CNGA3

cyclic nucleotide gated channel alpha 3
OMIM: 600053, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Red CNGA3 in Glaucoma (developmental)

Level 3: Anterior segment abnormalities
Level 2: Ophthalmological disorders
Version 1.45

review Not set
Sources
  • NHS GMS
  • Emory Genetics Laboratory
Phenotypes
  • Eye Disorders
Green CNGA3 in Retinal disorders

Level 3: Posterior segment abnormalities
Level 2: Ophthalmological disorders
Version 4.89
Latest signed off version: v4.0 (22 Mar 2023)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • Expert Review Green
Phenotypes
  • Achromatopsia
  • Achromatopsia-2, 216900
  • Eye Disorders
  • Achromatopsia, Cone, and Cone-rod Dystrophy
Red CNGA3 in Structural eye disease


Version 3.77
Latest signed off version: v3.0 (22 Mar 2023)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • Expert Review Red
Phenotypes
  • Achromatopsia-2, 216900
  • Eye Disorders