Source: ALL

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C2748572
Disease: SeSAME syndrome
SeSAME syndrome 		disease 1.000 strong 1.000 26 12 1997 2019
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C3538946
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT
DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT 		disease 0.600 strong 1.000 2 2 1997 2009
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C1863752
Disease: Enlarged Vestibular Aqueduct
Enlarged Vestibular Aqueduct 		phenotype 0.400 disputed 1.000 3 0 2004 2009
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C0271829
Disease: Pendred's syndrome
Pendred's syndrome 		disease 0.340 None 1.000 4 1 2009 2013
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		disease 0.310 None < 0.001 1 0 2011 2011
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		disease 0.300 None 1.000 1 0 2013 2013
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		disease 0.300 None 1.000 1 0 2014 2014
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C0751324
Disease: Multiple Sclerosis, Acute Fulminating
Multiple Sclerosis, Acute Fulminating 		disease 0.300 None 1.000 1 0 2013 2013
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		disease 0.210 None 1.000 2 0 2006 2012
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C0036572
Disease: Seizures
Seizures 		phenotype 0.200 None 1.000 11 3 2004 2018
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		disease 0.200 None 1.000 2 0 2011 2012
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C0007787
Disease: Transient Ischemic Attack
Transient Ischemic Attack 		disease 0.200 None 1.000 1 0 2010 2010
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C0035304
Disease: Retinal Degeneration
Retinal Degeneration 		phenotype 0.200 None 1.000 1 0 2012 2012
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C0035328
Disease: Retinal Vein Occlusion
Retinal Vein Occlusion 		disease 0.200 None 1.000 1 0 2011 2011
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C0018780
Disease: Hearing Loss, High-Frequency
Hearing Loss, High-Frequency 		disease 0.200 None 1.000 1 0 2014 2014
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C0018776
Disease: Hearing Loss, Central
Hearing Loss, Central 		disease 0.200 None 1.000 1 0 2014 2014
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C0042164
Disease: Uveitis
Uveitis 		disease 0.200 None 1.000 1 0 2007 2007
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C0014549
Disease: Tonic-Clonic Epilepsy
Tonic-Clonic Epilepsy 		disease 0.200 None 1.000 1 0 2013 2013
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C0162557
Disease: Liver Failure, Acute
Liver Failure, Acute 		disease 0.200 None 1.000 1 0 2011 2011
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C0270857
Disease: Epilepsy, Reflex
Epilepsy, Reflex 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C0038525
Disease: Subarachnoid Hemorrhage
Subarachnoid Hemorrhage 		disease 0.200 None 1.000 1 0 2012 2012
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia 		phenotype 0.120 None 1.000 2 1 2013 2018
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C0004134
Disease: Ataxia
Ataxia 		phenotype 0.120 None 1.000 2 0 2013 2018
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C0151723
Disease: Hypomagnesemia
Hypomagnesemia 		phenotype 0.110 None 1.000 1 0 2018 2018
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		group 0.110 None 1.000 1 2 2011 2011