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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
thymidine phosphorylase
Summary
- Gene Symbol
-
- TYMP
- Aliases
-
- gliostatin
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Angiogenesis
- Chemotaxis
- Developmental protein
- Differentiation
- Direct protein sequencing
- Disease variant
- Glycosyltransferase
- Growth factor
- Neuropathy
- Phosphoprotein
- Progressive external ophthalmoplegia
- Reference proteome
- Repeat
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| cell differentiation | ||
| dTMP catabolic process |
GO Hierarchy
- signal transduction
biological process
metabolic process [inference]
nitrogen compound metabolic process [inference]
cellular nitrogen compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
cellular nitrogen compound catabolic process [inference]
catabolic process [inference]
cellular catabolic process [inference]
organic substance catabolic process [inference]
cellular metabolic process [inference]
cellular aromatic compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
aromatic compound catabolic process [inference]
phosphorus metabolic process [inference]
phosphate-containing compound metabolic process [inference]
organophosphate metabolic process [inference]
cellular nitrogen compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
cellular nitrogen compound catabolic process [inference]
cellular catabolic process [inference]
heterocycle metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
heterocycle catabolic process [inference]
primary metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
small molecule metabolic process [inference]
organic substance metabolic process [inference]
organophosphate metabolic process [inference]
carbohydrate derivative metabolic process [inference]
organic cyclic compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
organic cyclic compound catabolic process [inference]
organonitrogen compound metabolic process [inference]
organic substance catabolic process [inference]
cellular process [inference]
cellular metabolic process [inference]
cellular aromatic compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
aromatic compound catabolic process [inference]
phosphorus metabolic process [inference]
phosphate-containing compound metabolic process [inference]
organophosphate metabolic process [inference]
cellular nitrogen compound metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
cellular nitrogen compound catabolic process [inference]
cellular catabolic process [inference]
heterocycle metabolic process [inference]
nucleobase-containing compound metabolic process [inference]
heterocycle catabolic process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| thymidine phosphorylase activity | ||
| protein homodimerization activity | ||
| growth factor activity | ||
| protein binding | ||
| pyrimidine-nucleoside phosphorylase activity |
|
GO Hierarchy
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:5076 | mixed glioma | |
| DOID:5077 | subependymal giant cell astrocytoma | |
| DOID:5082 | liver cirrhosis | |
| DOID:5162 | arteriolosclerosis | |
| DOID:539 | ophthalmoplegia | |
| DOID:5517 | stomach carcinoma | |
| DOID:5520 | head and neck squamous cell carcinoma | |
| DOID:5672 | large intestine cancer | |
| DOID:5675 | cribriform carcinoma | |
| DOID:574 | peripheral nervous system disease |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000044 | Hypogonadotropic hypogonadism |
| HP:0000407 | Sensorineural hearing impairment |
| HP:0000508 | Ptosis |
| HP:0000544 | External ophthalmoplegia |
| HP:0000590 | Progressive external ophthalmoplegia |
| HP:0000597 | Ophthalmoparesis |
| HP:0000651 | Diplopia |
| HP:0000726 | Dementia |
| HP:0000815 | Hypergonadotropic hypogonadism |
| Disease ID | Disease Name |
|---|---|
| ORPHA:298 |
|
| OMIM:603041 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 100552690 | ANOCA12161 | ||
| 107089065 | CYPVA12504 | ||
| 114037493 | VOMUR23004 | ||
| 100961589 | OTOGA17268 | ||
| 102784011 | NEOBR01259 | ||
| 102005582 | CHILA04697 | ||
| 105704872 | AOTNA39380 | ||
| 110205911 | PHACI28675 | ||
| 101043242 | SAIBB20939 | ||
| 111224845 | SERDU03500 |
