人 RAI2 (NM_001172739) cDNA克隆

Accession: NM_001172739
基因名称: RAI2
基因描述: Homo sapiens retinoic acid induced 2 (RAI2), transcript variant 3, mRNA.
种属: Human
CDS区长度: 1593 (查看编码区序列)
翻译后氨基酸长度: 530 (查看氨基酸序列)
Transcript Variant: This variant (3) differs in the 5' UTR compared to variant 1. Variants 1, 2 and 3 encode the same isoform (1).
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G112043 人 RAI2 (NM_001172739) cDNA克隆 pDONR223 2ug质粒 点击询价

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]