人 PLEKHG4 (NM_001129727) cDNA克隆

基本信息

Accession: NM_001129727
基因名称: PLEKHG4
基因别名: SCA4; PRTPHN1; ARHGEF44
基因描述: Homo sapiens pleckstrin homology domain containing, family G (with RhoGef domain) member 4 (PLEKHG4), transcript variant 2, mRNA.
种属: Human
CDS区长度: 3576 (查看编码区序列)
翻译后氨基酸长度: 1191 (查看氨基酸序列)
Transcript Variant: This variant (2) contains 2 spliced 5' non-coding exons, hence a different 5' UTR, compared to variant 1. Transcript variants 1-4 encode the same isoform.

订购信息

产品编号 产品名称 载体 规格 价格
G122496 人 PLEKHG4 (NM_001129727) 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 PLEKHG4 (NM_015432) cDNA克隆 transcript variant 1
人 PLEKHG4 (NM_001129727) cDNA克隆 transcript variant 2
人 PLEKHG4 (NM_001129728) cDNA克隆 transcript variant 3
人 PLEKHG4 (NM_001129729) cDNA克隆 transcript variant 4
人 PLEKHG4 (NM_001129731) cDNA克隆 transcript variant 5

基因简介

The protein encoded by this gene contains multiple domains suggestive of a role in intracellular signaling and cytoskeleton dynamics at the Golgi apparatus. Mutations in this gene are associated with spinocerebellar ataxia 16q22-linked. Several alternatively spliced transcript variants, differing only in the 5' UTR, or encoding a different isoform, have been found for this gene. [provided by RefSeq, Jul 2008]

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