蛋白质/抗原/多肽 >> 重组蛋白
重组卷曲螺旋结构域蛋白89
半岛bd体育手机客户端 介绍
基因名:
Ccdc89 半岛bd体育手机客户端 别名: 1700019B01Rik; AU022100; BOIP; Ccdc89; coiled-coil domain containing 89; coiled-coil domain containing 89; coiled-coil domain-containing protein 89; bc8 orange-interacting protein; 卷曲螺旋结构域蛋白89; 背景信息:
CCDC89 is a 374 amino acid cytoplasmic and nuclear protein that interacts with HRT1 and belongs to the CCDC89 family. The gene that encodes CCDC89 consists of more than 2,000 bases and maps to human chromosome 11q14.1. Chromosome 11, which comprises approximately 4% of the human genome, is considered a gene and disease association-dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations, while Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11-encoded genes.
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