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TRMT10A gene

Known as: RG9MTD2, RNA (GUANINE-9-)METHYLTRANSFERASE DOMAIN-CONTAINING PROTEIN 2, tRNA METHYLTRANSFERASE 10, S. CEREVISIAE, HOMOLOG OF, A 
National Institutes of Health

Related topics

Related topics

1 relation
TRMT10C gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Coordination of mRNA and tRNA methylations by TRMT10A
Significance It has been demonstrated that a diverse set of enzyme-mediated chemical modifications are found within RNAs, and… 
Highly Cited
2018
Highly Cited
2018
Pancreatic β-cell tRNA hypomethylation and fragmentation link TRMT10A deficiency with diabetes
Abstract Transfer RNAs (tRNAs) are non-coding RNA molecules essential for protein synthesis. Post-transcriptionally they are… 
2018
2018
A subcomplex of human mitochondrial RNase P is a bifunctional methyltransferase – extensive moonlighting in mitochondrial tRNA biogenesis
In 2012, we reported that all three human TRM10 homologues have tRNA methyltransferase activity. However, in a recent follow-up… 
2018
2018
University of Dundee Pancreatic-cell tRNA hypomethylation and fragmentation link TRMT 10 A deficiency with diabetes
Transfer RNAs (tRNAs) are non-coding RNA molecules essential for protein synthesis. Posttranscriptionally they are heavily… 
2018
2018
Syndromic Patients with Negative Islet Autoantibodies should be Tested for Mongenic Diabetes: Lessons from Patient with Trmt10a Mutation
Aim: Glucose metabolism can affect by several genes, and some of them represent distictive clinical and laboratory features. tRNA… 
2016
2016
Molecular portrait of a rare case of metastatic glioblastoma: somatic and germline mutations using whole-exome sequencing
for driver mutations. We found 4 variations in genes identified as tumor sup-pressors: RB1 deletion of 5 bases (Gln257fs), CREBBP… 
2016
2016
Structural and functional insights into tRNA binding and adenosine N 1-methylation by an archaeal Trm 10 homologue
Purine nucleosides on position 9 of eukaryal and archaeal tRNAs are frequently modified in vivo by the post-transcriptional… 
2015
2015
Case Report: Compound heterozygous nonsense mutations in TRMT10A are associated with microcephaly, delayed development, and periventricular white matter hyperintensities
Microcephaly is a fairly common feature observed in children with delayed development, defined as head circumference less than 2… 
2013
2013
Loss-of-function of TRMT10A causes young onset diabetes and microcephaly
2013
2013
Loss-of-function of the tRNA methyltransferase homolog gene TRMT10A causes young onset diabetes and primary microcephaly in humans
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