CACNG2

calcium voltage-gated channel auxiliary subunit gamma 2
OMIM: 602911, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red CACNG2 in Monogenic hearing loss


Level 2: Audiology
Version 6.41
Latest signed off version: v6.34 (12 Aug 2026)

Component of the following Super Panels:

  • Paediatric disorders
  • review Not set
    Sources
    • Expert
    Red CACNG2 in Intellectual disability


    Level 2: Developmental disorders
    Version 11.9
    Latest signed off version: v11.0 (12 Aug 2026)

    Component of the following Super Panels:

  • Hypotonic infant
  • Leukodystrophy, childhood onset
  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Red
    • Radboud University Medical Center, Nijmegen
    Phenotypes
    • ?Mental retardation, autosomal dominant 10 614256