tRNA methyltransferase 10C, mitochondrial RNase P subunit

Summary
Gene Symbol
  • TRMT10C
Organism
Homo sapiens (human)
NCBI Gene
54931
PubChem
54931
Alliance of Genome Resources
JoGo
TRMT10C
TogoVar
TRMT10C
Annotation
Keyword
  • 3D-structure
  • Coiled coil
  • Disease variant
  • Methyltransferase
  • Mitochondrion nucleoid
  • Phosphoprotein
  • Primary mitochondrial disease
  • Proteomics identification
  • Reference proteome
  • S-adenosyl-L-methionine
  • Transit peptide
  • tRNA processing
Proteins
Displaying 1 entry
UniProt Protein Name
Q7L0Y3
  • HBV pre-S2 trans-regulated protein 2
  • Mitochondrial ribonuclease P protein 1
  • RNA (guanine-9-)-methyltransferase domain-containing protein 1
  • Renal carcinoma antigen NY-REN-49
  • mRNA methyladenosine-N(1)-methyltransferase
  • tRNA (adenine(9)-N(1))-methyltransferase
  • tRNA (guanine(9)-N(1))-methyltransferase
Gene Ontology (GO)
GO Hierarchy
Displaying entries 1 - 5 of 12 in total
GO Term Evidence Code PMID
nucleus
nucleoplasm
nucleoplasm
mitochondrion
mitochondrion
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
tRNA methyltransferase
Functional Category
  • I: Lipid transport and metabolism
  • J: Translation, ribosomal structure and biogenesis
  • Q: Secondary metabolites biosynthesis, transport and catabolism
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:0111471 combined oxidative phosphorylation deficiency 30

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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