EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
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 | 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 | Microcephaly |
33448213 |
TRMT10A mutation in a child with diabetes, short stature, microcephaly and hypoplastic kidneys. |
causal interaction unassigned |
3 0 |
2.1.1.228 | Microcephaly |
34541035 |
Expanding the Phenotype of TRMT10A Mutations: Case Report and a Review of the Existing Cases. |
causal interaction unassigned |
4 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 |
2.1.1.228 | Microcephaly |
24204302 |
tRNA methyltransferase homolog gene TRMT10A mutation in young onset diabetes and primary microcephaly in humans. |
causal interaction ongoing research therapeutic application unassigned |
4 1 1 0 |
2.1.1.228 | Microcephaly |
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 |
2.1.1.228 | Microcephaly |
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 | Vitamin A Deficiency |
831816 |
The effect of vitamin A deficiency on testicular transfer RNA methyltransferase activity. |
causal interaction ongoing research unassigned |
2 3 0 |
2.1.1.228 | 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 |