人 SLC9A3R2 (NM_001252076) cDNA克隆

Accession: NM_001252076
基因名称: SLC9A3R2
基因别名: SIP1; OCTS2; SIP-1; TKA-1; E3KARP; NHERF2; NHE3RF2; NHERF-2
基因描述: Homo sapiens solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 2 (SLC9A3R2), transcript variant 5, mRNA.
种属: Human
CDS区长度: 648 (查看编码区序列)
翻译后氨基酸长度: 215 (查看氨基酸序列)
Transcript Variant: This variant (5) differs in the 5' UTR, uses an alternate splice site in the 3' coding region, lacks a portion of the 5' coding region and initiates translation at an alternate start codon, compared to variant 1. The encoded isoform (e) is shorter and has a distinct N-terminus, compared to isoform a.
产品编号 产品名称 载体 规格 价格
G167369 人 SLC9A3R2 (NM_001252076) cDNA克隆 pDONR223 2ug质粒 点击询价

This gene encodes a member of the NHERF family of PDZ scaffolding proteins. These proteins mediate many cellular processes by binding to and regulating the membrane expression and protein-protein interactions of membrane receptors and transport proteins. The encoded protein plays a role in intestinal sodium absorption by regulating the activity of the sodium/hydrogen exchanger 3, and may also regulate the cystic fibrosis transmembrane regulator (CFTR) ion channel. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]