EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   2.1.1.221 | Acidosis, Lactic |
27132592 |
Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies. |
causal interaction
unassigned |
1
0 |
| 2.1.1.221 | Carcinogenesis |
32833542 |
m1A Regulator TRMT10C Predicts Poorer Survival and Contributes to Malignant Behavior in Gynecological Cancers. |
causal interaction
diagnostic usage
ongoing research
unassigned |
2
3
4
0 |
| 2.1.1.221 | Deafness |
27132592 |
Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies. |
causal interaction
unassigned |
1
0 |
| 2.1.1.221 | Diabetes Mellitus |
26297882 |
Homozygous deletion of TRMT10A as part of a contiguous gene deletion in a syndrome of failure to thrive, delayed puberty, intellectual disability and diabetes mellitus. |
causal interaction
unassigned |
3
0 |
| 2.1.1.221 | Diabetes Mellitus |
26526202 |
tRNA methyltransferase homologue gene TRMT10A mutation in young adult-onset diabetes with intellectual disability, microcephaly and epilepsy. |
causal interaction
ongoing research
therapeutic application
unassigned |
4
1
3
0 |
| 2.1.1.221 | Diabetes Mellitus |
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 |
| 2.1.1.221 | Epilepsy |
26526202 |
tRNA methyltransferase homologue gene TRMT10A mutation in young adult-onset diabetes with intellectual disability, microcephaly and epilepsy. |
causal interaction
ongoing research
therapeutic application
unassigned |
4
1
3
0 |
| 2.1.1.221 | Hypoglycemia |
34541035 |
Expanding the Phenotype of TRMT10A Mutations: Case Report and a Review of the Existing Cases. |
causal interaction
unassigned |
4
0 |
| 2.1.1.221 | 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 |
| 2.1.1.221 | Intellectual Disability |
26297882 |
Homozygous deletion of TRMT10A as part of a contiguous gene deletion in a syndrome of failure to thrive, delayed puberty, intellectual disability and diabetes mellitus. |
causal interaction
unassigned |
3
0 |
