TRPM1

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

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green TRPM1 in Congenital Stationary Night Blindness


Level 2: Ophthalmological disorders
Version 1.0

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

Green TRPM1 in Congenital nystagmus


Level 2: Ophthalmological disorders
Version 2.0

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