2.1.1.228	Neoplasms	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=23381944&form=6&db=m	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	Microcephaly	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24204302&form=6&db=m	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	Neoplasms	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=24422464&form=6&db=m	A system of RNA modifications and biased codon use controls cellular stress response at the level of translation.	unassigned	-	
2.1.1.228	Neoplasms	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=25747896&form=6&db=m	Somatic cancer mutations in the DNMT2 tRNA methyltransferase alter its catalytic properties.	causal interaction,diagnostic usage,ongoing research,unassigned	4,1,4,0	
2.1.1.228	Diabetes Mellitus	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26526202&form=6&db=m	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	Epilepsy	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26526202&form=6&db=m	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	Intellectual Disability	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26526202&form=6&db=m	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	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=26526202&form=6&db=m	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	Intellectual Disability	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28784718&form=6&db=m	TRMT1-catalyzed tRNA modifications are required for redox homeostasis to ensure proper cellular proliferation and oxidative stress survival.	causal interaction,unassigned	3,0	
2.1.1.228	Ovarian Neoplasms	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=28829218&form=6&db=m	Association of tRNA methyltransferase NSUN2/IGF-II molecular signature with ovarian cancer survival.	causal interaction,diagnostic usage,ongoing research,unassigned	1,1,2,0