cell leak
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cytokine-dependent hematopoietic cell linker
MIST is a member trong>oftrong> the SLP76 family trong>oftrong> adaptors (see LCP2, MIM 601603; BLNK, MIM 604515). MIST plays a role in the trong>regulationtrong> trong>oftrong> immunoreceptor signaling, including PLC-gamma (PLCG1; MIM 172420)-mediated B cell antigen receptor (BCR) signaling and FC-epsilon R1 (see FCER1A, MIM 147140)-mediated mast cell degranulation (Cao et al., 1999 [PubMed 10562326]; Goitsuka et al., 2000, 2001 [PubMed 10744659] [PubMed 11463797]).[supplied by OMIM, Mar 2008]
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Thyroid carcinoma, nonmedullary, with cell oxyphilia
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cell division cycle 14C
This gene represents a retrogene trong>oftrong> cell division cycle 14B (CDC14B), which is located on chromosome 9. The introns in the coding sequence have been processed out relative to the CDC14B locus, but there is an intact open reading frame that is missing only some sequence at the N-terminus, including the nuclear localiztion signal, relative to proteins encoded by the CDC14B gene. There is a difference in the subcellular localization trong>oftrong> the protein encoded by this gene, relative to its parental gene product. While the parental gene product displays microtubular localization, GFP chimeras trong>oftrong> the protein encoded by this gene localize to the endoplasmic reticulum, indicating a possible new functional role for this gene. [provided by RefSeq, Nov 2017]
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cell division cycle 14B
The protein encoded by this gene is a member trong>oftrong> the dual specificity protein tyrosine phosphatase family. This protein is highly similar to Saccharomyces cerevisiae Cdc14, a protein tyrosine phosphatase involved in the exit trong>oftrong> cell mitosis and initiation trong>oftrong> DNA replication, which suggests the role in cell cycle control. This protein has been shown to interact with and dephosphorylates tumor suppressor protein p53, and is thought to regulate the function trong>oftrong> p53. Alternative splice trong>oftrong> this gene results in 3 transcript variants encoding distinct istrong>oftrong>orms. [provided by RefSeq, Jul 2008]
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cell division cycle 14A
The protein encoded by this gene is a member trong>oftrong> the dual specificity protein tyrosine phosphatase family. It is highly similar to Saccharomyces cerevisiae Cdc14, a protein tyrosine phosphatase involved in the exit trong>oftrong> cell mitosis and initiation trong>oftrong> DNA replication, suggesting a role in cell cycle control. This protein has been shown to interact with, and dephosphorylate tumor suppressor protein p53, and is thought to regulate the function trong>oftrong> p53. Alternative splicing trong>oftrong> this gene results in several transcript variants encoding distinct istrong>oftrong>orms. [provided by RefSeq, Jul 2008]
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carcinoembryonic antigen-related cell adhesion molecule 20
Predicted to enable protein tyrosine kinase binding activity. Predicted to be involved in trong>regulationtrong> trong>oftrong> immune system process and signal transduction. Predicted to be located in apical plasma membrane and microvillus membrane. Predicted to be active in cell surface and plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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carcinoembryonic antigen-related cell adhesion molecule 21
Predicted to be involved in T cell activation and immune response. Predicted to be located in membrane. Predicted to be active in external side trong>oftrong> plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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mucin 4, cell surface associated pseudogene
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islet cell autoantigen 1, 69kDa pseudogene
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dendritic cell protein pseudogene
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T cell receptor alpha variable 38-2/delta variable 8
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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islet cell autoantigen 1,69kDa-like
Predicted to enable protein domain specific binding activity. Predicted to be involved in trong>regulationtrong> trong>oftrong> transport. Predicted to act upstream trong>oftrong> or within spermatid development. Predicted to be located in acrosomal vesicle. Predicted to be active in Golgi apparatus. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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cell cycle control protein 50B-like
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speedy/RINGO cell cycle regulator family member E7, pseudogene
Predicted to enable protein kinase binding activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 6-4
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 6-1
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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cell division cycle 23
The protein encoded by this gene shares strong similarity with Saccharomyces cerevisiae Cdc23, a protein essential for cell cycle progression through the G2/M transition. This protein is a component trong>oftrong> anaphase-promoting complex (APC), which is composed trong>oftrong> eight protein subunits and highly conserved in eukaryotic cells. APC catalyzes the formation trong>oftrong> cyclin B-ubiquitin conjugate that is responsible for the ubiquitin-mediated proteolysis trong>oftrong> B-type cyclins. This protein and 3 other members trong>oftrong> the APC complex contain the TPR (tetratricopeptide repeat), a protein domain important for protein-protein interaction. [provided by RefSeq, Jul 2008]
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papillary renal cell carcinoma (translocation-associated)
This gene encodes a protein that may play a role in pre-mRNA splicing. Chromosomal translocations (X;1)(p11;q21) that result in fusion trong>oftrong> this gene to TFE3 (GeneID 7030) have been associated with papillary renal cell carcinoma. A PRCC-TFE3 fusion protein is expressed in affected carcinomas and is likely associated with altered gene transactivation. This fusion protein has also been associated with disruption trong>oftrong> the cell cycle.[provided by RefSeq, Aug 2010]
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V-set domain containing T cell activation inhibitor 1 pseudogene
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RCD1 required for cell differentiation1 homolog (S. pombe)
This gene encodes a member trong>oftrong> the highly conserved RCD1 protein family. The encoded protein is a transcriptional ctrong>oftrong>actor and a core protein trong>oftrong> the CCR4-NOT complex. It may be involved in signal transduction as well as retinoic acid-regulated cell differentiation and development. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Oct 2012]
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neural precursor cell expressed, developmentally down-regulated 8 pseudogene
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biorientation trong>oftrong> chromosomes in cell division 1-like 2
Predicted to be involved in cell division. Predicted to be located in centrosome; cytoplasm; and kinetochore. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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biorientation trong>oftrong> chromosomes in cell division 1-like 1
Involved in DNA damage response and replication fork processing. Located in nucleoplasm. Part trong>oftrong> Set1C/COMPASS complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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killer cell lectin-like receptor subfamily A pseudogene 1
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proliferating cell nuclear antigen pseudogene 2
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transcription factor 7 (T-cell specific, HMG-box)
This gene encodes a member trong>oftrong> the T-cell factor/lymphoid enhancer-binding factor family trong>oftrong> high mobility group (HMG) box transcriptional activators. This gene is expressed predominantly in T-cells and plays a critical role in natural killer cell and innate lymphoid cell development. The encoded protein forms a complex with beta-catenin and activates transcription through a Wnt/beta-catenin signaling pathway. Mice with a knockout trong>oftrong> this gene are viable and fertile, but display a block in T-lymphocyte differentiation. Alternative splicing results in multiple transcript variants. Naturally-occurring istrong>oftrong>orms lacking the N-terminal beta-catenin interaction domain may act as dominant negative regulators trong>oftrong> Wnt signaling. [provided by RefSeq, Oct 2016]
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cell division cycle 42 pseudogene
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cell division cycle 42 pseudogene
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proteoglycan 2, bone marrow (natural killer cell activator, eosinophil granule major basic protein)
The protein encoded by this gene is the predominant constituent trong>oftrong> the crystalline core trong>oftrong> the eosinophil granule. High levels trong>oftrong> the prtrong>oftrong>orm trong>oftrong> this protein are also present in placenta and pregnancy serum, where it exists as a complex with several other proteins including pregnancy-associated plasma protein A (PAPPA), angiotensinogen (AGT), and C3dg. This protein may be involved in antiparasitic defense mechanisms as a cytotoxin and helminthotoxin, and in immune hypersensitivity reactions. The encoded protein contains a peptide that displays potent antimicrobial activity against Gram-trong>positivetrong> bacteria, Gram-negative bacteria, and fungi. It is directly implicated in epithelial cell damage, exfoliation, and bronchospasm in allergic diseases. Alternatively spliced transcript variants encoding different istrong>oftrong>orms have been found for this gene. [provided by RefSeq, Nov 2014]
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mucosal vascular addressin cell adhesion molecule 1
The protein encoded by this gene is an endothelial cell adhesion molecule that interacts preferentially with the leukocyte beta7 integrin LPAM-1 (alpha4beta7), L-selectin, and VLA-4 (alpha4beta1) on myeloid cells to direct leukocytes into mucosal and inflamed tissues. It is a member trong>oftrong> the immunoglobulin family and is similar to ICAM1 and VCAM1. At least seven alternatively spliced transcripts encoding different protein istrong>oftrong>orms have been found for this gene, but the full-length nature trong>oftrong> some variants has not been determined. [provided by RefSeq, Jul 2008]
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programmed cell death 10 pseudogene
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intestinal cell (MAK-like) kinase
Eukaryotic protein kinases are enzymes that belong to a very extensive family trong>oftrong> proteins which share a conserved catalytic core common with both serine/threonine and tyrosine protein kinases. This gene encodes an intestinal serine/threonine kinase harboring a dual phosphorylation site found in mitogen-activating protein (MAP) kinases. The protein localizes to the intestinal crypt region and is thought to be important in intestinal epithelial cell proliferation and differentiation. Alternative splicing has been observed at this locus and two variants, encoding the same istrong>oftrong>orm, have been identified. [provided by RefSeq, Jul 2008]
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zyg-11 family member A, cell cycle regulator pseudogene 1
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neuroepithelial cell transforming 1
This gene is part trong>oftrong> the family trong>oftrong> Rho guanine nucleotide exchange factors. Members trong>oftrong> this family activate Rho proteins by catalyzing the exchange trong>oftrong> GDP for GTP. The protein encoded by this gene interacts with RhoA within the cell nucleus and may play a role in repairing DNA damage after ionizing radiation. Pseudogenes trong>oftrong> this gene are located on the long arms trong>oftrong> chromosomes 1, 7 and 18. Alternative splicing results in multiple transcript variants that encode different protein istrong>oftrong>orms. [provided by RefSeq, Jul 2012]
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T cell receptor beta variable 28
Predicted to enable peptide antigen binding activity. Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 26 (pseudogene)
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malignant T cell amplified sequence 2, pseudogene
This locus represents a retrogene copy trong>oftrong> MCTS1 (GeneID:28985) and contains an ORF similar to that parent gene. This locus is situated in a differentially methylated region (DMR) and transcripts in this region are imprinted. [provided by RefSeq, Nov 2021]
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Down syndrome cell adhesion molecule
This gene is a member trong>oftrong> the immunoglobulin superfamily trong>oftrong> cell adhesion molecules (Ig-CAMs), and is involved in human central and peripheral nervous system development. This gene is a candidate for Down syndrome and congenital heart disease (DSCHD). A gene encoding a similar Ig-CAM protein is located on chromosome 11. Alternatively spliced transcript variants encoding multiple istrong>oftrong>orms have been observed for this gene. [provided by RefSeq, Oct 2012]
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B-cell receptor-associated protein 31 pseudogene 1
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mucin 4, cell surface associated pseudogene
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mucin 4, cell surface associated pseudogene
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mucin 4, cell surface associated pseudogene
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suppressor trong>oftrong> cancer cell invasion
This gene encodes a regulator trong>oftrong> cell migration. The encoded protein appears to function in the RhoA (ras homolog gene family, member A)-Dia1 (diaphanous homolog 1) signal transduction pathway. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2010]
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sidekick cell adhesion molecule 1
The protein encoded by this gene is a member trong>oftrong> the immunoglobulin superfamily. The protein contains six immunoglobulin-like domains and thirteen fibronectin type III domains. Fibronectin type III domains are present in both extracellular and intracellular proteins and tandem repeats are known to contain binding sites for DNA, heparin and the cell surface. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2016]
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sidekick cell adhesion molecule 2
The protein encoded by this gene is a member trong>oftrong> the immunoglobulin superfamily. The protein contains two immunoglobulin domains and thirteen fibronectin type III domains. Fibronectin type III domains are present in both extracellular and intracellular proteins and tandem repeats are known to contain binding sites for DNA, heparin and the cell surface. This protein, and a homologous mouse sequence, are very similar to the Drosophila sidekick gene product but the specific function trong>oftrong> this superfamily member is not yet known. Evidence for alternative splicing at this gene locus has been observed but the full-length nature trong>oftrong> additional variants has not yet been determined. [provided by RefSeq, Jul 2008]
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T cell receptor alpha variable 31 (pseudogene)
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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pre-B-cell leukemia homeobox 4
This gene encodes a member trong>oftrong> the pre-B cell leukemia transcription factor family. These proteins are homeobox proteins that play critical roles in embryonic development and cellular differentiation both as Hox ctrong>oftrong>actors and through Hox-independent pathways. The encoded protein contains a homeobox DNA-binding domain, but specific functions trong>oftrong> the protein have not been determined. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, May 2011]
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pre-B-cell leukemia homeobox 2
This gene encodes a ubiquitously expressed member trong>oftrong> the TALE/PBX homeobox family. It was identified by its similarity to a homeobox gene which is involved in t(1;19) translocation in acute pre-B-cell leukemias. This protein is a transcriptional activator which binds to the TLX1 promoter. The gene is located within the major histocompatibility complex (MHC) on chromosome 6. [provided by RefSeq, Jul 2008]
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pre-B-cell leukemia homeobox 3
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in several processes, including eye development; nervous system development; and trong>regulationtrong> trong>oftrong> transcription by RNA polymerase II. Predicted to act upstream trong>oftrong> or within several processes, including adult locomotory behavior; dorsal spinal cord development; and trong>regulationtrong> trong>oftrong> respiratory gaseous exchange by nervous system process. Predicted to be located in chromatin. Predicted to be part trong>oftrong> transcription regulator complex. Predicted to be active in nucleus. Biomarker trong>oftrong> esophagus squamous cell carcinoma. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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pre-B-cell leukemia homeobox 1
This gene encodes a nuclear protein that belongs to the PBX homeobox family trong>oftrong> transcriptional factors. Studies in mice suggest that this gene may be involved in the trong>regulationtrong> trong>oftrong> osteogenesis and required for skeletal patterning and programming. A chromosomal translocation, t(1;19) involving this gene and TCF3/E2A gene, is associated with pre-B-cell acute lymphoblastic leukemia. The resulting fusion protein, in which the DNA binding domain trong>oftrong> E2A is replaced by the DNA binding domain trong>oftrong> this protein, transforms cells by constitutively activating transcription trong>oftrong> genes regulated by the PBX protein family. Alternatively spliced transcript variants encoding different istrong>oftrong>orms have been found for this gene. [provided by RefSeq, Jun 2017]
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T cell receptor alpha joining 30
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 31
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 33
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 34
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 35 (non-functional)
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 36
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 37
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 38
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 39
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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killer cell immunoglobulin-like receptor, three domains, short cytoplasmic tail, 1
Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets trong>oftrong> T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content trong>oftrong> the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number trong>oftrong> extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets trong>oftrong> HLA class I molecules; thus, KIR proteins are thought to play an important role in trong>regulationtrong> trong>oftrong> the immune response. Alternatively spliced transcript variants encoding different istrong>oftrong>orms have been found for this gene. [provided by RefSeq, Aug 2013]
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Tax1 (human T-cell leukemia virus type I) binding protein 1
This gene encodes a HTLV-1 tax1 binding protein. The encoded protein interacts with TNFAIP3, and inhibits TNF-induced apoptosis by mediating the TNFAIP3 anti-apoptotic activity. Degradation trong>oftrong> this protein by caspase-3-like family proteins is associated with apoptosis induced by TNF. This protein may also have a role in the inhibition trong>oftrong> inflammatory signaling pathways. Alternatively spliced transcript variants encoding different istrong>oftrong>orms have been found for this gene.[provided by RefSeq, May 2011]
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Tax1 (human T-cell leukemia virus type I) binding protein 3
This gene encodes a small, highly conserved protein with a single PDZ domain. PDZ (PSD-95/Discs large/ZO-1 homologous) domains promote protein-protein interactions that affect cell signaling, adhesion, protein scaffolding, and receptor and ion transporter functions. The encoded protein interacts with a large number trong>oftrong> target proteins that play roles in signaling pathways; for example, it interacts with Rho A and glutaminase L and also acts as a negative regulator trong>oftrong> the Wnt/beta-catenin signaling pathway. This protein was first identified as binding to the T-cell leukaemia virus (HTLV1) Tax oncoprotein. Overexpression trong>oftrong> this gene has been implicated in altered cancer cell adhesion, migration and metastasis. The encoded protein also modulates the localization and density trong>oftrong> inwardly rectifying potassium channel 2.3 (Kir2.3). To date, this protein has been shown to play a role in cell proliferation, development, stress response, and polarization. Alternative splicing results in multiple transcript variants encoding distinct istrong>oftrong>orms. [provided by RefSeq, Apr 2017]
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cell division cycle 73
This gene encodes a tumor suppressor that is involved in transcriptional and post-transcriptional control pathways. The protein is a component trong>oftrong> the the PAF protein complex, which associates with the RNA polymerase II subunit POLR2A and with a histone methyltransferase complex. This protein appears to facilitate the association trong>oftrong> 3' mRNA processing factors with actively-transcribed chromatin. Mutations in this gene have been linked to hyperparathyroidism-jaw tumor syndrome, familial isolated hyperparathyroidism, and parathyroid carcinoma. [provided by RefSeq, Jul 2009]
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T cell activation inhibitor, mitochondrial
Located in mitochondrion. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 20/OR9-2 (non-functional)
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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angio-associated, migratory cell protein
The gene is a member trong>oftrong> the immunoglobulin superfamily. The encoded protein is associated with angiogenesis, with potential roles in endothelial tube formation and the migration trong>oftrong> endothelial cells. It may also regulate smooth muscle cell migration via the RhoA pathway. The encoded protein can bind to heparin and may mediate heparin-sensitive cell adhesion. [provided by RefSeq, Oct 2014]
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cell division cycle 26 pseudogene 1
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T cell receptor alpha variable 2
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 3 (gene/pseudogene)
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 4
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 6
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 7
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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par-6 family cell polarity regulator gamma
Predicted to be involved in centrosome cycle; establishment or maintenance trong>oftrong> epithelial cell apical/basal polarity; and trong>regulationtrong> trong>oftrong> cellular localization. Predicted to be located in cytosol and plasma membrane. Predicted to be part trong>oftrong> PAR polarity complex. Predicted to be active in apical plasma membrane; cell cortex; and nucleus. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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par-6 family cell polarity regulator beta
This gene is a member trong>oftrong> the PAR6 family and encodes a protein with a PSD95/Discs-large/ZO1 (PDZ) domain, an OPR domain and a semi-Cdc42/Rac interactive binding (CRIB) domain. This cytoplasmic protein is involved in asymmetrical cell division and cell polarization processes as a member trong>oftrong> a multi-protein complex. [provided by RefSeq, Jul 2008]
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par-6 family cell polarity regulator alpha
This gene is a member trong>oftrong> the PAR6 family and encodes a protein with a PSD95/Discs-large/ZO1 (PDZ) domain and a semi-Cdc42/Rac interactive binding (CRIB) domain. This cell membrane protein is involved in asymmetrical cell division and cell polarization processes as a member trong>oftrong> a multi-protein complex. The protein also has a role in the epithelial-to-mesenchymal transition (EMT) that characterizes the invasive phenotype associated with metastatic carcinomas. Alternate transcriptional splice variants, encoding different istrong>oftrong>orms, have been characterized. [provided by RefSeq, Jul 2008]
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non-specific cytotoxic cell receptor protein 1 homolog (zebrafish)
Predicted to contribute to ubiquitin protein ligase activity. Involved in trong>positivetrong> trong>regulationtrong> trong>oftrong> cell population proliferation. Located in cytosol. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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mucin 20, cell surface associated
This gene encodes a member trong>oftrong> the mucin protein family. Mucins are high molecular weight glycoproteins secreted by many epithelial tissues to form an insoluble mucous barrier. The C-terminus trong>oftrong> this family member associates with the multifunctional docking site trong>oftrong> the MET proto-oncogene and suppresses activation trong>oftrong> some downstream MET signaling cascades. The protein features a mucin tandem repeat domain that varies between two and six copies in most individuals. Multiple variants encoding different istrong>oftrong>orms have been found for this gene. A related pseudogene, which is also located on chromosome 3, has been identified. [provided by RefSeq, Apr 2014]
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mucin 21, cell surface associated
