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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase
Summary
- Gene Symbol
-
- EHHADH
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Acetylation
- Alternative splicing
- Disease variant
- Fatty acid metabolism
- Isomerase
- Lyase
- Multifunctional enzyme
- NAD
- Oxidoreductase
- Peroxisome
- Phosphoprotein
- Reference proteome
- Proteins
| UniProt | Protein Name |
|---|---|
| Q08426 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| fatty acid beta-oxidation using acyl-CoA oxidase |
|
|
| fatty acid beta-oxidation |
GO Hierarchy
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| 3-hydroxyacyl-CoA dehydratase activity |
|
|
| enzyme binding | ||
| long-chain-3-hydroxyacyl-CoA dehydrogenase activity | ||
| enoyl-CoA hydratase activity | ||
| delta(3)-delta(2)-enoyl-CoA isomerase activity |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
KEGG BRITE Database
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050782 | Zollinger-Ellison syndrome | |
| DOID:0060235 | carnitine palmitoyltransferase II deficiency | |
| DOID:0060262 | gallbladder disease | |
| DOID:0070218 | familial hyperinsulinemic hypoglycemia 2 | |
| DOID:0070219 | familial hyperinsulinemic hypoglycemia 1 | |
| DOID:0080759 | Fanconi renotubular syndrome 3 | |
| DOID:0090031 | D-bifunctional protein deficiency | |
| DOID:0111040 | glycogen storage disease IXd | |
| DOID:0111041 | glycogen storage disease IXb | |
| DOID:0111042 | glycogen storage disease IXa |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002148 | Hypophosphatemia |
| HP:0002150 | Hypercalciuria |
| HP:0002206 | Pulmonary fibrosis |
| HP:0002653 | Bone pain |
| HP:0002659 | Increased susceptibility to fractures |
| HP:0002748 | Rickets |
| HP:0002749 | Osteomalacia |
| HP:0002900 | Hypokalemia |
| HP:0002909 | Generalized aminoaciduria |
| HP:0002979 | Bowing of the legs |
| Disease ID | Disease Name |
|---|---|
| OMIM:615605 |
|
| ORPHA:3337 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP002229
- Gene Name
- enoyl-CoA, hydratase/3-hydroxyacyl CoA dehydrogenase
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 101117635 | SHEEP01554 | ||
| 105999704 | DIPOR21890 | ||
| 100754698 | CRIGR12450 | ||
| 74147 | MGI:1277964 | MOUSE18983 | |
| 171142 | RGD:621441 | RATNO03711 | |
| 100135519 | CAVPO04594 | ||
| 101699730 | HETGA00486 | ||
| 101875701 | MELUD15280 | ||
| 100558466 | ANOCA04200 | ||
| 103676178 | URSMA08606 |
