菜单 基因医生

由该基因编码的蛋白质具有激酶活性,磷酸化调节参与信号转导。它磷酸化i kappa balpha、p105和c-jun,作为复合物介导磷酸化的对接位点。该基因位于17号染色体的Smith-Magenis综合征区域内。已经发现了一些编码不同亚型的转录变体。[由RefSeq提供,2015年10月]
The protein encoded by this gene possesses kinase activity that phosphorylates regulators involved in signal transduction. It phosphorylates I kappa-Balpha, p105, and c-Jun. It acts as a docking site for complex-mediated phosphorylation. The gene is located within the Smith-Magenis syndrome region on chromosome 17. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]

基因名:COPS3
别名:CSN3,SGN3
基因ID:8533
Chromosome:
(GRCh37)
17 Start: 17149938 End: 17184617 Strand: 
信号通路:  
COPS3 基因突变与药物