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 		0.600 GeneticVariation disease CLINVAR 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 		0.600 Biomarker disease GENOMICS_ENGLAND Assignment of the glial inwardly rectifying potassium channel KAB-2/Kir4.1 (Kcnj10) gene to the distal region of mouse chromosome 1. 9367690 1997
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		0.600 CausalMutation disease CLINVAR
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		0.600 Biomarker disease CTD_human