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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:0111041 | glycogen storage disease IXb | |
| DOID:0111042 | glycogen storage disease IXa | |
| DOID:0111043 | glycogen storage disease IXc | |
| DOID:0111338 | isolated elevated serum creatine phosphokinase levels | |
| DOID:1029 | familial periodic paralysis | |
| DOID:10908 | hydrocephalus | |
| DOID:11832 | visual epilepsy | |
| DOID:1289 | neurodegenerative disease | |
| DOID:13250 | diarrhea | |
| DOID:13884 | sick sinus syndrome |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0003234 | Decreased circulating carnitine concentration |
| HP:0003236 | Elevated circulating creatine kinase concentration |
| HP:0003394 | Muscle spasm |
| HP:0003473 | Fatigable weakness |
| HP:0003701 | Proximal muscle weakness |
| HP:0003738 | Exercise-induced myalgia |
| HP:0004326 | Cachexia |
| HP:0005684 | Distal arthrogryposis |
| HP:0007185 | Loss of consciousness |
| HP:0008309 | Medium chain 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 |
|---|---|---|---|
| 113576501 | ELEEL18629 | ||
| 115157647 | SALTR60989 | ||
| 115549069 | GADMO56601 | ||
| 100693621 | ORENI26704 | ||
| 446467 | Xenbase:XB-GENE-972941 | ||
| 447486 | Xenbase:XB-GENE-17339521 | ||
| 100494748 | Xenbase:XB-GENE-972935 | ||
| 101946138 | CHRPI15559 | ||
| 113436053 | PSETE07020 | ||
| 103815091 | SERCA08660 |
