GLT8D1:Ensemblv90

glycosyltransferase 8 domain containing 1
ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Amber GLT8D1 in Motor Neurone Disease


Level 2: Neurology and neurodevelopmental disorders
Version 1.39

Component of the following Super Panels:

  • Neurodegenerative disease - adult onset
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions
  • 2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Expert list
    Phenotypes
    • Amyotrophic lateral sclerosis

    Amber GLT8D1 in Incidentalome


    Version 0.370

    1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • ClinGen
    Phenotypes
    • amyotrophic lateral sclerosis MONDO:0004976

    Amber GLT8D1 in Motor Neurone Disease


    Level 2: Neurology and neurodevelopmental disorders
    Version 2.0

    2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert list
    • Expert Review Amber
    Phenotypes
    • Amyotrophic lateral sclerosis

    Amber GLT8D1 in Incidentalome


    Version 1.0

    1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • ClinGen
    • Expert Review Amber
    Phenotypes
    • amyotrophic lateral sclerosis MONDO:0004976