靶标:
C7orf50
产品别名:
YCR016W; C7orf50; chromosome 7 open reading frame 50; chromosome 7 open reading frame 50; uncharacterized protein C7orf50; 7号染色体开放阅读框50;
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 C7orf50 gene product has been provisionally designated C7orf50 pending further characterization.