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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:784 | chronic kidney disease | |
| DOID:83 | cataract | |
| DOID:8469 | influenza | |
| DOID:848 | arthritis | |
| DOID:8544 | chronic fatigue syndrome | |
| DOID:898 | autosomal dominant polycystic kidney disease | |
| DOID:9008 | psoriatic arthritis | |
| DOID:9256 | colorectal cancer | |
| DOID:9267 | urea cycle disorder | |
| DOID:934 | viral infectious disease |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001319 | Neonatal hypotonia |
| HP:0001320 | Cerebellar vermis hypoplasia |
| HP:0001324 | Muscle weakness |
| HP:0001397 | Hepatic steatosis |
| HP:0001399 | Hepatic failure |
| HP:0001403 | Macrovesicular hepatic steatosis |
| HP:0001522 | Death in infancy |
| HP:0001562 | Oligohydramnios |
| HP:0001637 | Abnormal myocardium morphology |
| HP:0001638 | Cardiomyopathy |
| 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 |
|---|---|---|---|
| 101076236 | TAKRU28570 | ||
| 102012746 | CHILA15786 | ||
| 105710437 | AOTNA02599 | ||
| 110209364 | PHACI35215 | ||
| 101033529 | SAIBB02998 | ||
| 101964466 | ICTTR15101 | ||
| 118318239 | SCOMX04891 | ||
| 102432707 | MYOLU04146 | ||
| 117026851 | RHIFE02326 | ||
| 100222209 | TAEGU28814 |
