Gene
dhcr24
- ID
- ZDB-GENE-041212-73
- Name
- 24-dehydrocholesterol reductase
- Symbol
- dhcr24 Nomenclature History
- Previous Names
-
- zgc:101638
- Type
- protein_coding_gene
- Location
- Chr: 20 Mapping Details/Browsers
- Description
- Predicted to enable delta24(24-1) sterol reductase activity. Predicted to be involved in steroid metabolic process. Predicted to be active in cytoplasm and membrane. Is expressed in cranial ganglion; lens; solid lens vesicle; telencephalon; and yolk syncytial layer. Human ortholog(s) of this gene implicated in lipid metabolism disorder. Orthologous to human DHCR24 (24-dehydrocholesterol reductase).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 7 figures from 2 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:101638 (8 images)
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
---|---|---|---|
Desmosterolosis | 602398 |
Domain, Family, and Site Summary
Type | InterPro ID | Name |
---|---|---|
Domain | IPR006094 | FAD linked oxidase, N-terminal |
Domain | IPR016166 | FAD-binding domain, PCMH-type |
Family | IPR040165 | Delta(24)-sterol reductase |
Homologous_superfamily | IPR016169 | FAD-binding, type PCMH, subdomain 2 |
Homologous_superfamily | IPR036318 | FAD-binding, type PCMH-like superfamily |
Domain Details Per Protein
Protein | Length | Delta(24)-sterol reductase | FAD-binding domain, PCMH-type | FAD-binding, type PCMH-like superfamily | FAD-binding, type PCMH, subdomain 2 | FAD linked oxidase, N-terminal |
---|---|---|---|---|---|---|
UniProtKB:Q5PRC9
|
516 |
Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
---|---|---|---|---|---|
mRNA |
dhcr24-201
(1)
|
Ensembl | 1,286 nt | ||
mRNA |
dhcr24-202
(1)
|
Ensembl | 1,828 nt |
Interactions and Pathways
No data available
Plasmids
No data available