×
Entrez Id:
2248
Gene Symbol:
FGF3
FGF3
0.730
Biomarker
disease
CLINGEN
Modeling human early otic sensory cell development with induced pluripotent stem cells.
29902227
2018
×
Entrez Id:
2248
Gene Symbol:
FGF3
FGF3
0.730
Biomarker
disease
CLINGEN
Spatial and temporal inhibition of FGFR2b ligands reveals continuous requirements and novel targets in mouse inner ear morphogenesis.
30504125
2018
×
Entrez Id:
2248
Gene Symbol:
FGF3
FGF3
0.730
Biomarker
disease
CLINGEN
Fgf3 and Fgf16 expression patterns define spatial and temporal domains in the developing chick inner ear.
26995070
2017
×
Entrez Id:
2248
Gene Symbol:
FGF3
FGF3
0.730
GeneticVariation
disease
BEFREE
LAMM syndrome with middle ear dysplasia associated with compound heterozygosity for FGF3 mutations.
21480479
2011
×
Entrez Id:
2248
Gene Symbol:
FGF3
FGF3
0.730
Biomarker
disease
CLINGEN
LAMM syndrome with middle ear dysplasia associated with compound heterozygosity for FGF3 mutations.
21480479
2011
×
Entrez Id:
2248
Gene Symbol:
FGF3
FGF3
0.730
Biomarker
disease
GENOMICS_ENGLAND
LAMM syndrome with middle ear dysplasia associated with compound heterozygosity for FGF3 mutations.
21480479
2011
×
Entrez Id:
2248
Gene Symbol:
FGF3
FGF3
0.730
GeneticVariation
disease
BEFREE
Molecular modeling result suggests a less drastic effect of p.R95W on FGF3 function compared with known missense mutations detected in fully penetrant LAMM syndrome .
21306635
2011
×
Entrez Id:
2248
Gene Symbol:
FGF3
FGF3
0.730
Biomarker
disease
CLINGEN
Molecular modeling result suggests a less drastic effect of p.R95W on FGF3 function compared with known missense mutations detected in fully penetrant LAMM syndrome .
21306635
2011
×
Entrez Id:
2248
Gene Symbol:
FGF3
FGF3
0.730
Biomarker
disease
CLINGEN
Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3).
18701883
2009
×
Entrez Id:
2248
Gene Symbol:
FGF3
FGF3
0.730
GeneticVariation
disease
UNIPROT
Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia .
18435799
2008
×
Entrez Id:
2248
Gene Symbol:
FGF3
FGF3
0.730
GeneticVariation
disease
BEFREE
Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia .
18435799
2008
×
Entrez Id:
2248
Gene Symbol:
FGF3
FGF3
0.730
Biomarker
disease
CLINGEN
Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia .
18435799
2008
×
Entrez Id:
2248
Gene Symbol:
FGF3
FGF3
0.730
Biomarker
disease
CLINGEN
Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia.
17236138
2007
×
Entrez Id:
2248
Gene Symbol:
FGF3
FGF3
0.730
GeneticVariation
disease
UNIPROT
Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia.
17236138
2007
×
Entrez Id:
2248
Gene Symbol:
FGF3
FGF3
0.730
Biomarker
disease
CLINGEN
Mice homozygous for a targeted disruption of the proto-oncogene int-2 have developmental defects in the tail and inner ear.
8223243
1993
×
Entrez Id:
2248
Gene Symbol:
FGF3
FGF3
0.730
Biomarker
disease
GENOMICS_ENGLAND
Potential oncogene product related to growth factors.
3574458
1987
×
Entrez Id:
2248
Gene Symbol:
FGF3
FGF3
0.730
CausalMutation
disease
CLINVAR
×
Entrez Id:
2248
Gene Symbol:
FGF3
FGF3
0.730
Biomarker
disease
GENOMICS_ENGLAND
×
Entrez Id:
2248
Gene Symbol:
FGF3
FGF3
0.730
Biomarker
disease
CTD_human
×
Entrez Id:
2248
Gene Symbol:
FGF3
FGF3
0.730
GeneticVariation
disease
CLINVAR