PanelApp (stage)
  1. Genes and Genomic Entities
  2. MRM2

MRM2

mitochondrial rRNA methyltransferase 2
OMIM: 606906, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green MRM2 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
Phenotypes
  • Mitochondrial DNA depletion syndrome 17, MIM# 618567

Green MRM2 in Mitochondrial disease


Level 2: Metabolic disorders
Version 0.927

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    Phenotypes
    • Mitochondrial DNA depletion syndrome 17, MIM# 618567

    Amber MRM2 in Liver Failure_Paediatric


    Level 2: Gastroenterological disorders
    Version 1.24

    Component of the following Super Panels:

  • Liverome Superpanel

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Expert list
    Phenotypes
    • Mitochondrial DNA depletion syndrome 17, MIM# 618567