Gene: WDR62 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 284403
Gene Symbol: WDR62
WDR62 		0.410 GeneticVariation disease BEFREE Patients with WDR62 mutation may have a wide range of malformations of cortical development in addition to congenital microcephaly. 30706430 2019
Entrez Id: 284403
Gene Symbol: WDR62
WDR62 		0.410 Biomarker disease CTD_human Identification and analysis of a novel dimerization domain shared by various members of c-Jun N-terminal kinase (JNK) scaffold proteins. 23341463 2013
Entrez Id: 284403
Gene Symbol: WDR62
WDR62 		0.410 CausalMutation disease CLINVAR