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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:0000006 | Autosomal dominant inheritance |
| HP:0000083 | Renal insufficiency |
| HP:0000117 | Renal phosphate wasting |
| HP:0001324 | Muscle weakness |
| HP:0001510 | Growth delay |
| HP:0001824 | Weight loss |
| HP:0001942 | Metabolic acidosis |
| HP:0001943 | Hypoglycemia |
| HP:0001944 | Dehydration |
| HP:0002049 | Proximal renal tubular acidosis |
| 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 |
|---|---|---|---|
| 177905 | WB:WBGene00001157 | ||
| 184065 | WB:WBGene00001158 | ||
| 100182913 | CIOIN15839 | ||
| 102355847 | LATCH11389 | ||
| 100000859 | ZFIN:ZDB-GENE-040426-2581 | DANRE45309 | |
| 103032907 | ASTMX15692 | ||
| 113574639 | ELEEL14399 | ||
| 115155396 | SALTR10742 | ||
| 115533260 | GADMO29881 | ||
| 101170799 | ORYLA09787 |
