IMPG1

interphotoreceptor matrix proteoglycan 1
OMIM: 602870, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green IMPG1 in Mendeliome


Version 1.1902

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Macular dystrophy, vitelliform, 4, OMIM:616151
  • Retinitis pigmentosa, MONDO:0019200
  • Retinitis pigmentosa 91, MIM# 153870

Amber IMPG1 in Retinitis pigmentosa_Autosomal Recessive/X-linked


Level 2: Ophthalmological disorders
Version 0.147

Component of the following Super Panels:

  • Retinal Disorders Superpanel
  • Retinitis Pigmentosa Superpanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Retinitis pigmentosa, MONDO:0019200
    • Retinitis pigmentosa 91, MIM# 153870

    Green IMPG1 in Retinitis pigmentosa_Autosomal Dominant


    Level 2: Ophthalmological disorders
    Version 0.57

    Component of the following Super Panels:

  • Retinal Disorders Superpanel
  • Retinitis Pigmentosa Superpanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Retinitis pigmentosa, MONDO:0019200

    Green IMPG1 in Macular Dystrophy/Stargardt Disease


    Level 2: Ophthalmological disorders
    Version 0.45

    Component of the following Super Panels:

  • Retinal Disorders Superpanel
  • review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Macular dystrophy, vitelliform, 4, OMIM:616151
    • Retinitis pigmentosa, MONDO:0019200