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MIRAGE
hydroxyacyl-CoA dehydrogenase
Summary
- Gene Symbol
-
- HADH
- Aliases
-
- HADH1
- SCHAD
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Alternative splicing
- Disease variant
- Fatty acid metabolism
- Hydroxylation
- Mitochondrion
- NAD
- Oxidoreductase
- Proteomics identification
- Reference proteome
- Spermatogenesis
- Transferase
- Transit peptide
- Proteins
| UniProt | Protein Name |
|---|---|
| A0A140VK76 |
|
| A0A0D9SFP2 |
|
| Q16836 |
|
| B3KTT6 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| fatty acid beta-oxidation | ||
| fatty acid beta-oxidation | ||
| fatty acid beta-oxidation | ||
| spermatogenesis | ||
| response to xenobiotic stimulus |
GO Hierarchy
biological process
metabolic process [inference]
cellular process [inference]
biological regulation [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| nucleoplasm | ||
| cytoplasm | ||
| mitochondrion | ||
| mitochondrion | ||
| mitochondrion |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| 3-hydroxyacyl-CoA dehydrogenase activity | ||
| 3-hydroxyacyl-CoA dehydrogenase activity | ||
| transferase activity | ||
| identical protein binding | ||
| NAD+ binding |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0070215 | familial hyperinsulinemic hypoglycemia 4 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001325 | Hypoglycemic coma |
| HP:0001397 | Hepatic steatosis |
| HP:0001508 | Failure to thrive |
| HP:0001510 | Growth delay |
| HP:0001511 | Intrauterine growth retardation |
| HP:0001639 | Hypertrophic cardiomyopathy |
| HP:0001644 | Dilated cardiomyopathy |
| HP:0001657 | Prolonged QT interval |
| HP:0001985 | Hypoketotic hypoglycemia |
| HP:0001987 | Hyperammonemia |
| Disease ID | Disease Name |
|---|---|
| OMIM:231530 |
|
| ORPHA:71212 |
|
| OMIM:609975 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP002407
- Gene Name
- hydroxyacyl-CoA dehydrogenase
