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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
acyl-CoA dehydrogenase short/branched chain
Summary
- Gene Symbol
-
- ACADSB
- Aliases
-
- ACAD7
- SBCAD
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Alternative splicing
- Disease variant
- FAD
- Fatty acid metabolism
- Mitochondrion
- Oxidoreductase
- Phosphoprotein
- Reference proteome
- Transit peptide
- Proteins
| UniProt | Protein Name |
|---|---|
| A0A0S2Z3P9 |
|
| P45954 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| fatty acid metabolic process | ||
| isoleucine catabolic process |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| mitochondrial matrix |
|
|
| mitochondrion |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| flavin adenine dinucleotide binding | ||
| butyryl-CoA dehydrogenase activity | ||
| isobutyryl-CoA:FAD oxidoreductase activity | ||
| acyl-CoA dehydrogenase activity | ||
| short-chain-acyl-CoA dehydrogenase activity |
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:11853 | monocular exotropia | |
| DOID:12849 | autistic disorder | |
| DOID:14692 | Smith-Lemli-Opitz syndrome | |
| DOID:1612 | breast cancer | |
| DOID:1826 | epilepsy | |
| DOID:1837 | diabetic ketoacidosis | |
| DOID:3459 | breast carcinoma | |
| DOID:3571 | liver cancer | |
| DOID:4090 | agnosia | |
| DOID:684 | hepatocellular carcinoma |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000252 | Microcephaly |
| HP:0000577 | Exotropia |
| HP:0001250 | Seizure |
| HP:0001252 | Hypotonia |
| HP:0001254 | Lethargy |
| HP:0001263 | Global developmental delay |
| HP:0001270 | Motor delay |
| HP:0001943 | Hypoglycemia |
| HP:0002045 | Hypothermia |
| Disease ID | Disease Name |
|---|---|
| OMIM:610006 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP001132
- Gene Name
- acyl-CoA dehydrogenase, short/branched chain
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 100171571 | PONAB01924 | ||
| 477856 | CANLF11554 | ||
| 112928830 | VULVU23724 | ||
| 123803910 | URSAM11914 | ||
| 100470228 | AILME00961 | ||
| 101092794 | FELCA26248 | ||
| 122202513 | PANLE03356 | ||
| 101332211 | TURTR10633 | ||
| 118882335 | BALMU14840 | ||
| 118898972 | BALMU08621 |
