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 |
|---|---|---|
| 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:0070135 | autosomal recessive cutis laxa type IA | |
| DOID:0070136 | autosomal dominant cutis laxa 2 | |
| DOID:0070137 | autosomal recessive cutis laxa type IIB | |
| DOID:0070138 | autosomal recessive cutis laxa type IIIB | |
| DOID:0070140 | autosomal recessive cutis laxa type IIC | |
| DOID:0070141 | autosomal recessive cutis laxa type II classic type | |
| DOID:0070142 | autosomal dominant cutis laxa | |
| DOID:0070145 | hereditary sensory and autonomic neuropathy type 5 | |
| DOID:0070195 | X-linked chronic granulomatous disease | |
| DOID:0080144 | childhood acute lymphocytic leukemia |
- 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 |
