IMPG2

interphotoreceptor matrix proteoglycan 2
OMIM: 607056, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Red IMPG2 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 IMPG2 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
  • Maculopathy, IMPG2 - related
  • Retinitis pigmentosa 56
  • Eye Disorders
  • Retinitis pigmentosa
  • Retinitis pigmentosa 56, 613581
  • Retinitis Pigmentosa, Recessive
Red IMPG2 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 56, 613581
  • Macular dystrophy, vitelliform, 5, 616152
  • Eye Disorders