首页 >> 半岛bd体育手机客户端
中心
蛋白质/抗原/多肽 >> 重组蛋白
重组FAM59A蛋白
半岛bd体育手机客户端
介绍 基因名: GAREM1 半岛bd体育手机客户端 别名: C18orf11; FAM59A; GAREM; Gm944; GAREM1; GRB2 associated regulator of MAPK1 subtype 1; GRB2 associated regulator of MAPK1 subtype 1; GRB2-associated and regulator of MAPK protein 1; GRB2 associated regulator of MAPK1 1; GRB2 associated, regulator of MAPK1; GRB2-associated and regulator of MAPK1; Grb2-associated and regulator of Erk/MAPK; family with sequence similarity 59, member A; protein FAM59A; FAM59A蛋白; 背景信息: Encoding over 300 genes, chromosome 18 contains about 76 million bases. Trisomy 18, or Edwards syndrome, is the second most common trisomy after Downs syndrome. Symptoms of Edwards syndrome include low birth weight, a variety of physical development defects, heart deformations and breathing difficulty. Translocation between chromosome 18 and 14 is the most common translocation in cancers and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18. The TGF∫ modulators, Smad2, Smad4 and Smad7 are encoded by chromosome 18. The FAM59A gene product has been provisionally designated FAM59A pending further characterization. 标签:His-tag |
相关半岛bd体育手机客户端
|