Gene: CRYGD ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1421
Gene Symbol: CRYGD
CRYGD 		0.320 GeneticVariation disease BEFREE We have identified a novel mutation, c.451_452insGACT, in CRYGD, which is associated with nuclear cataract. 26147294 2015
Entrez Id: 1421
Gene Symbol: CRYGD
CRYGD 		0.320 GermlineCausalMutation disease ORPHANET A Novel Insertion Variant of CRYGD Is Associated with Congenital Nuclear Cataract in a Chinese Family. 26147294 2015
Entrez Id: 1421
Gene Symbol: CRYGD
CRYGD 		0.320 GermlineCausalMutation disease ORPHANET Molecular genetics of congenital nuclear cataract. 24384146 2014
Entrez Id: 1421
Gene Symbol: CRYGD
CRYGD 		0.320 GermlineCausalMutation disease ORPHANET A novel CRYGD mutation (p.Trp43Arg) causing autosomal dominant congenital cataract in a Chinese family. 21031598 2011
Entrez Id: 1421
Gene Symbol: CRYGD
CRYGD 		0.320 GeneticVariation disease BEFREE Two affected siblings with nuclear cataract associated with a novel missense mutation in the CRYGD gene. 16943771 2006