人 C10orf2 (NM_021830) cDNA克隆

Accession: NM_021830
基因名称: C10orf2
基因别名: PEO; PEO1; SCA8; ATXN8; IOSCA; PEOA3; SANDO; TWINL; MTDPS7
基因描述: Homo sapiens chromosome 10 open reading frame 2 (C10orf2), transcript variant 1, mRNA.
种属: Human
CDS区长度: 2055 (查看编码区序列)
翻译后氨基酸长度: 684 (查看氨基酸序列)
Transcript Variant: This variant (1) encodes the longest isoform (A; also known as Twinkle).
产品编号 产品名称 载体 规格 价格
G121062 人 C10orf2 (NM_021830) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a hexameric DNA helicase which unwinds short stretches of double-stranded DNA in the 5' to 3' direction and, along with mitochondrial single-stranded DNA binding protein and mtDNA polymerase gamma, is thought to play a key role in mtDNA replication. The protein localizes to the mitochondrial matrix and mitochondrial nucleoids. Mutations in this gene cause infantile onset spinocerebellar ataxia (IOSCA) and progressive external ophthalmoplegia (PEO) and are also associated with several mitochondrial depletion syndromes. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Aug 2009]