人 SPG11 (NM_001160227) cDNA克隆

基本信息

Accession: NM_001160227
基因名称: SPG11
基因别名: KIAA1840
基因描述: Homo sapiens spastic paraplegia 11 (autosomal recessive) (SPG11), transcript variant 2, mRNA.
种属: Human
CDS区长度: 6993 (查看编码区序列)
翻译后氨基酸长度: 2330 (查看氨基酸序列)
Transcript Variant: This variant (2) lacks two alternate in-frame exons in the 3' coding region, compared to variant 1. The resulting isoform (2) lacks an internal segment, compared to isoform 1.

订购信息

产品编号 产品名称 载体 规格 价格
G118518 人 SPG11 (NM_001160227) cDNA克隆 pDONR223 2ug质粒 点击询价

载体信息

pDONR223载体图谱

相关转录本

人 SPG11 (NM_025137) cDNA克隆 transcript variant 1
人 SPG11 (NM_001160227) cDNA克隆 transcript variant 2

基因简介

The protein encoded by this gene is a potential transmembrane protein that is phosphorylated upon DNA damage. Defects in this gene are a cause of spastic paraplegia type 11 (SPG11). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]

相关产品