人 SLC6A8 (NM_001142805) cDNA克隆

基本信息

Accession: NM_001142805
基因名称: SLC6A8
基因别名: CRT; CT1; CRTR; CCDS1
基因描述: Homo sapiens solute carrier family 6 (neurotransmitter transporter), member 8 (SLC6A8), transcript variant 2, mRNA.
种属: Human
CDS区长度: 1878 (查看编码区序列)
翻译后氨基酸长度: 625 (查看氨基酸序列)
Transcript Variant: This variant (2) uses an alternate in-frame splice site in the central coding region, compared to variant 1. The resulting isoform (2) lacks a 10-aa segment but has the same N- and C-termini, compared to isoform 1.

订购信息

产品编号 产品名称 载体 规格 价格
G121619 人 SLC6A8 (NM_001142805) 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 SLC6A8 (NM_005629) cDNA克隆 transcript variant 1
人 SLC6A8 (NM_001142805) cDNA克隆 transcript variant 2
人 SLC6A8 (NM_001142806) cDNA克隆 transcript variant 3

基因简介

The protein encoded by this gene is a plasma membrane protein whose function is to transport creatine into and out of cells. Defects in this gene can result in X-linked creatine deficiency syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]

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