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: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:0000007 | Autosomal recessive inheritance |
| HP:0000252 | Microcephaly |
| HP:0000544 | External ophthalmoplegia |
| HP:0000648 | Optic atrophy |
| HP:0000708 | Atypical behavior |
| HP:0000709 | Psychosis |
| HP:0000750 | Delayed speech and language development |
| HP:0001250 | Seizure |
| HP:0001251 | Ataxia |
| HP:0001252 | Hypotonia |
| 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 |
|---|---|---|---|
| 41480 | FB:FBgn0037999 | ||
| 42364 | FB:FBgn0038742 | ||
| 102355418 | LATCH19585 | ||
| 445288 | ZFIN:ZDB-GENE-040808-64 | DANRE01113 | |
| 113583217 | ELEEL31849 | ||
| 115159775 | SALTR71100 | ||
| 115203884 | SALTR76760 | ||
| 115531828 | GADMO25681 | ||
| 101166811 | ORYLA02321 | ||
| 115592143 | SPAAU34733 |