This gene encodes a large membrane-bound glycoprotein which is a member trong>oftrong> the mucin family. Mucins are O-glycosylated proteins that play an essential role in forming protective mucous barriers on epithelial surfaces. These proteins also play a role in intracellular signaling. The encoded protein contains an N-terminal signal sequence, an extracellular mucin domain, a stem domain, a transmembrane domain, and a C-terminal cytoplasmic tail domain. The mucin domain contains O-glycosylation sites and is polymorphic with istrong>oftrong>orms containing a variable number trong>oftrong> nonidentical proline-, threonine-, and serine-rich tandem repeats trong>oftrong> 15 amino acids each. The aberrent expression trong>oftrong> this gene is associated with lung adenocarcinoma. [provided by RefSeq, May 2017]
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putative germ cell-specific gene 1-like protein 2
Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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inducible T-cell co-stimulator
The protein encoded by this gene belongs to the CD28 and CTLA-4 cell-surface receptor family. It forms homodimers and plays an important role in cell-cell signaling, immune responses, and trong>regulationtrong> trong>oftrong> cell proliferation. [provided by RefSeq, Jul 2008]
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epithelial cell adhesion molecule pseudogene
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cell division cycle associated 7 pseudogene
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speedy/RINGO cell cycle regulator family member E11
Enables acetylcholine receptor regulator activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T-cell tumor invasion and metastasis 1
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natural killer cell triggering receptor
This gene encodes a membrane-anchored protein with a hydrophobic amino terminal domain and a cyclophilin-like PPIase domain. It is present on the surface trong>oftrong> natural killer cells and facilitates their binding to targets. Its expression is regulated by IL2 activation trong>oftrong> the cells. [provided by RefSeq, Jul 2008]
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stromal cell-derived factor 2 pseudogene
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T cell receptor alpha variable 22
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 21
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 27
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 25
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 24
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 28 (pseudogene)
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor beta variable 25/OR9-2 (pseudogene)
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cell adhesion molecule L1-like
The protein encoded by this gene is a member trong>oftrong> the L1 gene family trong>oftrong> neural cell adhesion molecules. It is a neural recognition molecule that may be involved in signal transduction pathways. The deletion trong>oftrong> one copy trong>oftrong> this gene may be responsible for mental defects in patients with 3p- syndrome. This protein may also play a role in the growth trong>oftrong> certain cancers. Alternate splicing results in both coding and non-coding variants. [provided by RefSeq, Nov 2011]
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Basal cell carcinoma, susceptibility to, 4
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T cell receptor delta diversity 3
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor delta diversity 2
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor delta diversity 1
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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cell division cycle protein 27 homolog pseudogene
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T cell receptor delta constant
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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prostate stem cell antigen
This gene encodes a glycosylphosphatidylinositol-anchored cell membrane glycoprotein. In addition to being highly expressed in the prostate it is also expressed in the bladder, placenta, colon, kidney, and stomach. This gene is up-regulated in a large proportion trong>oftrong> prostate cancers and is also detected in cancers trong>oftrong> the bladder and pancreas. This gene includes a polymorphism that results in an upstream start codon in some individuals; this polymorphism is thought to be associated with a risk for certain gastric and bladder cancers. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]
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T cell receptor gamma locus antisense RNA 1
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activated leukocyte cell adhesion molecule
This gene encodes activated leukocyte cell adhesion molecule (ALCAM), also known as CD166 (cluster trong>oftrong> differentiation 166), which is a member trong>oftrong> a subfamily trong>oftrong> immunoglobulin receptors with five immunoglobulin-like domains (VVC2C2C2) in the extracellular domain. This protein binds to T-cell differentiation antigene CD6, and is implicated in the processes trong>oftrong> cell adhesion and migration. Multiple alternatively spliced transcript variants encoding different istrong>oftrong>orms have been found. [provided by RefSeq, Aug 2011]
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hematopoietic cell signal transducer
This gene encodes a transmembrane signaling adaptor that contains a YxxM motif in its cytoplasmic domain. The encoded protein may form part trong>oftrong> the immune recognition receptor complex with the C-type lectin-like receptor NKG2D. As part trong>oftrong> this receptor complex, this protein may activate phosphatidylinositol 3-kinase dependent signaling pathways through its intracytoplasmic YxxM motif. This receptor complex may have a role in cell survival and proliferation by activation trong>oftrong> NK and T cell responses. Alternative splicing results in two transcript variants encoding different istrong>oftrong>orms. [provided by RefSeq, Jul 2008]
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stromal cell derived factor 4
This gene encodes a stromal cell derived factor that is a member trong>oftrong> the CREC protein family. The encoded protein contains six EF-hand motifs and calcium-binding motifs. This protein localizes to the Golgi lumen and may be involved in regulating calcium dependent cellular activities. [provided by RefSeq, Sep 2011]
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stromal cell-derived factor 2
The protein encoded by this gene is believed to be a secretory protein. It has regions trong>oftrong> similarity to hydrophilic segments trong>oftrong> yeast mannosyltransferases. Its expression is ubiquitous and the gene appears to be relatively conserved among mammals. Alternate splicing results in both coding and non-coding variants. A pseudogene trong>oftrong> this gene is located on chromosome 15. [provided by RefSeq, Dec 2011]
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natural killer cell granule protein 7
Involved in defense response to protozoan. Located in cytolytic granule membrane and plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 22/OR9-2 (pseudogene)
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germ cell associated 2 (haspin)
Enables ATP binding activity and histone H3T3 kinase activity. Involved in several processes, including mitotic sister chromatid cohesion; mitotic spindle assembly checkpoint signaling; and protein localization to chromosome, centromeric region. Located in centrosome; nucleoplasm; and spindle. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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germ cell associated 1
Predicted to enable RNA polymerase binding activity. Predicted to be located in endoplasmic reticulum membrane. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor gamma variable 6 (pseudogene)
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T cell receptor gamma variable 7 (pseudogene)
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T cell receptor gamma variable 4
Predicted to be involved in adaptive immune response and innate immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in external side trong>oftrong> plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor gamma variable 5
Predicted to be involved in adaptive immune response and innate immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in external side trong>oftrong> plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor gamma variable 2
Predicted to be involved in adaptive immune response and innate immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in external side trong>oftrong> plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor gamma variable 3
Predicted to enable MHC protein binding activity and peptide antigen binding activity. Predicted to be involved in immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in external side trong>oftrong> plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor gamma variable 1 (non-functional)
Predicted to be involved in adaptive immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in external side trong>oftrong> plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor gamma variable 8
Predicted to be involved in adaptive immune response and innate immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in external side trong>oftrong> plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor gamma variable 9
Predicted to enable MHC protein binding activity and peptide antigen binding activity. Predicted to be involved in adaptive immune response and innate immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in external side trong>oftrong> plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor gamma variable B (pseudogene)
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T cell receptor gamma variable A (pseudogene)
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T cell receptor associated transmembrane adaptor 1
Predicted to enable transmembrane receptor protein tyrosine kinase adaptor activity. Acts upstream trong>oftrong> or within negative trong>regulationtrong> trong>oftrong> receptor recycling; negative trong>regulationtrong> trong>oftrong> transport; and trong>positivetrong> trong>regulationtrong> trong>oftrong> signal transduction. Located in centriolar satellite; mitotic spindle; and plasma membrane. Part trong>oftrong> T cell receptor complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 5B
Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets trong>oftrong> T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content trong>oftrong> the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number trong>oftrong> extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets trong>oftrong> HLA class I molecules; thus, KIR proteins are thought to play an important role in trong>regulationtrong> trong>oftrong> the immune response. [provided by RefSeq, Jul 2008]
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killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 5A
Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets trong>oftrong> T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content trong>oftrong> the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number trong>oftrong> extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets trong>oftrong> HLA class I molecules; thus, KIR proteins are thought to play an important role in trong>regulationtrong> trong>oftrong> the immune response. [provided by RefSeq, Jul 2008]
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T cell receptor alpha joining 58 (non-functional)
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 56
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 57
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 54
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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platelet/endothelial cell adhesion molecule 1
The protein encoded by this gene is found on the surface trong>oftrong> platelets, monocytes, neutrophils, and some types trong>oftrong> T-cells, and makes up a large portion trong>oftrong> endothelial cell intercellular junctions. The encoded protein is a member trong>oftrong> the immunoglobulin superfamily and is likely involved in leukocyte migration, angiogenesis, and integrin activation. [provided by RefSeq, May 2010]
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T-cell acute lymphocytic leukemia 1
Enables several functions, including E-box binding activity; RNA polymerase II-specific DNA-binding transcription factor binding activity; and histone deacetylase binding activity. Involved in several processes, including myeloid cell differentiation; trong>positivetrong> trong>regulationtrong> trong>oftrong> cellular component organization; and trong>positivetrong> trong>regulationtrong> trong>oftrong> erythrocyte differentiation. Located in chromatin and nucleoplasm. Part trong>oftrong> transcription regulator complex. Implicated in acute lymphoblastic leukemia. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T-cell acute lymphocytic leukemia 2
This intronless gene encodes a helix-loop-helix protein. Translocations between this gene on chromosome 9 and the T-cell receptor beta-chain locus on chromosome 7 have been associated with activation trong>oftrong> the T-cell acute lymphocytic leukemia 2 gene and T-cell acute lymphoblastic leukemia. [provided by RefSeq, Mar 2009]
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T cell receptor alpha variable 26-1
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 26-2
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor beta variable 22-1 (pseudogene)
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T cell receptor alpha variable 9-1
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 9-2
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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cell division cycle associated 4 pseudogene 2
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pre-B-cell leukemia homeobox 2 pseudogene 1
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T-cell leukemia homeobox 1
This gene encodes a nuclear transcription factor that belongs to the NK-linked or NK-like (NKL) subfamily trong>oftrong> homeobox genes. The encoded protein is required for normal development trong>oftrong> the spleen during embryogenesis. This protein is also involved in specification trong>oftrong> neuronal cell fates. Ectopic expression trong>oftrong> this gene due to chromosomal translocations is associated with certain T-cell acute lymphoblastic leukemias. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2010]
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T-cell leukemia homeobox 2
This gene is a member trong>oftrong> an orphan homeobox-containing transcription factor family. Studies trong>oftrong> the mouse ortholog have shown that the encoded protein is crucial for the development trong>oftrong> the enteric nervous system; in humans, loss-trong>oftrong>-function may play a role in tumorigenesis trong>oftrong> gastrointestinal stromal tumors. [provided by RefSeq, May 2010]
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T-cell leukemia homeobox 3
The protein encoded by this gene is an orphan homeobox protein that encodes a DNA-binding nuclear transcription factor. A translocation [t(5;14)(q35;q32)] involving this gene is associated with T-cell acute lymphoblastic leukemia (T-ALL) in children and young adults. [provided by RefSeq, Nov 2015]
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cell division cycle 37 pseudogene 1
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cell division cycle 37 pseudogene 2
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B-cell CLL/lymphoma 7C
This gene is identified by the similarity trong>oftrong> its product to the N-terminal region trong>oftrong> BCL7A protein. The BCL7A protein is encoded by the gene known to be directly involved in a three-way gene translocation in a Burkitt lymphoma cell line. The function trong>oftrong> this gene has not yet been determined. Two transcript variants encoding different istrong>oftrong>orms have been found for this gene. [provided by RefSeq, Nov 2013]
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B-cell CLL/lymphoma 7B
This gene encodes a member trong>oftrong> the BCL7 family including BCL7A, BCL7B and BCL7C proteins. This member is BCL7B, which contains a region that is highly similar to the N-terminal segment trong>oftrong> BCL7A or BCL7C proteins. The BCL7A protein is encoded by the gene known to be directly involved in a three-way gene translocation in a Burkitt lymphoma cell line. This gene is located at a chromosomal region commonly deleted in Williams syndrome. This gene is highly conserved from C. elegans to human. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Oct 2010]
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B-cell CLL/lymphoma 7A
This gene is directly involved, with Myc and IgH, in a three-way gene translocation in a Burkitt lymphoma cell line. As a result trong>oftrong> the gene translocation, the N-terminal region trong>oftrong> the gene product is disrupted, which is thought to be related to the pathogenesis trong>oftrong> a subset trong>oftrong> high-grade B cell non-Hodgkin lymphoma. The N-terminal segment involved in the translocation includes the region that shares a strong sequence similarity with those trong>oftrong> BCL7B and BCL7C. Two transcript variants encoding different istrong>oftrong>orms have been found for this gene. [provided by RefSeq, Jul 2008]
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B-cell translocation gene 1 pseudogene 1
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myelinating Schwann cell element
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glial cell derived neurotrophic factor
This gene encodes a secreted ligand trong>oftrong> the TGF-beta (transforming growth factor-beta) superfamily trong>oftrong> proteins. Ligands trong>oftrong> this family bind various TGF-beta receptors leading to recruitment and activation trong>oftrong> SMAD family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit trong>oftrong> the disulfide-linked homodimer. The recombinant form trong>oftrong> this protein, a highly conserved neurotrophic factor, was shown to promote the survival and differentiation trong>oftrong> dopaminergic neurons in culture, and was able to prevent apoptosis trong>oftrong> motor neurons induced by axotomy. This protein is a ligand for the product trong>oftrong> the RET (rearranged during transfection) protooncogene. Mutations in this gene may be associated with Hirschsprung disease and Tourette syndrome. This gene encodes multiple protein istrong>oftrong>orms that may undergo similar proteolytic processing. [provided by RefSeq, Aug 2016]
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cell division cycle 45
The protein encoded by this gene was identified by its strong similarity with Saccharomyces cerevisiae Cdc45, an essential protein required to the initiation trong>oftrong> DNA replication. Cdc45 is a member trong>oftrong> the highly conserved multiprotein complex including Cdc6/Cdc18, the minichromosome maintenance proteins (MCMs) and DNA polymerase, which is important for early steps trong>oftrong> DNA replication in eukaryotes. This protein has been shown to interact with MCM7 and DNA polymerase alpha. Studies trong>oftrong> the similar gene in Xenopus suggested that this protein play a pivotal role in the loading trong>oftrong> DNA polymerase alpha onto chromatin. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]
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cell division cycle 40
Pre-mRNA splicing occurs in two sequential transesterification steps. The protein encoded by this gene is found to be essential for the catalytic step II in pre-mRNA splicing process. It is found in the spliceosome, and contains seven WD repeats, which function in protein-protein interactions. This protein has a sequence similarity to yeast Prp17 protein, which functions in two different cellular processes: pre-mRNA splicing and cell cycle progression. It suggests that this protein may play a role in cell cycle progression. [provided by RefSeq, Jul 2008]
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cell division cycle 42
The protein encoded by this gene is a small GTPase trong>oftrong> the Rho-subfamily, which regulates signaling pathways that control diverse cellular functions including cell morphology, migration, endocytosis and cell cycle progression. This protein is highly similar to Saccharomyces cerevisiae Cdc 42, and is able to complement the yeast cdc42-1 mutant. The product trong>oftrong> oncogene Dbl was reported to specifically catalyze the dissociation trong>oftrong> GDP from this protein. This protein could regulate actin polymerization through its direct binding to Neural Wiskott-Aldrich syndrome protein (N-WASP), which subsequently activates Arp2/3 complex. Alternative splicing trong>oftrong> this gene results in multiple transcript variants. Pseudogenes trong>oftrong> this gene have been identified on chromosomes 3, 4, 5, 7, 8 and 20. [provided by RefSeq, Apr 2013]
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T-cell leukemia/lymphoma 1B
Enables protein kinase binding activity and protein serine/threonine kinase activator activity. Involved in intracellular signal transduction. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T-cell leukemia/lymphoma 1A
Overexpression trong>oftrong> the TCL1 gene in humans has been implicated in the development trong>oftrong> mature T cell leukemia, in which chromosomal rearrangements bring the TCL1 gene in close proximity to the T-cell antigen receptor (TCR)-alpha (MIM 186880) or TCR-beta (MIM 186930) regulatory elements (summarized by Virgilio et al., 1998 [PubMed 9520462]). In normal T cells TCL1 is expressed in CD4-/CD8- cells, but not in cells at later stages trong>oftrong> differentiation. TCL1 functions as a coactivator trong>oftrong> the cell survival kinase AKT (MIM 164730) (Laine et al., 2000 [PubMed 10983986]).[supplied by OMIM, Jul 2010]
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speedy/RINGO cell cycle regulator family member E13, pseudogene
Enables acetylcholine receptor regulator activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 11-2
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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killer cell immunoglobulin-like receptor 2DS1
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cell division cycle associated 7 pseudogene
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speedy/RINGO cell cycle regulator family member E21, pseudogene
Predicted to enable protein kinase binding activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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engulfment and cell motility 2 pseudogene 1
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cutaneous T-cell lymphoma-associated antigen 1 pseudogene
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LIM and senescent cell antigen-like domains 2 pseudogene
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inturned planar cell polarity protein
Predicted to enable phosphatidylinositol binding activity. Involved in embryonic digit morphogenesis; rotrong>oftrong> trong>oftrong> mouth development; and tongue morphogenesis. Located in ciliary basal body and motile cilium. Implicated in asphyxiating thoracic dystrophy and ortrong>oftrong>aciodigital syndrome XVII. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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cell adhesion associated, oncogene regulated pseudogene
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T-cell lymphoma invasion and metastasis 1
This gene encodes a RAC1-specific guanine nucleotide exchange factor (GEF). GEFs mediate the exchange trong>oftrong> guanosine diphosphate (GDP) for guanosine triphosphate (GTP). The binding trong>oftrong> GTP induces a conformational change in RAC1 that allows downstream effectors to bind and transduce a signal. This gene thus regulates RAC1 signaling pathways that affect cell shape, migration, adhesion, growth, survival, and polarity, as well as influencing actin cytoskeletal formation, endocytosis, and membrane trafficking. This gene thus plays an important role in cell invasion, metastasis, and carcinogenesis. In addition to RAC1, the encoded protein activates additional Rho-like GTPases such as CDC42, RAC2, RAC3 and RHOA. This gene encodes multiple protein istrong>oftrong>orms that experience a diverse array trong>oftrong> intramolecular, protein-protein, and phosphorylation interactions as well as phosphoinositide binding. Both the longer and shorter istrong>oftrong>orms have C-terminal Dbl homology (DH) and pleckstrin homology (PH) domains while only the longer istrong>oftrong>orms trong>oftrong> this gene have the N-terminal myristoylation site and the downstream N-terminal PH domain, ras-binding domain (RBD), and PSD-95/DlgA/ZO-1 (PDZ) domain. [provided by RefSeq, Jul 2017]
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T-cell lymphoma invasion and metastasis 2
This gene encodes a guanine nucleotide exchange factor. A highly similar mouse protein specifically activates ras-related C3 botulinum substrate 1, converting this Rho-like guanosine triphosphatase (GTPase) from a guanosine diphosphate-bound inactive state to a guanosine triphosphate-bound active state. The encoded protein may play a role in neural cell development. Alternatively spliced transcript variants encoding different istrong>oftrong>orms have been described. [provided by RefSeq, Jul 2008]
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T cell receptor beta variable 4-2
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 4-3
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 4-1
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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squamous cell carcinoma antigen recognized by T cells
This gene encodes two proteins, the SART1(800) protein expressed in the nucleus trong>oftrong> the majority trong>oftrong> proliferating cells, and the SART1(259) protein expressed in the cytosol trong>oftrong> epithelial cancers. The SART1(259) protein is translated by the mechanism trong>oftrong> -1 frameshifting during posttranscriptional trong>regulationtrong>; its full-length sequence is not published yet. The two encoded proteins are thought to be involved in the trong>regulationtrong> trong>oftrong> proliferation. Both proteins have tumor-rejection antigens. The SART1(259) protein possesses tumor epitopes capable trong>oftrong> inducing HLA-A2402-restricted cytotoxic T lymphocytes in cancer patients. This SART1(259) antigen may be useful in specific immunotherapy for cancer patients and may serve as a paradigmatic tool for the diagnosis and treatment trong>oftrong> patients with atopy. The SART1(259) protein is found to be essential for the recruitment trong>oftrong> the tri-snRNP to the pre-spliceosome in the spliceosome assembly pathway. [provided by RefSeq, Jul 2008]
