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: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome 		disease 0.700 None 0.980 251 43 1993 2020
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia 		phenotype 0.200 None 0.982 56 9 1994 2020
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C1141890
Disease: Congenital long QT syndrome
Congenital long QT syndrome 		disease 0.200 None 0.990 57 5 1996 2019
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C4551647
Disease: Long QT Syndrome 1
Long QT Syndrome 1 		disease 1.000 None 0.990 55 15 1996 2019
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C1560249
Disease: Adverse Event Associated with Cardiac Arrhythmia
Adverse Event Associated with Cardiac Arrhythmia 		phenotype 0.060 None 1.000 6 1 1996 2018
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C1865019
Disease: SHORT QT SYNDROME 2 (disorder)
SHORT QT SYNDROME 2 (disorder) 		disease 0.720 None 1.000 2 0 1996 2018
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C0022387
Disease: Jervell-Lange Nielsen Syndrome
Jervell-Lange Nielsen Syndrome 		disease 1.000 definitive 1.000 36 6 1997 2019
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C3150943
Disease: Long Qt Syndrome 2
Long Qt Syndrome 2 		disease 0.200 None 0.958 24 0 1997 2019
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C0004903
Disease: Beckwith-Wiedemann Syndrome
Beckwith-Wiedemann Syndrome 		disease 0.500 None 1.000 14 0 1997 2019
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C0085612
Disease: Ventricular arrhythmia
Ventricular arrhythmia 		disease 0.200 None 1.000 11 2 1997 2020
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C0035828
Disease: Romano-Ward Syndrome
Romano-Ward Syndrome 		disease 0.500 None 1.000 9 0 1997 2017
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C0339789
Disease: Congenital deafness
Congenital deafness 		disease 0.060 None 1.000 6 1 1997 2010
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C0152459
Disease: Linear atrophy
Linear atrophy 		disease 0.030 None 1.000 3 0 1997 2013
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C0741923
Disease: cardiac event
cardiac event 		phenotype 0.100 None 1.000 21 6 1998 2018
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		disease 0.070 None 0.857 7 1 1998 2013
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C0018799
Disease: Heart Diseases
Heart Diseases 		group 0.030 None 1.000 3 0 1998 2018
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C0751534
Disease: Syncopal Episode
Syncopal Episode 		phenotype 0.010 None 1.000 1 0 1998 1998
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C0391957
Disease: idiopathic epilepsy
idiopathic epilepsy 		disease 0.010 None 1.000 1 0 1998 1998
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		disease 0.200 None 1.000 36 9 1999 2020
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C0040479
Disease: Torsades de Pointes
Torsades de Pointes 		disease 0.180 None 0.875 7 3 1999 2013
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		group 0.050 None 1.000 5 0 1999 2014
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		group 0.050 None 1.000 5 0 1999 2014
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C0027708
Disease: Nephroblastoma
Nephroblastoma 		disease 0.120 None 1.000 2 0 1999 2015
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C0206743
Disease: Rhabdoid Tumor
Rhabdoid Tumor 		disease 0.010 None 1.000 1 0 1999 1999
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C1333015
Disease: Childhood Kidney Wilms Tumor
Childhood Kidney Wilms Tumor 		disease 0.010 None 1.000 1 0 1999 1999