RDH12 Products

Description

RDH12 is 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 3 (LCA3). [provided by RefSeq]

Bioinformatics

Entrez	145226 Human
Uniprot	NM_152443 Human NP_689656 Human Q96NR8 Human
Product By Gene ID	145226
Alternate Names	All-trans and 9-cis retinol dehydrogenase EC 1.1.1 EC 1.1.1.- EC 1.1.1.100 FLJ30273 LCA13retinol dehydrogenase 12, all-trans and 9-cis LCA3 retinol dehydrogenase 12 (all-trans and 9-cis) retinol dehydrogenase 12 (all-trans/9-cis/11-cis) retinol dehydrogenase 12 SDR7C2 short chain dehydrogenase/reductase family 7C, member 2

Research Areas for RDH12

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Vision