Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
0.070 GeneticVariation disease BEFREE Here we present 61 individuals from 20 unrelated families where coronal synostosis is due to an amino acid substitution (Pro250Arg) that results from a single point mutation in the fibroblast growth factor receptor 3 gene on chromosome 4p. 9042914 1997
Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
0.070 GeneticVariation disease BEFREE None of the 6 patients with nonsynostotic plagiocephaly and none of the 4 patients with additional suture synostosis had the FGFR3 mutation. 9580776 1998
Entrez Id: 57306
Gene Symbol: CUP2Q35
CUP2Q35
0.010 AlteredExpression disease BEFREE Mesoaxial complete syndactyly and synostosis with hypoplastic thumbs: an unusual combination or homozygous expression of syndactyly type I? 9783716 1998
Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
0.070 GeneticVariation disease BEFREE Fibroblast growth factor receptor 3 mutation in nonsyndromic coronal synostosis: clinical spectrum, prevalence, and surgical outcome. 10761652 2000
Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
0.070 GeneticVariation disease BEFREE At the authors' institution, mutations in FGFR3, located at chromosome 4p16, have been found to cause coronal synostosis. 11743367 2001
Entrez Id: 4745
Gene Symbol: NELL1
NELL1
0.010 Biomarker disease BEFREE Nell-1 transgenic animals exhibited CS-like phenotypes that ranged from simple to compound synostoses. 12235118 2002
Entrez Id: 2261
Gene Symbol: FGFR3
FGFR3
0.070 GeneticVariation disease LHGDN FGFR3 P250R mutation increases the risk of reoperation in apparent 'nonsyndromic' coronal craniosynostosis. 15915095 2005
Entrez Id: 7291
Gene Symbol: TWIST1
TWIST1
0.070 GeneticVariation disease BEFREE Saethre-Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome. 16251895 2006
Entrez Id: 7291
Gene Symbol: TWIST1
TWIST1
0.070 Biomarker disease BEFREE In Twist1(+/-) mice with coronal synostosis, we found that the frontal-parietal boundary is defective. 16540516 2006
Entrez Id: 7291
Gene Symbol: TWIST1
TWIST1
0.070 Biomarker disease LHGDN Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis. 16540516 2006
Entrez Id: 4488
Gene Symbol: MSX2
MSX2
0.020 Biomarker disease BEFREE This provides genetic evidence that Twist1, Msx2 and Efna4 function together in boundary formation and the pathogenesis of coronal synostosis. 16540516 2006
Entrez Id: 4488
Gene Symbol: MSX2
MSX2
0.020 Biomarker disease LHGDN Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis. 16540516 2006
Entrez Id: 1945
Gene Symbol: EFNA4
EFNA4
0.010 Biomarker disease LHGDN Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis. 16540516 2006
Entrez Id: 1945
Gene Symbol: EFNA4
EFNA4
0.010 GeneticVariation disease BEFREE Underlining the importance of ephrin-A4, we identified heterozygous mutations in the human orthologue, EFNA4, in three of 81 patients with non-syndromic coronal synostosis. 16540516 2006
Entrez Id: 3207
Gene Symbol: HOXA11
HOXA11
0.020 GeneticVariation disease BEFREE Previously, we identified an inherited syndrome of congenital amegakaryocytic thrombocytopenia and radio-ulnar synostosis that is associated with a point mutation in the third helix of HOXA11 homeodomain (HOXA11-DeltaH3). 16765069 2006
Entrez Id: 7291
Gene Symbol: TWIST1
TWIST1
0.070 Biomarker disease BEFREE We suggest that genetic testing of patients with isolated sagittal or coronal synostosis should include TWIST1 mutational analysis. 17343269 2007
Entrez Id: 1947
Gene Symbol: EFNB1
EFNB1
0.010 GeneticVariation disease BEFREE Syndromic synostosis has been found to be associated with mutations of the fibroblast growth factor receptor family (FGFR1, -R2, -R3), TWIST1, MSX2, and EFNB1. 17552943 2007
Entrez Id: 2260
Gene Symbol: FGFR1
FGFR1
0.010 GeneticVariation disease BEFREE Syndromic synostosis has been found to be associated with mutations of the fibroblast growth factor receptor family (FGFR1, -R2, -R3), TWIST1, MSX2, and EFNB1. 17552943 2007
Entrez Id: 9241
Gene Symbol: NOG
NOG
0.020 GeneticVariation disease BEFREE Mutations of the NOGGIN (NOG) gene in humans are associated with several autosomal dominant disorders such as proximal symphalangism and multiple synostoses. 18096605 2008
Entrez Id: 2317
Gene Symbol: FLNB
FLNB
0.010 GeneticVariation disease LHGDN Expanded clinical spectrum of spondylocarpotarsal synostosis syndrome and possible manifestation in a heterozygous father. 18257094 2008
Entrez Id: 9241
Gene Symbol: NOG
NOG
0.020 Biomarker disease BEFREE Mutations in the NOG gene which encodes the noggin protein, a bone morphogenetic protein antagonist, have been identified in TCS as well as in four other autosomal dominant disorders including proximal symphalangism (SYM1), multiple synostosis (SYNS1), Tarsal-Carpal coalition syndrome and brachydactyly type B (BDB). 18440889 2008
Entrez Id: 7291
Gene Symbol: TWIST1
TWIST1
0.070 GeneticVariation disease BEFREE All patients with either bicoronal synostosis or unicoronal synostosis with syndromic features should be screened for TWIST1 mutations, as this confers a greater risk than nonsyndromic synostosis of the same sutures. 19483581 2009
Entrez Id: 4488
Gene Symbol: MSX2
MSX2
0.020 Biomarker disease BEFREE Recently it has been proposed that an extra copy of MSX2 that maps to 5q35.2 causes premature synostosis of the sutures via the MSX2-mediated pathway of calvarial osteogenic differentiation. 19533795 2009
Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
0.020 GeneticVariation disease BEFREE RESULTS - Animals that received control osteoblasts, sham surgery, or no surgery demonstrated normal skull growth and coronal suture histology, whereas animals transplanted only with FGFR2 mutant osteoblasts showed evidence of bridging synostosis on the calvarial dural surface. 19627528 2009
Entrez Id: 3207
Gene Symbol: HOXA11
HOXA11
0.020 GeneticVariation disease BEFREE Proximal radio-ulnar synostosis with bone marrow failure syndrome in an infant without a HOXA11 mutation. 20562651 2010