Gene: B9D1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 27077
Gene Symbol: B9D1
B9D1 		0.410 Biomarker disease GENOMICS_ENGLAND Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome. 24886560 2014
Entrez Id: 27077
Gene Symbol: B9D1
B9D1 		0.410 Biomarker disease BEFREE Mice lacking B9d1 displayed polydactyly, kidney cysts, ductal plate malformations, and abnormal patterning of the neural tube, concomitant with compromised ciliogenesis, ciliary protein localization, and Hedgehog (Hh) signal transduction. 21763481 2011
Entrez Id: 27077
Gene Symbol: B9D1
B9D1 		0.410 GeneticVariation disease CLINVAR