Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2706
Gene Symbol: GJB2
GJB2 		0.600 Biomarker disease CTD_human
Entrez Id: 2706
Gene Symbol: GJB2
GJB2 		0.600 Biomarker disease MGD
Entrez Id: 2706
Gene Symbol: GJB2
GJB2 		0.600 CausalMutation disease CLINVAR
Entrez Id: 10804
Gene Symbol: GJB6
GJB6 		0.500 Biomarker disease MGD The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice. 20858605 2010
Entrez Id: 10804
Gene Symbol: GJB6
GJB6 		0.500 Biomarker disease MGD ATP release through connexin hemichannels and gap junction transfer of second messengers propagate Ca2+ signals across the inner ear. 19047635 2008
Entrez Id: 10804
Gene Symbol: GJB6
GJB6 		0.500 Biomarker disease MGD Connexin30 deficiency causes instrastrial fluid-blood barrier disruption within the cochlear stria vascularis. 17400755 2007
Entrez Id: 10804
Gene Symbol: GJB6
GJB6 		0.500 Biomarker disease MGD Restoration of connexin26 protein level in the cochlea completely rescues hearing in a mouse model of human connexin30-linked deafness. 17227867 2007
Entrez Id: 10804
Gene Symbol: GJB6
GJB6 		0.500 Biomarker disease MGD Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential. 12490528 2003
Entrez Id: 10804
Gene Symbol: GJB6
GJB6 		0.500 Biomarker disease CTD_human
Entrez Id: 2707
Gene Symbol: GJB3
GJB3 		0.300 Biomarker disease CTD_human