人 VSX1 (NM_001256271) cDNA克隆

基本信息

Accession: NM_001256271
基因名称: VSX1
基因别名: PPD; KTCN; PPCD; RINX; KTCN1; CAASDS
基因描述: Homo sapiens visual system homeobox 1 (VSX1), transcript variant 3, mRNA.
种属: Human
CDS区长度: 711 (查看编码区序列)
翻译后氨基酸长度: 236 (查看氨基酸序列)
Transcript Variant: This variant (3) differs in the 3' UTR and has coding region, compared to variant 1. The resulting protein (isoform c) has a distinct C-terminus and is shorter than isoform a.

订购信息

产品编号 产品名称 载体 规格 价格
G122212 人 VSX1 (NM_001256271) 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 VSX1 (NM_014588) cDNA克隆 transcript variant 1
人 VSX1 (NM_199425) cDNA克隆 transcript variant 2
人 VSX1 (NM_001256271) cDNA克隆 transcript variant 3
人 VSX1 (NM_001256272) cDNA克隆 transcript variant 4

基因简介

The protein encoded by this gene contains a paired-like homeodomain and binds to the core of the locus control region of the red/green visual pigment gene cluster. The encoded protein may regulate expression of the cone opsin genes early in development. Mutations in this gene can cause posterior polymorphous corneal dystrophy and keratoconus. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]

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