Source: ANIMAL_MODELS

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10
CUI: C2748572
Disease: SeSAME syndrome
SeSAME syndrome
1.000 Biomarker MGD Mutations in KCNJ10 cause a specific disorder, consisting of epilepsy, ataxia, sensorineural deafness, and tubulopathy. 19420365

2009

Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10
CUI: C2748572
Disease: SeSAME syndrome
SeSAME syndrome
1.000 Biomarker MGD Time course of inner ear degeneration and deafness in mice lacking the Kir4.1 potassium channel subunit. 12618319

2003

Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10
CUI: C2748572
Disease: SeSAME syndrome
SeSAME syndrome
1.000 Biomarker MGD KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential. 11788352

2002

Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10
CUI: C2748572
Disease: SeSAME syndrome
SeSAME syndrome
1.000 Biomarker MGD Kir4.1 potassium channel subunit is crucial for oligodendrocyte development and in vivo myelination. 11466414

2001

Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10
CUI: C2748572
Disease: SeSAME syndrome
SeSAME syndrome
1.000 Biomarker MGD Genetic inactivation of an inwardly rectifying potassium channel (Kir4.1 subunit) in mice: phenotypic impact in retina. 10908613

2000