Gene: CRB2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 286204
Gene Symbol: CRB2
CRB2 		0.110 GeneticVariation group BEFREE Furthermore, by complementation experiments in zebrafish, we demonstrate that CRB2 mutations result in loss of function and therefore constitute causative mutations leading to NS in humans. 25557779 2015
Entrez Id: 286204
Gene Symbol: CRB2
CRB2 		0.110 Biomarker group HPO