Entity Details
| Primary name |
RDH5_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q92781 |
| EntryName | RDH5_HUMAN |
| FullName | Retinol dehydrogenase 5 |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 318 |
| SequenceStatus | complete |
| DateCreated | 1997-11-01 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Endoplasmic reticulum membrane |
Domains
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| Domain | Name | Category | Type |
| IPR002347 | Short-chain dehydrogenase/reductase SDR | Family | Family |
| IPR036291 | NAD(P)-binding domain superfamily | Family | Homologous superfamily |
Diseases
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| Disease ID | Source | Name | Description |
| 136880 | OMIM | Retinitis punctata albescens (RPA) | A form of fleck retina disease characterized by aggregation of white flecks posteriorly in the retina, causing night blindness and delayed dark adaptation. It differs from fundus albipunctatus in being progressive and evolving to generalized atrophy of the retina. The disease is caused by variants affecting the gene represented in this entry. |
Drugs
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| Drug | Name | Source | Type |
| DB00157 | NADH | Drugbank | small molecule |
| DB00162 | Vitamin A | Drugbank | small molecule |
Interactions
4 interactions