PanelApp (stage)
  1. Genes and Genomic Entities
  2. NDUFA13

NDUFA13

NADH:ubiquinone oxidoreductase subunit A13
OMIM: 609435, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green NDUFA13 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Mitochondrial complex I deficiency, nuclear type 28, MIM# 618249

Green NDUFA13 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
    • Victorian Clinical Genetics Services
    • Australian Genomics Health Alliance Mitochondrial Flagship
    Phenotypes
    • Mitochondrial complex I deficiency, nuclear type 28, MIM# 618249

    Green NDUFA13 in Incidentalome_PREGEN_DRAFT


    Version 0.43

    		review Unknown
    Sources
    • NSW Health Pathology
    • Expert Review Green