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Protein structure
RDH5
Retinol dehydrogenase 5HSD17B9, RDH1, SDR9C5
This gene encodes an enzyme belonging to the short-chain dehydrogenases/reductases (SDR) family. This retinol dehydrogenase functions to catalyze the final step in the biosynthesis of 11-cis retinaldehyde, which is the universal chromophore of visual pigments. Mutations in this gene cause autosomal recessive fundus albipunctatus, a rare form of night blindness that is characterized by a delay in the regeneration of cone and rod photopigments. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the neighboring upstream BLOC1S1 (biogenesis of lysosomal organelles complex-1, subunit 1) gene. [provided by RefSeq, Dec 2010]
Top validated antibodies |
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| Everest Biotech |  EB10078 |
Polyclonal |
WB
EL
ICC
IHC
FC
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| Novus Biologicals | NBP1-52047 |
1 references | Polyclonal |
WB
EL
IHC
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| antibodies-online | ABIN568695 |
1 references | Polyclonal |
WB
EL
IHC
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| GeneTex | GTX88011 |
Polyclonal |
WB
ICC
IHC
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| NovoPro Bioscience Inc. | 118451 |
Polyclonal |
WB
EL
IHC
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