Source: CLINGEN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		0.620 Biomarker CLINGEN Functional characterization of CaVα2δ mutations associated with sudden cardiac death. 25527503

2015
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		0.620 Biomarker CLINGEN Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics. 24309898

2014
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		0.620 Biomarker CLINGEN CACNA1C, CACNB2b, and CACNA2D1 genes of 162 probands with BrS and BrS+SQT, 19 with IVF, and 24 with ERS were screened by direct sequencing. 20817017

2010
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder) 		0.620 Biomarker CLINGEN Targeted disruption of the voltage-dependent calcium channel alpha2/delta-1-subunit. 19429829

2009
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C0264893
Disease: Nodal rhythm disorder
Nodal rhythm disorder 		0.300 Biomarker CLINGEN Functional characterization of CaVα2δ mutations associated with sudden cardiac death. 25527503

2015
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C0348626
Disease: Other specified cardiac arrhythmias
Other specified cardiac arrhythmias 		0.300 Biomarker CLINGEN Functional characterization of CaVα2δ mutations associated with sudden cardiac death. 25527503

2015
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C0428908
Disease: Sinus Node Dysfunction (disorder)
Sinus Node Dysfunction (disorder) 		0.300 Biomarker CLINGEN Functional characterization of CaVα2δ mutations associated with sudden cardiac death. 25527503

2015
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C1399226
Disease: Ectopic rhythm
Ectopic rhythm 		0.300 Biomarker CLINGEN Functional characterization of CaVα2δ mutations associated with sudden cardiac death. 25527503

2015
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C2748542
Disease: CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder)
CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder) 		0.300 Biomarker CLINGEN Functional characterization of CaVα2δ mutations associated with sudden cardiac death. 25527503

2015
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C4551804
Disease: Brugada Syndrome 1
Brugada Syndrome 1 		0.300 Biomarker CLINGEN Functional characterization of CaVα2δ mutations associated with sudden cardiac death. 25527503

2015
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C0264893
Disease: Nodal rhythm disorder
Nodal rhythm disorder 		0.300 Biomarker CLINGEN Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics. 24309898

2014
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C0348626
Disease: Other specified cardiac arrhythmias
Other specified cardiac arrhythmias 		0.300 Biomarker CLINGEN Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics. 24309898

2014
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C0428908
Disease: Sinus Node Dysfunction (disorder)
Sinus Node Dysfunction (disorder) 		0.300 Biomarker CLINGEN Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics. 24309898

2014
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C1399226
Disease: Ectopic rhythm
Ectopic rhythm 		0.300 Biomarker CLINGEN Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics. 24309898

2014
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C2748542
Disease: CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder)
CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder) 		0.300 Biomarker CLINGEN Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics. 24309898

2014
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C4551804
Disease: Brugada Syndrome 1
Brugada Syndrome 1 		0.300 Biomarker CLINGEN Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics. 24309898

2014
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C0264893
Disease: Nodal rhythm disorder
Nodal rhythm disorder 		0.300 Biomarker CLINGEN Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death. 20817017

2010
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C0348626
Disease: Other specified cardiac arrhythmias
Other specified cardiac arrhythmias 		0.300 Biomarker CLINGEN Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death. 20817017

2010
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C0428908
Disease: Sinus Node Dysfunction (disorder)
Sinus Node Dysfunction (disorder) 		0.300 Biomarker CLINGEN Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death. 20817017

2010
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C1399226
Disease: Ectopic rhythm
Ectopic rhythm 		0.300 Biomarker CLINGEN Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death. 20817017

2010
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C2748542
Disease: CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder)
CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder) 		0.300 Biomarker CLINGEN Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death. 20817017

2010
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C4551804
Disease: Brugada Syndrome 1
Brugada Syndrome 1 		0.300 Biomarker CLINGEN Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death. 20817017

2010
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C0264893
Disease: Nodal rhythm disorder
Nodal rhythm disorder 		0.300 Biomarker CLINGEN Targeted disruption of the voltage-dependent calcium channel alpha2/delta-1-subunit. 19429829

2009
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C0348626
Disease: Other specified cardiac arrhythmias
Other specified cardiac arrhythmias 		0.300 Biomarker CLINGEN Targeted disruption of the voltage-dependent calcium channel alpha2/delta-1-subunit. 19429829

2009
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1
CUI: C0428908
Disease: Sinus Node Dysfunction (disorder)
Sinus Node Dysfunction (disorder) 		0.300 Biomarker CLINGEN Targeted disruption of the voltage-dependent calcium channel alpha2/delta-1-subunit. 19429829

2009