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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
catechol-O-methyltransferase
Summary
- Gene Symbol
-
- COMT
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative initiation
- Catecholamine metabolism
- Cell membrane
- Cytoplasm
- Direct protein sequencing
- Lipid metabolism
- Magnesium
- Metal-binding
- Methyltransferase
- Neurotransmitter degradation
- Phosphoprotein
- Reference proteome
- S-adenosyl-L-methionine
- Schizophrenia
- Signal-anchor
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| P21964 |
|
| A0A140VJG8 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| response to oxidative stress | ||
| cellular response to phosphate starvation | ||
| methylation | ||
| visual learning | ||
| response to wounding |
GO Hierarchy
biological process
metabolic process [inference]
cellular process [inference]
response to stimulus [inference]
localization [inference]
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| magnesium ion binding | ||
| L-dopa O-methyltransferase activity |
|
|
| orcinol O-methyltransferase activity |
|
|
| protein binding | ||
| catechol O-methyltransferase activity |
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:12400 | kleptomania | |
| DOID:12401 | intermittent explosive disorder | |
| DOID:12583 | velocardiofacial syndrome | |
| DOID:12678 | hypercalcemia | |
| DOID:12679 | nephrocalcinosis | |
| DOID:127 | leiomyoma | |
| DOID:12783 | migraine without aura | |
| DOID:12849 | autistic disorder | |
| DOID:12858 | Huntington's disease | |
| DOID:1287 | cardiovascular system disease |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0005562 | Multiple renal cysts |
| HP:0006510 | Chronic pulmonary obstruction |
| HP:0007018 | Attention deficit hyperactivity disorder |
| HP:0007086 | Social and occupational deterioration |
| HP:0007302 | Bipolar affective disorder |
| HP:0008872 | Feeding difficulties in infancy |
| HP:0011324 | Multiple suture craniosynostosis |
| HP:0011496 | Corneal neovascularization |
| HP:0011662 | Tricuspid atresia |
| HP:0012303 | Abnormal aortic arch morphology |
| Disease ID | Disease Name |
|---|---|
| OMIM:181500 |
|
| ORPHA:567 |
|
| OMIM:167870 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 102028906 | CHILA11645 | ||
| 105718485 | AOTNA30553 | ||
| 110215186 | PHACI30652 | ||
| 101035559 | SAIBB37198 | ||
| 101961744 | ICTTR10660 | ||
| 101595207 | JACJA22844 | ||
| 102428822 | MYOLU12064 | ||
| 117017474 | RHIFE28381 | ||
| 100223814 | TAEGU05974 | ||
| 103222988 | CHLSB07121 |
