Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 58
Gene Symbol: ACTA1
ACTA1 		0.600 Biomarker disease MGD Hypertrophy and dietary tyrosine ameliorate the phenotypes of a mouse model of severe nemaline myopathy. 22067542 2011
Entrez Id: 58
Gene Symbol: ACTA1
ACTA1 		0.600 Biomarker disease GENOMICS_ENGLAND Mutations and polymorphisms of the skeletal muscle alpha-actin gene (ACTA1). 19562689 2009
Entrez Id: 58
Gene Symbol: ACTA1
ACTA1 		0.600 CausalMutation disease CLINVAR
Entrez Id: 57822
Gene Symbol: GRHL3
GRHL3 		0.200 Biomarker disease MGD Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development. 24360809 2014
Entrez Id: 3664
Gene Symbol: IRF6
IRF6 		0.200 Biomarker disease MGD Identification of a Van der Woude syndrome mutation in the cleft palate 1 mutant mouse. 20196077 2010