Gene: TCF12 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6938
Gene Symbol: TCF12
TCF12 		0.440 GeneticVariation disease BEFREE This is the first study that reports the TCF12 mutations in Turkish patients with coronal suture synostosis. 31353793 2019
Entrez Id: 6938
Gene Symbol: TCF12
TCF12 		0.440 GeneticVariation disease BEFREE Variants were identified most frequently in TCF12 (N = 22) and EFNB1 (N = 8), typically in individuals with nonsyndromic coronal craniosynostosis or TWIST1-negative clinically suspected Saethre-Chotzen syndrome. 29215649 2018
Entrez Id: 6938
Gene Symbol: TCF12
TCF12 		0.440 GeneticVariation disease BEFREE This deletion leads to haploinsufficiency of TCF12 gene that can explain the coronal craniosynostosis described in the patient. 24648389 2014
Entrez Id: 6938
Gene Symbol: TCF12
TCF12 		0.440 Biomarker disease GENOMICS_ENGLAND Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis. 23354436 2013
Entrez Id: 6938
Gene Symbol: TCF12
TCF12 		0.440 GeneticVariation disease BEFREE Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis. 23354436 2013
Entrez Id: 6938
Gene Symbol: TCF12
TCF12 		0.440 GeneticVariation disease CLINVAR