该基因编码蛋白酪氨酸磷酸酶家族非受体4亚家族成员编码蛋白是一种淋巴特异性细胞内磷酸酶,与分子适配器蛋白CBL相关,可能参与调节T细胞受体信号途径中的CBL功能该基因突变可能与一系列自身免疫性疾病有关,包括1型糖尿病、类风湿关节炎、系统性红斑狼疮和Graves病另外,还描述了编码不同亚型的剪接转录变体。〔RefSeq,2009〕
This gene encodes of member of the non-receptor class 4 subfamily of the protein-tyrosine phosphatase family. The encoded protein is a lymphoid-specific intracellular phosphatase that associates with the molecular adapter protein CBL and may be involved in regulating CBL function in the T-cell receptor signaling pathway. Mutations in this gene may be associated with a range of autoimmune disorders including Type 1 Diabetes, rheumatoid arthritis, systemic lupus erythematosus and Graves' disease. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Mar 2009]
基因名: | PTPN22 |
别名: | LYP,PEP,LYP1,LYP2,PTPN8,PTPN22.5,PTPN22.6 |
基因ID: | 26191 |
Chromosome: (GRCh37) | 1 Start: 114356433 End: 114414375 Strand: |
信号通路: |