Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6495
Gene Symbol: SIX1
SIX1 		0.600 CausalMutation disease CLINVAR Biochemical and functional characterization of six SIX1 Branchio-oto-renal syndrome mutations. 19497856 2009
Entrez Id: 6495
Gene Symbol: SIX1
SIX1 		0.600 CausalMutation disease CLINVAR SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes. 15141091 2004
Entrez Id: 6495
Gene Symbol: SIX1
SIX1 		0.600 Biomarker disease GENOMICS_ENGLAND A novel locus (DFNA23) for prelingual autosomal dominant nonsyndromic hearing loss maps to 14q21-q22 in a Swiss German kindred. 10777717 2000
Entrez Id: 6495
Gene Symbol: SIX1
SIX1 		0.600 Biomarker disease GENOMICS_ENGLAND Abrogation of the G2 cell cycle checkpoint associated with overexpression of HSIX1: a possible mechanism of breast carcinogenesis. 9770533 1998
Entrez Id: 6495
Gene Symbol: SIX1
SIX1 		0.600 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 6495
Gene Symbol: SIX1
SIX1 		0.600 GeneticVariation disease CLINVAR
Entrez Id: 6495
Gene Symbol: SIX1
SIX1 		0.600 Biomarker disease CTD_human