Gene: FLNA ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2316
Gene Symbol: FLNA
FLNA 		0.110 GeneticVariation phenotype BEFREE Given that one putative FG locus (FGS2) is situated at Xq28, which is the location of the Filamin A gene (FLNA), and that a Filamin A mutation was reported in a boy with facial dysmorphism and constipation, it was hypothesized that Filamin A mutations could be one cause of FG syndrome. 17632775 2007
Entrez Id: 2316
Gene Symbol: FLNA
FLNA 		0.110 Biomarker phenotype HPO