EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
2.1.1.228 | Intellectual Disability |
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 |
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 | Infections |
4358158 |
Alteration in tRNA methyltransferase activity in mengovirus infection: host range specificity. |
causal interaction diagnostic usage unassigned |
1 1 0 |
2.1.1.228 | Adenocarcinoma |
6722163 |
Mature methyl-deficient tRNA isolated from a mammary adenocarcinoma. |
causal interaction unassigned |
4 0 |
2.1.1.228 | Adenocarcinoma |
7139605 |
Methyl-accepting RNA in 13762 mammary adenocarcinoma correlated with low adenine methyltransferase levels. |
causal interaction unassigned |
2 0 |
2.1.1.228 | Carcinogenesis |
17440925 |
Chromosome 8 BAC array comparative genomic hybridization and expression analysis identify amplification and overexpression of TRMT12 in breast cancer. |
unassigned |
0 |
2.1.1.228 | Carcinoma |
23381944 |
A human tRNA methyltransferase 9-like protein prevents tumour growth by regulating LIN9 and HIF1-?. |
diagnostic usage ongoing research therapeutic application unassigned |
3 1 1 0 |
2.1.1.228 | Carcinoma, Hepatocellular |
187335 |
Composition, associated tissue methyltransferase activity, and catabolic end products of transfer RNA from carcinogen-induced hepatoma and normal monkey livers. |
ongoing research unassigned |
1 0 |
2.1.1.228 | 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 |