TYMP - thymidine phosphorylase Gene
Also Known as TP; ECGF; ECGF1; MNGIE; MEDPS1; MTDPS1; PDECGF; hPD-ECGF
Species: Homo sapiens
About TYMP
This gene has 17 transcripts (splice variants), 174 orthologues and is associated with 2 phenotypes. Broad expression in appendix (RPKM 56.4), spleen (RPKM 37.3) and 21 other tissues.
Summary
This gene encodes an angiogenic factor which promotes angiogenesis in vivo and stimulates the in vitro growth of a variety of endothelial cells. It has a highly restricted target cell specificity acting only on endothelial cells. Mutations in this gene have been associated with mitochondrial neurogastrointestinal encephalomyopathy. Multiple alternatively spliced transcript variants have been identified. [provided by RefSeq, Apr 2012]
TYMP Products (5)
| mRNA | Protein | Name |
|---|---|---|
| NM_001113755.3 | NP_001107227.1 | thymidine phosphorylase isoform 1 precursor |
| NM_001113756.3 | NP_001107228.1 | thymidine phosphorylase isoform 1 precursor |
| NM_001257988.1 | NP_001244917.1 | thymidine phosphorylase isoform 1 precursor |
| NM_001257989.1 | NP_001244918.1 | thymidine phosphorylase isoform 2 |
| NM_001953.5 | NP_001944.1 | thymidine phosphorylase isoform 1 precursor |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
32296183 | GOA |
| enables protein homodimerization activity |
IDA
IDA: Inferred from direct assay
|
1590793 | GOA |
| enables thymidine phosphorylase activity |
IDA
IDA: Inferred from direct assay
|
1590793 | GOA |
| enables thymidine phosphorylase activity |
IMP
IMP: Inferred from mutant phenotype
|
9924029 | GOA |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| involved in mitochondrial genome maintenance |
IMP
IMP: Inferred from mutant phenotype
|
9924029 | GOA |
| involved in pyrimidine nucleoside metabolic process |
IDA
IDA: Inferred from direct assay
|
1590793 | GOA |
| involved in pyrimidine nucleoside metabolic process |
IMP
IMP: Inferred from mutant phenotype
|
9924029 | GOA |
| involved in regulation of gastric motility |
IMP
IMP: Inferred from mutant phenotype
|
9924029 | GOA |
| involved in regulation of myelination |
IMP
IMP: Inferred from mutant phenotype
|
9924029 | GOA |
| involved in regulation of transmission of nerve impulse |
IMP
IMP: Inferred from mutant phenotype
|
9924029 | GOA |
TYMP Protein Structure
Glycos_trans_3N: Glycosyl transferase family, helical bundle domain (36 - 99)
Glycos_transf_3: Glycosyl transferase family, a/b domain (110 - 340)
PYNP_C: Pyrimidine nucleoside phosphorylase C-terminal domain (389 - 447)
- 0
- 100
- 200
- 300
- 400
- 482 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
thymidine phosphorylase |
|
TYMP Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
TYMP | P19971 | ZMYND12 | Homo sapiens | Q9H0C1 | 32296183 | |
|
Intra
|
TYMP | P19971 | ZMYND12 | Homo sapiens | Q9H0C1 | 32296183 | |
|
Intra
|
TYMP | P19971 | ZMYND12 | Homo sapiens | Q9H0C1 | 32296183 | |
|
Intra
|
TYMP | P19971 | MESD | Homo sapiens | Q14696 | 32296183 | |
|
Intra
|
TYMP | P19971 | MESD | Homo sapiens | Q14696 | 32296183 | |
|
Intra
|
TYMP | P19971 | MESD | Homo sapiens | Q14696 | 32296183 |
TYMP Antibodies
| Cat. No. | Product Name | Application | Reactivity |
|---|---|---|---|
| HY-P810616 | Thymidine Phosphorylase Antibody (YA9878) | WB, IHC-P | Human |
| HY-P810617 | Thymidine Phosphorylase Antibody (YA9879) | WB, IHC-P | Human, Mouse, Rat |
| HY-P87125 | Thymidine Phosphorylase Antibody (YA6818) | WB, IHC-P | Human, Mouse, Rat |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Mitochondrial Dna Depletion Syndrome 1 |
|
|
| Mitochondrial Neurogastrointestinal Encephalomyopathy |
|
|
| Mitochondrial Dna Depletion Syndrome 4b |
|
|
| Myopia 6 |
|
|
| Fatal Infantile Cardioencephalomyopathy Due To Cytochrome C Oxidase Deficiency |
|
|
| Mitochondrial Complex Iv Deficiency, Nuclear Type 2 |
|
|
| Rectum Cancer |
|
|
| Chronic Progressive External Ophthalmoplegia |
|
|
| Pancreatic Ductal Carcinoma |
|
|
| Intestinal Pseudo-Obstruction |
|
|
| Cervical Squamous Cell Carcinoma |
|
|
| Mitochondrial Dna Depletion Syndrome |
|
|
| Adenocarcinoma |
|
|
| Bladder Cancer |
|
|
| Endometrial Cancer |
|
|
| Serous Cystadenocarcinoma |
|
|
| Colorectal Cancer |
|
|
| Dilated Cardiomyopathy |
|
|
| Kearns-Sayre Syndrome |
|
|
| Breast Cancer |
|
|
| Ptosis |
|
|
| Gastric Cancer |
|
|
| Pyloric Stenosis |
|
|
| Neuropathy |
|
|
| Lung Cancer |
|
|
| Pancreatic Adenocarcinoma |
|
|
| Gastric Adenocarcinoma |
|
|
| Ocular Motility Disease |
|
|
| Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis |
|
|
| Mitochondrial Dna Depletion Syndrome 6 |
|
|
| Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant 4 |
|
|
| Gallbladder Cancer |
|
|
| Superior Mesenteric Artery Syndrome |
|
|
| Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome 1 |
|
|
| Dihydropyrimidine Dehydrogenase Deficiency |
|
|
| Cervical Cancer |
|
|
| Oropharynx Cancer |
|
|
| Mitochondrial Dna Depletion Syndrome 4a |
|
|
| Pancreatic Cancer |
|
|
| Encephalopathy, Ethylmalonic |
|
|
| Esophageal Cancer |
|
|
| Mitochondrial Dna Depletion Syndrome 7 |
|
|
| Ovarian Cancer |
|
|
| Mitochondrial Myopathy |
|
|
| Mitochondrial Encephalomyopathy |
|
|
| Renal Cell Carcinoma, Nonpapillary |
|
|
| Myopathy |
|
|
| Hepatocellular Carcinoma |
|
|
| 3-Methylglutaconic Aciduria, Type Iii |
|
|
| Leukodystrophy |
|
|
| Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes |
|
|
| Leber Hereditary Optic Neuropathy, Modifier Of |
|
|
| Lung Cancer Susceptibility 3 |
|
|
| Leigh Syndrome |
|
|