×
Entrez Id:
2263
Gene Symbol:
FGFR2
FGFR2
0.740
Biomarker
disease
GENOMICS_ENGLAND
Whole-exome sequencing on deceased fetuses with ultrasound anomalies: expanding our knowledge of genetic disease during fetal development.
28425981
2017
×
Entrez Id:
2263
Gene Symbol:
FGFR2
FGFR2
0.740
Biomarker
disease
GENOMICS_ENGLAND
Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes.
27604308
2016
×
Entrez Id:
2263
Gene Symbol:
FGFR2
FGFR2
0.740
GeneticVariation
disease
BEFREE
Antley-Bixler syndrome (ABS) represents a group of heterogeneous disorders characterized by skeletal, cardiac, and urogenital abnormalities that have frequently been associated with mutations in fibroblast growth factor receptor 2 or cytochrome P450 reductase genes.
21705796
2011
×
Entrez Id:
2263
Gene Symbol:
FGFR2
FGFR2
0.740
GeneticVariation
disease
BEFREE
Antley-Bixler syndrome with normal steroidogenesis is caused by autosomal dominant gain-of-function mutations in fibroblast growth factor receptor 2 .
18259105
2008
×
Entrez Id:
2263
Gene Symbol:
FGFR2
FGFR2
0.740
Biomarker
disease
GENOMICS_ENGLAND
Mutations in different components of FGF signaling in LADD syndrome.
16501574
2006
×
Entrez Id:
2263
Gene Symbol:
FGFR2
FGFR2
0.740
GeneticVariation
disease
BEFREE
Although mouse Por gene ablation causes embryonic lethality, POR missense mutations cause disordered steroidogenesis, ambiguous genitalia, and Antley-Bixler syndrome (ABS), which has also been attributed to fibroblast growth factor receptor 2 (FGFR2 ) mutations.
15793702
2005
×
Entrez Id:
2263
Gene Symbol:
FGFR2
FGFR2
0.740
Biomarker
disease
GENOMICS_ENGLAND
Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain.
16061565
2005
×
Entrez Id:
2263
Gene Symbol:
FGFR2
FGFR2
0.740
GeneticVariation
disease
UNIPROT
Evidence for digenic inheritance in some cases of Antley-Bixler syndrome?
10633130
2000
×
Entrez Id:
2263
Gene Symbol:
FGFR2
FGFR2
0.740
GermlineCausalMutation
disease
ORPHANET
Evidence for digenic inheritance in some cases of Antley-Bixler syndrome?
10633130
2000
×
Entrez Id:
2263
Gene Symbol:
FGFR2
FGFR2
0.740
Biomarker
disease
CTD_human
We report the first case of ABS associated with an apparent dominant de novo mutation in the fibroblast growth factor receptor 2 (FGFR2 ) gene.
9605588
1998
×
Entrez Id:
2263
Gene Symbol:
FGFR2
FGFR2
0.740
Biomarker
disease
GENOMICS_ENGLAND
We report the first case of ABS associated with an apparent dominant de novo mutation in the fibroblast growth factor receptor 2 (FGFR2 ) gene.
9605588
1998
×
Entrez Id:
2263
Gene Symbol:
FGFR2
FGFR2
0.740
GermlineCausalMutation
disease
ORPHANET
We report the first case of ABS associated with an apparent dominant de novo mutation in the fibroblast growth factor receptor 2 (FGFR2 ) gene.
9605588
1998
×
Entrez Id:
2263
Gene Symbol:
FGFR2
FGFR2
0.740
GeneticVariation
disease
BEFREE
FGFR2 mutation associated with clinical manifestations consistent with Antley-Bixler syndrome .
9605588
1998
×
Entrez Id:
2263
Gene Symbol:
FGFR2
FGFR2
0.740
Biomarker
disease
GENOMICS_ENGLAND
Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome.
8696350
1996
×
Entrez Id:
2263
Gene Symbol:
FGFR2
FGFR2
0.740
CausalMutation
disease
CLINVAR
×
Entrez Id:
2263
Gene Symbol:
FGFR2
FGFR2
0.740
GeneticVariation
disease
CLINVAR
×
Entrez Id:
5447
Gene Symbol:
POR
POR
0.350
Biomarker
disease
CTD_human
Instability of the Human Cytochrome P450 Reductase A287P Variant Is the Major Contributor to Its Antley-Bixler Syndrome-like Phenotype.
27496950
2016
×
Entrez Id:
5447
Gene Symbol:
POR
POR
0.350
GeneticVariation
disease
BEFREE
Antley-Bixler syndrome (ABS) is an exceptionally rare craniosynostosis syndrome that can be accompanied by disordered steroidogenesis, and is mainly caused by mutations in the POR gene, inherited in an autosomal recessive manner.
26969897
2016
×
Entrez Id:
5447
Gene Symbol:
POR
POR
0.350
GeneticVariation
disease
BEFREE
46,XX DSD and Antley-Bixler syndrome due to novel mutations in the cytochrome P450 oxidoreductase gene.
23295302
2012
×
Entrez Id:
5447
Gene Symbol:
POR
POR
0.350
GeneticVariation
disease
BEFREE
Impairment of human CYP1A2-mediated xenobiotic metabolism by Antley-Bixler syndrome variants of cytochrome P450 oxidoreductase .
18455494
2008
×
Entrez Id:
5447
Gene Symbol:
POR
POR
0.350
Biomarker
disease
CTD_human
Mutations in POR (P450 (cytochrome) oxidoreductase , an essential electron donor to enzymes participating in cholesterol biosynthesis), have been identified in some patients with the ABS phenotype.
16906539
2006
×
Entrez Id:
5447
Gene Symbol:
POR
POR
0.350
GeneticVariation
disease
BEFREE
Cytochrome P450 oxidoreductase gene mutations and Antley-Bixler syndrome with abnormal genitalia and/or impaired steroidogenesis: molecular and clinical studies in 10 patients.
15483095
2005
×
Entrez Id:
5447
Gene Symbol:
POR
POR
0.350
GeneticVariation
disease
BEFREE
Although mouse Por gene ablation causes embryonic lethality, POR missense mutations cause disordered steroidogenesis, ambiguous genitalia, and Antley-Bixler syndrome (ABS), which has also been attributed to fibroblast growth factor receptor 2 (FGFR2) mutations.
15793702
2005
×
Entrez Id:
5447
Gene Symbol:
POR
POR
0.350
Biomarker
disease
CTD_human
Mutations of POR also affect drug-metabolizing P450 enzymes, explaining the association of ABS with maternal fluconazole ingestion.
14758361
2004
×
Entrez Id:
5447
Gene Symbol:
POR
POR
0.350
Biomarker
disease
CTD_human
Congenital adrenal hyperplasia caused by mutant P450 oxidoreductase and human androgen synthesis: analytical study.
15220035
2004