RRM1

ribonucleotide reductase catalytic subunit M1
OMIM: 180410, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red RRM1 in DDG2P


Version 7.1
Latest signed off version: v7.0 (6 May 2026)

Component of the following Super Panels:

  • Paediatric disorders
  • review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • DD-Gene2Phenotype
    Phenotypes
    • RRM1-related mitochondrial DNA depletion/deletions syndrome