人 RGS9 (NM_001165933) cDNA克隆

Accession: NM_001165933
基因名称: RGS9
基因别名: PERRS; RGS9L
基因描述: Homo sapiens regulator of G-protein signaling 9 (RGS9), transcript variant 3, mRNA.
种属: Human
CDS区长度: 1455 (查看编码区序列)
翻译后氨基酸长度: 484 (查看氨基酸序列)
Transcript Variant: This variant (3), also known as RGS9-1, uses an alternate in-frame splice site in the central coding region and differs in the 3' coding region, compared to variant 1. The resulting isoform (3) lacks a 3 amino acid segment and has a shorter and distinct C-terminus, compared to isoform 1. Isoform 3 includes a shorter C-terminal region and is referred to as the short form.
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G125697 人 RGS9 (NM_001165933) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a member of the RGS family of GTPase activating proteins that function in various signaling pathways by accelerating the deactivation of G proteins. This protein is anchored to photoreceptor membranes in retinal cells and deactivates G proteins in the rod and cone phototransduction cascades. Mutations in this gene result in bradyopsia. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]