Genomics England
GMS Panels
Panels
Genes and Entities

TRPM1

transient receptor potential cation channel subfamily M member 1
OMIM: 603576
PanelMode of inheritanceDetails
2 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 5.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C 613216
Green
in Retinal disorders
R-numbers: R32
Signed-off version 7.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Night blindness, congenital stationary (complete), 1C, autosomal recessive, Congenital Stationary Night Blindness, Night blindness, congenital stationary (complete), 1C, autosomal recessive, 613216