mitochondrial ribosomal protein S23

Summary
Gene Symbol
  • MRPS23
Organism
Homo sapiens (human)
NCBI Gene
51649
PubChem
51649
Alliance of Genome Resources
JoGo
MRPS23
TogoVar
MRPS23
Annotation
Keyword
  • 3D-structure
  • Acetylation
  • Disease variant
  • Mitochondrion
  • Primary mitochondrial disease
  • Proteomics identification
  • Reference proteome
  • Ribosomal protein
Proteins
Displaying 1 entry
UniProt Protein Name
Q9Y3D9
  • 28S ribosomal protein S23, mitochondrial
Gene Ontology (GO)
Displaying 1 entry
GO Term Evidence Code PMID
mitochondrial translation
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
mitochondrial ribosomal protein S23
Functional Category
  • J: Translation, ribosomal structure and biogenesis
  • O: Posttranslational modification, protein turnover, chaperones
  • T: Signal transduction mechanisms
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:0112115 combined oxidative phosphorylation deficiency 46

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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: April 6, 2026