Source: GENOMICS_ENGLAND

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: 3759
Gene Symbol: KCNJ2
KCNJ2 		potassium inwardly rectifying channel subfamily J member 2 0.572 0.731 0.31
CUI: C1563715
Disease: Andersen Syndrome
Andersen Syndrome 		disease 0.800 None 0.987 5 0 2001 2019
Entrez Id: 3759
Gene Symbol: KCNJ2
KCNJ2 		potassium inwardly rectifying channel subfamily J member 2 0.572 0.731 0.31
CUI: C1865018
Disease: Short QT Syndrome 3
Short QT Syndrome 3 		disease 0.740 strong 1.000 3 0 2001 2017
Entrez Id: 3759
Gene Symbol: KCNJ2
KCNJ2 		potassium inwardly rectifying channel subfamily J member 2 0.572 0.731 0.31
CUI: C3151431
Disease: ATRIAL FIBRILLATION, FAMILIAL, 9
ATRIAL FIBRILLATION, FAMILIAL, 9 		disease 0.700 strong 1.000 3 0 2002 2016
Entrez Id: 3759
Gene Symbol: KCNJ2
KCNJ2 		potassium inwardly rectifying channel subfamily J member 2 0.572 0.731 0.31
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		disease 0.470 strong 1.000 1 0 2005 2019
Entrez Id: 3759
Gene Symbol: KCNJ2
KCNJ2 		potassium inwardly rectifying channel subfamily J member 2 0.572 0.731 0.31
CUI: C0151879
Disease: Shortened QT interval
Shortened QT interval 		phenotype 0.400 strong 1.000 1 0 2015 2015
Entrez Id: 3759
Gene Symbol: KCNJ2
KCNJ2 		potassium inwardly rectifying channel subfamily J member 2 0.572 0.731 0.31
CUI: C0030443
Disease: Familial Periodic Paralysis
Familial Periodic Paralysis 		disease 0.400 None 1.000 1 0 2002 2015
Entrez Id: 3759
Gene Symbol: KCNJ2
KCNJ2 		potassium inwardly rectifying channel subfamily J member 2 0.572 0.731 0.31
CUI: C0008925
Disease: Cleft Palate
Cleft Palate 		disease 0.400 strong 1.000 1 0 2002 2002
Entrez Id: 3759
Gene Symbol: KCNJ2
KCNJ2 		potassium inwardly rectifying channel subfamily J member 2 0.572 0.731 0.31
CUI: C1279412
Disease: periodic paralysis (finding)
periodic paralysis (finding) 		disease 0.390 None 1.000 1 0 2002 2015
Entrez Id: 3759
Gene Symbol: KCNJ2
KCNJ2 		potassium inwardly rectifying channel subfamily J member 2 0.572 0.731 0.31
CUI: C1631597
Disease: VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder) 		disease 0.360 None 1.000 1 0 2009 2019
Entrez Id: 3759
Gene Symbol: KCNJ2
KCNJ2 		potassium inwardly rectifying channel subfamily J member 2 0.572 0.731 0.31
CUI: C2750061
Disease: Hypokalemic Periodic Paralysis, Type 2
Hypokalemic Periodic Paralysis, Type 2 		disease 0.300 None 1.000 1 0 2005 2005