RAX2

retina and anterior neural fold homeobox 2
OMIM: 610362, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Red RAX2 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 RAX2 in Retinal disorders

Level 3: Posterior segment abnormalities
Level 2: Ophthalmological disorders
Version 5.4
Latest signed off version: v5.0 (1 May 2024)

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • NHS GMS
  • Expert Review Green
Phenotypes
  • Cone-rod dystrophy 11, OMIM:610381
  • Retinitis pigmentosa 95, OMIM:620102
  • ?Macular degeneration, age-related, 6, OMIM:613757
Tags
  • Q1_24_MOI
Red RAX2 in Structural eye disease


Version 3.79
Latest signed off version: v3.0 (22 Mar 2023)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • NHS GMS
  • Expert Review Red
Phenotypes
  • Macular degeneration, age-related, 6, 613757
  • Cone-rod dystrophy 11, 610381
  • Eye Disorders