PanelApp
  1. Genes and Genomic Entities
  2. MRPL42

MRPL42

mitochondrial ribosomal protein L42
OMIM: 611847, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red MRPL42 in Mendeliome


Version 1.2374

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Other
Phenotypes
  • complex neurodevelopmental disorder MONDO:0100038

Red MRPL42 in Mitochondrial disease


Level 2: Metabolic disorders
Version 0.970

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Other
    Phenotypes
    • complex neurodevelopmental disorder MONDO:0100038