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
carnitine palmitoyltransferase 1A
Summary
- Gene Symbol
-
- CPT1A
- Aliases
-
- CPT1-L
- L-CPT1
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Acyltransferase
- Alternative splicing
- Disease variant
- Fatty acid metabolism
- Mitochondrion outer membrane
- Nitration
- Phosphoprotein
- Reference proteome
- Transmembrane helix
- Transport
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| triglyceride metabolic process | ||
| regulation of insulin secretion | ||
| fatty acid metabolic process | ||
| response to tetrachloromethane | ||
| response to xenobiotic stimulus |
GO Hierarchy
biological process
metabolic process [inference]
cellular process [inference]
response to stimulus [inference]
localization [inference]
biological regulation [inference]
regulation of biological process [inference]
regulation of metabolic process [inference]
positive regulation of biological process [inference]
regulation of response to stimulus [inference]
regulation of cellular process [inference]
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| palmitoleoyltransferase activity | ||
| carnitine O-palmitoyltransferase activity | ||
| protein-macromolecule adaptor activity | ||
| identical protein binding |
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:0080199 | colorectal carcinoma | |
| DOID:0080326 | familial hypertrophic cardiomyopathy | |
| DOID:0080348 | Alzheimer's disease 1 | |
| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | |
| DOID:0090031 | D-bifunctional protein deficiency | |
| DOID:0090129 | carnitine palmitoyltransferase I deficiency | |
| DOID:0110035 | Alzheimer's disease 2 | |
| DOID:0110037 | Alzheimer's disease 5 | |
| DOID:0110038 | Alzheimer's disease 6 | |
| DOID:0110039 | Alzheimer's disease 7 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001987 | Hyperammonemia |
| HP:0002014 | Diarrhea |
| HP:0002167 | Abnormality of speech or vocalization |
| HP:0002240 | Hepatomegaly |
| HP:0002910 | Elevated circulating hepatic transaminase concentration |
| HP:0002919 | Ketonuria |
| HP:0003202 | Skeletal muscle atrophy |
| HP:0003215 | Dicarboxylic aciduria |
| HP:0003236 | Elevated circulating creatine kinase concentration |
| HP:0004374 | Hemiplegia/hemiparesis |
| Disease ID | Disease Name |
|---|---|
| ORPHA:156 |
|
| OMIM:255120 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP002018
- Gene Name
- carnitine palmitoyltransferase 1A (liver)
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 174912 | WB:WBGene00012907 | ||
| 36109 | FB:FBgn0261862 | ||
| 102359458 | LATCH19062 | ||
| 560000 | ZFIN:ZDB-GENE-030131-3250 | DANRE45779 | |
| 321871 | ZFIN:ZDB-GENE-030131-590 | ||
| 550361 | ZFIN:ZDB-GENE-050417-155 | ||
| 558088 | ZFIN:ZDB-GENE-060503-925 | ||
| 103025592 | ASTMX00353 | ||
| 108275128 | ICTPU06614 | ||
| 113589507 | ELEEL43466 |
