靶标９�p style="text-indent: 2em;">Ssmem1

产品别名９�p style="text-indent: 2em;">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９�div style="text-indent: 2em;">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.