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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:47 | prostate disease | |
| DOID:4730 | vasomotor rhinitis | |
| DOID:4766 | embryoma | |
| DOID:4798 | aggressive systemic mastocytosis | |
| DOID:4840 | sebaceous carcinoma | |
| DOID:4851 | pilocytic astrocytoma | |
| DOID:4873 | anterior horn cell disease | |
| DOID:4896 | bile duct adenocarcinoma | |
| DOID:4897 | bile duct carcinoma | |
| DOID:4903 | granular cell carcinoma |
- 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 |
|---|---|---|---|
| 113573651 | ELEEL12713 | ||
| 115178817 | SALTR68548 | ||
| 115197208 | SALTR11809 | ||
| 115208531 | SALTR37384 | ||
| 115550587 | GADMO60759 | ||
| 101158017 | ORYLA14654 | ||
| 115586278 | SPAAU43303 | ||
| 380236 | Xenbase:XB-GENE-976961 | ||
| 495840 | Xenbase:XB-GENE-5918613 | ||
| 100125664 | Xenbase:XB-GENE-22041689 |
