Gene: FGFR3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3 		1.000 GeneticVariation disease UNIPROT A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome. 9042914 1997
Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3 		1.000 Biomarker disease GENOMICS_ENGLAND Fibroblast growth factor receptor 3 (FGFR3) transmembrane mutation in Crouzon syndrome with acanthosis nigricans. 7493034 1995
Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3 		1.000 Biomarker disease GENOMICS_ENGLAND Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia. 8078586 1994
Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3 		1.000 Biomarker disease GENOMICS_ENGLAND Stop codon FGFR3 mutations in thanatophoric dwarfism type 1. 7647778 1995
Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3 		1.000 Biomarker disease GENOMICS_ENGLAND Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes. 8841188 1996
Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3 		1.000 Biomarker disease GENOMICS_ENGLAND Muenke syndrome (FGFR3-related craniosynostosis): expansion of the phenotype and review of the literature. 18000976 2007