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Ask your administrator if you think this is wrong. ======= STAP1 ======= == Gene Information == * **<color #00a2e8>Official Symbol</color>**: STAP1 * **<color #00a2e8>Official Name</color>**: signal transducing adaptor family member 1 * **<color #00a2e8>Aliases and Previous Symbols</color>**: N/A * **<color #00a2e8>Entrez ID</color>**: [[https://www.ncbi.nlm.nih.gov/gene/?term=26228|26228]] * **<color #00a2e8>UniProt</color>**: [[https://www.uniprot.org/uniprot/Q9ULZ2|Q9ULZ2]] * **<color #00a2e8>Interactions</color>**: [[https://thebiogrid.org/search.php?search=STAP1&organism=9606|BioGRID]] * **<color #00a2e8>PubMed articles</color>**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20STAP1|Open PubMed]] * **<color #00a2e8>OMIM</color>**: [[https://omim.org/entry/604298|Open OMIM]] == Function Summary == * **<color #00a2e8>Entrez Summary</color>**: The protein encoded by this gene contains a proline-rich region, a pleckstrin homology (PH) domain, and a region in the carboxy terminal half with similarity to the Src Homology 2 (SH2) domain. This protein is a substrate of tyrosine-protein kinase Tec, and its interaction with tyrosine-protein kinase Tec is phosphorylation-dependent. This protein is thought to participate in a positive feedback loop by upregulating the activity of tyrosine-protein kinase Tec. Variants of this gene have been associated with autosomal-dominant hypercholesterolemia (ADH), which is characterized by elevated low-density lipoprotein cholesterol levels and in increased risk of coronary vascular disease. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2015]. * **<color #00a2e8>UniProt Summary</color>**: In BCR signaling, appears to function as a docking protein acting downstream of TEC and participates in a positive feedback loop by increasing the activity of TEC. {ECO:0000269|PubMed:10518561}. <button type='default' size='sm' modal='Pfam_Domains'>Pfam Domains</button> <button type='primary' size='sm' modal='GO_terms'>GO Terms</button> <modal id='Pfam_Domains' size='lg' title='Pfam Domains'> No Pfam Domain information is available for this gene. </modal> <modal id='GO_terms' size='lg' title='GO Terms'> |negative regulation of microglial cell migration| |negative regulation of macrophage colony-stimulating factor signaling pathway| |negative regulation of response to macrophage colony-stimulating factor| |negative regulation of cellular response to macrophage colony-stimulating factor stimulus| |regulation of microglial cell mediated cytotoxicity| |macrophage colony-stimulating factor receptor binding| |regulation of macrophage colony-stimulating factor signaling pathway| |positive regulation of microglial cell mediated cytotoxicity| |negative regulation of glial cell migration| |negative regulation of ruffle assembly| |regulation of cellular response to macrophage colony-stimulating factor stimulus| |regulation of response to macrophage colony-stimulating factor| |positive regulation of non-membrane spanning protein tyrosine kinase activity| |negative regulation of macrophage chemotaxis| |regulation of microglial cell migration| |regulation of non-membrane spanning protein tyrosine kinase activity| |positive regulation of microglial cell activation| |positive regulation of B cell receptor signaling pathway| |negative regulation of macrophage migration| |positive regulation of phagocytosis, engulfment| |transmembrane receptor protein tyrosine kinase adaptor activity| |positive regulation of membrane invagination| |positive regulation of neuroinflammatory response| |regulation of phagocytosis, engulfment| |regulation of glial cell migration| |regulation of membrane invagination| |negative regulation of leukocyte chemotaxis| |regulation of microglial cell activation| |positive regulation of actin cytoskeleton reorganization| |positive regulation of antigen receptor-mediated signaling pathway| |positive regulation of macrophage activation| |negative regulation of plasma membrane bounded cell projection assembly| |regulation of B cell receptor signaling pathway| |regulation of macrophage chemotaxis| |regulation of ruffle assembly| |regulation of neuroinflammatory response| |regulation of macrophage migration| |regulation of actin cytoskeleton reorganization| |phosphotyrosine residue binding| |negative regulation of gliogenesis| |negative regulation of leukocyte migration| |regulation of macrophage activation| |SH3/SH2 adaptor activity| |positive regulation of leukocyte mediated cytotoxicity| |positive regulation of protein tyrosine kinase activity| |negative regulation of chemotaxis| |negative regulation of cytokine-mediated signaling pathway| |regulation of antigen receptor-mediated signaling pathway| |negative regulation of response to cytokine stimulus| |positive regulation of cell killing| |positive regulation of phagocytosis| |regulation of leukocyte mediated cytotoxicity| |regulation of protein tyrosine kinase activity| |regulation of phagocytosis| |positive regulation of endocytosis| |regulation of cell killing| |phospholipid binding| |regulation of leukocyte chemotaxis| |regulation of gliogenesis| |positive regulation of inflammatory response| |regulation of cytokine-mediated signaling pathway| |regulation of response to cytokine stimulus| |negative regulation of cell projection organization| |cellular response to lipopolysaccharide| |positive regulation of peptidyl-tyrosine phosphorylation| |cellular response to molecule of bacterial origin| |regulation of leukocyte migration| |regulation of plasma membrane bounded cell projection assembly| |regulation of cell projection assembly| |regulation of endocytosis| |regulation of