Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 284403
Gene Symbol: WDR62
WDR62
0.110 GeneticVariation disease BEFREE Here we demonstrate the use of whole-exome sequencing to overcome these obstacles by identifying recessive mutations in WD repeat domain 62 (WDR62) as the cause of a wide spectrum of severe cerebral cortical malformations including microcephaly, pachygyria with cortical thickening as well as hypoplasia of the corpus callosum. 20729831 2010
Entrez Id: 284403
Gene Symbol: WDR62
WDR62
0.110 Biomarker disease HPO