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 1.45

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • Emory Genetics Laboratory
Phenotypes
  • Retinitis pigmentosa 49, OMIM:613756
Green CNGA1 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 BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • Expert Review Green
Phenotypes
  • Retinitis pigmentosa 49, OMIM:613756
Tags
  • Q1_24_MOI
Red CNGA1 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
  • Retinitis pigmentosa 49, OMIM:613756