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  1. Genes and Genomic Entities
  2. MT-ND6

MT-ND6

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

5 panels

Panel Reviews Mode of inheritance Details
5 panels

No list MT-ND6 in Early-onset Parkinson disease


Level 2: Neurology and neurodevelopmental disorders
Version 2.43

Component of the following Super Panels:

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

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

    Green MT-ND6 in Mendeliome


    Version 1.3512

    		1 review MITOCHONDRIAL
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Mitochondrial disease (MONDO:0044970), MT-ND6-related
    Tags
    • mtDNA

    Green MT-ND6 in Mitochondrial disease


    Level 2: Metabolic disorders
    Version 0.1085

    Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions

    		•  1 review MITOCHONDRIAL
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Mitochondrial disease (MONDO:0044970), MT-ND6-related
    Tags
    • mtDNA

    Red MT-ND6 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

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

    Red MT-ND6 in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.140

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