- 商品货号:F112044
- accession:NM_001172743
- 基因别名:RAI2
- 基因描述:Homo sapiens retinoic acid induced 2 (RAI2), transcript variant 1, mRNA.
- 载体: 现货载体
- CDS区长度:1593
- 翻译后氨基酸长度:530
- TranscriptVariant:This variant (1) encodes the longer isoform. Variants 1, 2 and 3 encode the same isoform (1).
- 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]
- 载体信息:自有图片地址
- 规格:10ul 质粒
CDS区参考序列: 点击查看序列翻译后氨基酸参数序列: 点击查看序列