Gene: FBN1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2200
Gene Symbol: FBN1
FBN1 		0.140 GeneticVariation disease BEFREE Novel FBN1 mutation causes Marfan syndrome with bilateral ectopia lentis and refractory glaucoma. 22034023 2012
Entrez Id: 2200
Gene Symbol: FBN1
FBN1 		0.140 GeneticVariation disease LHGDN Late-onset bilateral lens dislocation and glaucoma associated with a novel mutation in FBN1. 18615205 2008
Entrez Id: 2200
Gene Symbol: FBN1
FBN1 		0.140 GeneticVariation disease BEFREE Late-onset bilateral lens dislocation and glaucoma associated with a novel mutation in FBN1. 18615205 2008
Entrez Id: 2200
Gene Symbol: FBN1
FBN1 		0.140 GeneticVariation disease BEFREE Juvenile bilateral lens dislocation and glaucoma associated with a novel mutation in the fibrillin 1 gene. 16971892 2006
Entrez Id: 2200
Gene Symbol: FBN1
FBN1 		0.140 AlteredExpression disease BEFREE There was no detectable upregulation of fibrillin-1 mRNA in glaucoma. 10870517 2000
Entrez Id: 2200
Gene Symbol: FBN1
FBN1 		0.140 Biomarker disease HPO