蛋白质/抗原/多肽 >> 重组蛋白
重组7号染色体开放阅读框29蛋白
产品介绍 基因名: ZBED10P 产品别名: C7orf29; ZBED6CL; ZBED10P; zinc finger BED-type containing 10, pseudogene; zinc finger BED-type containing 10, pseudogene; ZBED6 C-terminal like; 7号染色体开放阅读框29; 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 C7orf29 gene product has been provisionally designated C7orf29 pending further characterization. 标签:His-tag |
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