UNC79

unc-79 homolog, NALCN channel complex subunit
OMIM: 616884, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red UNC79 in DDG2P


Version 7.1
Latest signed off version: v7.0 (6 May 2026)

Component of the following Super Panels:

  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • DD-Gene2Phenotype
    • Expert Review Red
    Phenotypes
    • UNC79-related intellectual disability with focal motor seizures