Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10413
Gene Symbol: YAP1
YAP1 		0.300 GermlineCausalMutation disease ORPHANET Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects. 24462371 2014