EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    2.7.8.15 | adenylate kinase deficiency |
16835905 |
Missense mutation in the N-acetylglucosamine-1-phosphotransferase gene (GNPTA) in a patient with mucolipidosis II induces changes in the size and cellular distribution of GNPTG. |
causal interaction
ongoing research
unassigned |
4
1
0 |
| 2.7.8.15 | Brain Diseases |
30117111 |
DPAGT1 Deficiency with Encephalopathy (DPAGT1-CDG): Clinical and Genetic Description of 11 New Patients. |
causal interaction
diagnostic usage
unassigned |
4
2
0 |
| 2.7.8.15 | Carcinoma |
19549906 |
Overexpression of DPAGT1 leads to aberrant N-glycosylation of E-cadherin and cellular discohesion in oral cancer. |
causal interaction
ongoing research
therapeutic application
unassigned |
1
4
2
0 |
| 2.7.8.15 | Carcinoma |
22341307 |
Aberrant amplification of the crosstalk between canonical Wnt signaling and N-glycosylation gene DPAGT1 promotes oral cancer. |
causal interaction
ongoing research
therapeutic application
unassigned |
4
4
3
0 |
| 2.7.8.15 | Carcinoma, Hepatocellular |
1648948 |
Elevated carbohydrate phosphotransferase activity in human hepatoma and phosphorylation of cathepsin D. |
causal interaction
diagnostic usage
ongoing research
unassigned |
3
3
2
0 |
| 2.7.8.15 | Carcinoma, Squamous Cell |
19549906 |
Overexpression of DPAGT1 leads to aberrant N-glycosylation of E-cadherin and cellular discohesion in oral cancer. |
causal interaction
ongoing research
therapeutic application
unassigned |
1
4
2
0 |
| 2.7.8.15 | Carcinoma, Squamous Cell |
20693288 |
N-glycosylation gene DPAGT1 is a target of the Wnt/beta-catenin signaling pathway. |
ongoing research
unassigned |
4
0 |
| 2.7.8.15 | Carcinoma, Squamous Cell |
22341307 |
Aberrant amplification of the crosstalk between canonical Wnt signaling and N-glycosylation gene DPAGT1 promotes oral cancer. |
causal interaction
ongoing research
therapeutic application
unassigned |
4
4
3
0 |
| 2.7.8.15 | Congenital Disorders of Glycosylation |
28712839 |
Congenital myasthenia and congenital disorders of glycosylation caused by mutations in the DPAGT1 gene. |
causal interaction
unassigned |
2
0 |
| 2.7.8.15 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
12872255 |
Deficiency of UDP-GlcNAc:Dolichol Phosphate N-Acetylglucosamine-1 Phosphate Transferase (DPAGT1) causes a novel congenital disorder of Glycosylation Type Ij. |
causal interaction
unassigned |
4
0 |
