PanelApp (staging)
  1. Genes and Genomic Entities
  2. LRIT3

LRIT3

leucine rich repeat, Ig-like and transmembrane domains 3
OMIM: 615004, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green LRIT3 in Mendeliome


Version 1.2302

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Night blindness, congenital stationary (complete), 1F, autosomal recessive, MIM# 615058

Green LRIT3 in Congenital Stationary Night Blindness


Level 2: Ophthalmological disorders
Version 0.23

Component of the following Super Panels:

  • Retinal Disorders Superpanel

    		•  2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Night blindness, congenital stationary (complete), 1F, autosomal recessive, 615058

    Red LRIT3 in Congenital nystagmus


    Level 2: Ophthalmological disorders
    Version 1.22

    		2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert Review Red
    • Royal Melbourne Hospital
    • Victorian Clinical Genetics Services
    Phenotypes
    • Night blindness, congenital stationary (complete), 1F, autosomal recessive, 615058