EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   2.4.1.232 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
34467644 |
A novel homozygous mutation in the human ALG12 gene results in an aberrant profile of oligomannose N-glycans in patient's serum. |
causal interaction
unassigned |
1
0 |
| 2.4.1.232 | Influenza, Human |
8601597 |
Localization of a yeast early Golgi mannosyltransferase, Och1p, involves retrograde transport. |
unassigned |
0 |
| 2.4.1.232 | Metabolic Diseases |
34467644 |
A novel homozygous mutation in the human ALG12 gene results in an aberrant profile of oligomannose N-glycans in patient's serum. |
causal interaction
unassigned |
1
0 |
| 2.4.1.232 | Tuberculosis |
11964144 |
Characterization of a putative alpha-mannosyltransferase involved in phosphatidylinositol trimannoside biosynthesis in Mycobacterium tuberculosis. |
ongoing research
unassigned |
3
0 |
