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Invitrogen
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Immunogen sequence: DSPFLKAFQA SSSSSPETLT DVGTSSQVSS LRRPEEDDMA FFERRYQERM KMEKAAKWKG KAPLPSATK
Highest antigen sequence identity to the following orthologs: Mouse - 63%, Rat - 67%.
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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: family with sequence similarity 221, member A; Protein FAM221A; uncharacterized protein C7orf46
基因别名: C7orf46; FAM221A
UniProt ID: (Human) A4D161
Entrez Gene ID: (Human) 340277