EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   2.4.99.18 | Adenocarcinoma |
15157669 |
Role of the Sec14-like domain of Dbl family exchange factors in the regulation of Rho family GTPases in different subcellular sites. |
ongoing research
unassigned |
3
0 |
| 2.4.99.18 | Congenital Disorders of Glycosylation |
23842455 |
Mutations in STT3A and STT3B cause two congenital disorders of glycosylation. |
unassigned |
0 |
| 2.4.99.18 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
23842455 |
Mutations in STT3A and STT3B cause two congenital disorders of glycosylation. |
unassigned |
0 |
| 2.4.99.18 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
32267060 |
Oligosaccharyltransferase complex-congenital disorders of glycosylation: A novel congenital disorder of glycosylation. |
causal interaction
therapeutic application
unassigned |
1
1
0 |
| 2.4.99.18 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
32451662 |
An Update on XMEN Disease. |
causal interaction
unassigned |
3
0 |
| 2.4.99.18 | Dengue |
28720733 |
Dengue Virus Hijacks a Noncanonical Oxidoreductase Function of a Cellular Oligosaccharyltransferase Complex. |
causal interaction
ongoing research
therapeutic application
unassigned |
4
2
3
0 |
| 2.4.99.18 | Dengue |
31414286 |
The major oligosaccharyl transferase complex genes are not involved in dengue virus replication in Aedes aegypti mosquitoes. |
unassigned |
0 |
| 2.4.99.18 | Epilepsies, Partial |
32267060 |
Oligosaccharyltransferase complex-congenital disorders of glycosylation: A novel congenital disorder of glycosylation. |
causal interaction
therapeutic application
unassigned |
1
1
0 |
| 2.4.99.18 | Glioma |
29967251 |
Oligosaccharyltransferase inhibition Reduces Receptor Tyrosine Kinase Activation and Enhances Glioma Radiosensitivity. |
causal interaction
ongoing research
therapeutic application
unassigned |
4
2
3
0 |
| 2.4.99.18 | Heart Defects, Congenital |
32267060 |
Oligosaccharyltransferase complex-congenital disorders of glycosylation: A novel congenital disorder of glycosylation. |
causal interaction
therapeutic application
unassigned |
1
1
0 |
