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Intellectual_disability

Gene: FBN1

Red List (low evidence)

FBN1 (fibrillin 1)
EnsemblGeneIds (GRCh38): ENSG00000166147
EnsemblGeneIds (GRCh37): ENSG00000166147
OMIM: 134797, Gene2Phenotype
FBN1 is in 14 panels

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Details

Sources
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Marfan syndrome, 154700Ectopia lentis, familial, 129600MASS syndrome, 604308Weill-Marchesani syndrome 2, dominant, 608328Aortic aneurysm, ascending, and dissectionStiff skin syndrome, 184900Acromicric dysplasia, 102370Geleophysic dysplasia 2, 614185
OMIM
134797
Clinvar variants
Variants in FBN1
Penetrance
Complete
Panels with this gene

History Filter Activity

8 Oct 2015, Gel status: 1

Added New Source

Ellen McDonagh (Genomics England Curator)

FBN1 was added to Intellectual_disabilitypanel. Sources: Radboud University Medical Center, Nijmegen