Gene: KCNJ10 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		0.400 Biomarker phenotype CLINGEN Mutations of KCNJ10 together with mutations of SLC26A4 cause digenic nonsyndromic hearing loss associated with enlarged vestibular aqueduct syndrome. 19426954 2009
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		0.400 Biomarker phenotype CLINGEN Free radical stress-mediated loss of Kcnj10 protein expression in stria vascularis contributes to deafness in Pendred syndrome mouse model. 17959752 2008
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		0.400 Biomarker phenotype CLINGEN Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model. 15320950 2004
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		0.400 Biomarker phenotype HPO