蛋白质/抗原/多肽 >> 重组蛋白
重组FAM118B蛋白
半岛bd体育手机客户端 介绍
基因名:
FAM118B 半岛bd体育手机客户端 别名: FAM118B; family with sequence similarity 118 member B; family with sequence similarity 118 member B; protein FAM118B; FAM118B蛋白; 背景信息:
With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4% of human genomic DNA and 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. 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. The FAM118B gene product has been provisionally designated FAM118B pending further characterization.
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