Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
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:0060765 | autosomal dominant Robinow syndrome 2 | |
| DOID:0060766 | autosomal dominant Robinow syndrome 1 | |
| DOID:0060767 | autosomal dominant Robinow syndrome 3 | |
| DOID:0080153 | medium chain acyl-CoA dehydrogenase deficiency | |
| DOID:0080154 | short chain acyl-CoA dehydrogenase deficiency | |
| DOID:1029 | familial periodic paralysis | |
| DOID:11328 | schizophreniform disorder | |
| DOID:11725 | Cornelia de Lange syndrome | |
| DOID:11832 | visual epilepsy | |
| DOID:11983 | Prader-Willi syndrome |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001254 | Lethargy |
| HP:0001263 | Global developmental delay |
| HP:0001276 | Hypertonia |
| HP:0001332 | Dystonia |
| HP:0001371 | Flexion contracture |
| HP:0001397 | Hepatic steatosis |
| HP:0001508 | Failure to thrive |
| HP:0001511 | Intrauterine growth retardation |
| HP:0001638 | Cardiomyopathy |
| HP:0001942 | Metabolic acidosis |
| 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 |
|---|---|---|---|
| 100557906 | ANOCA14929 | ||
| 114043226 | VOMUR16676 | ||
| 113907415 | BOBOX33303 | ||
| 105866975 | MICMU11895 | ||
| 100963935 | OTOGA11928 | ||
| 102019142 | CHILA14347 | ||
| 105728538 | AOTNA01561 | ||
| 110222822 | PHACI23795 | ||
| 101049174 | SAIBB20240 | ||
| 101975440 | ICTTR04304 |
