GPR179

G protein-coupled receptor 179
OMIM: 614515, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Red GPR179 in Glaucoma (developmental)

Level 3: Anterior segment abnormalities
Level 2: Ophthalmological disorders
Version 1.7

review Not set
Sources
  • Emory Genetics Laboratory
Phenotypes
  • Eye Disorders

Amber GPR179 in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 3.66
Signed off v.3.2 on 13 Feb 2020

Component of the following Super Panels:

  • Hypotonic infant
  • Paediatric disorders
  • White matter disorders - childhood onset
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • BRIDGE study SPEED NEURO Tier1 Gene
    Phenotypes
    • Night blindness, congenital stationary (complete), 1E, autosomal
    • recessive, 614565

    Green GPR179 in Retinal disorders

    Level 3: Posterior segment abnormalities
    Level 2: Ophthalmological disorders
    Version 2.13
    Signed off v.2.7 on 25 Feb 2020

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • NHS GMS
    • Expert Review Green
    Phenotypes
    • Congenital Stationary Night Blindness
    • Night blindness, congenital stationary (complete), 1E, autosomal recessive, 614565

    Red GPR179 in Structural eye disease


    Version 1.5
    Signed off v.1.3 on 4 Mar 2020

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • NHS GMS
    • Expert Review Red
    Phenotypes
    • Night blindness, congenital stationary (complete), 1E, autosomal recessive, 614565
    • Eye Disorders

    Green GPR179 in Severe Paediatric Disorders


    Version 1.6

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Next Generation Children Project
    • Expert Review Green
    • Expert list
    Phenotypes
    • Night blindness, congenital stationary (complete), 1E, autosomal recessive, 614565