Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
THANATOPHORIC DYSPLASIA, TYPE I (disorder)
0.800 GeneticVariation UNIPROT We examined 22 cases of TD variants for the presence of missense mutations in the fibroblast growth factor receptor 3 (FGFR3) gene. 10360402

1999

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
THANATOPHORIC DYSPLASIA, TYPE I (disorder)
0.800 GeneticVariation UNIPROT In conclusion, we have identified the G370C mutation in the FGFR3 gene in a Japanese TD1 patient. 9790257

1998

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
THANATOPHORIC DYSPLASIA, TYPE I (disorder)
0.800 GeneticVariation UNIPROT Lys650Met substitution in the tyrosine kinase domain of the fibroblast growth factor receptor gene causes thanatophoric dysplasia Type I. Mutations in brief no. 199. Online. 10671061

1998

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
THANATOPHORIC DYSPLASIA, TYPE I (disorder)
0.800 GeneticVariation UNIPROT Here, we report the identification of FGFR3 mutations in 25/26 TD cases. 8845844

1996

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
THANATOPHORIC DYSPLASIA, TYPE I (disorder)
0.800 GeneticVariation UNIPROT A sporadic mutation causing a Lys650Glu change in the tyrosine kinase domain of FGFR3 was found in 16 of 16 individuals with one type of TD. 7773297

1995

Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
THANATOPHORIC DYSPLASIA, TYPE I (disorder)
0.800 GeneticVariation UNIPROT Another mutation that results in the substitution of an unpaired cysteine residue in the extracellular domain of FGFR3 in thanatophoric dysplasia type I. 8589699

1995