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T cell receptor alpha joining 61 (non-functional)
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 60 (pseudogene)
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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CDC14 cell division cycle 14 C-like
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T cell receptor alpha variable 18
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 19
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 10
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 11 (pseudogene)
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 16
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 17
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 15 (pseudogene)
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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speedy/RINGO cell cycle regulator family member E4
Predicted to enable protein kinase binding activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor alpha variable 8-1
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 8-3
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 8-2
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 8-5 (pseudogene)
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 8-4
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 8-7 (non-functional)
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 8-6
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor beta variable 5-7 (non-functional)
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 5-6
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 5-5
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 5-4
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 5-3 (non-functional)
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 5-2 (pseudogene)
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T cell receptor beta variable 5-1
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 5-8
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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B-cell CLL/lymphoma 9 pseudogene 1
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transcription factor 7-like 1 (T-cell specific, HMG-box)
This gene encodes a member trong>oftrong> the T cell factor/lymphoid enhancer factor family trong>oftrong> transcription factors. These transcription factors are activated by beta catenin, mediate the Wnt signaling pathway and are antagonized by the transforming growth factor beta signaling pathway. The encoded protein contains a high mobility group-box DNA binding domain and participates in the trong>regulationtrong> trong>oftrong> cell cycle genes and cellular senescence. [provided by RefSeq, Nov 2010]
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transcription factor 7-like 2 (T-cell specific, HMG-box)
This gene encodes a high mobility group (HMG) box-containing transcription factor that plays a key role in the Wnt signaling pathway. The protein has been implicated in blood glucose homeostasis. Genetic variants trong>oftrong> this gene are associated with increased risk trong>oftrong> type 2 diabetes. Several transcript variants encoding multiple different istrong>oftrong>orms have been found for this gene.[provided by RefSeq, Oct 2010]
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T cell receptor alpha constant
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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cell division cycle 123
Enables ATP binding activity and magnesium ion binding activity. Involved in eukaryotic translation initiation factor 2 complex assembly. Located in cytoplasm. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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killer cell lectin-like receptor subfamily D, member 1
Natural killer (NK) cells are a distinct lineage trong>oftrong> lymphocytes that mediate cytotoxic activity and secrete cytokines upon immune stimulation. Several genes trong>oftrong> the C-type lectin superfamily, including members trong>oftrong> the NKG2 family, are expressed by NK cells and may be involved in the trong>regulationtrong> trong>oftrong> NK cell function. KLRD1 (CD94) is an antigen preferentially expressed on NK cells and is classified as a type II membrane protein because it has an external C terminus. Several transcript variants encoding different istrong>oftrong>orms have been found for this gene. [provided by RefSeq, May 2017]
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engulfment and cell motility 1
This gene encodes a member trong>oftrong> the engulfment and cell motility protein family. These proteins interact with dedicator trong>oftrong> cytokinesis proteins to promote phagocytosis and cell migration. Increased expression trong>oftrong> this gene and dedicator trong>oftrong> cytokinesis 1 may promote glioma cell invasion, and single nucleotide polymorphisms in this gene may be associated with diabetic nephropathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]
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engulfment and cell motility 2
The protein encoded by this gene interacts with the dedicator trong>oftrong> cyto-kinesis 1 protein. Similarity to a C. elegans protein suggests that this protein may function in phagocytosis trong>oftrong> apoptotic cells and in cell migration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]
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engulfment and cell motility 3
The protein encoded by this gene is similar to a C. elegans protein that functions in phagocytosis trong>oftrong> apoptotic cells and in cell migration. Other members trong>oftrong> this small family trong>oftrong> engulfment and cell motility (ELMO) proteins have been shown to interact with the dedicator trong>oftrong> cyto-kinesis 1 protein to promote phagocytosis and effect cell shape changes. [provided by RefSeq, Jul 2008]
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cell cycle progression 1
Involved in trong>positivetrong> trong>regulationtrong> trong>oftrong> cell cycle and trong>positivetrong> trong>regulationtrong> trong>oftrong> cell population proliferation. Predicted to be active in membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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mast cell immunoglobulin-like receptor 1
Predicted to enable transmembrane signaling receptor activity. Predicted to be involved in cell surface receptor signaling pathway; mast cell degranulation; and negative trong>regulationtrong> trong>oftrong> mast cell activation. Predicted to be located in plasma membrane. Predicted to be active in external side trong>oftrong> plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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endothelial cell surface expressed chemotaxis and apoptosis regulator
The protein encoded by this gene is primarily found in endothelial cells and blood vessels, where it is involved in cell shape changes and EGF-induced cell migration. It can enhance the activation trong>oftrong> vascular endothelial growth factor receptor-2/kinase insert domain receptor and also promote the proteolysis trong>oftrong> internalized kinase insert domain receptor. This gene may play a role in angiogenesis-related diseases. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]
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programmed cell death 2-like
Predicted to be involved in apoptotic process. Located in membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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dendritic cell-associated nuclear protein
This intronless gene is specifically expressed in dendritic cells (DCs), which are potent antigen-presenting cells involved in activating naive T cells to initiate antigen-specific immune response. The encoded protein is localized mainly in the perinucleus. One trong>oftrong> the alleles (A/T) trong>oftrong> this gene, that causes premature translation termination at aa 117, has been associated with an increased prevalence trong>oftrong> major depression in humans. [provided by RefSeq, Jul 2008]
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mucin 1, cell surface associated
This gene encodes a membrane-bound protein that is a member trong>oftrong> the mucin family. Mucins are O-glycosylated proteins that play an essential role in forming protective mucous barriers on epithelial surfaces. These proteins also play a role in intracellular signaling. This protein is expressed on the apical surface trong>oftrong> epithelial cells that line the mucosal surfaces trong>oftrong> many different tissues including lung, breast stomach and pancreas. This protein is proteolytically cleaved into alpha and beta subunits that form a heterodimeric complex. The N-terminal alpha subunit functions in cell-adhesion and the C-terminal beta subunit is involved in cell signaling. Overexpression, aberrant intracellular localization, and changes in glycosylation trong>oftrong> this protein have been associated with carcinomas. This gene is known to contain a highly polymorphic variable number tandem repeats (VNTR) domain. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Feb 2011]
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cell division cycle associated 4 pseudogene 4
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cell division cycle associated 4 pseudogene 1
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cell division cycle associated 4 pseudogene 3
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speedy/RINGO cell cycle regulator family member E22, pseudogene
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cell division cycle 27 homolog pseudogene
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T cell receptor beta diversity 2
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killer cell lectin-like receptor subfamily K, member 1
Natural killer (NK) cells are lymphocytes that can mediate lysis trong>oftrong> certain tumor cells and virus-infected cells without previous activation. They can also regulate specific humoral and cell-mediated immunity. NK cells preferentially express several calcium-dependent (C-type) lectins, which have been implicated in the trong>regulationtrong> trong>oftrong> NK cell function. The NKG2 gene family is located within the NK complex, a region that contains several C-type lectin genes preferentially expressed in NK cells. This gene encodes a member trong>oftrong> the NKG2 family. The encoded transmembrane protein is characterized by a type II membrane orientation (has an extracellular C terminus) and the presence trong>oftrong> a C-type lectin domain. It binds to a diverse family trong>oftrong> ligands that include MHC class I chain-related A and B proteins and UL-16 binding proteins, where ligand-receptor interactions can result in the activation trong>oftrong> NK and T cells. The surface expression trong>oftrong> these ligands is important for the recognition trong>oftrong> stressed cells by the immune system, and thus this protein and its ligands are therapeutic targets for the treatment trong>oftrong> immune diseases and cancers. Read-through transcription exists between this gene and the upstream KLRC4 (killer cell lectin-like receptor subfamily C, member 4) family member in the same cluster. [provided by RefSeq, Dec 2010]
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Basal cell carcinoma, susceptibility to, 1
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Basal cell carcinoma, susceptibility to, 2
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Basal cell carcinoma, susceptibility to, 3
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meteorin, glial cell differentiation regulator-like
Predicted to enable hormone activity. Predicted to be involved in several processes, including brown fat cell differentiation; trong>positivetrong> trong>regulationtrong> trong>oftrong> brown fat cell differentiation; and response to muscle activity. Located in extracellular exosome. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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VANGL planar cell polarity protein 2
The protein encoded by this gene is a membrane protein involved in the trong>regulationtrong> trong>oftrong> planar cell polarity, especially in the stereociliary bundles trong>oftrong> the cochlea. The encoded protein transmits directional signals to individual cells or groups trong>oftrong> cells in epithelial sheets. This protein is also involved in the development trong>oftrong> the neural plate. [provided by RefSeq, Sep 2011]
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T cell receptor beta variable 8-2 (pseudogene)
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T cell receptor beta variable 8-1 (pseudogene)
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T cell receptor beta variable 26/OR9-2 (pseudogene)
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programmed cell death 2 pseudogene
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T cell receptor alpha locus
Enables signaling receptor activity. Contributes to peptide antigen binding activity. Involved in T cell activation involved in immune response; T cell mediated cytotoxicity directed against tumor cell target; and detection trong>oftrong> tumor cell. Located in cell surface. Part trong>oftrong> alpha-beta T cell receptor complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta locus
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor beta locus. The beta locus includes V (variable), J (joining), diversity (D), and C (constant) segments. During T cell development, the beta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Several V segments and one J segment trong>oftrong> the beta locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. The beta locus also includes eight trypsinogen genes, three trong>oftrong> which encode functional proteins and five trong>oftrong> which are pseudogenes. Chromosomal abnormalities involving the T-cell receptor beta locus have been associated with T-cell lymphomas. [provided by RefSeq, Jul 2008]
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T cell receptor delta locus
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T cell receptor gamma locus
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor gamma locus. The gamma locus includes V (variable), J (joining), and C (constant) segments. During T cell development, the gamma chain is synthesized by a recombination event at the DNA level joining a V segment with a J segment; the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random addition trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Several V segments trong>oftrong> the gamma locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. Somatic rearrangement trong>oftrong> the gamma locus has been observed in T cells derived from patients with T cell leukemia and ataxia telangiectasia. [provided by RefSeq, Jul 2008]
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cell division cycle 42 pseudogene 4
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cell division cycle 42 pseudogene 6
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cell division cycle 42 pseudogene 1
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cell division cycle 42 pseudogene 2
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cutaneous T-cell lymphoma-associated antigen 1 pseudogene
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cell cycle exit and neuronal differentiation 1 pseudogene 1
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cell cycle exit and neuronal differentiation 1 pseudogene 2
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epithelial cell transforming 2
The protein encoded by this gene is a guanine nucleotide exchange factor and transforming protein that is related to Rho-specific exchange factors and yeast cell cycle regulators. The expression trong>oftrong> this gene is elevated with the onset trong>oftrong> DNA synthesis and remains elevated during G2 and M phases. In situ hybridization analysis showed that expression is at a high level in cells undergoing mitosis in regenerating liver. Thus, this protein is expressed in a cell cycle-dependent manner during liver regeneration, and is thought to have an important role in the trong>regulationtrong> trong>oftrong> cytokinesis. Several transcript variants encoding different istrong>oftrong>orms have been found for this gene. [provided by RefSeq, Mar 2017]
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T cell receptor delta joining 4
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor delta joining 1
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor delta joining 3
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor delta joining 2
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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speedy/RINGO cell cycle regulator family member E14, pseudogene
Predicted to enable protein kinase binding activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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killer cell lectin-like receptor subfamily C, member 1
Natural killer (NK) cells are lymphocytes that can mediate lysis trong>oftrong> certain tumor cells and virus-infected cells without previous activation. They can also regulate specific humoral and cell-mediated immunity. The protein encoded by this gene belongs to the killer cell lectin-like receptor family, also called NKG2 family, which is a group trong>oftrong> transmembrane proteins preferentially expressed in NK cells. This family trong>oftrong> proteins is characterized by the type II membrane orientation and the presence trong>oftrong> a C-type lectin domain. This protein forms a complex with another family member, KLRD1/CD94, and has been implicated in the recognition trong>oftrong> the MHC class I HLA-E molecules in NK cells. The genes trong>oftrong> NKG2 family members form a killer cell lectin-like receptor gene cluster on chromosome 12. Multiple alternatively spliced transcript variants encoding distinct istrong>oftrong>orms have been observed. [provided by RefSeq, Jan 2015]
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killer cell lectin-like receptor subfamily C, member 3
Natural killer (NK) cells are lymphocytes that can mediate lysis trong>oftrong> certain tumor cells and virus-infected cells without previous activation. They can also regulate specific humoral and cell-mediated immunity. NK cells preferentially express several calcium-dependent (C-type) lectins, which have been implicated in the trong>regulationtrong> trong>oftrong> NK cell function. KLRC3 is a member trong>oftrong> the NKG2 group which are expressed primarily in natural killer (NK) cells and encodes a family trong>oftrong> transmembrane proteins characterized by a type II membrane orientation (extracellular C terminus) and the presence trong>oftrong> a C-type lectin domain. The NKG2 gene family is located within the NK complex, a region that contains several C-type lectin genes preferentially expressed on NK cells. Alternative splicing results in multiple transcript variants encoding different istrong>oftrong>orms. [provided by RefSeq, Jul 2008]
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killer cell lectin-like receptor subfamily C, member 2
Natural killer (NK) cells are lymphocytes that can mediate lysis trong>oftrong> certain tumor cells and virus-infected cells without previous activation. They can also regulate specific humoral and cell-mediated immunity. NK cells preferentially express several calcium-dependent (C-type) lectins, which have been implicated in the trong>regulationtrong> trong>oftrong> NK cell function. The group, designated KLRC (NKG2) are expressed primarily in natural killer (NK) cells and encodes a family trong>oftrong> transmembrane proteins characterized by a type II membrane orientation (extracellular C terminus) and the presence trong>oftrong> a C-type lectin domain. The KLRC (NKG2) gene family is located within the NK complex, a region that contains several C-type lectin genes preferentially expressed on NK cells. KLRC2 alternative splice variants have been described but their full-length nature has not been determined. [provided by RefSeq, Jul 2008]
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killer cell lectin-like receptor subfamily C, member 4
Natural killer (NK) cells are lymphocytes that can mediate lysis trong>oftrong> certain tumor cells and virus-infected cells without previous activation. They can also regulate specific humoral and cell-mediated immunity. NK cells preferentially express several calcium-dependent (C-type) lectins, which have been implicated in the trong>regulationtrong> trong>oftrong> NK cell function. This gene is a member trong>oftrong> the NKG2 group trong>oftrong> genes that are expressed primarily in natural killer (NK) cells. These family members encode transmembrane proteins that are characterized by a type II membrane orientation (have an extracellular C-terminus) and the presence trong>oftrong> a C-type lectin domain. This family member is located within the NK complex, a region that contains several C-type lectin genes preferentially expressed in NK cells. Read-through transcription exists between this gene and the downstream KLRK1 (killer cell lectin-like receptor subfamily K, member 1) family member. [provided by RefSeq, Dec 2010]
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mal, T-cell differentiation protein-like
This gene encodes an element trong>oftrong> the machinery for raft-mediated trafficking in endothelial cells. The encoded protein, a member trong>oftrong> the MAL proteolipid family, predominantly localizes in glycolipid- and cholesterol-enriched membrane (GEM) rafts. It interacts with caveolin-1. [provided by RefSeq, Jul 2008]
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mal, T-cell differentiation protein 2 (gene/pseudogene)
This gene encodes a multispan transmembrane protein belonging to the MAL proteolipid family. The protein is a component trong>oftrong> lipid rafts and, in polarized cells, it primarily localizes to endosomal structures beneath the apical membrane. It is required for transcytosis, an intracellular transport pathway used to deliver membrane-bound proteins and exogenous cargos from the basolateral to the apical surface. [provided by RefSeq, Jul 2008]
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MCF.2 cell line derived transforming sequence-like
This gene encodes a guanine nucleotide exchange factor that interacts specifically with the GTP-bound Rac1 and plays a role in the Rho/Rac signaling pathways. A variant in this gene was associated with osteoarthritis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]
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par-6 family cell polarity regulator beta pseudogene
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T cell receptor beta joining 1-6
Predicted to be involved in adaptive immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta joining 1-5
Predicted to be involved in adaptive immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta joining 1-4
Predicted to be involved in adaptive immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta joining 1-3
Predicted to be involved in adaptive immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta joining 1-2
Predicted to be involved in adaptive immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta joining 1-1
Predicted to be involved in adaptive immune response. Predicted to be located in plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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taste receptor cell protein 1-like
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zyg-11 related, cell cycle regulator
This gene encodes a subunit trong>oftrong> an E3 ubiquitin ligase complex that may be involved in meiosis. The encoded protein contains three leucine-rich repeat motifs. [provided by RefSeq, Nov 2012]
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cutaneous T-cell lymphoma-associated antigen 1 pseudogene
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T cell receptor beta variable 23-1 (non-functional)
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be located in immunological synapse. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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neuroepithelial cell transforming 1 pseudogene
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neuroepithelial cell transforming 1 pseudogene
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T cell receptor alpha joining 59 (non-functional)
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 52
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 53
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 50
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 51 (pseudogene)
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 55 (pseudogene)
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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BCL2-associated agonist trong>oftrong> cell death
The protein encoded by this gene is a member trong>oftrong> the BCL-2 family. BCL-2 family members are known to be regulators trong>oftrong> programmed cell death. This protein trong>positivetrong>ly regulates cell apoptosis by forming heterodimers with BCL-xL (B-cell lymphoma-extra large) and BCL-2, and reversing their death repressor activity. Proapoptotic activity trong>oftrong> this protein is regulated through its phosphorylation. Protein kinases AKT and MAP kinase, as well as protein phosphatase calcineurin were found to be involved in the trong>regulationtrong> trong>oftrong> this protein. Alternative splicing trong>oftrong> this gene results in two transcript variants which encode the same istrong>oftrong>orm. [provided by RefSeq, Dec 2019]
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T cell receptor alpha variable 41
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 40
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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host cell factor C2 pseudogene 1
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mast cell-expressed membrane protein 1
This gene encodes a single-pass transmembrane protein. Based on its expression pattern, it is speculated to be involved in regulating mast cell differentiation or immune responses. [provided by RefSeq, Jul 2008]
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cell division cycle 16
The protein encoded by this gene functions as a protein ubiquitin ligase and is a component trong>oftrong> the multiprotein APC complex. The APC complex is a cyclin degradation system that governs exit from mitosis by targeting cell cycle proteins for degredation by the 26S proteasome. Each component protein trong>oftrong> the APC complex is highly conserved among eukaryotic organisms. This protein, and other APC complex proteins, contain a tetratricopeptide repeat (TPR) domain; a protein domain that is trong>oftrong>ten involved in protein-protein interactions and the assembly trong>oftrong> multiprotein complexes. Multiple alternatively spliced transcript variants, encoding distinct proteins, have been identified. [provided by RefSeq, Jan 2016]
