Gene: WNT2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7472
Gene Symbol: WNT2
WNT2 		0.010 Biomarker disease BEFREE Novel mutations in the ferritin-L iron-responsive element that only mildly impair IRP binding cause hereditary hyperferritinaemia cataract syndrome. 23421845 2013