Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
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:0110156 | Charcot-Marie-Tooth disease type 2B1 | |
| DOID:0110157 | Charcot-Marie-Tooth disease type 2J | |
| DOID:0110158 | Charcot-Marie-Tooth disease type 2I | |
| DOID:0110159 | Charcot-Marie-Tooth disease type 2B | |
| DOID:0110160 | Charcot-Marie-Tooth disease axonal type 2T | |
| DOID:0110161 | Charcot-Marie-Tooth disease type 2R | |
| DOID:0110163 | Charcot-Marie-Tooth disease axonal type 2F | |
| DOID:0110164 | Charcot-Marie-Tooth disease type 2D | |
| DOID:0110165 | Charcot-Marie-Tooth disease type 2E | |
| DOID:0110166 | Charcot-Marie-Tooth disease axonal type 2H |
- 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 |
|---|---|---|---|
| 100223841 | TAEGU26276 | ||
| 103237927 | CHLSB00535 | ||
| 108513829 | RHIBE14100 | ||
| 104658349 | RHIRO00498 | ||
| 100584637 | NOMLE10789 | ||
| 107560000 | SINGR46301 | ||
| 107573156 | SINGR99800 | ||
| 106837498 | EQUAS28731 | ||
| 116819161 | CHEAB18652 | ||
| 115056011 | ECHNA53221 |