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B-cell receptor-associated protein 29
Involved in osteoblast differentiation. Located in membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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epithelial cell transforming 2 like
Predicted to enable guanyl-nucleotide exchange factor activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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speedy/RINGO cell cycle regulator family member E9, pseudogene
Enables acetylcholine receptor regulator activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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speedy/RINGO cell cycle regulator family member E5
Predicted to enable protein kinase binding activity. Predicted to be involved in trong>positivetrong> trong>regulationtrong> trong>oftrong> cyclin-dependent protein serine/threonine kinase activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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speedy/RINGO cell cycle regulator family member E6
This gene encodes a cell cycle regulatory protein which plays an important role in cell cycle progression by binding and activating cyclin-dependent kinases. The encoded protein belongs to a family trong>oftrong> cyclin-dependent kinase regulators that contain a speedy box domain which is required for cyclin-dependent kinase activation. [provided by RefSeq, Jul 2017]
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speedy/RINGO cell cycle regulator family member E1
This gene is located at chromosome 7p13 which is close to the Williams Beuren syndrome chromosome region 7q11.23. [provided by RefSeq, Jul 2008]
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speedy/RINGO cell cycle regulator family member E3
Predicted to enable protein kinase binding activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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speedy/RINGO cell cycle regulator family member E2
Predicted to enable protein kinase binding activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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ES cell expressed Ras
This gene encodes a constitutively active member trong>oftrong> the small GTPase Ras protein family. The encoded protein activates the phosphatidylinositol 3-kinase signal transduction pathway in undifferentiated stem cells, but is not expressed in differentiated cells. This gene may be involved in cancer and chemotherapy resistance. [provided by RefSeq, Dec 2012]
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testicular germ cell tumor susceptibility 1
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islet cell autoantigen 1, 69kDa
This gene encodes a protein with an arfaptin homology domain that is found both in the cytosol and as membrane-bound form on the Golgi complex and immature secretory granules. This protein is believed to be an autoantigen in insulin-dependent diabetes mellitus and primary Sjogren's syndrome. Several transcript variants encoding two different istrong>oftrong>orms have been found for this gene. [provided by RefSeq, Feb 2013]
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cell division cycle associated 8 pseudogene
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cell division cycle 6
The protein encoded by this gene is highly similar to Saccharomyces cerevisiae Cdc6, a protein essential for the initiation trong>oftrong> DNA replication. This protein functions as a regulator at the early steps trong>oftrong> DNA replication. It localizes in cell nucleus during cell cyle G1, but translocates to the cytoplasm at the start trong>oftrong> S phase. The subcellular translocation trong>oftrong> this protein during cell cyle is regulated through its phosphorylation by Cdks. Transcription trong>oftrong> this protein was reported to be regulated in response to mitogenic signals through transcriptional control mechanism involving E2F proteins. [provided by RefSeq, Jul 2008]
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cell division cycle 7
This gene encodes a cell division cycle protein with kinase activity that is critical for the G1/S transition. The yeast homolog is also essential for initiation trong>oftrong> DNA replication as cell division occurs. Overexpression trong>oftrong> this gene product may be associated with neoplastic transformation for some tumors. Multiple alternatively spliced transcript variants that encode the same protein have been detected. [provided by RefSeq, Aug 2008]
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T cell receptor alpha variable 1-1
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 1-2
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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carcinoembryonic antigen-related cell adhesion molecule pseudogene 10
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carcinoembryonic antigen-related cell adhesion molecule pseudogene 11
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IL2-inducible T-cell kinase
This gene encodes an intracellular tyrosine kinase expressed in T-cells. The protein contains both SH2 and SH3 domains which are trong>oftrong>ten found in intracellular kinases. It is thought to play a role in T-cell proliferation and differentiation. [provided by RefSeq, Jul 2008]
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B-cell CLL/lymphoma 9-like
Enables beta-catenin binding activity. Involved in several processes, including negative trong>regulationtrong> trong>oftrong> transforming growth factor beta receptor signaling pathway; trong>positivetrong> trong>regulationtrong> trong>oftrong> epithelial to mesenchymal transition; and trong>positivetrong> trong>regulationtrong> trong>oftrong> transcription by RNA polymerase II. Located in fibrillar center and nucleoplasm. Part trong>oftrong> beta-catenin-TCF complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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speedy/RINGO cell cycle regulator family member E18
Predicted to enable protein kinase binding activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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endothelial cell-specific molecule 1
This gene encodes a secreted protein which is mainly expressed in the endothelial cells in human lung and kidney tissues. The expression trong>oftrong> this gene is regulated by cytokines, suggesting that it may play a role in endothelium-dependent pathological disorders. The transcript contains multiple polyadenylation and mRNA instability signals. Two transcript variants encoding different istrong>oftrong>orms have been found for this gene. [provided by RefSeq, Oct 2008]
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male germ cell-associated kinase
The product trong>oftrong> this gene is a serine/threonine protein kinase related to kinases involved in cell cycle trong>regulationtrong>. Studies trong>oftrong> the mouse and rat homologs have localized the kinase to the chromosomes during meiosis in spermatogenesis, specifically to the synaptonemal complex that exists while homologous chromosomes are paired. Mutations in this gene have been associated with ciliary defects resulting in retinitis pigmentosa 62. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]
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mal, T-cell differentiation protein
The protein encoded by this gene is a highly hydrophobic integral membrane protein belonging to the MAL family trong>oftrong> proteolipids. The protein has been localized to the endoplasmic reticulum trong>oftrong> T-cells and is a candidate linker protein in T-cell signal transduction. In addition, this proteolipid is localized in compact myelin trong>oftrong> cells in the nervous system and has been implicated in myelin biogenesis and/or function. The protein plays a role in the formation, stabilization and maintenance trong>oftrong> glycosphingolipid-enriched membrane microdomains. Down-trong>regulationtrong> trong>oftrong> this gene has been associated with a variety trong>oftrong> human epithelial malignancies. Alternative splicing produces four transcript variants which vary from each other by the presence or absence trong>oftrong> alternatively spliced exons 2 and 3. [provided by RefSeq, May 2012]
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cell division cycle 37-like 1
CDC37L1 is a cytoplasmic phosphoprotein that exists in complex with HSP90 (HSPCA; MIM 140571) as well as several other proteins involved in HSP90-mediated protein folding (Scholz et al., 2001 [PubMed 11413142]).[supplied by OMIM, Mar 2008]
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carcinoembryonic antigen-related cell adhesion molecule pseudogene 8
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carcinoembryonic antigen-related cell adhesion molecule pseudogene 9
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carcinoembryonic antigen-related cell adhesion molecule pseudogene 2
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carcinoembryonic antigen-related cell adhesion molecule pseudogene 3
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carcinoembryonic antigen-related cell adhesion molecule pseudogene 1
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carcinoembryonic antigen-related cell adhesion molecule pseudogene 6
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carcinoembryonic antigen-related cell adhesion molecule pseudogene 7
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carcinoembryonic antigen-related cell adhesion molecule pseudogene 4
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carcinoembryonic antigen-related cell adhesion molecule pseudogene 5
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killer cell immunoglobulin-like receptor 2DS3
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proliferating cell nuclear antigen pseudogene 3
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neuroepithelial cell transforming 1 pseudogene
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inducible T-cell co-stimulator ligand
Enables identical protein binding activity and receptor ligand activity. Involved in T follicular helper cell differentiation. Located in intracellular membrane-bounded organelle. Is active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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Down syndrome cell adhesion molecule like 1
The protein encoded by this gene is a member trong>oftrong> the Ig superfamily trong>oftrong> cell adhesion molecules and is involved in neuronal differentiation. The encoded membrane-bound protein localizes to the cell surface, where it forms aggregates that repel neuronal processes trong>oftrong> the same cell type. [provided by RefSeq, Sep 2016]
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cell death-inducing DFFA-like effector b
Enables identical protein binding activity. Involved in lipid droplet fusion and trong>positivetrong> trong>regulationtrong> trong>oftrong> apoptotic process. Acts upstream trong>oftrong> or within apoptotic process. Located in cytosol and perinuclear region trong>oftrong> cytoplasm. Is active in lipid droplet. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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carcinoembryonic antigen-related cell adhesion molecule 22, pseudogene
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T-cell activation antigen p250
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MCF.2 cell line derived transforming sequence-like 2
Predicted to enable guanyl-nucleotide exchange factor activity. Predicted to be located in cytosol. Predicted to be active in cytoplasm. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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cell growth regulator with EF-hand domain 1
Predicted to enable calcium ion binding activity. Predicted to be involved in negative trong>regulationtrong> trong>oftrong> cell population proliferation. Predicted to be located in extracellular region. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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mucin 20, cell surface associated pseudogene
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B-cell CLL/lymphoma 10
This gene was identified by its translocation in a case trong>oftrong> mucosa-associated lymphoid tissue (MALT) lymphoma. The protein encoded by this gene contains a caspase recruitment domain (CARD), and has been shown to induce apoptosis and to activate NF-kappaB. This protein is reported to interact with other CARD domain containing proteins including CARD9, 10, 11 and 14, which are thought to function as upstream regulators in NF-kappaB signaling. This protein is found to form a complex with MALT1, a protein encoded by another gene known to be translocated in MALT lymphoma. MALT1 and this protein are thought to synergize in the activation trong>oftrong> NF-kappaB, and the detrong>regulationtrong> trong>oftrong> either trong>oftrong> them may contribute to the same pathogenetic process that leads to the malignancy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2016]
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L1 cell adhesion molecule
The protein encoded by this gene is an axonal glycoprotein belonging to the immunoglobulin supergene family. The ectodomain, consisting trong>oftrong> several immunoglobulin-like domains and fibronectin-like repeats (type III), is linked via a single transmembrane sequence to a conserved cytoplasmic domain. This cell adhesion molecule plays an important role in nervous system development, including neuronal migration and differentiation. Mutations in the gene cause X-linked neurological syndromes known as CRASH (corpus callosum hypoplasia, retardation, aphasia, spastic paraplegia and hydrocephalus). Alternative splicing trong>oftrong> this gene results in multiple transcript variants, some trong>oftrong> which include an alternate exon that is considered to be specific to neurons. [provided by RefSeq, May 2013]
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Temperature sensitivity complementation, cell cycle specific
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T cell receptor beta variable 27
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor alpha variable 38-1
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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cell cycle associated protein 1
Enables several functions, including ATP binding activity; molecular condensate scaffold activity; and signaling adaptor activity. Involved in membraneless organelle assembly; trong>positivetrong> trong>regulationtrong> trong>oftrong> stress granule assembly; and trong>regulationtrong> trong>oftrong> gene expression. Located in cell leading edge and cytosol. Is active in intracellular membraneless organelle. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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embryonic stem cell related (non-protein coding)
Part trong>oftrong> nucleus. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 3-2 (pseudogene)
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killer cell lectin-like receptor subfamily F, member 2
Enables protein homodimerization activity. Predicted to be involved in natural killer cell degranulation and trong>positivetrong> trong>regulationtrong> trong>oftrong> cytokine production. Predicted to act upstream trong>oftrong> or within natural killer cell activation and trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell mediated cytotoxicity. Located in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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killer cell lectin-like receptor subfamily F, member 1
KLRF1, an activating homodimeric C-type lectin-like receptor (CTLR), is expressed on nearly all natural killer (NK) cells and stimulates their cytoxicity and cytokine release (Kuttruff et al., 2009 [PubMed 18922855]).[supplied by OMIM, Oct 2009]
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speedy/RINGO cell cycle regulator family member E19, pseudogene
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Fas cell surface death receptor
The protein encoded by this gene is a member trong>oftrong> the TNF-receptor superfamily. This receptor contains a death domain. It has been shown to play a central role in the physiological trong>regulationtrong> trong>oftrong> programmed cell death, and has been implicated in the pathogenesis trong>oftrong> various malignancies and diseases trong>oftrong> the immune system. The interaction trong>oftrong> this receptor with its ligand allows the formation trong>oftrong> a death-inducing signaling complex that includes Fas-associated death domain protein (FADD), caspase 8, and caspase 10. The autoproteolytic processing trong>oftrong> the caspases in the complex triggers a downstream caspase cascade, and leads to apoptosis. This receptor has been also shown to activate NF-kappaB, MAPK3/ERK1, and MAPK8/JNK, and is found to be involved in transducing the proliferating signals in normal diploid fibroblast and T cells. Several alternatively spliced transcript variants have been described, some trong>oftrong> which are candidates for nonsense-mediated mRNA decay (NMD). The istrong>oftrong>orms lacking the transmembrane domain may negatively regulate the apoptosis mediated by the full length istrong>oftrong>orm. [provided by RefSeq, Mar 2011]
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squamous cell carcinoma antigen recognized by T cells 3
The protein encoded by this gene is an RNA-binding nuclear protein that is a tumor-rejection antigen. This antigen possesses tumor epitopes capable trong>oftrong> inducing HLA-A24-restricted and tumor-specific cytotoxic T lymphocytes in cancer patients and may be useful for specific immunotherapy. This gene product is found to be an important cellular factor for HIV-1 gene expression and viral replication. It also associates transiently with U6 and U4/U6 snRNPs during the recycling phase trong>oftrong> the spliceosome cycle. This encoded protein is thought to be involved in the trong>regulationtrong> trong>oftrong> mRNA splicing. [provided by RefSeq, Jul 2008]
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leukocyte cell derived chemotaxin 1
This gene encodes a glycosylated transmembrane protein that is cleaved to form a mature, secreted protein. The N-terminus trong>oftrong> the precursor protein shares characteristics with other surfactant proteins and is sometimes called chondrosurfactant protein although no biological activity has yet been defined for it. The C-terminus trong>oftrong> the precursor protein contains a 25 kDa mature protein called leukocyte cell-derived chemotaxin-1 or chondromodulin-1. The mature protein promotes chondrocyte growth and inhibits angiogenesis. This gene is expressed in the avascular zone trong>oftrong> prehypertrophic cartilage and its expression decreases during chondrocyte hypertrophy and vascular invasion. The mature protein likely plays a role in endochondral bone development by permitting cartilaginous anlagen to be vascularized and replaced by bone. It may be involved also in the broad control trong>oftrong> tissue vascularization during development. Alternative splicing results in multiple transcript variants encoding different istrong>oftrong>orms. [provided by RefSeq, Jul 2008]
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leukocyte cell-derived chemotaxin 2
This gene encodes a secreted, 16 kDa protein that acts as a chemotactic factor to neutrophils and stimulates the growth trong>oftrong> chondrocytes and osteoblasts. This protein has high sequence similarity to the chondromodulin repeat regions trong>oftrong> the chicken myb-induced myeloid 1 protein. A polymorphism in this gene may be associated with rheumatoid arthritis. [provided by RefSeq, Jul 2008]
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opioid binding protein/cell adhesion molecule-like
This gene encodes a member trong>oftrong> the IgLON subfamily in the immunoglobulin protein superfamily trong>oftrong> proteins. The encoded preprotein is proteolytically processed to generate the mature protein. This protein is localized in the plasma membrane and may have an accessory role in opioid receptor function. This gene has an ortholog in rat and bovine. The opioid binding-cell adhesion molecule encoded by the rat gene binds opioid alkaloids in the presence trong>oftrong> acidic lipids, exhibits selectivity for mu ligands and acts as a GPI-anchored protein. Since the encoded protein is highly conserved in species during evolution, it may have a fundamental role in mammalian systems. Alternative splicing results in multiple transcript variants, at least one trong>oftrong> which encodes an istrong>oftrong>orm that is proteolytically processed. [provided by RefSeq, Jan 2016]
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WD repeat containing planar cell polarity effector
This gene encodes a cytoplasmic WD40 repeat protein. A similar gene in frogs encodes a planar cell polarity protein that plays a critical role in collective cell movement and ciliogenesis by mediating septin localization. Mutations in this gene are associated with Bardet-Biedl syndrome 15 and may also play a role in Meckel-Gruber syndrome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2014]
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cell adhesion associated, oncogene regulated pseudogene
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speedy/RINGO cell cycle regulator family member E17
Enables acetylcholine receptor regulator activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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speedy/RINGO cell cycle regulator family member E16
Predicted to enable protein kinase binding activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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speedy/RINGO cell cycle regulator family member A
Enables protein kinase activator activity and protein kinase binding activity. Involved in several processes, including G1/S transition trong>oftrong> mitotic cell cycle; trong>positivetrong> trong>regulationtrong> trong>oftrong> cell population proliferation; and trong>positivetrong> trong>regulationtrong> trong>oftrong> protein kinase activity. Located in nucleoplasm. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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speedy/RINGO cell cycle regulator family member C
Enables protein kinase binding activity. Predicted to be located in nucleus. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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B-cell acute lymphoblastic leukemia expressed
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T cell receptor beta variable 12-4
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 12-5
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 12-1 (pseudogene)
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T cell receptor beta variable 12-2 (pseudogene)
Predicted to be involved in immune system process. Predicted to be located in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 12-3
Predicted to enable MHC protein binding activity and peptide antigen binding activity. Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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programmed cell death 2-like pseudogene
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cell adhesion associated, oncogene regulated pseudogene
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killer cell immunoglobulin-like receptor, three domains, pseudogene 1
Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets trong>oftrong> T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content trong>oftrong> the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number trong>oftrong> extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets trong>oftrong> HLA class I molecules; thus, KIR proteins are thought to play an important role in trong>regulationtrong> trong>oftrong> the immune response. This gene is one trong>oftrong> the `framework` loci that is present on all haplotypes. This gene is considered to be a pseudogene based on the absence trong>oftrong> transcription and it lacks several functional domains compared to other killer cell immunoglobulin-like receptors. A rare haplotype, the result trong>oftrong> a recombinantion event, has two copies trong>oftrong> this gene, one trong>oftrong> which may encode a secreted protein. (PMID: 15580659)[provided by RefSeq, Mar 2011]
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smooth muscle and endothelial cell enriched migration/differentiation-associated long non-coding RNA
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B-cell linker
This gene encodes a cytoplasmic linker or adaptor protein that plays a critical role in B cell development. This protein bridges B cell receptor-associated kinase activation with downstream signaling pathways, thereby affecting various biological functions. The phosphorylation trong>oftrong> five tyrosine residues is necessary for this protein to nucleate distinct signaling effectors following B cell receptor activation. Mutations in this gene cause hypoglobulinemia and absent B cells, a disease in which the pro- to pre-B-cell transition is developmentally blocked. Deficiency in this protein has also been shown in some cases trong>oftrong> pre-B acute lymphoblastic leukemia. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, May 2012]
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T cell-interacting, activating receptor on myeloid cells 1
Enables immunoglobulin receptor binding activity. Involved in negative trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell activation. Located in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T-cell immunoglobulin and mucin domain containing 4
Predicted to enable phosphatidylserine binding activity. Predicted to be involved in apoptotic cell clearance and cytoskeletal rearrangement involved in phagocytosis, engulfment. Predicted to be located in extracellular region and plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 9
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 2
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor beta variable 1 (pseudogene)
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T cell receptor beta variable C
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T cell receptor beta variable B (pseudogene)
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T cell receptor beta variable A (pseudogene)
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mediator trong>oftrong> cell motility 1 pseudogene
