Gene: MSX1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.700 Biomarker disease BEFREE To evaluate the association of transforming growth factor β3 ( TGFβ3), muscle segment homeobox 1 ( MSX1), Metalloproteinases 3 ( MMP3), and MMP9 genes as candidates for nonsyndromic cleft lip and/or palate in an Indian population. 29738289 2019
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.700 Biomarker disease GENOMICS_ENGLAND Mutations in the MSX1 gene in Turkish children with non-syndromic tooth agenesis and other dental anomalies. 25565750 2014
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.700 GeneticVariation disease BEFREE The patients with non-syndromic cleft lip and/or palate were characterized by similar distribution of MSX1 genotypes and allele in comparison to subjects without oral clefts (P > 0.05). 23130753 2013
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.700 GeneticVariation disease BEFREE Conclusion : Our data suggest that CDH1 and MSX1 gene polymorphisms are risk factors for susceptibility to NS-CL/P in a sample of the Iranian population. 23231047 2013
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.700 GeneticVariation disease BEFREE Our findings suggest that the nonsense mutation in MSX1 might have resulted in rapid degradation of the mutated transcript and caused the phenotype of tooth agenesis with cleft lip in the Chinese family. 22813217 2012
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.700 GeneticVariation disease BEFREE No significant association was found between NSOC and rs3821949 or rs12532 in MSX1 gene, whereas an association was observed between the P147Q variant and cleft lip with cleft palate in the case-control analysis. 21689018 2011
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.700 GeneticVariation disease LHGDN MSX1 polymorphism associated with risk of oral cleft in Korea: evidence from case-parent trio and case-control studies. 17326252 2007
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.700 Biomarker disease LHGDN [Association study on microsatellite polymorphisms of MSX1 gene and nonsyndromic cleft lip and palate]. 17557248 2007
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.700 GeneticVariation disease LHGDN Association of MSX1 with nonsyndromic cleft lip and palate in a Colombian population. 18177186 2007
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.700 GeneticVariation disease BEFREE MSX1 mutations contribute to nonsyndromic cleft lip in a Thai population. 16868654 2006
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.700 Biomarker disease LHGDN Linkage disequilibrium between MSX1 and non-syndromic cleft lip/palate in the Chilean population. 15381719 2004
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.700 Biomarker disease BEFREE With likelihood ratio test analysis, "cleft lip only" showed association with MSX1 (p = 0.04) and "cleft palate only" with TGFB3 (p = 0.02). 12651933 2003
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.700 SusceptibilityMutation disease ORPHANET MSX1 has been proposed as a gene in which mutations may contribute to non-syndromic forms of cleft lip and/or cleft palate. 12807959 2003
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.700 GeneticVariation disease BEFREE MSX1 has been proposed as a gene in which mutations may contribute to non-syndromic forms of cleft lip and/or cleft palate. 12807959 2003
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.700 Biomarker disease BEFREE Cleft lip and/or palate with hypodontia outside the cleft region was positively associated with both TGFB3 and MSX1, compared with noncleft controls. 12733956 2003
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.700 GeneticVariation disease LHGDN MSX1 has been proposed as a gene in which mutations may contribute to non-syndromic forms of cleft lip and/or cleft palate. 12807959 2003
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.700 Biomarker disease LHGDN Cleft lip and/or palate with hypodontia outside the cleft region was positively associated with both TGFB3 and MSX1, compared with noncleft controls. 12733956 2003
Entrez Id: 4487
Gene Symbol: MSX1
MSX1 		0.700 Biomarker disease HPO