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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 activity | ||
| ureteric bud development | ||
| response to vitamin E | ||
| osteoblast differentiation | ||
| aerobic respiration |
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:6543 | acne | |
| DOID:657 | adenoma | |
| DOID:6683 | X-linked Aarskog syndrome | |
| DOID:6688 | autoimmune lymphoproliferative syndrome | |
| DOID:6713 | cerebrovascular disease | |
| DOID:6725 | spinal stenosis | |
| DOID:6726 | fibrillary astrocytoma | |
| DOID:674 | cleft palate | |
| DOID:676 | juvenile rheumatoid arthritis | |
| DOID:6811 | juvenile pilocytic astrocytoma |
- 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 |
|---|---|---|---|
| 403474 | CANLF05641 | ||
| 123799428 | URSAM10797 | ||
| 100473949 | AILME11380 | ||
| 101682593 | MUSPF12018 | ||
| 101093891 | FELCA25335 | ||
| 122199436 | PANLE13909 | ||
| 101331217 | TURTR03221 | ||
| 118899997 | BALMU09075 | ||
| 100673484 | LOXAF12429 | ||
| 397568 | PIGXX17441 |
