人 SLC24A1 (NM_001254740) cDNA克隆

基本信息

Accession: NM_001254740
基因名称: SLC24A1
基因别名: NCKX; RODX; NCKX1; CSNB1D; HsT17412
基因描述: Homo sapiens solute carrier family 24 (sodium/potassium/calcium exchanger), member 1 (SLC24A1), transcript variant 2, mRNA.
种属: Human
CDS区长度: 1281 (查看编码区序列)
翻译后氨基酸长度: 426 (查看氨基酸序列)
Transcript Variant: This variant (2) differs in the 5' UTR, lacks a portion of the 5' coding region and initiates translation at an alternate start codon, compared to variant 1. The encoded isoform (2) is shorter and has a distinct N-terminus, compared to isoform 1.

订购信息

产品编号 产品名称 载体 规格 价格
G122519 人 SLC24A1 (NM_001254740) 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 SLC24A1 (NM_004727) cDNA克隆 transcript variant 1
人 SLC24A1 (NM_001254740) cDNA克隆 transcript variant 2

基因简介

This gene encodes a member of the potassium-dependent sodium/calcium exchanger protein family. The encoded protein plays an important role in sodium/calcium exchange in retinal rod and cone photoreceptors by mediating the extrusion of one calcium ion and one potassium ion in exchange for four sodium ions. Mutations in this gene may play a role in congenital stationary night blindness. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]

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