CNGA1

cyclic nucleotide gated channel alpha 1
OMIM: 123825, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Red CNGA1 in Glaucoma (developmental)

Level 3: Anterior segment abnormalities
Level 2: Ophthalmological disorders
Version 1.47

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • Emory Genetics Laboratory
Phenotypes
  • Retinitis pigmentosa 49, OMIM:613756
Green CNGA1 in Retinal disorders


Level 2: Ophthalmology
Version 9.3
Latest signed off version: v9.0 (6 May 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • Expert Review Green
Phenotypes
  • Retinitis pigmentosa 49, OMIM:613756
Red CNGA1 in Structural eye disease


Level 2: Ophthalmology
Version 5.6
Latest signed off version: v5.0 (6 May 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • Expert Review Red
Phenotypes
  • Retinitis pigmentosa 49, OMIM:613756