Source: BEFREE

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: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
DIABETES MELLITUS, PERMANENT NEONATAL
disease 1.000 strong 0.984 35 6 2001 2018
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
Diabetes Mellitus, Non-Insulin-Dependent
disease 0.900 strong 0.943 91 11 1996 2019
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C3888018
Disease: Congenital Hyperinsulinism
Congenital Hyperinsulinism
disease 0.700 None 1.000 44 4 2001 2019
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
Maturity onset diabetes mellitus in young
disease 0.660 strong 1.000 6 1 2009 2019
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
MATURITY-ONSET DIABETES OF THE YOUNG, TYPE 13
disease 0.610 None 1.000 1 1 2011 2017
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
Developmental Delay, Epilepsy, and Neonatal Diabetes
disease 0.570 None 1.000 7 4 2006 2018
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0158981
Disease: Neonatal diabetes mellitus
Neonatal diabetes mellitus
disease 0.500 None 0.988 80 10 2004 2019
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C4303593
Disease: DEND syndrome
DEND syndrome
disease 0.490 strong 1.000 9 6 2007 2017
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0036572
Disease: Seizures
Seizures
phenotype 0.430 None 1.000 3 1 2007 2018
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
Diabetes Mellitus, Insulin-Dependent
disease 0.380 None 0.889 8 1 2004 2018
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C3888631
Disease: Monogenic diabetes
Monogenic diabetes
disease 0.340 strong 1.000 4 0 2009 2018
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
Diabetes Mellitus, Transient Neonatal, 1
disease 0.330 None 1.000 3 1 2005 2012
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0362046
Disease: Prediabetes syndrome
Prediabetes syndrome
disease 0.230 None 1.000 3 2 2007 2018
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
group 0.210 None 1.000 1 1 2005 2007
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
group 0.200 None 0.985 61 12 2003 2019
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C1864903
Disease: Hyperinsulinemic hypoglycemia
Hyperinsulinemic hypoglycemia
disease 0.200 None 1.000 10 1 2011 2016
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0020615
Disease: Hypoglycemia
Hypoglycemia
disease 0.190 None 0.889 8 1 2003 2019
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism
disease 0.190 None 1.000 8 0 2000 2017
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
disease 0.170 None 1.000 7 7 2005 2016
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
phenotype 0.150 None 0.800 4 1 2005 2013
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia
disease 0.150 None 1.000 1 3 2002 2016
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
Transient neonatal diabetes mellitus
disease 0.130 None 1.000 3 0 2008 2012
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0028754
Disease: Obesity
Obesity
disease 0.110 None < 0.001 1 2 2014 2014
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0011847
Disease: Diabetes
Diabetes
disease 0.100 None 0.981 54 12 2003 2019
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
potassium inwardly rectifying channel subfamily J member 11 0.529 0.615 1.1E-02
CUI: C0014544
Disease: Epilepsy
Epilepsy
disease 0.090 None 0.889 6 6 2004 2015