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mucin 3A, cell surface associated
The mucin genes encode epithelial glycoproteins, some trong>oftrong> which are secreted and some membrane bound. Each trong>oftrong> the genes contains at least one large domain trong>oftrong> tandemly repeated sequence that encodes the peptide sequence rich in serine and/or threonine residues, which carries most trong>oftrong> the O-linked glycosylation (Gendler and Spicer, 1995 [PubMed 7778880]).[supplied by OMIM, Aug 2008]
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mucin 3B, cell surface associated
Predicted to be located in Golgi lumen and plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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defender against cell death 1
DAD1, the defender against apoptotic cell death, was initially identified as a negative regulator trong>oftrong> programmed cell death in the temperature sensitive tsBN7 cell line. The DAD1 protein disappeared in temperature-sensitive cells following a shift to the nonpermissive temperature, suggesting that loss trong>oftrong> the DAD1 protein triggered apoptosis. DAD1 is believed to be a tightly associated subunit trong>oftrong> oligosaccharyltransferase both in the intact membrane and in the purified enzyme, thus reflecting the essential nature trong>oftrong> N-linked glycosylation in eukaryotes. [provided by RefSeq, Jul 2008]
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host cell factor C2
This gene encodes one trong>oftrong> two proteins which interact with VP16, a herpes simplex virus protein that initiates virus infection. Both the encoded protein and the original Herpes host cell factor interact with VP16 through a beta-propeller domain. The original Herpes host cell factor, however, is effective at initiating viral infection while the encoded protein is not. Transcripts trong>oftrong> varying length due to alternative polyadenylation signals have been described. [provided by RefSeq, Jul 2008]
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host cell factor C1
This gene is a member trong>oftrong> the host cell factor family and encodes a protein with five Kelch repeats, a fibronectin-like motif, and six HCF repeats, each trong>oftrong> which contains a highly specific cleavage signal. This nuclear coactivator is proteolytically cleaved at one trong>oftrong> the six possible sites, resulting in the creation trong>oftrong> an N-terminal chain and the corresponding C-terminal chain. The final form trong>oftrong> this protein consists trong>oftrong> noncovalently bound N- and C-terminal chains. The protein is involved in control trong>oftrong> the cell cycle and transcriptional trong>regulationtrong> during herpes simplex virus infection. Alternatively spliced variants which encode different protein istrong>oftrong>orms have been described; however, not all variants have been fully characterized. [provided by RefSeq, Jul 2008]
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B-cell receptor-associated protein 31 pseudogene 2
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Pancreatic beta cell, agenesis trong>oftrong>
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membrane-spanning 4-domains, subfamily A, member 3 (hematopoietic cell-specific)
This gene encodes a member trong>oftrong> the membrane-spanning 4A gene family. Members trong>oftrong> this protein family are characterized by common structural features and similar intron/exon splice boundaries and display unique expression patterns among hematopoietic cells and nonlymphoid tissues. This family member likely plays a role in signal transduction and may function as a subunit associated with receptor complexes. The gene encoding this protein is localized to 11q12, among a cluster trong>oftrong> related family members. Alternative splicing may result in multiple transcript variants; however, not all variants have been fully described. [provided by RefSeq, Jul 2008]
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T cell receptor alpha variable 34
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 35
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 37 (pseudogene)
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 30
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 32 (pseudogene)
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 33 (pseudogene)
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 39
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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killer cell immunoglobulin-like receptor, two domains, pseudogene 1
Predicted to be involved in immune response-regulating signaling pathway. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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testicular cell adhesion molecule 1, pseudogene
This pseudogene is located downstream from the growth hormone locus on chromosome 17. This locus evolved by a series trong>oftrong> partial duplications that have disrupted the human gene. A homologous gene in mouse encodes a testis-specific cell adhesion protein that may play a role in germ cell-Sertoli cell interactions. [provided by RefSeq, Apr 2012]
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bone marrow stromal cell antigen 1
Bone marrow stromal cell antigen-1 is a stromal cell line-derived glycosylphosphatidylinositol-anchored molecule that facilitates pre-B-cell growth. The deduced amino acid sequence exhibits 33% similarity with CD38. BST1 expression is enhanced in bone marrow stromal cell lines derived from patients with rheumatoid arthritis. The polyclonal B-cell abnormalities in rheumatoid arthritis may be, at least in part, attributed to BST1 overexpression in the stromal cell population. [provided by RefSeq, Jul 2008]
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bone marrow stromal cell antigen 2
Bone marrow stromal cells are involved in the growth and development trong>oftrong> B-cells. The specific function trong>oftrong> the protein encoded by the bone marrow stromal cell antigen 2 is undetermined; however, this protein may play a role in pre-B-cell growth and in rheumatoid arthritis. [provided by RefSeq, Jul 2008]
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Purkinje cell protein 4 like 1
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T cell receptor beta variable 29/OR9-2 (non-functional)
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programmed cell death 6 interacting protein
This gene encodes a protein that functions within the ESCRT pathway in the abscission stage trong>oftrong> cytokinesis, in intralumenal endosomal vesicle formation, and in enveloped virus budding. Studies using mouse cells have shown that overexpression trong>oftrong> this protein can block apoptosis. In addition, the product trong>oftrong> this gene binds to the product trong>oftrong> the PDCD6 gene, a protein required for apoptosis, in a calcium-dependent manner. This gene product also binds to endophilins, proteins that regulate membrane shape during endocytosis. Overexpression trong>oftrong> this gene product and endophilins results in cytoplasmic vacuolization, which may be partly responsible for the protection against cell death. Several alternatively spliced transcript variants encoding different istrong>oftrong>orms have been found for this gene. Related pseudogenes have been identified on chromosome 15. [provided by RefSeq, Jan 2012]
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T cell receptor beta variable 24/OR9-2 (pseudogene)
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T cell receptor gamma variable 11 (non-functional)
Predicted to be involved in adaptive immune response. Predicted to be located in external side trong>oftrong> plasma membrane. Predicted to be part trong>oftrong> T cell receptor complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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neural precursor cell expressed, developmentally down-regulated 4, E3 ubiquitin protein ligase
This gene is the founding member trong>oftrong> the NEDD4 family trong>oftrong> HECT ubiquitin ligases that function in the ubiquitin proteasome system trong>oftrong> protein degradation. The encoded protein contains an N-terminal calcium and phospholipid binding C2 domain followed by multiple tryptophan-rich WW domains and, a C-terminal HECT ubiquitin ligase catalytic domain. It plays critical role in the trong>regulationtrong> trong>oftrong> a number trong>oftrong> membrane receptors, endocytic machinery components and the tumor suppressor PTEN. [provided by RefSeq, Jul 2016]
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T cell receptor alpha variable 12-1
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 12-3
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 12-2
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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speedy/RINGO cell cycle regulator family member E20, pseudogene
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undifferentiated embryonic cell transcription factor 1
The protein encoded by this gene is a leucine zipper-containing transcriptional coactivator that may link the upstream activator ATF2 with the basal transcription complex. The encoded protein is closely associated with chromatin and is required for the proper differentiation trong>oftrong> embryonic carcinoma and embryonic stem cells. Found nearly exclusively in pluripotent cells, this protein can also serve as a transcriptional repressor. [provided by RefSeq, Nov 2015]
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carcinoembryonic antigen-related cell adhesion molecule 1 (biliary glycoprotein)
This gene encodes a member trong>oftrong> the carcinoembryonic antigen (CEA) gene family, which belongs to the immunoglobulin superfamily. Two subgroups trong>oftrong> the CEA family, the CEA cell adhesion molecules and the pregnancy-specific glycoproteins, are located within a 1.2 Mb cluster on the long arm trong>oftrong> chromosome 19. Eleven pseudogenes trong>oftrong> the CEA cell adhesion molecule subgroup are also found in the cluster. The encoded protein was originally described in bile ducts trong>oftrong> liver as biliary glycoprotein. Subsequently, it was found to be a cell-cell adhesion molecule detected on leukocytes, epithelia, and endothelia. The encoded protein mediates cell adhesion via homophilic as well as heterophilic binding to other proteins trong>oftrong> the subgroup. Multiple cellular activities have been attributed to the encoded protein, including roles in the differentiation and arrangement trong>oftrong> tissue three-dimensional structure, angiogenesis, apoptosis, tumor suppression, metastasis, and the modulation trong>oftrong> innate and adaptive immune responses. Multiple transcript variants encoding different istrong>oftrong>orms have been reported, but the full-length nature trong>oftrong> all variants has not been defined. [provided by RefSeq, May 2010]
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carcinoembryonic antigen-related cell adhesion molecule 3
This gene encodes a member trong>oftrong> the family trong>oftrong> carcinoembryonic antigen-related cell adhesion molecules (CEACAMs), which are used by several bacterial pathogens to bind and invade host cells. The encoded transmembrane protein directs phagocytosis trong>oftrong> several bacterial species that is dependent on the small GTPase Rac. It is thought to serve an important role in controlling human-specific pathogens by the innate immune system. Alternatively spliced transcript variants have been described. [provided by RefSeq, Mar 2013]
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carcinoembryonic antigen-related cell adhesion molecule 5
This gene encodes a cell surface glycoprotein that represents the founding member trong>oftrong> the carcinoembryonic antigen (CEA) family trong>oftrong> proteins. The encoded protein is used as a clinical biomarker for gastrointestinal cancers and may promote tumor development through its role as a cell adhesion molecule. Additionally, the encoded protein may regulate differentiation, apoptosis, and cell polarity. This gene is present in a CEA family gene cluster on chromosome 19. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]
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carcinoembryonic antigen-related cell adhesion molecule 4
Predicted to enable protein tyrosine kinase binding activity. Involved in phagocytosis. Predicted to be located in membrane. Predicted to be active in cell surface and plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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carcinoembryonic antigen-related cell adhesion molecule 7
This gene encodes a cell surface glycoprotein and member trong>oftrong> the carcinoembryonic antigen (CEA) family trong>oftrong> proteins. Expression trong>oftrong> this gene may be downregulated in colon and rectal cancer. Additionally, lower expression levels trong>oftrong> this gene may be predictive trong>oftrong> rectal cancer recurrence. This gene is present in a CEA family gene cluster on chromosome 19. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]
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carcinoembryonic antigen-related cell adhesion molecule 6 (non-specific cross reacting antigen)
This gene encodes a protein that belongs to the carcinoembryonic antigen (CEA) family whose members are glycosyl phosphatidyl inositol (GPI) anchored cell surface glycoproteins. Members trong>oftrong> this family play a role in cell adhesion and are widely used as tumor markers in serum immunoassay determinations trong>oftrong> carcinoma. This gene affects the sensitivity trong>oftrong> tumor cells to adenovirus infection. The protein encoded by this gene acts as a receptor for adherent-invasive E. coli adhesion to the surface trong>oftrong> ileal epithelial cells in patients with Crohn's disease. This gene is clustered with genes and pseudogenes trong>oftrong> the cell adhesion molecules subgroup trong>oftrong> the CEA family on chromosome 19. [provided by RefSeq, Apr 2014]
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carcinoembryonic antigen-related cell adhesion molecule 8
Enables protein heterodimerization activity. Involved in heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules. Located in cell surface and extracellular space. Biomarker trong>oftrong> severe acute respiratory syndrome. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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histone cell cycle regulator pseudogene 1
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cell division cycle 42 pseudogene 3
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T cell receptor alpha variable 13-1
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha variable 13-2
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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basal cell adhesion molecule (Lutheran blood group)
This gene encodes Lutheran blood group glycoprotein, a member trong>oftrong> the immunoglobulin superfamily and a receptor for the extracellular matrix protein, laminin. The protein contains five extracellular immunoglobulin domains, a single transmembrane domain, and a short C-terminal cytoplasmic tail. This protein may play a role in epithelial cell cancer and in vaso-occlusion trong>oftrong> red blood cells in sickle cell disease. Polymorphisms in this gene define some trong>oftrong> the antigens in the Lutheran system and also the Auberger system. Inactivating variants trong>oftrong> this gene result in the recessive Lutheran null phenotype, Lu(a-b-), trong>oftrong> the Lutheran blood group. Two transcript variants encoding different istrong>oftrong>orms have been found for this gene. [provided by RefSeq, May 2012]
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CWF19-like 1, cell cycle control (S. pombe)
This gene encodes a member trong>oftrong> the CWF19 protein family. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia-17 and mild cognitive disability. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2014]
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CWF19-like 2, cell cycle control (S. pombe)
Predicted to be involved in mRNA splicing, via spliceosome. Predicted to be located in nucleoplasm. Predicted to be part trong>oftrong> post-mRNA release spliceosomal complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 3
Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets trong>oftrong> T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content trong>oftrong> the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number trong>oftrong> extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets trong>oftrong> HLA class I molecules; thus, KIR proteins are thought to play an important role in trong>regulationtrong> trong>oftrong> the immune response. [provided by RefSeq, Jul 2008]
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killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 2
Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets trong>oftrong> T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content trong>oftrong> the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number trong>oftrong> extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets trong>oftrong> HLA class I molecules; thus, KIR proteins are thought to play an important role in trong>regulationtrong> trong>oftrong> the immune response. [provided by RefSeq, Jul 2008]
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killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 1
Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets trong>oftrong> T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content trong>oftrong> the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number trong>oftrong> extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets trong>oftrong> HLA class I molecules; thus, KIR proteins are thought to play an important role in trong>regulationtrong> trong>oftrong> the immune response. [provided by RefSeq, Jul 2008]
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killer cell immunoglobulin-like receptor, two domains, long cytoplasmic tail, 4
Killer cell immunoglobulin-like receptors (KIRs) are transmembrane glycoproteins expressed by natural killer cells and subsets trong>oftrong> T cells. The KIR genes are polymorphic and highly homologous and they are found in a cluster on chromosome 19q13.4 within the 1 Mb leukocyte receptor complex (LRC). The gene content trong>oftrong> the KIR gene cluster varies among haplotypes, although several `framework` genes are found in all haplotypes (KIR3DL3, KIR3DP1, KIR3DL4, KIR3DL2). The KIR proteins are classified by the number trong>oftrong> extracellular immunoglobulin domains (2D or 3D) and by whether they have a long (L) or short (S) cytoplasmic domain. KIR proteins with the long cytoplasmic domain transduce inhibitory signals upon ligand binding via an immune tyrosine-based inhibitory motif (ITIM), while KIR proteins with the short cytoplasmic domain lack the ITIM motif and instead associate with the TYRO protein tyrosine kinase binding protein to transduce activating signals. The ligands for several KIR proteins are subsets trong>oftrong> HLA class I molecules; thus, KIR proteins are thought to play an important role in trong>regulationtrong> trong>oftrong> the immune response. This gene is one trong>oftrong> the `framework` loci that is present on all haplotypes. Alternate alleles trong>oftrong> this gene are represented on multiple alternate reference loci (ALT_REF_LOCs). Alternative splicing results in multiple transcript variants, some trong>oftrong> which may not be annotated on the primary reference assembly. [provided by RefSeq, Jul 2016]
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cell division cycle 73, Paf1/RNA polymerase II complex component, homolog (S. cerevisiae) pseudogene
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T cell receptor beta variable 29-1
Predicted to be involved in cell surface receptor signaling pathway. Predicted to be part trong>oftrong> T cell receptor complex. Predicted to be active in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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T cell receptor alpha joining 4
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 5
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 6
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 7
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 1 (non-functional)
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 2 (non-functional)
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 3
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 8
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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T cell receptor alpha joining 9
T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface trong>oftrong> antigen presenting cells (APC). Each T cell receptor is a dimer consisting trong>oftrong> one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization trong>oftrong> the T cell receptor alpha and delta loci. Both the alpha and delta loci include V (variable), J (joining), and C (constant) segments and the delta locus also includes diversity (D) segments. The delta locus is situated within the alpha locus, between the alpha V and J segments. During T cell development, the delta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The alpha chain is synthesized by recombination joining a single V segment with a J segment. For both chains, the C segment is later joined by splicing at the RNA level. Recombination trong>oftrong> many different V segments with several J segments provides a wide range trong>oftrong> antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional trong>oftrong> nucleotides by terminal deoxynucleotidyltransferase. Five variable segments can be used in either alpha or delta chains and are described by TRAV/DV symbols. Several V and J segments trong>oftrong> the alpha locus are known to be incapable trong>oftrong> encoding a protein and are considered pseudogenes. [provided by RefSeq, Aug 2016]
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germ cell-less, spermatogenesis associated 1
This gene encodes a nuclear envelope protein that appears to be involved in spermatogenesis, either directly or by influencing genes that play a more direct role in the process. This multi-exon locus is the homolog trong>oftrong> the mouse and drosophila germ cell-less gene but the human genome also contains a single-exon locus on chromosome 5 that contains an open reading frame capable trong>oftrong> encoding a highly-related protein. [provided by RefSeq, Jul 2008]
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cell adhesion molecule 4
Enables vascular endothelial growth factor receptor 2 binding activity. Involved in several processes, including negative trong>regulationtrong> trong>oftrong> protein phosphorylation; trong>regulationtrong> trong>oftrong> Rac protein signal transduction; and trong>regulationtrong> trong>oftrong> wound healing. Located in cell leading edge and cell-cell contact zone. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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cell adhesion molecule 2
This gene encodes a member trong>oftrong> the synaptic cell adhesion molecule 1 (SynCAM) family which belongs to the immunoglobulin (Ig) superfamily. The encoded protein has three Ig-like domains and a cytosolic protein 4.1 binding site near the C-terminus. Proteins belonging to the protein 4.1 family crosslink spectrin and interact with other cytoskeletal proteins. Multiple transcript variants encoding different istrong>oftrong>orms have been found for this gene. [provided by RefSeq, Feb 2012]
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cell adhesion molecule 3
The protein encoded by this gene is a calcium-independent cell-cell adhesion protein that can form homodimers or heterodimers with other nectin proteins. The encoded protein has both homophilic and heterophilic cell-cell adhesion activity. This gene is reported to be a tumor suppressor gene. [provided by RefSeq, Oct 2016]
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cell adhesion molecule 1
Enables signaling receptor binding activity. Involved in several processes, including cell recognition; trong>positivetrong> trong>regulationtrong> trong>oftrong> cytokine production; and susceptibility to natural killer cell mediated cytotoxicity. Located in plasma membrane. Implicated in breast carcinoma and prostate cancer. Biomarker trong>oftrong> cervix uteri carcinoma in situ. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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cell death activator CIDE-3-like
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vegetative cell wall protein gp1-like
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chymase 1, mast cell
This gene encodes a chymotryptic serine proteinase that belongs to the peptidase family S1. It is expressed in mast cells and is thought to function in the degradation trong>oftrong> the extracellular matrix, the trong>regulationtrong> trong>oftrong> submucosal gland secretion, and the generation trong>oftrong> vasoactive peptides. In the heart and blood vessels, this protein, rather than angiotensin converting enzyme, is largely responsible for converting angiotensin I to the vasoactive peptide angiotensin II. Alternative splicing results in multiple variants. [provided by RefSeq, Apr 2015]
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B-cell CLL/lymphoma 11A (zinc finger protein)
This gene encodes a C2H2 type zinc-finger protein by its similarity to the mouse Bcl11a/Evi9 protein. The corresponding mouse gene is a common site trong>oftrong> retroviral integration in myeloid leukemia, and may function as a leukemia disease gene, in part, through its interaction with BCL6. During hematopoietic cell differentiation, this gene is down-regulated. It is possibly involved in lymphoma pathogenesis since translocations associated with B-cell malignancies also deregulates its expression. Multiple transcript variants encoding several different istrong>oftrong>orms have been found for this gene. [provided by RefSeq, Jul 2008]
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B-cell CLL/lymphoma 11B (zinc finger protein)
This gene encodes a C2H2-type zinc finger protein and is closely related to BCL11A, a gene whose translocation may be associated with B-cell malignancies. Although the specific function trong>oftrong> this gene has not been determined, the encoded protein is known to be a transcriptional repressor, and is regulated by the NURD nucleosome remodeling and histone deacetylase complex. Four alternatively spliced transcript variants encoding distinct istrong>oftrong>orms have been found for this gene. [provided by RefSeq, Aug 2013]
