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Results 1 - 10 of 36 > >>
EC Number Disease PubMed ID Title of Publication Category Confidence Level
Display the word mapDisplay the reaction diagram Show all sequences 2.1.1.228Intellectual Disability 28784718 TRMT1-catalyzed tRNA modifications are required for redox homeostasis to ensure proper cellular proliferation and oxidative stress survival. causal interaction
unassigned
3
0
Display the word mapDisplay the reaction diagram Show all sequences 2.1.1.228Intellectual Disability 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
Display the word mapDisplay the reaction diagram Show all sequences 2.1.1.228Intellectual Disability 33448213 TRMT10A mutation in a child with diabetes, short stature, microcephaly and hypoplastic kidneys. causal interaction
unassigned
3
0
Display the word mapDisplay the reaction diagram Show all sequences 2.1.1.228Intellectual Disability 34541035 Expanding the Phenotype of TRMT10A Mutations: Case Report and a Review of the Existing Cases. causal interaction
unassigned
4
0
Display the word mapDisplay the reaction diagram Show all sequences 2.1.1.228Neoplasms 7139605 Methyl-accepting RNA in 13762 mammary adenocarcinoma correlated with low adenine methyltransferase levels. causal interaction
unassigned
2
0
Display the word mapDisplay the reaction diagram Show all sequences 2.1.1.228Neoplasms 25747896 Somatic cancer mutations in the DNMT2 tRNA methyltransferase alter its catalytic properties. causal interaction
diagnostic usage
ongoing research
unassigned
4
1
4
0
Display the word mapDisplay the reaction diagram Show all sequences 2.1.1.228Neoplasms 30415557 tRNA Methyltransferase Defects and Intellectual Disability. diagnostic usage
ongoing research
therapeutic application
unassigned
2
1
1
0
Display the word mapDisplay the reaction diagram Show all sequences 2.1.1.228Insulin 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
Display the word mapDisplay the reaction diagram Show all sequences 2.1.1.228Intellectual 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
Display the word mapDisplay the reaction diagram Show all sequences 2.1.1.228Intellectual Disability 30415557 tRNA Methyltransferase Defects and Intellectual Disability. diagnostic usage
ongoing research
therapeutic application
unassigned
2
1
1
0
Results 1 - 10 of 36 > >>