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  1. Genes and Genomic Entities
  2. MT-ND1

MT-ND1

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

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Green MT-ND1 in Mendeliome


Version 1.3795

1 review MITOCHONDRIAL
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Mitochondrial respiratory chain complex deficiency, MONDO:0000066, MT-ND1-related
Tags
  • mtDNA

Green MT-ND1 in Optic Atrophy


Level 2: Ophthalmological disorders
Version 1.64

Component of the following Super Panels:

  • Retinal Disorders Superpanel

    		•  1 review MITOCHONDRIAL
    Sources
    • Expert Review Green
    • Expert list
    • Expert list
    Phenotypes
    • Mitochondrial respiratory chain complex deficiency, MONDO:0000066, MT-ND1-related
    Tags
    • mtDNA

    Green MT-ND1 in Mitochondrial disease


    Level 2: Metabolic disorders
    Version 0.1275

    Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions

    		•  1 review MITOCHONDRIAL
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Mitochondrial respiratory chain complex deficiency, MONDO:0000066, MT-ND1-related
    Tags
    • mtDNA

    Green MT-ND1 in Stroke


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.38

    		1 review MITOCHONDRIAL
    Sources
    • Expert Review Green
    • Expert list
    • Expert list
    Phenotypes
    • Mitochondrial respiratory chain complex deficiency, MONDO:0000066, MT-ND1-related
    Tags
    • mtDNA

    Red MT-ND1 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-ND1 in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.141

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