methionyl-tRNA synthetase 2, mitochondrial

Summary
Gene Symbol
  • MARS2
Organism
Homo sapiens (human)
NCBI Gene
92935
PubChem
92935
Alliance of Genome Resources
Annotation
Keyword
  • ATP-binding
  • Aminoacyl-tRNA synthetase
  • Deafness
  • Disease variant
  • Mitochondrion
  • Neurodegeneration
  • Primary mitochondrial disease
  • Protein biosynthesis
  • Reference proteome
  • Transit peptide
Proteins
Displaying 1 entry
UniProt Protein Name
Q96GW9
  • Methionyl-tRNA synthetase 2
  • Mitochondrial methionyl-tRNA synthetase
Gene Ontology (GO)
GO Hierarchy
Displaying all 2 entries
GO Term Evidence Code PMID
methionine-tRNA ligase activity
ATP binding
GO Hierarchy
Disease
Disease Ontology
Displaying all 4 entries
DO ID Disease Name Source
DOID:0050942 spastic ataxia 3
DOID:0111468 combined oxidative phosphorylation deficiency 25
DOID:1289 neurodegenerative disease
DOID:700 mitochondrial metabolism disease

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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