人 AFG3L2 (NM_006796) cDNA克隆

Accession: NM_006796
基因名称: AFG3L2
基因别名: SCA28; SPAX5
基因描述: Homo sapiens AFG3-like AAA ATPase 2 (AFG3L2), mRNA.
种属: Human
CDS区长度: 2394 (查看编码区序列)
翻译后氨基酸长度: 797 (查看氨基酸序列)
产品编号 产品名称 载体 规格 价格
G127546 人 AFG3L2 (NM_006796) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a protein localized in mitochondria and closely related to paraplegin. The paraplegin gene is responsible for an autosomal recessive form of hereditary spastic paraplegia. This gene is a candidate gene for other hereditary spastic paraplegias or neurodegenerative disorders. [provided by RefSeq, Jul 2008]