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 		0.300 GermlineCausalMutation disease ORPHANET Ciliary disorder of the skeleton. 22791528 2012
Entrez Id: 57539
Gene Symbol: WDR35
WDR35 		0.300 GermlineCausalMutation disease ORPHANET Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis. 21473986 2011