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 		0.310 Biomarker disease GENOMICS_ENGLAND Joubert syndrome: genotyping a Northern European patient cohort. 25920555 2016
Entrez Id: 27077
Gene Symbol: B9D1
B9D1 		0.310 GeneticVariation disease BEFREE 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 		0.310 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 		0.310 Biomarker disease GENOMICS_ENGLAND B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysis. 21493627 2011
Entrez Id: 27077
Gene Symbol: B9D1
B9D1 		0.310 Biomarker disease GENOMICS_ENGLAND