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biorientation trong>oftrong> chromosomes in cell division 1 pseudogene 2
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biorientation trong>oftrong> chromosomes in cell division 1 pseudogene 1
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Natural killer cell deficiency, familial isolated
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cell division cycle 42 pseudogene
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fizzy/cell division cycle 20 related 1 (Drosophila)
Enables ubiquitin-like ligase-substrate adaptor activity. Involved in anaphase-promoting complex-dependent catabolic process; mitotic G2 DNA damage checkpoint signaling; and trong>positivetrong> trong>regulationtrong> trong>oftrong> ubiquitin protein ligase activity. Located in nuclear membrane and nucleoplasm. Implicated in developmental and epileptic encephalopathy 109. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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RHO family interacting cell polarization regulator 1
Enables 14-3-3 protein binding activity. Involved in several processes, including establishment trong>oftrong> Golgi localization; negative trong>regulationtrong> trong>oftrong> Rho guanyl-nucleotide exchange factor activity; and negative trong>regulationtrong> trong>oftrong> Rho protein signal transduction. Located in Golgi apparatus; cell leading edge; and membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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nectin cell adhesion molecule 1
This gene encodes an adhesion protein that plays a role in the organization trong>oftrong> adherens junctions and tight junctions in epithelial and endothelial cells. The protein is a calcium(2+)-independent cell-cell adhesion molecule that belongs to the immunoglobulin superfamily and has 3 extracellular immunoglobulin-like loops, a single transmembrane domain (in some istrong>oftrong>orms), and a cytoplasmic region. This protein acts as a receptor for glycoprotein D (gD) trong>oftrong> herpes simplex viruses 1 and 2 (HSV-1, HSV-2), and pseudorabies virus (PRV) and mediates viral entry into epithelial and neuronal cells. Mutations in this gene cause cleft lip and palate/ectodermal dysplasia 1 syndrome (CLPED1) as well as non-syndromic cleft lip with or without cleft palate (CL/P). Alternative splicing results in multiple transcript variants encoding proteins with distinct C-termini. [provided by RefSeq, Oct 2009]
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cell migration inducing hyaluronidase 2
This gene encodes a type II transmembrane protein that belongs to the interferon-induced transmembrane (IFITM) protein superfamily. The encoded protein functions as a cell surface hyaluronidase that cleaves extracellular high molecular weight hyaluronan into intermediate size fragments before internalization and degradation in the lysosome. It also has an interferon-mediated antiviral function in humans through activation trong>oftrong> the JAK STAT signaling pathway. The activation trong>oftrong> this gene by transcription factor SOX4 in breast cancer cells has been shown to mediate the pathological effects trong>oftrong> SOX4 on cancer progression. Naturally occurring mutations in this gene are associated with autosomal recessive non-syndromic hearing loss. [provided by RefSeq, Mar 2017]
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nectin cell adhesion molecule 4
This gene encodes a member trong>oftrong> the nectin family. The encoded protein contains two immunoglobulin-like (Ig-like) C2-type domains and one Ig-like V-type domain. It is involved in cell adhesion through trans-homophilic and -heterophilic interactions. It is a single-pass type I membrane protein. The soluble form is produced by proteolytic cleavage at the cell surface by the metalloproteinase ADAM17/TACE. The secreted form is found in both breast tumor cell lines and breast tumor patients. Mutations in this gene are the cause trong>oftrong> ectodermal dysplasia-syndactyly syndrome type 1, an autosomal recessive disorder. Alternatively spliced transcript variants have been found but the full-length nature trong>oftrong> the variant has not been determined.[provided by RefSeq, Jan 2011]
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nectin cell adhesion molecule 2
This gene encodes a single-pass type I membrane glycoprotein with two Ig-like C2-type domains and an Ig-like V-type domain. This protein is one trong>oftrong> the plasma membrane components trong>oftrong> adherens junctions. It also serves as an entry for certain mutant strains trong>oftrong> herpes simplex virus and pseudorabies virus, and it is involved in cell to cell spreading trong>oftrong> these viruses. Variations in this gene have been associated with differences in the severity trong>oftrong> multiple sclerosis. Alternate transcriptional splice variants, encoding different istrong>oftrong>orms, have been characterized. [provided by RefSeq, Jul 2008]
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PATJ crumbs cell polarity complex component
This gene encodes a protein with multiple PDZ domains. PDZ domains mediate protein-protein interactions, and proteins with multiple PDZ domains trong>oftrong>ten organize multimeric complexes at the plasma membrane. This protein localizes to tight junctions and to the apical membrane trong>oftrong> epithelial cells. A similar protein in Drosophila is a scaffolding protein which tethers several members trong>oftrong> a multimeric signaling complex in photoreceptors. [provided by RefSeq, Jul 2008]
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nectin cell adhesion molecule 3
This gene encodes a member trong>oftrong> the nectin family trong>oftrong> proteins, which function as adhesion molecules at adherens junctions. This family member interacts with other nectin-like proteins and with afadin, a filamentous actin-binding protein involved in the trong>regulationtrong> trong>oftrong> directional motility, cell proliferation and survival. This gene plays a role in ocular development involving the ciliary body. Mutations in this gene are believed to result in congenital ocular defects. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2011]
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RHO family interacting cell polarization regulator 2
This gene encodes an atypical inhibitor trong>oftrong> the small G protein RhoA. Inhibition trong>oftrong> RhoA activity by the encoded protein mediates myoblast fusion and polarization trong>oftrong> T cells and neutrophils. The encoded protein is a component trong>oftrong> hair cell stereocilia that is essential for hearing. A splice site mutation in this gene results in hearing loss in human patients. [provided by RefSeq, Sep 2016]
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alkaline phosphatase, germ cell
There are at least four distinct but related alkaline phosphatases: intestinal, placental, placental-like, and liver/bone/kidney (tissue non-specific). The product trong>oftrong> this gene is a membrane bound glycosylated enzyme, localized to testis, thymus and certain germ cell tumors, that is closely related to both the placental and intestinal forms trong>oftrong> alkaline phosphatase. [provided by RefSeq, Jul 2008]
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germ cell-less 2, spermatogenesis associated
This locus shares a high degree trong>oftrong> identity with the multi-exon germ cell-less gene on chromosome 2. Despite its single-exon nature, this chromosome 5 locus contains an open reading frame that could putatively encode a full-length germ cell-less related protein. [provided by RefSeq, Jul 2008]
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cell cycle regulator trong>oftrong> NHEJ
Predicted to enable molecular adaptor activity. Involved in double-strand break repair via nonhomologous end joining and negative trong>regulationtrong> trong>oftrong> double-strand break repair via nonhomologous end joining. Located in cytoplasm and nucleus. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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DAP3 binding cell death enhancer 1
Enables protein kinase binding activity and protein serine/threonine kinase activator activity. Involved in several processes, including HRI-mediated signaling; trong>positivetrong> trong>regulationtrong> trong>oftrong> mitophagy; and response to iron ion starvation. Located in mitochondrial inner membrane. Is active in cytosol and mitochondrial outer membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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speedy/RINGO cell cycle regulator family member E9
Enables acetylcholine receptor regulator activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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pancreatic progenitor cell differentiation and proliferation factor like
Predicted to be involved in cell differentiation. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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speedy/RINGO cell cycle regulator family member E10
Enables acetylcholine receptor regulator activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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germ cell nuclear acidic peptidase
Enables SUMO polymer binding activity. Involved in protein-DNA covalent cross-linking repair. Located in PML body. Implicated in X-linked spermatogenic failure 4. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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speedy/RINGO cell cycle regulator family member E21
Predicted to enable protein kinase binding activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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regulator trong>oftrong> hemoglobinization and erythroid cell expansion
Enables erythropoietin receptor binding activity. Involved in erythropoietin-mediated signaling pathway and trong>positivetrong> trong>regulationtrong> trong>oftrong> erythrocyte differentiation. Located in plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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speedy/RINGO cell cycle regulator family member E12
Predicted to enable protein kinase binding activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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killer cell lectin like receptor A1, pseudogene
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NOTCH1 associated lncRNA in T cell acute lymphoblastic leukemia 1
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cell death inducing DFFA like effector c pseudogene 1
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mucin 20, cell surface associated pseudogene 1
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P38 inhibited cutaneous squamous cell carcinoma associated lincRNA
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NELL2 interacting cell ontogeny regulator 1
Predicted to enable mRNA 3'-UTR binding activity. Predicted to be involved in 3'-UTR-mediated mRNA stabilization and spermatogenesis. Predicted to be located in perinuclear region trong>oftrong> cytoplasm. Predicted to be active in extracellular space. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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lysosome cell death regulator
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stem cell inhibitory RNA transcript
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speedy/RINGO cell cycle regulator family member E13
Enables acetylcholine receptor regulator activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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speedy/RINGO cell cycle regulator family member E8
Enables acetylcholine receptor regulator activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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speedy/RINGO cell cycle regulator family member E14
Predicted to enable protein kinase binding activity. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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cell division cycle 50 P4-ATPase accessory subunit A
Enables aminophospholipid flippase activity and structural molecule activity. Involved in several processes, including phospholipid transport; trong>positivetrong> trong>regulationtrong> trong>oftrong> transport; and xenobiotic transmembrane transport. Located in endoplasmic reticulum and plasma membrane. Part trong>oftrong> early endosome membrane; late endosome membrane; and phospholipid-translocating ATPase complex. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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cell division cycle 50 P4-ATPase accessory subunit B
Enables aminophospholipid flippase activity. Involved in aminophospholipid transport and trong>positivetrong> trong>regulationtrong> trong>oftrong> protein exit from endoplasmic reticulum. Part trong>oftrong> phospholipid-translocating ATPase complex and plasma membrane. [provided by Alliance trong>oftrong> Genome Resources, Mar 2025]
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killer cell immunoglobulin-like receptor 2DL4-like
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t cell costimulation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell costimulation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell costimulation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cd4-trong>positivetrong>, alpha-beta t cell costimulation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell costimulation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell costimulation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>regulationtrong> trong>oftrong> cd4-trong>positivetrong>, alpha-beta t cell costimulation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2023
genes participating in the negative trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell costimulation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell costimulation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2025
genes participating in the negative trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell costimulation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell costimulation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2015
genes participating in the cd4-trong>positivetrong>, alpha-beta t cell costimulation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2023
genes participating in the CD4-trong>positivetrong>, alpha-beta T cell costimulation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2025
genes participating in the CD4-trong>positivetrong>, alpha-beta T cell costimulation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>regulationtrong> trong>oftrong> t cell costimulation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2023
genes participating in the negative trong>regulationtrong> trong>oftrong> T cell costimulation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>regulationtrong> trong>oftrong> T cell costimulation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2025
genes participating in the negative trong>regulationtrong> trong>oftrong> T cell costimulation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>regulationtrong> trong>oftrong> T cell costimulation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GeneRIF Biological Term Annotations
genes co-occuring with the biological term costimulation in literature-supported statements describing functions trong>oftrong> genes from the GeneRIF Biological Term Annotations dataset.
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From Reactome Pathways 2014
proteins participating in the Costimulation by the CD28 family pathway from the Reactome Pathways dataset.
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From Reactome Pathways 2024
proteins participating in the Costimulation by the CD28 family pathway from the Reactome Pathways 2024 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cd4-trong>positivetrong>, cd25-trong>positivetrong>, alpha-beta regulatory t cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell differentiation involved in immune response biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell differentiation involved in immune response biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From ClinVar Gene-Phenotype Associations
genes associated with the Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-trong>positivetrong>, NK cell-trong>positivetrong> phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
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From CTD Gene-Disease Associations
genes/proteins associated with the disease Severe Combined Immunodeficiency, Autosomal Recessive, T Cell Negative, B Cell trong>Positivetrong>, NK Cell trong>Positivetrong> from the curated CTD Gene-Disease Associations dataset.
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From MGI Mouse Phenotype Associations 2023
gene mutations causing the increased KLRG1-trong>positivetrong> CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
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From IMPC Knockout Mouse Phenotypes
gene knockouts causing the increased KLRG1-trong>positivetrong> CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell number phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
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From GO Biological Process Annotations 2015
genes participating in the cerebellar purkinje cell-granule cell precursor cell signaling involved in trong>regulationtrong> trong>oftrong> granule cell precursor cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2023
genes participating in the cerebellar Purkinje cell-granule cell precursor cell signaling involved in trong>regulationtrong> trong>oftrong> granule cell precursor cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t cell activation via t cell receptor contact with antigen bound to mhc molecule on antigen presenting cell biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell activation via T cell receptor contact with antigen bound to MHC molecule on antigen presenting cell biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell activation via T cell receptor contact with antigen bound to MHC molecule on antigen presenting cell biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> ryanodine-sensitive calcium-release channel activity by adrenergic receptor signaling pathway involved in trong>positivetrong> trong>regulationtrong> trong>oftrong> cardiac muscle contraction biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> gluconeogenesis by trong>positivetrong> trong>regulationtrong> trong>oftrong> transcription from rna polymerase ii promoter biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> fever generation by trong>positivetrong> trong>regulationtrong> trong>oftrong> prostaglandin secretion biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> fever generation by trong>positivetrong> trong>regulationtrong> trong>oftrong> prostaglandin secretion biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> pseudohyphal growth by trong>positivetrong> trong>regulationtrong> trong>oftrong> transcription from RNA polymerase II promoter biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> fever generation by trong>positivetrong> trong>regulationtrong> trong>oftrong> prostaglandin secretion biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>regulationtrong> trong>oftrong> cd4-trong>positivetrong>, cd25-trong>positivetrong>, alpha-beta regulatory t cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cd8-trong>positivetrong>, alpha-beta t cell activation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cd4-trong>positivetrong>, alpha-beta t cell activation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cd8-trong>positivetrong>, alpha-beta t cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cd4-trong>positivetrong>, alpha-beta t cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cd8-trong>positivetrong>, alpha-beta t cell extravasation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cd8-trong>positivetrong>, alpha-beta t cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cd8-trong>positivetrong>, alpha-beta cytotoxic t cell extravasation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cd4-trong>positivetrong>, alpha-beta t cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell activation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> CD8-trong>positivetrong>, alpha-beta T cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> CD8-trong>positivetrong>, alpha-beta T cell activation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> CD8-trong>positivetrong>, alpha-beta T cell extravasation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> CD8-trong>positivetrong>, alpha-beta T cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> CD8-trong>positivetrong>, alpha-beta cytotoxic T cell extravasation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> activated CD8-trong>positivetrong>, alpha-beta T cell apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell differentiation involved in immune response biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell activation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> CD8-trong>positivetrong>, alpha-beta T cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> CD8-trong>positivetrong>, alpha-beta T cell activation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> CD8-trong>positivetrong>, alpha-beta T cell extravasation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> CD8-trong>positivetrong>, alpha-beta T cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> CD8-trong>positivetrong>, alpha-beta cytotoxic T cell extravasation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> activated CD8-trong>positivetrong>, alpha-beta T cell apoptotic process biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell differentiation involved in immune response biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> ubiquitin-protein ligase activity involved in trong>regulationtrong> trong>oftrong> mitotic cell cycle transition biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> trong>regulationtrong> trong>oftrong> vascular associated smooth muscle cell membrane depolarization biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> trong>regulationtrong> trong>oftrong> vascular associated smooth muscle cell membrane depolarization biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GAD Gene-Disease Associations
genes associated with the disease adenocarcinoma; carcinoma, large cell; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm trong>oftrong> lung ; small cell carcinoma trong>oftrong> lung; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> calcium-independent cell-cell adhesion biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> calcium-dependent cell-cell adhesion biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell mediated immune response to tumor cell biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> homotypic cell-cell adhesion biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> heterotypic cell-cell adhesion biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell-cell adhesion biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell mediated cytotoxicity directed against tumor cell target biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell-cell adhesion mediated by cadherin biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell-cell adhesion mediated by integrin biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell growth involved in cardiac muscle cell development biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> leukocyte cell-cell adhesion biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t cell mediated immune response to tumor cell biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the canonical wnt signaling pathway involved in trong>positivetrong> trong>regulationtrong> trong>oftrong> cell-cell adhesion biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> activated T cell autonomous cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell-cell adhesion mediated by integrin biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell-cell adhesion biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> homotypic cell-cell adhesion biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> heterotypic cell-cell adhesion biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell-cell adhesion mediated by cadherin biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell mediated cytotoxicity directed against tumor cell target biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell mediated immune response to tumor cell biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> substrate-dependent cell migration, cell attachment to substrate biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell growth involved in cardiac muscle cell development biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> leukocyte cell-cell adhesion biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> protein localization to cell-cell junction biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> calcium-independent cell-cell adhesion biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell mediated cytotoxicity directed against tumor cell target biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell mediated immune response to tumor cell biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> activated T cell autonomous cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell-cell adhesion mediated by integrin biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> homotypic cell-cell adhesion biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell-cell adhesion mediated by cadherin biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> protein localization to cell-cell junction biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> heterotypic cell-cell adhesion biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell-cell adhesion biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell mediated cytotoxicity directed against tumor cell target biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell mediated immune response to tumor cell biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> substrate-dependent cell migration, cell attachment to substrate biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell growth involved in cardiac muscle cell development biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> leukocyte cell-cell adhesion biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> calcium-independent cell-cell adhesion biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell mediated cytotoxicity directed against tumor cell target biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell mediated immune response to tumor cell biological process from the curated GO Biological Process Annotations 2025 dataset.
