重组7号染色体开放阅读框45蛋白
交货期:1周
产品别名:Recombinant Ssmem1
Recombinant serine-rich single-pass membrane protein 1 protein
基因名:
Ssmem1
产品别名:
1700016K02Rik; 1700025E21Rik; Ssmem1; serine-rich single-pass membrane protein 1; serine-rich single-pass membrane protein 1; 7号染色体开放阅读框45;
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 C7orf45 gene product has been provisionally designated C7orf45 pending further characterization.
产品发布日期:2025.05.16