Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 80776
Gene Symbol: B9D2
B9D2 		0.500 Biomarker disease GENOMICS_ENGLAND Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity. 26092869 2015
Entrez Id: 80776
Gene Symbol: B9D2
B9D2 		0.500 GeneticVariation disease UNIPROT Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity. 26092869 2015
Entrez Id: 80776
Gene Symbol: B9D2
B9D2 		0.500 Biomarker disease GENOMICS_ENGLAND Disruption of a ciliary B9 protein complex causes Meckel syndrome. 21763481 2011
Entrez Id: 80776
Gene Symbol: B9D2
B9D2 		0.500 GeneticVariation disease UNIPROT Disruption of a ciliary B9 protein complex causes Meckel syndrome. 21763481 2011