Gene: CACNA2D1 ×
Source: CURATED ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1 		0.620 Biomarker disease CLINGEN Functional characterization of CaVα2δ mutations associated with sudden cardiac death. 25527503 2015
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1 		0.620 Biomarker disease 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 		0.620 SusceptibilityMutation disease ORPHANET 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 		0.620 Biomarker disease 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 		0.620 Biomarker disease CLINGEN Targeted disruption of the voltage-dependent calcium channel alpha2/delta-1-subunit. 19429829 2009
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1 		0.620 SusceptibilityMutation disease ORPHANET Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death. 17224476 2007
Entrez Id: 781
Gene Symbol: CACNA2D1
CACNA2D1 		0.620 Biomarker disease GENOMICS_ENGLAND Short QT syndrome. 16301704 2005