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重组7号染色体开放阅读框46蛋白
交货期:1周

产品名称
Recombinant Fam221a
Recombinant family with sequence similarity 221, member A protein
产品介绍
基因名:

Fam221a


产品别名:

D330028D13Rik; Fam221a; family with sequence similarity 221, member A; family with sequence similarity 221, member A; protein FAM221A; uncharacterized protein C7orf46 homolog; 7号染色体开放阅读框46;


背景信息:
Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf46 gene product has been provisionally designated C7orf46 pending further characterization.
广州伟伯科技有限公司
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