mitochondrial tRNA translation optimization 1

Summary
Gene Symbol
  • MTO1
Organism
Homo sapiens (human)
NCBI Gene
25821
PubChem
25821
Alliance of Genome Resources
Annotation
Keyword
  • Alternative splicing
  • Cardiomyopathy
  • Disease variant
  • FAD
  • Methylation
  • Mitochondrion
  • Primary mitochondrial disease
  • Reference proteome
  • Transit peptide
  • tRNA processing
Proteins
Displaying 1 entry
UniProt Protein Name
Q9Y2Z2
Gene Ontology (GO)
Displaying all 2 entries
GO Term Evidence Code PMID
mitochondrial tRNA wobble uridine modification
tRNA methylation
GO Hierarchy
Disease
Disease Ontology
Displaying all 3 entries
DO ID Disease Name Source
DOID:0050563 nonsyndromic deafness
DOID:0060286 combined oxidative phosphorylation deficiency
DOID:0111480 combined oxidative phosphorylation deficiency 10

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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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Last updated: December 9, 2024