2017-5-4
英文名称 Anti-C7orf64
中文名称 7号染色体开放阅读框64抗体
别 名 C7orf64; RBM48_HUMAN; DKFZP564O0523; DKFZp686D1651; HSPC304; Hypothetical protein LOC84060; OTTHUMP00000215752; UPF0712 protein C7orf64.
详细介绍:
相关资料:
产品介绍 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 C7orf64 gene product has been provisionally designated C7orf64 pending further characterization.
Similarity : Belongs to the RBM48 family.
Contains 1 RRM (RNA recognition motif) domain.
Database links : UniProtKB/Swiss-Prot: Q5RL73.1
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