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
3-oxoacid CoA-transferase 1
Summary
- Gene Symbol
-
- OXCT1
- Aliases
-
- SCOT
- Succinyl-CoA:3-ketoacid-CoA transferase
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Direct protein sequencing
- Disease variant
- Lipid metabolism
- Mitochondrion
- Phosphoprotein
- Reference proteome
- Signal
- Transferase
- Transit peptide
- Proteins
| UniProt | Protein Name |
|---|---|
| P55809 |
|
| A0A024R040 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| cellular ketone body metabolic process | ||
| ketone catabolic process | ||
| ketone body catabolic process |
| GO Term | Evidence Code | PMID |
|---|---|---|
| mitochondrial matrix |
|
|
| mitochondrion |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| succinyl-CoA:3-oxo-acid CoA-transferase activity |
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:10923 | sickle cell anemia | |
| DOID:11476 | osteoporosis | |
| DOID:13739 | nutmeg liver | |
| DOID:14723 | beta-ketothiolase deficiency | |
| DOID:162 | cancer | |
| DOID:1811 | reflex sympathetic dystrophy | |
| DOID:1936 | atherosclerosis | |
| DOID:2348 | arteriosclerotic cardiovascular disease | |
| DOID:2978 | carbohydrate metabolic disorder | |
| DOID:3070 | high grade glioma |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0002013 | Vomiting |
| HP:0002789 | Tachypnea |
| HP:0002919 | Ketonuria |
| HP:0003623 | Neonatal onset |
| HP:0005974 | Episodic ketoacidosis |
| Disease ID | Disease Name |
|---|---|
| OMIM:245050 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP001815
- Gene Name
- 3-oxoacid CoA transferase 1
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 115398391 | SALFA06154 | ||
| 109046059 | CYPCA135364 | ||
| 103741342 | NANGA03572 | ||
| 116437606 | CORMO28049 | ||
| 103252461 | CARSF25105 | ||
| 115619513 | STRHB08594 |
