EC Number   |
Disease |
PubMed ID  |
Title of Publication |
Category |
Confidence Level |
|---|
   2.1.1.228 | Ovarian Neoplasms |
29085442 |
Ovarian cancer proliferation and apoptosis are regulated by human transfer RNA methyltransferase 9-likevia LIN9. |
unassigned |
0 |
| 2.1.1.228 | Retinoblastoma |
29085442 |
Ovarian cancer proliferation and apoptosis are regulated by human transfer RNA methyltransferase 9-likevia LIN9. |
unassigned |
0 |
| 2.1.1.228 | Microcephaly |
30247717 |
Pancreatic ?-cell tRNA hypomethylation and fragmentation link TRMT10A deficiency with diabetes. |
causal interaction
ongoing research
unassigned |
4
2
0 |
| 2.1.1.228 | Intellectual Disability |
30289604 |
Mutations in the tRNA methyltransferase 1 gene TRMT1 cause congenital microcephaly, isolated inferior vermian hypoplasia and cystic leukomalacia in addition to intellectual disability. |
unassigned |
0 |
| 2.1.1.228 | Microcephaly |
30289604 |
Mutations in the tRNA methyltransferase 1 gene TRMT1 cause congenital microcephaly, isolated inferior vermian hypoplasia and cystic leukomalacia in addition to intellectual disability. |
unassigned |
0 |
| 2.1.1.228 | Intellectual Disability |
30415557 |
tRNA Methyltransferase Defects and Intellectual Disability. |
diagnostic usage
ongoing research
therapeutic application
unassigned |
2
1
1
0 |
| 2.1.1.228 | Neoplasms |
30415557 |
tRNA Methyltransferase Defects and Intellectual Disability. |
diagnostic usage
ongoing research
therapeutic application
unassigned |
2
1
1
0 |
| 2.1.1.228 | Nervous System Diseases |
30415557 |
tRNA Methyltransferase Defects and Intellectual Disability. |
diagnostic usage
ongoing research
therapeutic application
unassigned |
2
1
1
0 |
| 2.1.1.228 | Epilepsy |
33067246 |
tRNA methyltransferase 10 homologue A (TRMT10A) mutation in a Chinese patient with diabetes, insulin resistance, intellectual deficiency and microcephaly. |
causal interaction
ongoing research
unassigned |
4
1
0 |
| 2.1.1.228 | Insulin Resistance |
33067246 |
tRNA methyltransferase 10 homologue A (TRMT10A) mutation in a Chinese patient with diabetes, insulin resistance, intellectual deficiency and microcephaly. |
causal interaction
ongoing research
unassigned |
4
1
0 |
