PanelApp (stage)
  1. Genes and Genomic Entities
  2. MT-ND6

MT-ND6

mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6
OMIM: 516006, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

No list MT-ND6 in Early-onset Parkinson disease


Level 2: Neurology and neurodevelopmental disorders
Version 2.3

Component of the following Super Panels:

  • Neurodegenerative disease - adult onset
  • Progressive Neurological Conditions
  • Tremors_Superpanel

    		•  review MITOCHONDRIAL
    Sources
    • Literature
    Phenotypes
    • Leber Optic Atrophy
    • Parkinsonism
    • OMIM 516006
    Tags
    • mtDNA

    Green MT-ND6 in Mitochondrial disease


    Level 2: Metabolic disorders
    Version 0.927

    Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions

    		•  review MITOCHONDRIAL
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Mitochondrial cardiomyopathy complex I deficiency
    • Leber's optic neuropathy
    • MELAS
    • Dystonia
    • Striatal necrosis, bilateral
    Tags
    • mtDNA

    Red MT-ND6 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    		review MITOCHONDRIAL
    Sources
    • Expert Review Red
    • BabySeq Category C gene
    Phenotypes
    • Leber hereditary optic neuropathy

    Red MT-ND6 in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.113

    		review MITOCHONDRIAL
    Sources
    • BabySeq Category C gene
    • Expert Review Red
    Phenotypes
    • Leber hereditary optic neuropathy