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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
acyl-CoA dehydrogenase medium chain
Summary
- Gene Symbol
-
- ACADM
- Aliases
-
- ACAD1
- MCAD
- MCADH
- medium-chain acyl-CoA dehydrogenase
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Alternative splicing
- Direct protein sequencing
- Disease variant
- FAD
- Fatty acid metabolism
- Mitochondrion
- Oxidoreductase
- Phosphoprotein
- Proteomics identification
- Reference proteome
- Transit peptide
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| medium-chain fatty acid metabolic process | ||
| response to cold | ||
| carnitine biosynthetic process | ||
| regulation of gluconeogenesis | ||
| fatty acid beta-oxidation |
GO Hierarchy
biological process
metabolic process [inference]
cellular process [inference]
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| flavin adenine dinucleotide binding | ||
| medium-chain-acyl-CoA dehydrogenase activity | ||
| acyl-CoA dehydrogenase activity | ||
| identical protein 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:2862 | glucosephosphate dehydrogenase deficiency | |
| DOID:3459 | breast carcinoma | |
| DOID:3650 | lactic acidosis | |
| DOID:409 | liver disease | |
| DOID:423 | myopathy | |
| DOID:4450 | renal cell carcinoma | |
| DOID:4451 | renal carcinoma | |
| DOID:4464 | collecting duct carcinoma | |
| DOID:4465 | papillary renal cell carcinoma | |
| DOID:4467 | clear cell renal cell carcinoma |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002069 | Bilateral tonic-clonic seizure |
| HP:0002181 | Cerebral edema |
| HP:0002240 | Hepatomegaly |
| HP:0002373 | Febrile seizure (within the age range of 3 months to 6 years) |
| HP:0002875 | Exertional dyspnea |
| HP:0002910 | Elevated circulating hepatic transaminase concentration |
| HP:0003108 | Hyperglycinuria |
| HP:0003198 | Myopathy |
| HP:0003202 | Skeletal muscle atrophy |
| HP:0003215 | Dicarboxylic aciduria |
| Disease ID | Disease Name |
|---|---|
| OMIM:201450 |
|
| ORPHA:42 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP000167
- Gene Name
- acyl-CoA dehydrogenase, C-4 to C-12 straight chain
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 103746470 | NANGA14567 | ||
| 116439115 | CORMO00074 | ||
| 116447738 | CORMO26287 |
