Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6833
Gene Symbol: ABCC8
ABCC8
0.100 GeneticVariation group CLINVAR
Entrez Id: 25
Gene Symbol: ABL1
ABL1
0.100 CausalMutation group CLINVAR Germline mutations in ABL1 cause an autosomal dominant syndrome characterized by congenital heart defects and skeletal malformations. 28288113 2017
Entrez Id: 25
Gene Symbol: ABL1
ABL1
0.100 Biomarker group HPO
Entrez Id: 58
Gene Symbol: ACTA1
ACTA1
0.010 Biomarker group BEFREE The Cardiac α actin 1 gene (ACTC1) has been related to familial atrial septal defects. 20962418 2010
Entrez Id: 59
Gene Symbol: ACTA2
ACTA2
0.030 GeneticVariation group BEFREE (2007) Am J Med Genet 143: 2662-2667 Alpha-cardiac actin mutations produce atrial septal defects Matsson et al.(2008) Hum Mol Genet 17: 256-265. 18400036 2008
Entrez Id: 59
Gene Symbol: ACTA2
ACTA2
0.030 GeneticVariation group BEFREE Alpha-cardiac actin mutations produce atrial septal defects. 17947298 2008
Entrez Id: 59
Gene Symbol: ACTA2
ACTA2
0.030 GeneticVariation group BEFREE In the present study, we further searched for mutations in human α-cardiac actin (ACTC1) and smooth muscle α-actin (ACTA2) genes as a possible cause of atrial septum defect type II (ASDII) and PDA. 25861618 2015
Entrez Id: 60
Gene Symbol: ACTB
ACTB
0.020 Biomarker group BEFREE In the present study, we further searched for mutations in human α-cardiac actin (ACTC1) and smooth muscle α-actin (ACTA2) genes as a possible cause of atrial septum defect type II (ASDII) and PDA. 25861618 2015
Entrez Id: 60
Gene Symbol: ACTB
ACTB
0.020 GeneticVariation group BEFREE We combined a genome-wide linkage analysis with cell biology, microscopy, and molecular biology tools to characterize a novel ACTC1 (cardiac α-actin) mutation identified in association with ASD and late-onset dilated cardiomyopathy in a large, multi-generational family. 31430208 2019
Entrez Id: 70
Gene Symbol: ACTC1
ACTC1
0.190 GeneticVariation group BEFREE Our results provide further evidence supporting a causative role for ACTC1 mutations in ASD. 24461919 2014
Entrez Id: 70
Gene Symbol: ACTC1
ACTC1
0.190 Biomarker group BEFREE The Cardiac α actin 1 gene (ACTC1) has been related to familial atrial septal defects. 20962418 2010
Entrez Id: 70
Gene Symbol: ACTC1
ACTC1
0.190 Biomarker group HPO
Entrez Id: 70
Gene Symbol: ACTC1
ACTC1
0.190 GeneticVariation group BEFREE (2007) Am J Med Genet 143: 2662-2667 Alpha-cardiac actin mutations produce atrial septal defects Matsson et al.(2008) Hum Mol Genet 17: 256-265. 18400036 2008
Entrez Id: 70
Gene Symbol: ACTC1
ACTC1
0.190 GeneticVariation group BEFREE The frequencies of II (Insertion/Insertion) genotype in the ASD and VSD patients were significantly higher than that of controls (p=0.004 for ASD Vs. controls, and p=0.009 for VSD Vs. controls, respectively), and the frequencies for I allele in CHD patients were also significantly higher than that in controls (p=0.01 for ASD Vs. controls, and p=0.009 for VSD Vs. controls, respectively). 23299027 2013
Entrez Id: 70
Gene Symbol: ACTC1
ACTC1
0.190 GeneticVariation group BEFREE In the present study, we further searched for mutations in human α-cardiac actin (ACTC1) and smooth muscle α-actin (ACTA2) genes as a possible cause of atrial septum defect type II (ASDII) and PDA. 25861618 2015
Entrez Id: 70
Gene Symbol: ACTC1
ACTC1
0.190 GeneticVariation group LHGDN The combined results indicate, for the first time, that ACTC1 mutations or reduced ACTC1 levels may lead to ASD without signs of cardiomyopathy. 17947298 2008
Entrez Id: 70
Gene Symbol: ACTC1
ACTC1
0.190 GeneticVariation group BEFREE The combined results indicate, for the first time, that ACTC1 mutations or reduced ACTC1 levels may lead to ASD without signs of cardiomyopathy. 17947298 2008
Entrez Id: 70
Gene Symbol: ACTC1
ACTC1
0.190 GeneticVariation group BEFREE We recently identified a novel, heterozygous, and non-synonymous ACTC1 mutation (p.Gly247Asp or G247D) in a large, multi-generational family, causing atrial-septal defect followed by late-onset dilated cardiomyopathy (DCM). 31434612 2019
Entrez Id: 70
Gene Symbol: ACTC1
ACTC1
0.190 GeneticVariation group BEFREE Using a genome-wide linkage analysis, the ASD disease locus was mapped to chromosome 15q14 harboring the ACTC1 gene. 31430208 2019
Entrez Id: 70
Gene Symbol: ACTC1
ACTC1
0.190 GeneticVariation group BEFREE A gain-of-function ACTC1 3'UTR mutation that introduces a miR-139-5p target site may be associated with a dominant familial atrial septal defect. 27139165 2016
Entrez Id: 86
Gene Symbol: ACTL6A
ACTL6A
0.100 GeneticVariation group CLINVAR
Entrez Id: 81
Gene Symbol: ACTN4
ACTN4
0.010 GeneticVariation group BEFREE ASD-associated mutations induced changes in the localization of α-actinin-4, which localized less to dendritic spines, and for SWAP-70 and SrGAP3, which localized more to dendritic spines. 30123108 2018
Entrez Id: 84890
Gene Symbol: ADO
ADO
0.010 Biomarker group BEFREE Among the 114 patients submitted to ADO II-AS implantation at our institution, 12 received this device as off-label treatment of paravalvular leak (n = 5), sinus of Valsalva fissuration (n = 2), accessory atrial septal defect (n = 2), muscular ventricular septal defect (n = 1), bleeding bronchial artery aneurysm (n = 1) and reverse shunt due to abnormal origin of left subclavian artery from pulmonary artery (n = 1). 27898501 2017
Entrez Id: 55109
Gene Symbol: AGGF1
AGGF1
0.100 Biomarker group HPO
Entrez Id: 139285
Gene Symbol: AMER1
AMER1
0.100 Biomarker group HPO