人 RAI2 (NM_001172732) cDNA克隆

基本信息

Accession: NM_001172732
基因名称: RAI2
基因描述: Homo sapiens retinoic acid induced 2 (RAI2), transcript variant 4, mRNA.
种属: Human
CDS区长度: 1443 (查看编码区序列)
翻译后氨基酸长度: 480 (查看氨基酸序列)
Transcript Variant: This variant (4) differs in the 5' UTR and lacks a segment in the coding region, compared to variant 1. The resulting protein (isoform 2) is shorter than isoform 1.

订购信息

产品编号 产品名称 载体 规格 价格
G112042 人 RAI2 (NM_001172732) 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 RAI2 (NM_001172743) cDNA克隆 transcript variant 1
人 RAI2 (NM_021785) cDNA克隆 transcript variant 2
人 RAI2 (NM_001172739) cDNA克隆 transcript variant 3
人 RAI2 (NM_001172732) cDNA克隆 transcript variant 4

基因简介

Retinoic acid plays a critical role in development, cellular growth, and differentiation. The specific function of this retinoic acid-induced gene has not yet been determined but it may play a role in development. The chromosomal location of this gene designates it to be a candidate for diseases such as Nance-Horan syndrome, sensorineural deafness, non-specific X-linked mental retardation, oral-facial-digital syndrome, and Fried syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]

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