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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 |
|---|---|---|
| response to estradiol | ||
| response to reactive oxygen species |
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:0110167 | Charcot-Marie-Tooth disease axonal type 2K | |
| DOID:0110168 | Charcot-Marie-Tooth disease type 2Y | |
| DOID:0110169 | Charcot-Marie-Tooth disease axonal type 2P | |
| DOID:0110170 | Charcot-Marie-Tooth disease axonal type 2Q | |
| DOID:0110173 | Charcot-Marie-Tooth disease axonal type 2U | |
| DOID:0110174 | Charcot-Marie-Tooth disease axonal type 2L | |
| DOID:0110175 | Charcot-Marie-Tooth disease axonal type 2O | |
| DOID:0110177 | Charcot-Marie-Tooth disease axonal type 2N | |
| DOID:0110179 | Charcot-Marie-Tooth disease type 2B2 | |
| DOID:0110182 | Charcot-Marie-Tooth disease axonal type 2C |
- 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 |
|---|---|---|---|
| 101707368 | HETGA18798 | ||
| 101872372 | MELUD12773 | ||
| 100031495 | MONDO27903 | ||
| 102459642 | PELSI16844 | ||
| 100566382 | ANOCA15979 | ||
| 103659323 | URSMA15153 | ||
| 114024686 | VOMUR18590 | ||
| 102545088 | VICPA04743 | ||
| 105866203 | MICMU15682 | ||
| 100942335 | OTOGA19418 |
