EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   2.4.1.109 | Brain Diseases |
18646561 |
Muscular dystrophies due to defective glycosylation of dystroglycan. |
causal interaction
unassigned |
3
0 |
| 2.4.1.109 | Brain Diseases |
18647264 |
Genetic alterations of protein-o-mannosyltransferase-1 in glioneuronal and glial brain tumors with subarachnoid spread. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
3
2
0 |
| 2.4.1.109 | Brain Neoplasms |
18647264 |
Genetic alterations of protein-o-mannosyltransferase-1 in glioneuronal and glial brain tumors with subarachnoid spread. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
3
2
0 |
| 2.4.1.109 | Breast Neoplasms |
30760814 |
Genome-wide expression analysis reveals six contravened targets of EZH2 associated with breast cancer patient survival. |
causal interaction
diagnostic usage
ongoing research
unassigned |
3
3
1
0 |
| 2.4.1.109 | Candidiasis |
26268065 |
Vaccination with Recombinant Non-transmembrane Domain of Protein Mannosyltransferase 4 Improves Survival during Murine Disseminated Candidiasis. |
ongoing research
therapeutic application
unassigned |
2
2
0 |
| 2.4.1.109 | Cardiomyopathies |
22549409 |
Cardiomyopathy in patients with POMT1-related congenital and limb-girdle muscular dystrophy. |
causal interaction
therapeutic application
unassigned |
4
1
0 |
| 2.4.1.109 | Cleft Lip |
18640039 |
Walker-Warburg Syndrome with POMT1 mutations can be associated with cleft lip and cleft palate. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
1
2
0 |
| 2.4.1.109 | Cleft Palate |
18640039 |
Walker-Warburg Syndrome with POMT1 mutations can be associated with cleft lip and cleft palate. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
1
2
0 |
| 2.4.1.109 | Cobblestone Lissencephaly |
22323514 |
Cobblestone lissencephaly: neuropathological subtypes and correlations with genes of dystroglycanopathies. |
causal interaction
unassigned |
1
0 |
| 2.4.1.109 | Cobblestone Lissencephaly |
32973946 |
Novel compound variants of the TMTC3 gene cause cobblestone lissencephaly-like syndrome: A case report. |
causal interaction
therapeutic application
unassigned |
1
1
0 |
