Genomics England
GMS Panels
Panels
Genes and Entities

CLRN1

clarin 1
OMIM: 606397
PanelMode of inheritanceDetails
2 panels
Green
in Monogenic hearing loss
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R67
Signed-off version 4.57
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
hearing loss, #276902:Usher syndrome, type 3A, Retinitis pigmentosa 61, 614180
Green
in Retinal disorders
R-numbers: R32
Signed-off version 7.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Eye Disorders, ?Usher syndrome, type 3A, 276902, Retinitis pigmentosa 61, 614180