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]
人 RGS9 (NM_001081955) cDNA克隆
| Accession: | NM_001081955 |
|---|---|
| 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 2, mRNA. |
| 种属: | Human |
| CDS区长度: | 2016 (查看编码区序列) |
| 翻译后氨基酸长度: | 671 (查看氨基酸序列) |
| Transcript Variant: | This variant (2), also known as RGS9-2, uses an alternate in-frame splice site in the central coding region, compared to variant 1. The resulting isoform (2) lacks a 3 amino acid segment, compared to isoform 1. Isoforms 1 and 2 include a longer C-terminal domain and are collectively referred to as the long form. |
| 人 RGS9 (NM_003835) cDNA克隆 | transcript variant 1 |
| 人 RGS9 (NM_001081955) cDNA克隆 | transcript variant 2 |
| 人 RGS9 (NM_001165933) cDNA克隆 | transcript variant 3 |
扫一扫 加微信
联系我们
- 客服热线:
0731-84158353 - 订货邮箱:
order@youbio.cn - 技术支持:
tech@youbio.cn 
QQ：2605877374