chemotaxis| |cellular response to biotic stimulus| |positive regulation of cytoskeleton organization| |regulation of peptidyl-tyrosine phosphorylation| |negative regulation of cell migration| |negative regulation of cell motility| |negative regulation of neurogenesis| |negative regulation of cellular component movement| |negative regulation of nervous system development| |response to lipopolysaccharide| |negative regulation of locomotion| |response to molecule of bacterial origin| |negative regulation of cell development| |regulation of inflammatory response| |regulation of actin cytoskeleton organization| |negative regulation of response to external stimulus| |regulation of actin filament-based process| |positive regulation of leukocyte activation| |positive regulation of cell activation| |negative regulation of immune system process| |negative regulation of phosphorylation| |protein kinase binding| |positive regulation of defense response| |transmembrane receptor protein tyrosine kinase signaling pathway| |cellular response to lipid| |positive regulation of protein kinase activity| |regulation of cytoskeleton organization| |regulation of vesicle-mediated transport| |negative regulation of phosphate metabolic process| |negative regulation of phosphorus metabolic process| |positive regulation of kinase activity| |protein-containing complex| |positive regulation of response to external stimulus| |regulation of leukocyte activation| |positive regulation of organelle organization| |regulation of cell activation| |positive regulation of transferase activity| |intracellular membrane-bounded organelle| |response to bacterium| |regulation of plasma membrane bounded cell projection organization| |negative regulation of cellular component organization| |regulation of cell projection organization| |negative regulation of cell differentiation| |enzyme linked receptor protein signaling pathway| |regulation of defense response| |regulation of protein kinase activity| |regulation of neurogenesis| |regulation of cell migration| |response to lipid| |positive regulation of immune response| |regulation of kinase activity| |regulation of cell motility| |regulation of nervous system development| |regulation of cell development| |negative regulation of developmental process| |regulation of cellular component biogenesis| |regulation of transferase activity| |regulation of locomotion| |positive regulation of transport| |regulation of cellular component movement| |positive regulation of protein phosphorylation| |cellular response to oxygen-containing compound| |positive regulation of phosphorylation| |regulation of response to external stimulus| |positive regulation of phosphate metabolic process| |positive regulation of phosphorus metabolic process| |regulation of immune response| |positive regulation of immune system process| |negative regulation of multicellular organismal process| |positive regulation of cellular component organization| |positive regulation of protein modification process| |mitochondrion| |negative regulation of signal transduction| |regulation of organelle organization| |response to other organism| |response to external biotic stimulus| |response to biotic stimulus| |negative regulation of cell communication| |negative regulation of signaling| |positive regulation of catalytic activity| |regulation of protein phosphorylation| |regulation of response to stress| |generation of neurons| |response to oxygen-containing compound| |regulation of phosphorylation| |positive regulation of cellular protein metabolic process| |negative regulation of response to stimulus| |neurogenesis| |positive regulation of signal transduction| |regulation of immune system process| |positive regulation of protein metabolic process| |positive regulation of molecular function| |regulation of phosphate metabolic process| |regulation of phosphorus metabolic process| |regulation of cell differentiation| |positive regulation of cell communication| |positive regulation of signaling| |regulation of protein modification process| |regulation of transport| |positive regulation of gene expression| </modal> \\ === CRISPR Data === <button type='default' size='small' modal='Compound_Hit'>Compound Hit</button> <button type='default' size='small' modal='Most_Correlated_Genes'>Most Correlated Genes in Chemogenomics</button> <button type='primary' size='small' modal='Essential_Avana'>Tissues where Essential in the Avana Dataset (DepMap 20Q1)</button> <modal id='Compound_Hit' size='lg' title='Compound Hit'> No hits were found. </modal> <modal id='Most_Correlated_Genes' size='lg' title='Most Correlated Genes in Chemogenomics'> No correlation found to any other genes in chemogenomics. </modal> <modal id='Essential_Avana' size='lg' title='Tissues where Essential in the Avana Dataset (DepMap 20Q1)'> Global Fraction of Cell Lines Where Essential: 0/739 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|0/28| |blood|0/28| |bone|0/26| |breast|0/33| |central nervous system|0/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|0/16| |kidney|0/21| |liver|0/20| |lung|0/75| |lymphocyte|0/16| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|0/15| |prostate|0/1| |skin|0/24| |soft tissue|0/9| |thyroid|0/2| |upper aerodigestive|0/22| |urinary tract|0/29| |uterus|0/5| </modal> == Essentiality in NALM6 == * **<color #00a2e8>Essentiality Rank</color>**: 15243 * **<color #00a2e8>Expression level (log2 read counts)</color>**: 6.9 <button type='primary' size='small' modal='Dist_expr'>Expression Distribution</button> <modal id='Dist_expr' size='lg' title='STAP1 Expression in NALM6 Cells: 6.9'> {{:chemogenomics:nalm6 dist.png?nolink |}} </modal> Last modified: 2026/01/07 22:37by 127.0.0.1