菜单 基因医生

该基因编码的蛋白参与多种途径,包括src家族激酶的调控。它通过与蛋白酪氨酸磷酸酶(ptpn22)基因编码的蛋白结合,在t细胞活化中发挥重要作用。该蛋白也在多种底物上磷酸化C末端酪氨酸残基,包括SRC原癌基因、非受体酪氨酸激酶基因编码的蛋白质磷酸化抑制src家族酪氨酸激酶的激酶活性。该基因的内含子多态性(rs34933034)已被发现影响b细胞的活化,并与系统性红斑狼疮(sle)有关。选择性剪接导致多个转录变体[由RefSeq提供,2017年8月]
The protein encoded by this gene is involved in multiple pathways, including the regulation of Src family kinases. It plays an important role in T-cell activation through its association with the protein encoded by the protein tyrosine phosphatase, non-receptor type 22 (PTPN22) gene. This protein also phosphorylates C-terminal tyrosine residues on multiple substrates, including the protein encoded by the SRC proto-oncogene, non-receptor tyrosine kinase gene. Phosphorylation suppresses the kinase activity of the Src family tyrosine kinases. An intronic polymorphism (rs34933034) in this gene has been found to affect B-cell activation and is associated with systemic lupus erythematosus (SLE). Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2017]

基因名:CSK
别名:
基因ID:1445
Chromosome:
(GRCh37)
15 Start: 75074425 End: 75095539 Strand: 
信号通路:  
CSK 基因突变与药物