Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 84667
Gene Symbol: HES7
HES7 		0.600 GeneticVariation disease UNIPROT Two novel missense mutations in HAIRY-AND-ENHANCER-OF-SPLIT-7 in a family with spondylocostal dysostosis. 20087400 2010
Entrez Id: 84667
Gene Symbol: HES7
HES7 		0.600 GeneticVariation disease UNIPROT Mutation of Hairy-and-Enhancer-of-Split-7 in humans causes spondylocostal dysostosis. 18775957 2008
Entrez Id: 84667
Gene Symbol: HES7
HES7 		0.600 GeneticVariation disease CLINVAR
Entrez Id: 84667
Gene Symbol: HES7
HES7 		0.600 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 134701
Gene Symbol: RIPPLY2
RIPPLY2 		0.200 Biomarker disease MGD Ripply2 is essential for precise somite formation during mouse early development. 17531978 2007
Entrez Id: 10683
Gene Symbol: DLL3
DLL3 		0.200 Biomarker disease MGD Axial skeletal defects caused by mutation in the spondylocostal dysplasia/pudgy gene Dll3 are associated with disruption of the segmentation clock within the presomitic mesoderm. 11923214 2002
Entrez Id: 6911
Gene Symbol: TBX6
TBX6 		0.200 Biomarker disease MGD Development of rib-vertebrae: a new mutation in the house mouse with accessory caudal duplications. 4073528 1985