Gene: B9D2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 80776
Gene Symbol: B9D2
B9D2 		0.410 GeneticVariation disease BEFREE We identified presumed causal variants in 62% of pedigrees, including the first B9D2 mutations associated with JS. 26092869 2015
Entrez Id: 80776
Gene Symbol: B9D2
B9D2 		0.410 Biomarker disease GENOMICS_ENGLAND We identified presumed causal variants in 62% of pedigrees, including the first B9D2 mutations associated with JS. 26092869 2015
Entrez Id: 80776
Gene Symbol: B9D2
B9D2 		0.410 CausalMutation disease CLINVAR We identified presumed causal variants in 62% of pedigrees, including the first B9D2 mutations associated with JS. 26092869 2015
Entrez Id: 80776
Gene Symbol: B9D2
B9D2 		0.410 Biomarker disease GENOMICS_ENGLAND Disruption of a ciliary B9 protein complex causes Meckel syndrome. 21763481 2011
Entrez Id: 80776
Gene Symbol: B9D2
B9D2 		0.410 GeneticVariation disease CLINVAR