ALG10B

ALG10 alpha-1,2-glucosyltransferase B
OMIM: 603313, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red ALG10B in Incidentalome


Version 1.2

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • ClinGen
Phenotypes
  • long QT syndrome MONDO:0002442

Red ALG10B in Long QT Syndrome


Level 2: Cardiovascular disorders
Version 1.0

Component of the following Super Panels:

  • Adult Cardiac SuperPanel
  • Arrhythmia_SuperPanel
  • 1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • ClinGen
    • ClinGen
    Phenotypes
    • long QT syndrome MONDO:0002442