人 SLC6A8 (NM_005629) cDNA克隆

Accession: NM_005629
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 1, mRNA.
种属: Human
CDS区长度: 1908 (查看编码区序列)
翻译后氨基酸长度: 635 (查看氨基酸序列)
Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (1).
产品编号 产品名称 载体 规格 价格
G121621 人 SLC6A8 (NM_005629) cDNA克隆 pDONR223 2ug质粒 点击询价

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]