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From ClinVar Gene-Phenotype Associations
genes associated with the Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-trong>positivetrong>, NK cell-negative phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
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From CTD Gene-Disease Associations
genes/proteins associated with the disease Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-trong>Positivetrong>, NK Cell-Negative from the curated CTD Gene-Disease Associations dataset.
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From CTD Gene-Disease Associations
genes/proteins associated with the disease Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, NK Cell-trong>Positivetrong> from the curated CTD Gene-Disease Associations dataset.
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From OMIM Gene-Disease Associations
genes associated with the severe combined immunodeficiency, t cell-negative, b-cell/natural killer-cell trong>positivetrong> phenotype from the curated OMIM Gene-Disease Associations dataset.
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From OMIM Gene-Disease Associations
genes associated with the severe combined immunodeficiency, t-cell negative, b-cell/natural killer cell-trong>positivetrong> type phenotype from the curated OMIM Gene-Disease Associations dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> biosynthetic process trong>oftrong> antibacterial peptides active against gram-trong>positivetrong> bacteria biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> trong>positivetrong> chemotaxis biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> trong>positivetrong> chemotaxis biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> trong>positivetrong> chemotaxis biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2015
genes participating in the cd4-trong>positivetrong>, cd25-trong>positivetrong>, alpha-beta regulatory t cell lineage commitment biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the cd4-trong>positivetrong> or cd8-trong>positivetrong>, alpha-beta t cell lineage commitment biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the cd4-trong>positivetrong>, cd25-trong>positivetrong>, alpha-beta regulatory t cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From MPO Gene-Phenotype Associations
gene mutations causing the abnormal cd4-trong>positivetrong>, cd25-trong>positivetrong>, alpha-beta regulatory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
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From MPO Gene-Phenotype Associations
gene mutations causing the abnormal cd4-trong>positivetrong>, cd25-trong>positivetrong>, alpha-beta regulatory t cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
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From MPO Gene-Phenotype Associations
gene mutations causing the decreased cd4-trong>positivetrong>, cd25-trong>positivetrong>, alpha-beta regulatory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
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From MPO Gene-Phenotype Associations
gene mutations causing the increased cd4-trong>positivetrong>, cd25-trong>positivetrong>, alpha-beta regulatory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
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From GO Biological Process Annotations 2023
genes participating in the CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell lineage commitment biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the CD4-trong>positivetrong> or CD8-trong>positivetrong>, alpha-beta T cell lineage commitment biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From MGI Mouse Phenotype Associations 2023
gene mutations causing the abnormal CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
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From MGI Mouse Phenotype Associations 2023
gene mutations causing the decreased CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
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From MGI Mouse Phenotype Associations 2023
gene mutations causing the increased CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
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From MGI Mouse Phenotype Associations 2023
gene mutations causing the increased memory CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
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From MGI Mouse Phenotype Associations 2023
gene mutations causing the decreased memory CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
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From MGI Mouse Phenotype Associations 2023
gene mutations causing the decreased CD5-trong>positivetrong> Ly6C-trong>positivetrong> T cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
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From MGI Mouse Phenotype Associations 2023
gene mutations causing the increased CD8-trong>positivetrong>, CD25-trong>positivetrong> alpha-beta T cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
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From MGI Mouse Phenotype Associations 2023
gene mutations causing the increased CD4-trong>positivetrong>, CD25-trong>positivetrong> NK T cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
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From MGI Mouse Phenotype Associations 2023
gene mutations causing the abnormal CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
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From IMPC Knockout Mouse Phenotypes
gene knockouts causing the increased CD8-trong>positivetrong>, CD25-trong>positivetrong> alpha-beta T cell number phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
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From IMPC Knockout Mouse Phenotypes
gene knockouts causing the increased CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell number phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
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From IMPC Knockout Mouse Phenotypes
gene knockouts causing the increased CD4-trong>positivetrong>, CD25-trong>positivetrong> NK T cell number phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
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From IMPC Knockout Mouse Phenotypes
gene knockouts causing the increased memory CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell number phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
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From IMPC Knockout Mouse Phenotypes
gene knockouts causing the decreased CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell number phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
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From IMPC Knockout Mouse Phenotypes
gene knockouts causing the decreased CD5-trong>positivetrong> Ly6C-trong>positivetrong> T cell number phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
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From IMPC Knockout Mouse Phenotypes
gene knockouts causing the decreased memory CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell number phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
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From GO Biological Process Annotations 2025
genes participating in the CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell lineage commitment biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the CD4-trong>positivetrong> or CD8-trong>positivetrong>, alpha-beta T cell lineage commitment biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the CD4-trong>positivetrong>, CD25-trong>positivetrong>, alpha-beta regulatory T cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2015
genes participating in the negative trong>regulationtrong> trong>oftrong> cell-cell adhesion by negative trong>regulationtrong> trong>oftrong> transcription from rna polymerase ii promoter biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>regulationtrong> trong>oftrong> t cell activation via t cell receptor contact with antigen bound to mhc molecule on antigen presenting cell biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the negative trong>regulationtrong> trong>oftrong> t cell activation via t cell receptor contact with antigen bound to mhc molecule on antigen presenting cell biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2023
genes participating in the negative trong>regulationtrong> trong>oftrong> T cell activation via T cell receptor contact with antigen bound to MHC molecule on antigen presenting cell biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>regulationtrong> trong>oftrong> T cell activation via T cell receptor contact with antigen bound to MHC molecule on antigen presenting cell biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2025
genes participating in the negative trong>regulationtrong> trong>oftrong> T cell activation via T cell receptor contact with antigen bound to MHC molecule on antigen presenting cell biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>regulationtrong> trong>oftrong> T cell activation via T cell receptor contact with antigen bound to MHC molecule on antigen presenting cell biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> skeletal muscle contraction by trong>regulationtrong> trong>oftrong> release trong>oftrong> sequestered calcium ion biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>regulationtrong> trong>oftrong> glycolytic by trong>positivetrong> trong>regulationtrong> trong>oftrong> transcription from rna polymerase ii promoter biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>regulationtrong> trong>oftrong> cellular ketone metabolic process by trong>positivetrong> trong>regulationtrong> trong>oftrong> transcription from rna polymerase ii promoter biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>regulationtrong> trong>oftrong> lipid transport by trong>positivetrong> trong>regulationtrong> trong>oftrong> transcription from rna polymerase ii promoter biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> heart induction by negative trong>regulationtrong> trong>oftrong> canonical wnt signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> heart induction by negative trong>regulationtrong> trong>oftrong> canonical Wnt signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> skeletal muscle contraction by trong>regulationtrong> trong>oftrong> release trong>oftrong> sequestered calcium ion biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> skeletal muscle contraction by trong>regulationtrong> trong>oftrong> release trong>oftrong> sequestered calcium ion biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GAD Gene-Disease Associations
genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; neoplasms, second primary; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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From GAD Gene-Disease Associations
genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; cocarcinogenesis; neoplasms, radiation-induced; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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From GAD Gene-Disease Associations
genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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From GAD Gene-Disease Associations
genes associated with the disease b-cell lymphomas; lymphoma, b-cell; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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From GAD Gene-Disease Associations
genes associated with the disease adenocarcinoma; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm trong>oftrong> lung ; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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From GAD Gene-Disease Associations
genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; dna damage; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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From GAD Gene-Disease Associations
genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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From GAD Gene-Disease Associations
genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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From GAD Gene-Disease Associations
genes associated with the disease adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm trong>oftrong> lung ; small cell carcinoma trong>oftrong> lung; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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From GAD Gene-Disease Associations
genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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From GAD Gene-Disease Associations
genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; melanoma; postoperative complications; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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From GAD Gene-Disease Associations
genes associated with the disease adenocarcinoma; carcinoma, giant cell; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm recurrence, local in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
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From GO Biological Process Annotations 2015
genes participating in the cell-cell signaling involved in cell-cell junction organization biological process from the curated GO Biological Process Annotations 2015 dataset.
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From PhosphoSitePlus Phosphosite-Disease Associations
proteins associated with the disease non-small cell large cell lung carcinoma; non-small cell squamous cell lung carcinoma from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t-helper 17 cell lineage commitment biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mast cell cytokine production biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mitotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell cycle process biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell communication by electrical coupling biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> fat cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> hematopoietic stem cell migration biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mitotic cell cycle biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> apoptotic cell clearance biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t-helper 2 cell activation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> b cell apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell cycle biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>regulationtrong> trong>oftrong> cd8-trong>positivetrong>, alpha-beta t cell activation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell chemotaxis by vegf-activated vascular endothelial growth factor receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> pigment cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> metanephric glomerular visceral epithelial cell development biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell adhesion biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> lung goblet cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> transcription from rna polymerase ii promoter involved in smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> stem cell maintenance biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> epithelial cell migration biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell morphogenesis involved in differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> b cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> pancreatic stellate cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mesodermal cell fate specification biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> nk t cell activation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> dendritic cell dendrite assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> regulatory t cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> brown fat cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell killing biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> muscle cell apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> necrotic cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mesenchymal cell proliferation involved in ureter development biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell maturation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mesenchymal stem cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> epithelial cell proliferation involved in prostate gland development biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> smooth muscle cell chemotaxis biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the negative trong>regulationtrong> trong>oftrong> trong>positivetrong> thymic t cell selection biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>regulationtrong> trong>oftrong> cd8-trong>positivetrong>, alpha-beta t cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> immature t cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mast cell activation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> central b cell tolerance induction biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mast cell activation involved in immune response biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell volume biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> blood vessel endothelial cell migration biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>regulationtrong> trong>oftrong> cd4-trong>positivetrong>, alpha-beta t cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> by organism trong>oftrong> programmed cell death in other organism involved in symbiotic interaction biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the negative trong>regulationtrong> trong>oftrong> cd4-trong>positivetrong>, alpha-beta t cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> secretion by cell biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell cycle checkpoint biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> glial cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> dendritic cell cytokine production biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t cell migration biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the fibroblast growth factor receptor signaling pathway involved in trong>positivetrong> trong>regulationtrong> trong>oftrong> cell proliferation in bone marrow biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t cell tolerance induction biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> hematopoietic progenitor cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> satellite cell activation involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> epithelial cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t-helper cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> male germ cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> inner ear receptor cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the canonical wnt signaling pathway involved in trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell migration biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mast cell degranulation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mesenchymal cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> hair follicle cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> hematopoietic stem cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> glomerular metanephric mesangial cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell proliferation by vegf-activated platelet derived growth factor receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the negative trong>regulationtrong> trong>oftrong> cd4-trong>positivetrong>, alpha-beta t cell activation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> type b pancreatic cell apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> schwann cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell communication by electrical coupling involved in cardiac conduction biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> tendon cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> memory t cell activation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> hematopoietic stem cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> urothelial cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> transcription involved in g1/s transition trong>oftrong> mitotic cell cycle biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell proliferation involved in kidney development biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> white fat cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell cycle phase transition biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> histamine secretion by mast cell biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> b cell tolerance induction biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> nk t cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell communication biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t-helper 1 cell cytokine production biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell migration biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> dendritic cell apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t cell cytokine production biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cardiac muscle cell apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell mediated cytotoxicity biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> ureter smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> gamma-delta t cell activation involved in immune response biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell chemotaxis biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell-substrate adhesion biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t-helper 2 cell cytokine production biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cardiac muscle cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t cell chemotaxis biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> neuroepithelial cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> smooth muscle cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> pro-t cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell development biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> alpha-beta t cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> myeloid cell apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> kidney smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t cell mediated immunity biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mast cell chemotaxis biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> nephron tubule epithelial cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell fate commitment biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> g2/m transition trong>oftrong> mitotic cell cycle biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell communication by chemical coupling biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell size biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t cell receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> striated muscle cell apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> myeloid dendritic cell chemotaxis biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> homophilic cell adhesion biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t cell mediated cytotoxicity biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> alpha-beta t cell activation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell degranulation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mitotic cell cycle, embryonic biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> alpha-beta t cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> stem cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>regulationtrong> trong>oftrong> cd8-trong>positivetrong>, alpha-beta t cell extravasation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>regulationtrong> trong>oftrong> cd4-trong>positivetrong>, alpha-beta t cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell migration by vascular endothelial growth factor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell aging biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> dendritic cell chemotaxis biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> b cell chemotaxis biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mononuclear cell migration biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> by symbiont trong>oftrong> host programmed cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell chemotaxis to fibroblast growth factor biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell migration involved in sprouting angiogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> b cell receptor signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> skeletal muscle cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell adhesion molecule production biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> lens epithelial cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell-matrix adhesion biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> meiotic cell cycle biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> metanephric dct cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell growth biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mast cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> memory t cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>regulationtrong> trong>oftrong> cd4-trong>positivetrong>, alpha-beta t cell activation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> activated t cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> viral entry into host cell biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell chemotaxis biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> smooth muscle cell migration biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> lung ciliated cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t-helper 17 cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> glial cell line-derived neurotrophic factor secretion biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell development biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell activation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>regulationtrong> trong>oftrong> trong>positivetrong> thymic t cell selection biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> b cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the canonical wnt signaling pathway involved in trong>positivetrong> trong>regulationtrong> trong>oftrong> cardiac outflow tract cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell adhesion mediated by integrin biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> epithelial cell differentiation involved in kidney development biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> activation-induced cell death trong>oftrong> t cells biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mammary gland epithelial cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mononuclear cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t cell anergy biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> tongue muscle cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> by host trong>oftrong> viral release from host cell biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t-helper 1 cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell death biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> response to tumor cell biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> schwann cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t cell differentiation in thymus biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> neural precursor cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> muscle cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> immune response to tumor cell biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mitotic cell cycle spindle assembly checkpoint biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the negative trong>regulationtrong> trong>oftrong> cd4-trong>positivetrong>, alpha-beta t cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> myeloid cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> metanephric cap mesenchymal cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t cell apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> nk t cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> polarized epithelial cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mesenchymal stem cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> gamma-delta t cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>regulationtrong> trong>oftrong> cd8-trong>positivetrong>, alpha-beta cytotoxic t cell extravasation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> dendritic cell antigen processing and presentation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> epithelial cell proliferation involved in wound healing biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> by virus trong>oftrong> viral protein levels in host cell biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> stem cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cerebellar granule cell precursor proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> gamma-delta t cell activation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> metanephric mesenchymal cell migration biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mast cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> plasma cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mesenchymal cell apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> fat cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell activation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell cycle g1/s phase transition biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell motility biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> blood vessel endothelial cell proliferation involved in sprouting angiogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> dendritic cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> peripheral t cell tolerance induction biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> b cell activation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> trophoblast cell migration biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> viral release from host cell biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> epithelial cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t-helper 2 cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell mediated immunity biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell cycle g2/m phase transition biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cyclin-dependent protein serine/threonine kinase activity involved in g2/m transition trong>oftrong> mitotic cell cycle biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> substrate adhesion-dependent cell spreading biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> sodium ion export from cell biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> protein localization to cell surface biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> metaphase/anaphase transition trong>oftrong> cell cycle biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cardiac muscle cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> canonical wnt signaling pathway involved in cardiac muscle cell fate commitment biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cardiac vascular smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell fate specification biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the negative trong>regulationtrong> trong>oftrong> cd8-trong>positivetrong>, alpha-beta t cell activation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> metanephric mesenchymal cell migration by platelet-derived growth factor receptor-beta signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> macrophage derived foam cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> photoreceptor cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> glial cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cytotoxic t cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>regulationtrong> trong>oftrong> cd8-trong>positivetrong>, alpha-beta t cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell proliferation involved in heart valve morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> auditory receptor cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> myeloid dendritic cell activation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell proliferation involved in heart morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t cell extravasation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell projection organization biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell cytokine production biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> epidermal cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> smooth muscle cell apoptotic process biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell cycle arrest biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> membrane depolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell migration biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> wnt signaling pathway, planar cell polarity pathway biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> immature t cell proliferation in thymus biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> transcription from rna polymerase ii promoter involved in myocardial precursor cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell division biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> engulfment trong>oftrong> apoptotic cell biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> striated muscle cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> g1/s transition trong>oftrong> mitotic cell cycle biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> epithelial cell proliferation involved in lung morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> brown fat cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> nuclear cell cycle dna replication biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> glomerular mesangial cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> canonical wnt signaling pathway involved in controlling type b pancreatic cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> type b pancreatic cell development biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> neutrophil mediated killing trong>oftrong> symbiont cell biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> hepatic stellate cell activation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> t cell activation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell proliferation in bone marrow biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cyclin-dependent protein serine/threonine kinase activity involved in g1/s transition trong>oftrong> mitotic cell cycle biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> b cell mediated immunity biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> skeletal muscle cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
|
From GO Biological Process Annotations 2015
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
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From GO Biological Process Annotations 2023
