PanelApp (test)
  1. Genes and Genomic Entities
  2. TRPM1

TRPM1

transient receptor potential cation channel subfamily M member 1
OMIM: 603576, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green TRPM1 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Night blindness, congenital stationary (complete), 1C, autosomal recessive, MIM# 613216

Green TRPM1 in Congenital Stationary Night Blindness


Level 2: Ophthalmological disorders
Version 0.23

Component of the following Super Panels:

  • Retinal Disorders Superpanel

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Night blindness, congenital stationary (complete), 1C, autosomal recessive, 613216

    Green TRPM1 in Congenital nystagmus


    Level 2: Ophthalmological disorders
    Version 1.21

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Night blindness, congenital stationary (complete), 1C, autosomal recessive, 613216