PanelApp
  1. Genes and Genomic Entities
  2. ALG10

ALG10

ALG10, alpha-1,2-glucosyltransferase
OMIM: 603313, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red ALG10 in Congenital Disorders of Glycosylation


Level 2: Metabolic disorders
Version 1.78

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Congenital disorder of glycosylation, MONDO:0015286, ALG10-related

    Red ALG10 in Mendeliome


    Version 1.3512

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Congenital disorder of glycosylation, MONDO:0015286, ALG10-related

    Red ALG10 in Genetic Epilepsy


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.267

    Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Congenital disorder of glycosylation, MONDO:0015286, ALG10-related