Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
0.320 Biomarker group CTD_human [Genetic origin of non-syndromic cleft lip and palate. TWIST, a candidate gene? Research protocol]. 18082115 2007
Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
0.320 Biomarker group CTD_human Syndromic craniosynostosis with elbow joint contracture. 16465081 2006
Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
0.320 Biomarker group CTD_human An important role for the IIIb isoform of fibroblast growth factor receptor 2 (FGFR2) in mesenchymal-epithelial signalling during mouse organogenesis. 10631169 2000
Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
0.320 AlteredExpression group BEFREE Since FGF8 maps to the same chromosomal region as FGFR2, has indeed been shown to be a ligand for FGFR2, and has an expression pattern consistent with limb and craniofacial anomalies, we have screened two kindreds with Pfeiffer syndrome that were previously linked to markers from 10q24-25 and a large number of individuals with craniosynostosis and limb anomalies for mutations in the coding sequence of FGF8. 9332670 1997
Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
0.320 GeneticVariation group BEFREE This study demonstrates that FGFR2 mutations can result in a spectrum of craniofacial abnormalities even within one family. 8957519 1996