PanelApp (staging)
  1. Genes and Genomic Entities
  2. GNAT1

GNAT1

G protein subunit alpha transducin 1
OMIM: 139330, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green GNAT1 in Mendeliome


Version 1.2302

2 reviews BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Night blindness, congenital stationary, autosomal dominant 3, MIM# 610444
  • Night blindness, congenital stationary, type 1G, MIM# 616389

Green GNAT1 in Congenital Stationary Night Blindness


Level 2: Ophthalmological disorders
Version 0.23

Component of the following Super Panels:

  • Retinal Disorders Superpanel

    		•  1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Night blindness, congenital stationary, autosomal dominant 3, 610444

    Red GNAT1 in Congenital nystagmus


    Level 2: Ophthalmological disorders
    Version 1.22

    		1 review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Royal Melbourne Hospital
    Phenotypes
    • Night blindness, congenital stationary, autosomal dominant 3, IM# 610444
    • Night blindness, congenital stationary, type 1G, MIM# 616389