Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 147912
Gene Symbol: SIX5
SIX5 		0.700 GeneticVariation disease UNIPROT Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome. 17357085 2007
Entrez Id: 147912
Gene Symbol: SIX5
SIX5 		0.700 Biomarker disease GENOMICS_ENGLAND Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome. 17357085 2007
Entrez Id: 147912
Gene Symbol: SIX5
SIX5 		0.700 Biomarker disease GENOMICS_ENGLAND Characterization of the expression of DMPK and SIX5 in the human eye and implications for pathogenesis in myotonic dystrophy. 9949207 1999
Entrez Id: 147912
Gene Symbol: SIX5
SIX5 		0.700 Biomarker disease GENOMICS_ENGLAND
Entrez Id: 147912
Gene Symbol: SIX5
SIX5 		0.700 Biomarker disease CTD_human
Entrez Id: 147912
Gene Symbol: SIX5
SIX5 		0.700 CausalMutation disease CLINVAR
Entrez Id: 7020
Gene Symbol: TFAP2A
TFAP2A 		0.300 Biomarker disease CTD_human Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulators. 19685247 2009
Entrez Id: 2138
Gene Symbol: EYA1
EYA1 		0.300 Biomarker disease CTD_human Thymus, kidney and craniofacial abnormalities in Six 1 deficient mice. 12834866 2003
Entrez Id: 6495
Gene Symbol: SIX1
SIX1 		0.300 Biomarker disease CTD_human