Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2697
Gene Symbol: GJA1
GJA1
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.320 GeneticVariation BEFREE Mutations in GJB6 and GJA1 are not a major cause of nonsyndromic deafness in this group of Africans from Cameroon and South Africa. 24785695

2014
Entrez Id: 2697
Gene Symbol: GJA1
GJA1
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.320 Biomarker CLINGEN Connexin 43 and hearing: possible implications for retrocochlear auditory processing. 23817980

2013
Entrez Id: 2697
Gene Symbol: GJA1
GJA1
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.320 Biomarker BEFREE Novel mutations in the connexin43 (GJA1) and GJA1 pseudogene may contribute to nonsyndromic hearing loss. 20130915

2010
Entrez Id: 2697
Gene Symbol: GJA1
GJA1
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.320 Biomarker CLINGEN Expression of the connexin43- and connexin45-encoding genes in the developing and mature mouse inner ear. 14986102

2004
Entrez Id: 2697
Gene Symbol: GJA1
GJA1
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.320 Biomarker CLINGEN Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness. 11741837

2001