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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: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:0001315 | Reduced tendon reflexes |
| HP:0001397 | Hepatic steatosis |
| HP:0001410 | Decreased liver function |
| HP:0001640 | Cardiomegaly |
| HP:0001942 | Metabolic acidosis |
| HP:0001943 | Hypoglycemia |
| HP:0001946 | Ketosis |
| HP:0001987 | Hyperammonemia |
| HP:0002013 | Vomiting |
| HP:0002014 | Diarrhea |
| 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 |
|---|---|---|---|
| 114598843 | PODMU05655 | ||
| 107584839 | SINGR01561 | ||
| 107584851 | SINGR01561 | ||
| 107602542 | SINGR66425 | ||
| 106836523 | EQUAS18461 | ||
| 115057400 | ECHNA34685 | ||
| 115406002 | SALFA34123 | ||
| 113483021 | ATHCN10431 | ||
| 109049067 | CYPCA42654 | ||
| 109101178 | CYPCA70696 |
