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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
carnitine palmitoyltransferase 2
Summary
- Gene Symbol
-
- CPT2
- Aliases
-
- CPTASE
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Acetylation
- Acyltransferase
- Direct protein sequencing
- Disease variant
- Fatty acid metabolism
- Mitochondrion inner membrane
- Proteomics identification
- Reference proteome
- Transit peptide
- Transport
- Proteins
| UniProt | Protein Name |
|---|---|
| A0A1B0GTB8 |
|
| P23786 |
|
| A0A140VK13 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| positive regulation of cold-induced thermogenesis | ||
| fatty acid beta-oxidation | ||
| carnitine shuttle |
|
|
| in utero embryonic development | ||
| long-chain fatty acid metabolic process |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| mitochondrial inner membrane | ||
| mitochondrion | ||
| nucleolus | ||
| nucleoplasm |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| carnitine O-palmitoyltransferase activity | ||
| acyltransferase activity | ||
| protein binding | ||
| carnitine O-octanoyltransferase activity |
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:10908 | hydrocephalus | |
| DOID:1094 | attention deficit hyperactivity disorder | |
| DOID:11111 | hydronephrosis | |
| DOID:11612 | polycystic ovary syndrome | |
| DOID:1168 | familial hyperlipidemia | |
| DOID:11832 | visual epilepsy | |
| DOID:11836 | clubfoot | |
| DOID:11847 | coronary thrombosis | |
| DOID:11984 | hypertrophic cardiomyopathy | |
| DOID:12241 | beta thalassemia |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001970 | Tubulointerstitial nephritis |
| HP:0001985 | Hypoketotic hypoglycemia |
| HP:0001987 | Hyperammonemia |
| HP:0002013 | Vomiting |
| HP:0002014 | Diarrhea |
| HP:0002093 | Respiratory insufficiency |
| HP:0002104 | Apnea |
| HP:0002119 | Ventriculomegaly |
| HP:0002126 | Polymicrogyria |
| HP:0002134 | Abnormal basal ganglia morphology |
| Disease ID | Disease Name |
|---|---|
| OMIM:608836 |
|
| OMIM:255110 |
|
| ORPHA:228308 |
|
| OMIM:614212 |
|
| ORPHA:228305 |
|
| ORPHA:228302 |
|
| OMIM:600649 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP000790
- Gene Name
- carnitine palmitoyltransferase 2
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 105298970 | PTEVA11811 | ||
| 115042276 | ECHNA37235 | ||
| 115382081 | SALFA43287 | ||
| 113483174 | ATHCN10599 | ||
| 105806351 | PROCO02410 | ||
| 851285 | SGD:S000000080 | ||
| 103730274 | NANGA17595 | ||
| 116448008 | CORMO26940 | ||
| 103255442 | CARSF21189 |
