Gene: CRYBB2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1415
Gene Symbol: CRYBB2
CRYBB2 		0.310 GermlineCausalMutation disease ORPHANET Molecular genetics of congenital nuclear cataract. 24384146 2014
Entrez Id: 1415
Gene Symbol: CRYBB2
CRYBB2 		0.310 GermlineCausalMutation disease ORPHANET Mutation analysis of congenital cataract in a Basotho family identified a new missense allele in CRYBB2. 19649175 2009
Entrez Id: 1415
Gene Symbol: CRYBB2
CRYBB2 		0.310 GeneticVariation disease BEFREE However, a substitution (W151C in exon 6 of CRYBB2) was identified as the most likely causative mutation underlying the phenotype of central nuclear cataract in all affected members of family C176. 15452067 2004