Gene
hacd1
- ID
- ZDB-GENE-170413-2
- Name
- 3-hydroxyacyl-CoA dehydratase 1
- Symbol
- hacd1 Nomenclature History
- Previous Names
- None
- Type
- protein_coding_gene
- Location
- Chr: 7 Mapping Details/Browsers
- Description
- Predicted to enable 3-hydroxyacyl-CoA dehydratase activity. Predicted to be involved in fatty acid elongation; sphingolipid biosynthetic process; and very long-chain fatty acid biosynthetic process. Predicted to act upstream of or within fatty acid metabolic process. Predicted to be located in endoplasmic reticulum and membrane. Predicted to be active in endoplasmic reticulum membrane. Human ortholog(s) of this gene implicated in congenital myopathy. Orthologous to human HACD1 (3-hydroxyacyl-CoA dehydratase 1).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- No data available
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
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 |
|---|---|---|---|
| Congenital myopathy 11 | 619967 |
Domain, Family, and Site Summary
| Type | InterPro ID | Name |
|---|---|---|
| Family | IPR007482 | Protein-tyrosine phosphatase-like, PTPLA |
Domain Details Per Protein
| Protein | Length | Protein-tyrosine phosphatase-like, PTPLA |
|---|---|---|
|
UniProtKB:A0A0G2L0Q2
|
||
|
UniProtKB:A0A8M2BE05
|
195 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available