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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:0060583 | Noonan syndrome 5 | |
| DOID:0060584 | Noonan syndrome 6 | |
| DOID:0060585 | Noonan syndrome 7 | |
| DOID:0060586 | Noonan syndrome 8 | |
| DOID:0060587 | Noonan syndrome 9 | |
| DOID:0060588 | Noonan syndrome 10 | |
| DOID:0060600 | obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum | |
| DOID:0060608 | microcephalic osteodysplastic primordial dwarfism type I | |
| DOID:0060609 | microcephalic osteodysplastic primordial dwarfism type II | |
| DOID:0060642 | recessive dystrophic epidermolysis bullosa |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0006357 | Premature loss of permanent teeth |
| HP:0012517 | Reduced circulating catalase activity |
| HP:0012531 | Pain |
| HP:0100605 | Neoplasm of the larynx |
| HP:0100651 | Type I diabetes mellitus |
| HP:0100753 | Schizophrenia |
| HP:0100758 | Gangrene |
| 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 |
|---|---|---|---|
| 175085 | WB:WBGene00000831 | ||
| 175086 | WB:WBGene00013220 | ||
| 259738 | WB:WBGene00000830 | ||
| 34198 | FB:FBgn0032061 | ||
| 40048 | FB:FBgn0000261 | ||
| 103186029 | CALMI33690 | ||
| 102347899 | LATCH09316 | ||
| 30068 | ZFIN:ZDB-GENE-000210-20 | DANRE26876 | |
| 103032916 | ASTMX02137 | ||
| 108275217 | ICTPU07003 |
