人 STRA6 (NM_001199042) cDNA克隆

基本信息

Accession: NM_001199042
基因名称: STRA6
基因别名: MCOPS9; MCOPCB8; PP14296
基因描述: Homo sapiens stimulated by retinoic acid 6 (STRA6), transcript variant 8, mRNA.
种属: Human
CDS区长度: 2121 (查看编码区序列)
翻译后氨基酸长度: 706 (查看氨基酸序列)
Transcript Variant: This variant (8) represents the longest transcript and encodes the longest isoform (f).

订购信息

产品编号 产品名称 载体 规格 价格
G157822 人 STRA6 (NM_001199042) 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 STRA6 (NM_001142617) cDNA克隆 transcript variant 1
人 STRA6 (NM_022369) cDNA克隆 transcript variant 2
人 STRA6 (NM_001142618) cDNA克隆 transcript variant 3
人 STRA6 (NM_001142619) cDNA克隆 transcript variant 4
人 STRA6 (NM_001142620) cDNA克隆 transcript variant 5
人 STRA6 (NM_001199040) cDNA克隆 transcript variant 6
人 STRA6 (NM_001199041) cDNA克隆 transcript variant 7
人 STRA6 (NM_001199042) cDNA克隆 transcript variant 8

基因简介

The protein encoded by this gene is a membrane protein involved in the metabolism of retinol. The encoded protein acts as a receptor for retinol/retinol binding protein complexes. This protein removes the retinol from the complex and transports it across the cell membrane. Defects in this gene are a cause of syndromic microphthalmia type 9 (MCOPS9). Several transcript variants encoding a few different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]

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