Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / OrganismsTools
SugarDrawer
GlycanBuilder
Glycan Converters
GlycoMaple
GlycomeAtlas
LM-GlycomeAtlas
GALAXY
MCAW
GlycoSim
GRable
Guidelines
MIRAGE
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 |
|---|---|---|
| long-chain fatty acid metabolic process | ||
| in utero embryonic development | ||
| fatty acid beta-oxidation | ||
| fatty acid beta-oxidation | ||
| fatty acid beta-oxidation |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| nucleoplasm | ||
| nucleolus | ||
| mitochondrion | ||
| mitochondrion | ||
| mitochondrion |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| carnitine O-palmitoyltransferase activity | ||
| carnitine O-palmitoyltransferase activity | ||
| carnitine O-palmitoyltransferase activity | ||
| carnitine O-palmitoyltransferase activity | ||
| protein binding |
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Carnitine
- Functional Category
-
- E: Amino acid transport and metabolism
- M: Cell wall/membrane/envelope biogenesis
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| transferase 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:0080000 | muscular disease | |
| DOID:3146 | lipid metabolism disorder | |
| DOID:936 | brain disease |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000006 | Autosomal dominant inheritance |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000073 | Ureteral duplication |
| HP:0000083 | Renal insufficiency |
| HP:0000105 | Enlarged kidney |
| HP:0000110 | Renal dysplasia |
| HP:0000113 | Polycystic kidney dysplasia |
| HP:0000126 | Hydronephrosis |
| HP:0000189 | Narrow palate |
| HP:0000218 | High palate |
| Disease ID | Disease Name |
|---|---|
| OMIM:608836 |
|
| OMIM:600649 |
|
| ORPHA:228302 |
|
| OMIM:614212 |
|
| ORPHA:228305 |
|
| OMIM:255110 |
|
| ORPHA:228308 |
|
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 |
|---|---|---|---|
| 1376 | Xenbase:XB-GENE-963400 | ||
| 12896 | Xenbase:XB-GENE-963400 | MOUSE39931 | |
| 25413 | Xenbase:XB-GENE-963400 | RATNO33907 | |
| 38355 | Xenbase:XB-GENE-963400 | ||
| 489585 | CANLF15696 | ||
| 504502 | BOVIN26922 | ||
| 714150 | MACMU22625 | ||
| 737945 | PANTR21132 | ||
| 100005717 | DANRE43307 | ||
| 100017404 | MONDO13148 |
