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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 |
|---|---|---|
| cellular response to growth factor stimulus | ||
| response to fatty acid | ||
| hemoglobin metabolic process | ||
| response to lead ion | ||
| response to hypoxia |
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:0110206 | Charcot-Marie-Tooth disease dominant intermediate F | |
| DOID:0110207 | Charcot-Marie-Tooth disease X-linked dominant 6 | |
| DOID:0110208 | Charcot-Marie-Tooth disease X-linked recessive 2 | |
| DOID:0110209 | Charcot-Marie-Tooth disease X-linked dominant 1 | |
| DOID:0110210 | Charcot-Marie-Tooth disease X-linked recessive 5 | |
| DOID:0110211 | Charcot-Marie-Tooth disease X-linked recessive 3 | |
| DOID:0110212 | Charcot-Marie-Tooth disease X-linked recessive 4 | |
| DOID:0110213 | isolated cleft palate | |
| DOID:0110425 | dilated cardiomyopathy 1A | |
| DOID:0110741 | type 1 diabetes mellitus 2 |
- 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 |
|---|---|---|---|
| 115391988 | SALFA29646 | ||
| 105814601 | PROCO06381 | ||
| 851843 | SGD:S000002664 | ||
| 852979 | SGD:S000003320 | ||
| 103749495 | NANGA09866 | ||
| 116445326 | CORMO22993 | ||
| 103258675 | CARSF15784 | ||
| 115606104 | STRHB09069 |
