The protein encoded by this gene is an NADPH-dependent retinal reductase whose highest activity is toward 9-cis and all-trans-retinol. The encoded enzyme also plays a role in the metabolism of short-chain aldehydes but does not exhibit steroid dehydrogenase activity. Defects in this gene are a cause of Leber congenital amaurosis type 13 and Retinitis Pigmentosa 53. [provided by RefSeq, Sep 2015]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| RDH12-20-RE | 20 (40 μL) | 200 μL |  |
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| RDH12-20-OR | 20 (40 μL) | 200 μL |  |
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| RDH12-20-GO | 20 (40 μL) | 200 μL |  |
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| RDH12-20-GR | 20 (40 μL) | 200 μL |  |
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| RDH12-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is an NADPH-dependent retinal reductase whose highest activity is toward 9-cis and all-trans-retinol. The encoded enzyme also plays a role in the metabolism of short-chain aldehydes but does not exhibit steroid dehydrogenase activity. Defects in this gene are a cause of Leber congenital amaurosis type 13 and Retinitis Pigmentosa 53. [provided by RefSeq, Sep 2015]
Gene Symbol : RDH12
Gene Name : Retinol dehydrogenase 12 (all-trans/9-cis/11-cis)
Chromosome : CHR 14: 677,018,85-677,344,50
Locus : 14q24.1
Alt. Genes : CELA3A
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