genes participating in the negative trong>regulationtrong> trong>oftrong> CD8-trong>positivetrong>, alpha-beta T cell activation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> epithelial cell proliferation involved in wound healing biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell differentiation in thymus biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> G1/S transition trong>oftrong> mitotic cell cycle biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell activation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell population proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell migration biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell activation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> neural precursor cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the negative trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell activation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell migration by vascular endothelial growth factor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> viral entry into host cell biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> dendritic cell chemotaxis biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the negative trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> dendritic cell apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> dendritic cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> epidermal cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell adhesion biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> nuclear cell cycle DNA replication biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> G2/M transition trong>oftrong> mitotic cell cycle biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> skeletal muscle cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell migration biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell migration involved in sprouting angiogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell growth biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell migration biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell-matrix adhesion biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> dendritic cell antigen processing and presentation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell chemotaxis biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell adhesion mediated by integrin biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell motility biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> myeloid dendritic cell chemotaxis biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> vascular associated smooth muscle cell apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> stem cell population maintenance biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> stem cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell cycle biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mitotic cell cycle biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mitotic cell cycle spindle assembly checkpoint biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> smooth muscle cell migration biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> substrate adhesion-dependent cell spreading biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell mediated immunity biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell mediated cytotoxicity biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> smooth muscle cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cardiac muscle cell contraction biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the negative trong>regulationtrong> trong>oftrong> CD8-trong>positivetrong>, alpha-beta T cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> brown fat cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> macrophage derived foam cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> lung ciliated cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> epithelial cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> regulatory T cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell mediated cytotoxicity biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> urothelial cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> epithelial cell migration biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> epithelial cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> hair follicle cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> blood vessel endothelial cell migration biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> vascular endothelial cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell junction assembly biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> lymphoid progenitor cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cytotoxic T cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell cytokine production biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell chemotaxis to fibroblast growth factor biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mesenchymal cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> tongue muscle cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> nephron tubule epithelial cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> protein localization to cell cortex biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell degranulation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell cycle G2/M phase transition biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> stem cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> pro-B cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> microglial cell mediated cytotoxicity biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> protein localization to cell surface biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mast cell chemotaxis biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> satellite cell activation involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> immune response to tumor cell biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> fat cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell-substrate adhesion biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> NK T cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> activated T cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T-helper 1 cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> transcription involved in G1/S transition trong>oftrong> mitotic cell cycle biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endodermal cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> vascular associated smooth muscle cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mitotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>regulationtrong> trong>oftrong> trong>positivetrong> thymic T cell selection biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> Wnt signaling pathway, planar cell polarity pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> leukocyte adhesion to vascular endothelial cell biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell cycle process biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> histamine secretion by mast cell biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> hematopoietic stem cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cardiac muscle cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell proliferation involved in heart morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> transcription involved in G2/M transition trong>oftrong> mitotic cell cycle biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>regulationtrong> trong>oftrong> CD8-trong>positivetrong>, alpha-beta T cell activation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> myeloid dendritic cell cytokine production biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> by virus trong>oftrong> viral protein levels in host cell biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> aortic smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> smooth muscle cell-matrix adhesion biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell cytokine production biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mast cell cytokine production biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> alpha-beta T cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> establishment trong>oftrong> T cell polarity biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> apoptotic cell clearance biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> metanephric cap mesenchymal cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> metanephric mesenchymal cell migration by platelet-derived growth factor receptor-beta signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> glomerular mesangial cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> vascular associated smooth muscle cell migration biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> vascular associated smooth muscle cell dedifferentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> metanephric mesenchymal cell migration biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cardiac muscle cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> programmed cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> glial cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mononuclear cell migration biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> leukocyte adhesion to arterial endothelial cell biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> smooth muscle cell apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell mediated immunity biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell adhesion molecule production biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T-helper 1 cell cytokine production biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> memory T cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> B cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> vascular associated smooth muscle cell differentiation involved in phenotypic switching biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> memory T cell activation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell chemotaxis by VEGF-activated vascular endothelial growth factor receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell chemotaxis biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the negative trong>regulationtrong> trong>oftrong> CD8-trong>positivetrong>, alpha-beta T cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> trophectodermal cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T-helper 2 cell cytokine production biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell division biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> B cell activation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> type B pancreatic cell apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell size biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> long-chain fatty acid import into cell biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> B cell receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> myeloid dendritic cell activation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> myeloid cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> muscle cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mast cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell cycle G1/S phase transition biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> hematopoietic stem cell migration biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell fate specification biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> lens fiber cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the negative trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> blood vessel endothelial cell proliferation involved in sprouting angiogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mononuclear cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> microglial cell migration biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell proliferation by VEGF-activated platelet derived growth factor receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mast cell degranulation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> trophoblast cell migration biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> microglial cell activation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell chemotaxis biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T-helper 2 cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell-matrix adhesion via fibronectin biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> dendritic cell cytokine production biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> vascular associated smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>regulationtrong> trong>oftrong> CD8-trong>positivetrong>, alpha-beta T cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> Schwann cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell proliferation involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> glial cell-derived neurotrophic factor production biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell cycle phase transition biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mesodermal cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell tolerance induction biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the negative trong>regulationtrong> trong>oftrong> trong>positivetrong> thymic T cell selection biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> B cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> plasma cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> glomerular metanephric mesangial cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> hematopoietic progenitor cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> smooth muscle cell chemotaxis biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> epithelial cell proliferation involved in lung morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the fibroblast growth factor receptor signaling pathway involved in trong>positivetrong> trong>regulationtrong> trong>oftrong> cell proliferation in bone marrow biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell fate determination biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> B cell apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> alpha-beta T cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mesenchymal stem cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> necrotic cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cardiac muscle cell apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell activation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> NK T cell activation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T-helper 17 cell lineage commitment biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell development biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the canonical Wnt signaling pathway involved in trong>positivetrong> trong>regulationtrong> trong>oftrong> cardiac outflow tract cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> lung goblet cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mesenchymal stem cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> lens epithelial cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> B cell tolerance induction biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> NK T cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell killing biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> glial cell migration biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> B cell chemotaxis biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> phosphatidylserine exposure on apoptotic cell surface biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> type B pancreatic cell development biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell proliferation in bone marrow biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> autophagic cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> gamma-delta T cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> amacrine cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mesodermal cell fate specification biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> striated muscle cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> metanephric DCT cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T-helper 2 cell activation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> epithelial cell apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> integrin activation by cell surface receptor linked signal transduction biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> hematopoietic stem cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell communication by electrical coupling biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> membrane depolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell communication by electrical coupling involved in cardiac conduction biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell proliferation involved in heart valve morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> hydrogen peroxide-induced cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mitotic cell cycle, embryonic biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> chorionic trophoblast cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell activation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> hepatic stellate cell activation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> immature T cell proliferation in thymus biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> ureter smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> kidney smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mesenchymal cell proliferation involved in ureter development biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mast cell activation biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> myeloid cell apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
|
From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> type B pancreatic cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> voltage-gated potassium channel activity involved in atrial cardiac muscle cell action potential repolarization biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> fat cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> engulfment trong>oftrong> apoptotic cell biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> polarized epithelial cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell projection organization biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell anergy biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> gamma-delta T cell activation involved in immune response biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T-helper 17 cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> white fat cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> atrial cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> pigment cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mast cell activation by Fc-epsilon receptor signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mammary gland epithelial cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> central B cell tolerance induction biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cardiac vascular smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> dendritic cell dendrite assembly biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> male germ cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cardiac neural crest cell migration involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell maturation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> homophilic cell adhesion biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> gamma-delta T cell activation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mast cell activation involved in immune response biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>regulationtrong> trong>oftrong> activated CD4-trong>positivetrong>, alpha-beta T cell apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> tolerance induction to tumor cell biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> hydrogen peroxide-mediated programmed cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mesenchymal stem cell migration biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> pro-T cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>regulationtrong> trong>oftrong> CD8-trong>positivetrong>, alpha-beta cytotoxic T cell extravasation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> G2/MI transition trong>oftrong> meiotic cell cycle biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cilium-dependent cell motility biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> meiotic cell cycle biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> plasma membrane bounded cell projection assembly biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> protein localization to cell periphery biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> secretion by cell biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> glial cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell development biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> metaphase/anaphase transition trong>oftrong> cell cycle biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell morphogenesis involved in differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell-substrate junction organization biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>regulationtrong> trong>oftrong> CD8-trong>positivetrong>, alpha-beta T cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell cycle checkpoint biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell chemotaxis to fibroblast growth factor biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> epithelial cell differentiation involved in kidney development biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> response to tumor cell biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> membrane repolarization during ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T-helper cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell communication biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> alpha-beta T cell activation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell proliferation involved in kidney development biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> muscle cell apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell differentiation involved in phenotypic switching biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> neutrophil mediated killing trong>oftrong> symbiont cell biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> neuroepithelial cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell fate commitment biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> B cell mediated immunity biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> striated muscle cell apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell extravasation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>regulationtrong> trong>oftrong> CD8-trong>positivetrong>, alpha-beta T cell extravasation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cerebellar granule cell precursor proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> immature T cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> membrane repolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> germ cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>regulationtrong> trong>oftrong> activated CD8-trong>positivetrong>, alpha-beta T cell apoptotic process biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2023
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> meiotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2023 dataset.
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From GO Biological Process Annotations 2025
genes participating in the negative trong>regulationtrong> trong>oftrong> CD8-trong>positivetrong>, alpha-beta T cell activation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> epithelial cell proliferation involved in wound healing biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell differentiation in thymus biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> neural precursor cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> G1/S transition trong>oftrong> mitotic cell cycle biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell activation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell population proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell migration biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell activation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell apoptotic process biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell-substrate adhesion biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the negative trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell activation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> viral entry into host cell biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell migration biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> dendritic cell chemotaxis biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the negative trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> dendritic cell apoptotic process biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> dendritic cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> epidermal cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell adhesion biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> nuclear cell cycle DNA replication biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> G2/M transition trong>oftrong> mitotic cell cycle biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> skeletal muscle cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell migration biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell migration involved in sprouting angiogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell anergy biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> stem cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> tendon cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell growth biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell-matrix adhesion biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> dendritic cell antigen processing and presentation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell chemotaxis biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell adhesion mediated by integrin biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell motility biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> myeloid dendritic cell chemotaxis biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> vascular associated smooth muscle cell apoptotic process biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell-matrix adhesion via fibronectin biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> stem cell population maintenance biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> stem cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell cycle biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mitotic cell cycle biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mitotic cell cycle spindle assembly checkpoint biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> smooth muscle cell migration biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> substrate adhesion-dependent cell spreading biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell mediated immunity biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell mediated cytotoxicity biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> smooth muscle cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cardiac muscle cell contraction biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the negative trong>regulationtrong> trong>oftrong> CD8-trong>positivetrong>, alpha-beta T cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> brown fat cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> macrophage derived foam cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> lung ciliated cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> epithelial cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> regulatory T cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell mediated cytotoxicity biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> urothelial cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> epithelial cell migration biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> epithelial cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> hair follicle cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> blood vessel endothelial cell migration biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> vascular endothelial cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> lymphoid progenitor cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cytotoxic T cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell cytokine production biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell chemotaxis to fibroblast growth factor biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mesenchymal cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> tongue muscle cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> nephron tubule epithelial cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> protein localization to cell cortex biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell degranulation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell cycle G2/M phase transition biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> pro-B cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> microglial cell mediated cytotoxicity biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> protein localization to cell surface biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mast cell chemotaxis biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> satellite cell activation involved in skeletal muscle regeneration biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T-helper 17 cell lineage commitment biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> immune response to tumor cell biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> fat cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> NK T cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> membrane repolarization during ventricular cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> activated T cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T-helper 1 cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endodermal cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> vascular associated smooth muscle cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell junction assembly biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mitotic cell cycle phase transition biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>regulationtrong> trong>oftrong> trong>positivetrong> thymic T cell selection biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> Wnt signaling pathway, planar cell polarity pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> leukocyte adhesion to vascular endothelial cell biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell cycle process biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> histamine secretion by mast cell biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> hematopoietic stem cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cardiac muscle cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell proliferation involved in heart morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>regulationtrong> trong>oftrong> CD8-trong>positivetrong>, alpha-beta T cell activation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> myeloid dendritic cell cytokine production biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> by virus trong>oftrong> viral protein levels in host cell biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> aortic smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> smooth muscle cell-matrix adhesion biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell cytokine production biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell apoptotic process biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mast cell cytokine production biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> alpha-beta T cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> establishment trong>oftrong> T cell polarity biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> apoptotic cell clearance biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> metanephric cap mesenchymal cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> metanephric mesenchymal cell migration by platelet-derived growth factor receptor-beta signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> glomerular mesangial cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> vascular associated smooth muscle cell migration biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> vascular associated smooth muscle cell dedifferentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> metanephric mesenchymal cell migration biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mesenchymal stem cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cardiac muscle cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> programmed cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> glial cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mononuclear cell migration biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> leukocyte adhesion to arterial endothelial cell biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> smooth muscle cell apoptotic process biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell mediated immunity biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell adhesion molecule production biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T-helper 1 cell cytokine production biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> memory T cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> B cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> vascular associated smooth muscle cell differentiation involved in phenotypic switching biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> memory T cell activation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell chemotaxis biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the negative trong>regulationtrong> trong>oftrong> CD8-trong>positivetrong>, alpha-beta T cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> trophectodermal cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T-helper 2 cell cytokine production biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell division biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> B cell activation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> type B pancreatic cell apoptotic process biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell size biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> long-chain fatty acid import into cell biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> myeloid dendritic cell activation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> myeloid cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> muscle cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mast cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell cycle G1/S phase transition biological process from the curated GO Biological Process Annotations 2025 dataset.
|
From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> hematopoietic stem cell migration biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell fate specification biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> lens fiber cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the negative trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> blood vessel endothelial cell proliferation involved in sprouting angiogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mononuclear cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> microglial cell migration biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell proliferation by VEGF-activated platelet derived growth factor receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mast cell degranulation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> trophoblast cell migration biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> microglial cell activation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell chemotaxis biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T-helper 2 cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> dendritic cell cytokine production biological process from the curated GO Biological Process Annotations 2025 dataset.
|
From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> vascular associated smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
|
From GO Biological Process Annotations 2025
genes participating in the trong>regulationtrong> trong>oftrong> CD8-trong>positivetrong>, alpha-beta T cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> Schwann cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell activation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> glial cell-derived neurotrophic factor production biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell chemotaxis by VEGF-activated vascular endothelial growth factor receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell cycle phase transition biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mesodermal cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T cell tolerance induction biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the negative trong>regulationtrong> trong>oftrong> trong>positivetrong> thymic T cell selection biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> B cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> plasma cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> glomerular metanephric mesangial cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> hematopoietic progenitor cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
|
From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> smooth muscle cell chemotaxis biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> epithelial cell proliferation involved in lung morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the fibroblast growth factor receptor signaling pathway involved in trong>positivetrong> trong>regulationtrong> trong>oftrong> cell proliferation in bone marrow biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell fate determination biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> B cell apoptotic process biological process from the curated GO Biological Process Annotations 2025 dataset.
|
From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> alpha-beta T cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> B cell receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell proliferation in bone marrow biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cardiac muscle cell apoptotic process biological process from the curated GO Biological Process Annotations 2025 dataset.
|
From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> NK T cell activation biological process from the curated GO Biological Process Annotations 2025 dataset.
|
From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> natural killer cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell development biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell proliferation in midbrain biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> lung goblet cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mesenchymal stem cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> lens epithelial cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
|
From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> B cell tolerance induction biological process from the curated GO Biological Process Annotations 2025 dataset.
|
From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> NK T cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
|
From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> protein localization to cell periphery biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell killing biological process from the curated GO Biological Process Annotations 2025 dataset.
|
From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> glial cell migration biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> B cell chemotaxis biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> phosphatidylserine exposure on apoptotic cell surface biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> type B pancreatic cell development biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> autophagic cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> gamma-delta T cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> amacrine cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mesodermal cell fate specification biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> endothelial cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> striated muscle cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> metanephric DCT cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T-helper 2 cell activation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> transformation trong>oftrong> host cell by virus biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> epithelial cell apoptotic process biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> integrin activation by cell surface receptor linked signal transduction biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> hematopoietic stem cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell communication by electrical coupling biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> membrane depolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell communication by electrical coupling involved in cardiac conduction biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell proliferation involved in heart valve morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> programmed necrotic cell death biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mitotic cell cycle, embryonic biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> chorionic trophoblast cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell activation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> hepatic stellate cell activation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> immature T cell proliferation in thymus biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> ureter smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> kidney smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mesenchymal cell proliferation involved in ureter development biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mast cell activation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> myeloid cell apoptotic process biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> type B pancreatic cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> membrane repolarization during cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> fat cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>regulationtrong> trong>oftrong> CD4-trong>positivetrong>, alpha-beta T cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> engulfment trong>oftrong> apoptotic cell biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> retinal ganglion cell axon guidance biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> polarized epithelial cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell projection organization biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> gamma-delta T cell activation involved in immune response biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> T-helper 17 cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> white fat cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> atrial cardiac muscle cell action potential biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> pigment cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mast cell activation by Fc-epsilon receptor signaling pathway biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> mammary gland epithelial cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> central B cell tolerance induction biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cardiac vascular smooth muscle cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> dendritic cell dendrite assembly biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> male germ cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cardiac neural crest cell migration involved in outflow tract morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
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From GO Biological Process Annotations 2025
genes participating in the trong>positivetrong> trong>regulationtrong> trong>oftrong> cell maturation biological process from the curated GO Biological Process Annotations 2025 dataset.
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