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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:4471 | chromophobe renal cell carcinoma | |
| DOID:4473 | sarcomatoid renal cell carcinoma | |
| DOID:4724 | brain edema | |
| DOID:5672 | large intestine cancer | |
| DOID:6000 | congestive heart failure | |
| DOID:655 | inherited metabolic disorder | |
| DOID:7327 | pseudosarcomatous fibromatosis | |
| DOID:769 | neuroblastoma | |
| DOID:8677 | perinatal necrotizing enterocolitis | |
| DOID:9007 | sudden infant death syndrome |
- 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 |
|---|---|---|---|
| 490207 | CANLF16989 | ||
| 123795304 | URSAM09606 | ||
| 100480578 | AILME15185 | ||
| 101088421 | FELCA19346 | ||
| 122227609 | PANLE10081 | ||
| 118879993 | BALMU23239 | ||
| 100673289 | LOXAF13480 | ||
| 397104 | PIGXX30121 | ||
| 505968 | BOVIN26700 | ||
| 102179380 | CAPHI21937 |
