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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:9008 | psoriatic arthritis | |
| DOID:9256 | colorectal cancer | |
| DOID:9266 | cystinuria | |
| DOID:9267 | urea cycle disorder | |
| DOID:9281 | phenylketonuria | |
| DOID:9452 | steatotic liver disease | |
| DOID:9870 | galactosemia | |
| DOID:9970 | obesity | |
| DOID:9993 | hypoglycemia |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000256 | Macrocephaly |
| HP:0000750 | Delayed speech and language development |
| HP:0001250 | Seizure |
| HP:0001251 | Ataxia |
| HP:0001252 | Hypotonia |
| HP:0001254 | Lethargy |
| HP:0001259 | Coma |
| HP:0001263 | Global developmental delay |
| HP:0001290 | Generalized hypotonia |
| 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 |
