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Ask your administrator if you think this is wrong. ======= STAT6 ======= == Gene Information == * **<color #00a2e8>Official Symbol</color>**: STAT6 * **<color #00a2e8>Official Name</color>**: signal transducer and activator of transcription 6 * **<color #00a2e8>Aliases and Previous Symbols</color>**: N/A * **<color #00a2e8>Entrez ID</color>**: [[https://www.ncbi.nlm.nih.gov/gene/?term=6778|6778]] * **<color #00a2e8>UniProt</color>**: [[https://www.uniprot.org/uniprot/P42226|P42226]] * **<color #00a2e8>Interactions</color>**: [[https://thebiogrid.org/search.php?search=STAT6&organism=9606|BioGRID]] * **<color #00a2e8>PubMed articles</color>**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20STAT6|Open PubMed]] * **<color #00a2e8>OMIM</color>**: [[https://omim.org/entry/601512|Open OMIM]] == Function Summary == * **<color #00a2e8>Entrez Summary</color>**: The protein encoded by this gene is a member of the STAT family of transcription factors. In response to cytokines and growth factors, STAT family members are phosphorylated by the receptor associated kinases, and then form homo- or heterodimers that translocate to the cell nucleus where they act as transcription activators. This protein plays a central role in exerting IL4 mediated biological responses. It is found to induce the expression of BCL2L1/BCL-X(L), which is responsible for the anti-apoptotic activity of IL4. Knockout studies in mice suggested the roles of this gene in differentiation of T helper 2 (Th2) cells, expression of cell surface markers, and class switch of immunoglobulins. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]. * **<color #00a2e8>UniProt Summary</color>**: Carries out a dual function: signal transduction and activation of transcription. Involved in IL4/interleukin-4- and IL3/interleukin-3-mediated signaling. {ECO:0000269|PubMed:17210636}. <button type='primary' 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'> |STAT int| |STAT alpha| |STAT bind| |SH2| </modal> <modal id='GO_terms' size='lg' title='GO Terms'> |T-helper 1 cell lineage commitment| |positive regulation of isotype switching to IgE isotypes| |interleukin-4-mediated signaling pathway| |regulation of isotype switching to IgE isotypes| |T-helper 1 cell differentiation| |T-helper cell lineage commitment| |CD4-positive, alpha-beta T cell lineage commitment| |mammary gland epithelial cell proliferation| |alpha-beta T cell lineage commitment| |negative regulation of type 2 immune response| |growth hormone receptor signaling pathway via JAK-STAT| |CD4-positive or CD8-positive, alpha-beta T cell lineage commitment| |T-helper 1 type immune response| |cellular response to reactive nitrogen species| |growth hormone receptor signaling pathway| |T cell lineage commitment| |cellular response to growth hormone stimulus| |positive regulation of isotype switching| |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| |cellular response to interleukin-4| |regulation of type 2 immune response| |response to interleukin-4| |T cell differentiation involved in immune response| |regulation of isotype switching| |response to growth hormone| |CD4-positive, alpha-beta T cell differentiation| |positive regulation of immunoglobulin mediated immune response| |positive regulation of B cell mediated immunity| |receptor signaling pathway via JAK-STAT| |CD4-positive, alpha-beta T cell activation| |T cell selection| |positive regulation of DNA recombination| |receptor signaling pathway via STAT| |mammary gland morphogenesis| |positive regulation of immunoglobulin production| |alpha-beta T cell differentiation| |regulation of B cell mediated immunity| |regulation of immunoglobulin mediated immune response| |mammary gland epithelium development| |alpha-beta T cell activation| |regulation of immunoglobulin production| |T cell activation involved in immune response| |cellular response to hydrogen peroxide| |positive regulation of type I interferon production| |protein phosphatase binding| |epithelial cell proliferation| |positive regulation of production of molecular mediator of immune response| |positive regulation of cold-induced thermogenesis| |gland morphogenesis| |positive regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains| |regulation of DNA recombination| |positive regulation of lymphocyte mediated immunity| |positive regulation of adaptive immune response| |lymphocyte activation involved in immune response| |cellular response to antibiotic| |response to hydrogen peroxide| |regulation of type I interferon production| |mammary gland development| |cellular response to reactive oxygen species| |positive regulation of leukocyte mediated immunity| |T cell differentiation| |regulation of production of molecular mediator of immune response| |regulation of cold-induced thermogenesis| |regulation of adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains| |negative regulation of immune response| |regulation of lymphocyte mediated immunity| |regulation of adaptive immune response| |positive regulation of B cell activation| |positive regulation of DNA metabolic process| |response