人 PLEKHG4 (NM_015432) cDNA克隆

Accession: NM_015432
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 1, 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 (1) represents the longest transcript and encodes the longer isoform (1). Transcript variants 1-4 encode the same isoform.
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G122500 人 PLEKHG4 (NM_015432) cDNA克隆 pDONR223 2ug质粒 点击询价

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]