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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 |
|---|---|---|
| intramolecular oxidoreductase activity, transposing C=C bonds | ||
| protein binding | ||
| 3-hydroxyacyl-CoA dehydrogenase activity | ||
| 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
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:0003076 | Glycosuria |
| HP:0003081 | Increased urinary potassium |
| HP:0003109 | Hyperphosphaturia |
| HP:0003126 | Low-molecular-weight proteinuria |
| HP:0003149 | Hyperuricosuria |
| HP:0003234 | Decreased circulating carnitine concentration |
| HP:0003259 | Elevated circulating creatinine concentration |
| HP:0003355 | Aminoaciduria |
| HP:0003537 | Hypouricemia |
| HP:0003593 | Infantile onset |
| 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 |
|---|---|---|---|
| 100174685 | PONAB25252 | ||
| 488110 | CANLF13544 | ||
| 112926276 | VULVU20545 | ||
| 100468058 | AILME16401 | ||
| 101685945 | MUSPF16488 | ||
| 122198473 | PANLE23508 | ||
| 118894255 | BALMU18019 | ||
| 100677184 | LOXAF11074 | ||
| 448846 | PIGXX05298 | ||
| 102179598 | CAPHI12159 |
