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 GeneticVariation disease BEFREE Furthermore, we report a case with heterozygous mutations in CC2D2A and B9D1, a gene associated with the more severe Meckel-Gruber syndrome that was recently published as a potential new JBS gene, and discuss the significance of this finding. 25920555 2016
Entrez Id: 27077
Gene Symbol: B9D1
B9D1 		0.410 GermlineCausalMutation disease ORPHANET 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 		0.410 CausalMutation disease CLINVAR B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysis. 21493627 2011