to reactive oxygen species| |regulation of leukocyte mediated immunity| |regulation of B cell activation| |cellular response to toxic substance| |positive regulation of immune effector process| |membrane raft| |T cell activation| |lymphocyte differentiation| |nuclear chromatin| |nuclear membrane| |cellular response to oxidative stress| |cell fate commitment| |cellular response to peptide hormone stimulus| |adaptive immune response based on somatic recombination of immune receptors built from immunoglobulin superfamily domains| |response to antibiotic| |RNA polymerase II regulatory region sequence-specific DNA binding| |cellular response to peptide| |leukocyte differentiation| |regulation of DNA metabolic process| |positive regulation of lymphocyte activation| |lymphocyte activation| |response to oxidative stress| |response to peptide hormone| |cellular response to drug| |positive regulation of leukocyte activation| |gland development| |positive regulation of cell activation| |negative regulation of immune system process| |DNA-binding transcription activator activity, RNA polymerase II-specific| |positive regulation of cytokine production| |regulation of immune effector process| |response to peptide| |RNA polymerase II proximal promoter sequence-specific DNA binding| |response to toxic substance| |transmembrane receptor protein tyrosine kinase signaling pathway| |regulation of lymphocyte activation| |response to inorganic substance| |cell population proliferation| |hemopoiesis| |cellular response to organonitrogen compound| |regulation of leukocyte activation| |cellular response to hormone stimulus| |hematopoietic or lymphoid organ development| |adaptive immune response| |leukocyte activation involved in immune response| |cell activation involved in immune response| |regulation of cell activation| |immune system development| |cellular response to nitrogen compound| |cytokine-mediated signaling pathway| |DNA-binding transcription factor activity| |regulation of cytokine production| |enzyme linked receptor protein signaling pathway| |negative regulation of transcription by RNA polymerase II| |positive regulation of immune response| |response to hormone| |leukocyte activation| |animal organ morphogenesis| |response to organonitrogen compound| |cellular response to cytokine stimulus| |response to drug| |cellular response to oxygen-containing compound| |identical protein binding| |cell activation| |response to nitrogen compound| |immune effector process| |response to cytokine| |epithelium development| |regulation of immune response| |positive regulation of immune system process| |negative regulation of transcription, DNA-templated| |positive regulation of transcription by RNA polymerase II| |cellular response to endogenous stimulus| |negative regulation of nucleic acid-templated transcription| |negative regulation of RNA biosynthetic process| |negative regulation of RNA metabolic process| |defense response| |positive regulation of developmental process| |negative regulation of cellular macromolecule biosynthetic process| |negative regulation of nucleobase-containing compound metabolic process| |negative regulation of macromolecule biosynthetic process| |response to endogenous stimulus| |negative regulation of cellular biosynthetic process| |positive regulation of transcription, DNA-templated| |negative regulation of biosynthetic process| |response to oxygen-containing compound| |DNA-binding transcription factor activity, RNA polymerase II-specific| |regulation of cell population proliferation| |negative regulation of response to stimulus| |positive regulation of nucleic acid-templated transcription| |positive regulation of RNA biosynthetic process| |regulation of immune system process| |cellular response to stress| |negative regulation of gene expression| |positive regulation of RNA metabolic process| |positive regulation of multicellular organismal process| |tissue development| |immune response| |positive regulation of nucleobase-containing compound metabolic process| |positive regulation of macromolecule biosynthetic process| |positive regulation of cellular biosynthetic process| |positive regulation of gene expression| |positive regulation of biosynthetic process| </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:exp112|S-DABN 8μM R03 exp112]]|-2.35| |[[:results:exp90|WYE-354 6μM R02 exp90]]|-1.82| |[[:results:exp293|Myriocin 25μM R06 exp293]]|-1.77| |[[:results:exp320|ABT-702 5μM plus CoCl2 18μM R07 exp320]]|-1.76| |[[:results:exp450|Artemisinin 50μM R08 exp450]]|1.71| |[[:results:exp321|ABT-702 5μM plus Deferoxamine 11μM R07 exp321]]|2.03| </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: 1/739 ^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|1/16| |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>**: 9411 * **<color #00a2e8>Expression level (log2 read counts)</color>**: 7.61 <button type='primary' size='small' modal='Dist_expr'>Expression Distribution</button> <modal id='Dist_expr' size='lg' title='STAT6 Expression in NALM6 Cells: 7.61'> {{:chemogenomics:nalm6 dist.png?nolink |}} </modal> Last modified: 2026/01/07 22:37by 127.0.0.1