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	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	Intellectual Disability	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30289604&form=6&db=m	Mutations in the tRNA methyltransferase 1 gene TRMT1 cause congenital microcephaly, isolated inferior vermian hypoplasia and cystic leukomalacia in addition to intellectual disability.	unassigned	-	
2.1.1.228	Intellectual Disability	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30415557&form=6&db=m	tRNA Methyltransferase Defects and Intellectual Disability.	diagnostic usage,ongoing research,therapeutic application,unassigned	2,1,1,0	
2.1.1.228	Intellectual Disability	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33067246&form=6&db=m	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	Intellectual Disability	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33448213&form=6&db=m	TRMT10A mutation in a child with diabetes, short stature, microcephaly and hypoplastic kidneys.	causal interaction,unassigned	3,0	
2.1.1.228	Intellectual Disability	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=34541035&form=6&db=m	Expanding the Phenotype of TRMT10A Mutations: Case Report and a Review of the Existing Cases.	causal interaction,unassigned	4,0	
2.1.1.228	Leukemia	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=3855480&form=6&db=m	Differences in activity of N2-guanine tRNA methyltransferase II among several inbred strains of mice.	diagnostic usage,ongoing research,unassigned	1,3,0	
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	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