MRPS25

mitochondrial ribosomal protein S25
OMIM: 611987, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red MRPS25 in Mitochondrial disorders


Level 2: Mitochondrial
Version 10.23
Latest signed off version: v10.18 (12 Aug 2026)

Component of the following Super Panels:

  • Leukodystrophy, childhood onset
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • ?Combined oxidative phosphorylation deficiency 50, OMIM:619025