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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
catalase
Summary
- Gene Symbol
-
- CAT
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Direct protein sequencing
- Heme
- Hydrogen peroxide
- Mitogen
- NADP
- Peroxisome
- Phosphoprotein
- Reference proteome
- Proteins
| UniProt | Protein Name |
|---|---|
| P04040 |
|
| A0A384P5Q0 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| UV protection | ||
| response to hydrogen peroxide | ||
| response to ethanol | ||
| response to insulin | ||
| cholesterol metabolic process |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| catalase complex | ||
| intracellular membrane-bounded organelle | ||
| cytosol |
|
|
| extracellular region |
|
|
| cytoplasm |
| GO Term | Evidence Code | PMID |
|---|---|---|
| catalase activity | ||
| enzyme binding | ||
| protein homodimerization activity | ||
| oxidoreductase activity, acting on peroxide as acceptor | ||
| aminoacylase 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:0050741 | alcohol dependence | |
| DOID:0050745 | diffuse large B-cell lymphoma | |
| DOID:0050753 | cerebellar ataxia | |
| DOID:0050771 | pheochromocytoma | |
| DOID:0050853 | chronic venous insufficiency | |
| DOID:0050865 | tongue squamous cell carcinoma | |
| DOID:0050954 | spinocerebellar ataxia type 1 | |
| DOID:0050955 | spinocerebellar ataxia type 2 | |
| DOID:0060041 | autism spectrum disorder | |
| DOID:0060058 | lymphoma |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000155 | Oral ulcer |
| HP:0000166 | Severe periodontitis |
| HP:0000225 | Gingival bleeding |
| HP:0000230 | Gingivitis |
| HP:0001045 | Vitiligo |
| HP:0001300 | Parkinsonism |
| HP:0001935 | Microcytic anemia |
| HP:0002634 | Arteriosclerosis |
| HP:0005978 | Type II diabetes mellitus |
| Disease ID | Disease Name |
|---|---|
| OMIM:614097 |
|
| ORPHA:926 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 108715227 | Xenbase:XB-GENE-17329948 | ||
| 108715253 | Xenbase:XB-GENE-22041690 | ||
| 548403 | Xenbase:XB-GENE-976955 | ||
| 549470 | Xenbase:XB-GENE-5918489 | ||
| 101937020 | CHRPI34979 | ||
| 109321334 | CROPO08275 | ||
| 100541757 | MELGA10729 | ||
| 103822227 | SERCA16612 | ||
| 100921016 | SARHA15650 | ||
| 100388372 | CALJA04269 |
