Gene: WDR35 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 57539
Gene Symbol: WDR35
WDR35 		0.410 GeneticVariation disease BEFREE We review 39 patients including two new patients, one with compound heterozygous novel mutations in WDR35 and a previously unreported multisutural craniosynostosis that may be a part of Sensenbrenner syndrome. 24123776 2013
Entrez Id: 57539
Gene Symbol: WDR35
WDR35 		0.410 Biomarker disease CTD_human Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome. 20817137 2010
Entrez Id: 57539
Gene Symbol: WDR35
WDR35 		0.410 Biomarker disease HPO