蛋白质/抗原/多肽 >> 重组蛋白
重组7号染色体开放阅读框57蛋白
半岛bd体育手机客户端 介绍
基因名:
C7orf57 半岛bd体育手机客户端 别名: C7orf57; chromosome 7 open reading frame 57; chromosome 7 open reading frame 57; uncharacterized protein C7orf57; 7号染色体开放阅读框57; 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 C7orf57 gene product has been provisionally designated C7orf57 pending further characterization.
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