×
Entrez Id:
3766
Gene Symbol:
KCNJ10
KCNJ10
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
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
SeSAME syndrome
1.000
Biomarker
MGD
KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential.
11788352
2002
×
Entrez Id:
3766
Gene Symbol:
KCNJ10
KCNJ10
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
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
×
Entrez Id:
3766
Gene Symbol:
KCNJ10
KCNJ10
Sensorineural Hearing Loss (disorder)
0.300
Biomarker
RGD
Long-lasting changes in the cochlear K+ recycling structures after acute energy failure.
23827367
2014
×
Entrez Id:
3766
Gene Symbol:
KCNJ10
KCNJ10
Amyotrophic Lateral Sclerosis
0.210
Biomarker
RGD
Changes in the astrocytic aquaporin-4 and inwardly rectifying potassium channel expression in the brain of the amyotrophic lateral sclerosis SOD1(G93A) rat model.
22987392
2012
×
Entrez Id:
3766
Gene Symbol:
KCNJ10
KCNJ10
Epilepsy, Reflex
0.200
Biomarker
RGD
Down-Regulation of Astrocytic Kir4.1 Channels during the Audiogenic Epileptogenesis in Leucine-Rich Glioma-Inactivated 1 (Lgi1 ) Mutant Rats.
30813600
2019
×
Entrez Id:
3766
Gene Symbol:
KCNJ10
KCNJ10
Hearing Loss, Central
0.200
Biomarker
RGD
Long-lasting changes in the cochlear K+ recycling structures after acute energy failure.
23827367
2014
×
Entrez Id:
3766
Gene Symbol:
KCNJ10
KCNJ10
Hearing Loss, High-Frequency
0.200
Biomarker
RGD
Long-lasting changes in the cochlear K+ recycling structures after acute energy failure.
23827367
2014
×
Entrez Id:
3766
Gene Symbol:
KCNJ10
KCNJ10
Tonic-Clonic Epilepsy
0.200
Biomarker
RGD
Expressional analysis of inwardly rectifying Kir4.1 channels in Noda epileptic rat (NER).
23603404
2013
×
Entrez Id:
3766
Gene Symbol:
KCNJ10
KCNJ10
Diabetic Retinopathy
0.200
Therapeutic
RGD
Protection against methylglyoxal-derived AGEs by regulation of glyoxalase 1 prevents retinal neuroglial and vasodegenerative pathology.
22143324
2012
×
Entrez Id:
3766
Gene Symbol:
KCNJ10
KCNJ10
Retinal Degeneration
0.200
Biomarker
RGD
The changes of potassium currents in RCS rat Müller cell during retinal degeneration.
22055109
2012
×
Entrez Id:
3766
Gene Symbol:
KCNJ10
KCNJ10
Subarachnoid Hemorrhage
0.200
Therapeutic
RGD
p53-induced uncoupling expression of aquaporin-4 and inwardly rectifying K+ 4.1 channels in cytotoxic edema after subarachnoid hemorrhage.
22420318
2012
×
Entrez Id:
3766
Gene Symbol:
KCNJ10
KCNJ10
Diabetic Retinopathy
0.200
Therapeutic
RGD
Expression of aquaporin 4 and Kir4.1 in diabetic rat retina: treatment with minocycline.
21672350
2011
×
Entrez Id:
3766
Gene Symbol:
KCNJ10
KCNJ10
Retinal Vein Occlusion
0.200
Biomarker
RGD
Effects of intravitreal triamcinolone acetonide on retinal gene expression in a rat model of central retinal vein occlusion.
21487926
2011
×
Entrez Id:
3766
Gene Symbol:
KCNJ10
KCNJ10
Liver Failure, Acute
0.200
Biomarker
RGD
Down-regulation of Kir4.1 in the cerebral cortex of rats with liver failure and in cultured astrocytes treated with glutamine: Implications for astrocytic dysfunction in hepatic encephalopathy.
21538466
2011
×
Entrez Id:
3766
Gene Symbol:
KCNJ10
KCNJ10
Transient Ischemic Attack
0.200
Biomarker
RGD
Impact of global cerebral ischemia on K+ channel expression and membrane properties of glial cells in the rat hippocampus.
20833221
2010
×
Entrez Id:
3766
Gene Symbol:
KCNJ10
KCNJ10
Uveitis
0.200
Biomarker
RGD
Differential expression of Kir4.1 and aquaporin 4 in the retina from endotoxin-induced uveitis rat.
17356517
2007