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 cognitive disability, oral-facial-digital syndrome, and Fried syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| RAI2-20-RE | 20 (40 μL) | 200 μL |  |
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| RAI2-20-OR | 20 (40 μL) | 200 μL |  |
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| RAI2-20-GO | 20 (40 μL) | 200 μL |  |
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| RAI2-20-GR | 20 (40 μL) | 200 μL |  |
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| RAI2-20-AQ | 20 (40 μL) | 200 μL |  |
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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 cognitive disability, oral-facial-digital syndrome, and Fried syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]
Gene Symbol : RAI2
Gene Name : Retinoic acid induced 2
Chromosome : CHR X: 178,613,45-178,000,48
Locus : Xp22.13
Alt. Genes : HIPK3
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