EC Number   |
Disease |
PubMed ID |
Title of Publication  |
Category |
Confidence Level |
|---|
   2.4.99.6 | Carcinoma |
31747460 |
"Aberrant sialylation plays a significant role in oral squamous cell carcinoma progression". |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
4
4
0 |
| 2.4.99.6 | Mouth Neoplasms |
31747460 |
"Aberrant sialylation plays a significant role in oral squamous cell carcinoma progression". |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
4
4
0 |
| 2.4.99.6 | Neoplasm Metastasis |
31747460 |
"Aberrant sialylation plays a significant role in oral squamous cell carcinoma progression". |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
4
4
0 |
| 2.4.99.6 | Adenocarcinoma |
23726834 |
?2,3-sialyltransferase ST3Gal IV promotes migration and metastasis in pancreatic adenocarcinoma cells and tends to be highly expressed in pancreatic adenocarcinoma tissues. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
3
4
0 |
| 2.4.99.6 | Neoplasm Metastasis |
23726834 |
?2,3-sialyltransferase ST3Gal IV promotes migration and metastasis in pancreatic adenocarcinoma cells and tends to be highly expressed in pancreatic adenocarcinoma tissues. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
3
4
0 |
| 2.4.99.6 | Neoplasms |
23726834 |
?2,3-sialyltransferase ST3Gal IV promotes migration and metastasis in pancreatic adenocarcinoma cells and tends to be highly expressed in pancreatic adenocarcinoma tissues. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
3
4
0 |
| 2.4.99.6 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
31584066 |
A novel nonsense and inactivating variant of ST3GAL3 in two infant siblings suffering severe epilepsy and expressing circulating CA19.9. |
unassigned |
0 |
| 2.4.99.6 | Epilepsy |
31584066 |
A novel nonsense and inactivating variant of ST3GAL3 in two infant siblings suffering severe epilepsy and expressing circulating CA19.9. |
unassigned |
0 |
| 2.4.99.6 | Intellectual Disability |
32666583 |
A novel variant of ST3GAL3 causes non-syndromic autosomal recessive intellectual disability in Iranian patients. |
causal interaction
unassigned |
3
0 |
| 2.4.99.6 | n-acetyllactosaminide alpha-2,3-sialyltransferase deficiency |
30089820 |
A patient-specific induced pluripotent stem cell model for West syndrome caused by ST3GAL3 deficiency. |
causal interaction
diagnostic usage
ongoing research
unassigned |
3
2
4
0 |
