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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
acyl-CoA dehydrogenase short chain
Summary
- Gene Symbol
-
- ACADS
- Aliases
-
- ACAD3
- SCAD
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- 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 |
|---|---|---|
| butyrate catabolic process | ||
| fatty acid beta-oxidation | ||
| fatty acid beta-oxidation using acyl-CoA dehydrogenase |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| nucleus | ||
| centrosome | ||
| mitochondrial matrix | ||
| mitochondrion | ||
| nucleoplasm |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| flavin adenine dinucleotide binding | ||
| butyryl-CoA dehydrogenase activity | ||
| acyl-CoA dehydrogenase activity |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050185 | erythema multiforme | |
| DOID:0050426 | Stevens-Johnson syndrome | |
| DOID:0050569 | Seckel syndrome | |
| DOID:0050700 | cardiomyopathy | |
| DOID:0060249 | scoliosis | |
| DOID:0060254 | Robinow syndrome | |
| DOID:0060578 | Noonan syndrome 1 | |
| DOID:0060580 | Noonan syndrome 2 | |
| DOID:0060581 | Noonan syndrome 3 | |
| DOID:0060582 | Noonan syndrome 4 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001999 | Abnormal facial shape |
| HP:0002098 | Respiratory distress |
| HP:0002500 | Abnormal cerebral white matter morphology |
| HP:0002650 | Scoliosis |
| HP:0003198 | Myopathy |
| HP:0003219 | Ethylmalonic aciduria |
| HP:0003593 | Infantile onset |
| HP:0003623 | Neonatal onset |
| HP:0004911 | Episodic metabolic acidosis |
| HP:0006929 | Hypoglycemic encephalopathy |
| Disease ID | Disease Name |
|---|---|
| ORPHA:26792 |
|
| OMIM:201470 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP001974
- Gene Name
- acyl-CoA dehydrogenase, C-2 to C-3 short chain
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 115614826 | STRHB20194 |
