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Ask your administrator if you think this is wrong. ======= LY9 ======= == Gene Information == * **<color #00a2e8>Official Symbol</color>**: LY9 * **<color #00a2e8>Official Name</color>**: lymphocyte antigen 9 * **<color #00a2e8>Aliases and Previous Symbols</color>**: N/A * **<color #00a2e8>Entrez ID</color>**: [[https://www.ncbi.nlm.nih.gov/gene/?term=4063|4063]] * **<color #00a2e8>UniProt</color>**: [[https://www.uniprot.org/uniprot/Q9HBG7|Q9HBG7]] * **<color #00a2e8>Interactions</color>**: [[https://thebiogrid.org/search.php?search=LY9&organism=9606|BioGRID]] * **<color #00a2e8>PubMed articles</color>**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20LY9|Open PubMed]] * **<color #00a2e8>OMIM</color>**: [[https://omim.org/entry/600684|Open OMIM]] == Function Summary == * **<color #00a2e8>Entrez Summary</color>**: N/A * **<color #00a2e8>UniProt Summary</color>**: Self-ligand receptor of the signaling lymphocytic activation molecule (SLAM) family. SLAM receptors triggered by homo- or heterotypic cell-cell interactions are modulating the activation and differentiation of a wide variety of immune cells and thus are involved in the regulation and interconnection of both innate and adaptive immune response. Activities are controlled by presence or absence of small cytoplasmic adapter proteins, SH2D1A/SAP and/or SH2D1B/EAT-2. May participate in adhesion reactions between T lymphocytes and accessory cells by homophilic interaction. Promotes T-cell differentiation into a helper T-cell Th17 phenotype leading to increased IL-17 secretion; the costimulatory activity requires SH2D1A (PubMed:22184727). Promotes recruitment of RORC to the IL-17 promoter (PubMed:22989874). May be involved in the maintenance of peripheral cell tolerance by serving as a negative regulator of the immune response. May disable autoantibody responses and inhibit IFN-gamma secretion by CD4(+) T-cells. May negatively regulate the size of thymic innate CD8(+) T-cells and the development of invariant natural killer T (iNKT) cells (By similarity). {ECO:0000250|UniProtKB:Q01965, ECO:0000269|PubMed:22184727, ECO:0000269|PubMed:22989874}. <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'> |T-helper 17 cell lineage commitment| |T-helper 17 cell differentiation| |T-helper 17 type immune response| |T-helper cell lineage commitment| |CD4-positive, alpha-beta T cell lineage commitment| |alpha-beta T cell lineage commitment| |CD4-positive or CD8-positive, alpha-beta T cell lineage commitment| |positive regulation of interleukin-17 production| |T cell lineage commitment| |positive T cell selection| |T-helper cell differentiation| |CD4-positive, alpha-beta T cell differentiation involved in immune response| |alpha-beta T cell differentiation involved in immune response| |alpha-beta T cell activation involved in immune response| |regulation of interleukin-17 production| |T cell differentiation involved in immune response| |CD4-positive, alpha-beta T cell differentiation| |CD4-positive, alpha-beta T cell activation| |T cell selection| |alpha-beta T cell differentiation| |alpha-beta T cell activation| |T cell activation involved in immune response| |lymphocyte activation involved in immune response| |T cell differentiation| |T cell activation| |lymphocyte differentiation| |cell fate commitment| |adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains| |leukocyte differentiation| |lymphocyte activation| |positive regulation of cytokine production| |hemopoiesis| |hematopoietic or lymphoid organ development| |adaptive immune response| |cell surface| |leukocyte activation involved in immune response| |cell activation involved in immune response| |immune system development| |regulation of cytokine production| |molecular function| |innate immune response| |leukocyte activation| |cell adhesion| |biological adhesion| |defense response to other organism| |cell activation| |immune effector process| |response to other organism| |response to external biotic stimulus| |response to biotic stimulus| |defense response| |positive regulation of multicellular organismal process| |immune response| </modal> \\ === CRISPR Data === <button type='primary' 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'> ^Screen^Score^ |[[:results:exp301|VER-155008 3.9μM R06 exp301]]|1.94| </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>**: 4822 * **<color #00a2e8>Expression level (log2 read counts)</color>**: 3.56 <button type='primary' size='small' modal='Dist_expr'>Expression Distribution</button> <modal id='Dist_expr' size='lg' title='LY9 Expression in NALM6 Cells: 3.56'> {{:chemogenomics:nalm6 dist.png?nolink |}} </modal> Last modified: 2025/12/10 20:19by 127.0.0.1