蛋白质/抗原/多肽 >> 重组蛋白
重组FAM160B1蛋白
产品介绍 基因名: FHIP2A 产品别名: FAM160B1; KIAA1600; bA106M7.3; FHIP2A; FHF complex subunit HOOK interacting protein 2A; FHF complex subunit HOOK interacting protein 2A; FHF complex subunit HOOK interacting protein 2A; family with sequence similarity 160 member B1; protein FAM160B1; FAM160B1蛋白; 背景信息: FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which 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. 标签:His-tag |
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