人 ALS2 (NM_001135745) cDNA克隆

Accession: NM_001135745
基因名称: ALS2
基因别名: ALSJ; PLSJ; IAHSP; ALS2CR6
基因描述: Homo sapiens amyotrophic lateral sclerosis 2 (juvenile) (ALS2), transcript variant 2, mRNA.
种属: Human
CDS区长度: 1191 (查看编码区序列)
翻译后氨基酸长度: 396 (查看氨基酸序列)
Transcript Variant: This variant (2) uses an internal polyA site resulting in a substantially shorter transcript with a unique 3' coding region, compared to variant 1. The encoded isoform (2), also known as the short form, is substantially shorter and has a unique C-terminus, compared to isoform 1.
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G113905 人 ALS2 (NM_001135745) cDNA克隆 pDONR223 2ug质粒 点击询价

The protein encoded by this gene contains an ATS1/RCC1-like domain, a RhoGEF domain, and a vacuolar protein sorting 9 (VPS9) domain, all of which are guanine-nucleotide exchange factors that activate members of the Ras superfamily of GTPases. The protein functions as a guanine nucleotide exchange factor for the small GTPase RAB5. The protein localizes with RAB5 on early endosomal compartments, and functions as a modulator for endosomal dynamics. Mutations in this gene result in several forms of juvenile lateral sclerosis and infantile-onset ascending spastic paralysis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]