Genomics England
GMS Panels
Panels
Genes and Entities

CRYGC

crystallin gamma C
OMIM: 123680
PanelMode of inheritanceDetails
4 panels
Green
in Bilateral congenital or childhood onset cataracts
R-numbers: R31
Signed-off version 4.14
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Cataract 2, multiple types, 604307, cataract autosomal dominant, cataract coppock-like, Cataract 2, multiple types
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.3
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CATARACT AUTOSOMAL DOMINANT 604219, CATARACT COPPOCK-LIKE 604307
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 4.0
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CATARACT AUTOSOMAL DOMINANT
Green
in Structural eye disease
R-numbers: R36
Signed-off version 3.79
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Cataract 2, multiple types (often with microcornea), 604307