Source: GENOMICS_ENGLAND

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10060
Gene Symbol: ABCC9
ABCC9
CUI: C0795905
Disease: Cantu syndrome
Cantu syndrome 		0.800 Biomarker GENOMICS_ENGLAND

Entrez Id: 10060
Gene Symbol: ABCC9
ABCC9
CUI: C0795905
Disease: Cantu syndrome
Cantu syndrome 		0.800 Biomarker GENOMICS_ENGLAND

Entrez Id: 10060
Gene Symbol: ABCC9
ABCC9
CUI: C1837839
Disease: CARDIOMYOPATHY, DILATED, 1O
CARDIOMYOPATHY, DILATED, 1O 		0.700 Biomarker GENOMICS_ENGLAND Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples. 27532257

2017
Entrez Id: 10060
Gene Symbol: ABCC9
ABCC9
CUI: C3279695
Disease: ATRIAL FIBRILLATION, FAMILIAL, 12
ATRIAL FIBRILLATION, FAMILIAL, 12 		0.700 Biomarker GENOMICS_ENGLAND Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples. 27532257

2017
Entrez Id: 10060
Gene Symbol: ABCC9
ABCC9
CUI: C1837839
Disease: CARDIOMYOPATHY, DILATED, 1O
CARDIOMYOPATHY, DILATED, 1O 		0.700 Biomarker GENOMICS_ENGLAND ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene. 24439875

2014
Entrez Id: 10060
Gene Symbol: ABCC9
ABCC9
CUI: C3279695
Disease: ATRIAL FIBRILLATION, FAMILIAL, 12
ATRIAL FIBRILLATION, FAMILIAL, 12 		0.700 Biomarker GENOMICS_ENGLAND ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene. 24439875

2014
Entrez Id: 10060
Gene Symbol: ABCC9
ABCC9
CUI: C1837839
Disease: CARDIOMYOPATHY, DILATED, 1O
CARDIOMYOPATHY, DILATED, 1O 		0.700 Biomarker GENOMICS_ENGLAND Short QT syndrome. 16301704

2005
Entrez Id: 10060
Gene Symbol: ABCC9
ABCC9
CUI: C3279695
Disease: ATRIAL FIBRILLATION, FAMILIAL, 12
ATRIAL FIBRILLATION, FAMILIAL, 12 		0.700 Biomarker GENOMICS_ENGLAND Short QT syndrome. 16301704

2005
Entrez Id: 10060
Gene Symbol: ABCC9
ABCC9
CUI: C1837839
Disease: CARDIOMYOPATHY, DILATED, 1O
CARDIOMYOPATHY, DILATED, 1O 		0.700 Biomarker GENOMICS_ENGLAND ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating. 15034580

2004
Entrez Id: 10060
Gene Symbol: ABCC9
ABCC9
CUI: C3279695
Disease: ATRIAL FIBRILLATION, FAMILIAL, 12
ATRIAL FIBRILLATION, FAMILIAL, 12 		0.700 Biomarker GENOMICS_ENGLAND ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating. 15034580

2004
Entrez Id: 10060
Gene Symbol: ABCC9
ABCC9
CUI: C0042514
Disease: Tachycardia, Ventricular
Tachycardia, Ventricular 		0.600 Biomarker GENOMICS_ENGLAND Short QT syndrome. 16301704

2005
Entrez Id: 10060
Gene Symbol: ABCC9
ABCC9
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		0.510 Biomarker GENOMICS_ENGLAND ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene. 24439875

2014
Entrez Id: 10060
Gene Symbol: ABCC9
ABCC9
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		0.420 Biomarker GENOMICS_ENGLAND ABCC9 is a novel Brugada and early repolarization syndrome susceptibility gene. 24439875

2014
Entrez Id: 10060
Gene Symbol: ABCC9
ABCC9
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		0.400 Biomarker GENOMICS_ENGLAND

Entrez Id: 10060
Gene Symbol: ABCC9
ABCC9
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.310 Biomarker GENOMICS_ENGLAND Short QT syndrome. 16301704

2005
Entrez Id: 10060
Gene Symbol: ABCC9
ABCC9
CUI: C0151879
Disease: Shortened QT interval
Shortened QT interval 		0.300 Biomarker GENOMICS_ENGLAND Short QT syndrome. 16301704

2005