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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 catabolic process | ||
| response to starvation | ||
| fatty acid beta-oxidation using acyl-CoA dehydrogenase | ||
| liver development | ||
| glycogen biosynthetic process |
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:0014667 | disease of metabolism | |
| DOID:0050387 | nonpapillary renal cell carcinoma | |
| DOID:0050646 | distal arthrogryposis | |
| DOID:0060262 | gallbladder disease | |
| DOID:0080153 | medium chain acyl-CoA dehydrogenase deficiency | |
| DOID:0080199 | colorectal carcinoma | |
| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | |
| DOID:0090031 | D-bifunctional protein deficiency | |
| DOID:0090129 | carnitine palmitoyltransferase I deficiency | |
| DOID:0111040 | glycogen storage disease IXd |
- 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 |
