PanelApp (stage)
  1. Genes and Genomic Entities
  2. MT-ND1

MT-ND1

mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1
OMIM: 516000, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green MT-ND1 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 complex I deficiency
    • Leber's optic neuropathy
    • Deafness
    • Dystonia
    Tags
    • mtDNA

    Red MT-ND1 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-ND1 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