DHRS3 dehydrogenase/reductase 3
Gene ID: 9249, updated on 28-Oct-2024Gene type: protein coding
Also known as: SDR1; RDH17; Rsdr1; DD83.1; SDR16C1; retSDR1; CNALPTC1
- See all available tests in GTR for this gene
- Go to complete Gene record for DHRS3
- Go to Variation Viewer for DHRS3 variants
Summary
Predicted to enable all-trans-retinol dehydrogenase (NAD+) activity. Predicted to be involved in regulation of retinoic acid receptor signaling pathway and retinoid metabolic process. Predicted to act upstream of or within several processes, including heart morphogenesis; negative regulation of retinoic acid receptor signaling pathway; and regulation of ossification. Predicted to be located in endoplasmic reticulum membrane and photoreceptor outer segment membrane. Predicted to be active in lipid droplet. [provided by Alliance of Genome Resources, Oct 2024]
Genomic context
- Location:
- 1p36.21
- Sequence:
- Chromosome: 1; NC_000001.11 (12567910..12618210, complement)
- Total number of exons:
- 9
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for DHRS3 variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- Variation ViewerRelated Variants
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