Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4607
Gene Symbol: MYBPC3
MYBPC3
0.100 CausalMutation disease CLINVAR
Entrez Id: 54795
Gene Symbol: TRPM4
TRPM4
0.040 AlteredExpression disease BEFREE Transient receptor potential cation channel subfamily melastatin member 4 (TRPM4), a Ca2+-activated nonselective cation channel abundantly expressed in the heart, has been implicated in conduction block and other arrhythmic propensities associated with cardiac remodelling and injury. 28898995 2017
Entrez Id: 54795
Gene Symbol: TRPM4
TRPM4
0.040 AlteredExpression disease BEFREE This study suggests that in Purkinje fibers, TRPM4 channels may account for sodium background current (I<sub>Nab</sub>), and that a heterogeneous expression of TRPM4 channels in the His/Purkinje system is required for type II heart block, as seen clinically. 30598284 2019
Entrez Id: 93649
Gene Symbol: MYOCD
MYOCD
0.010 AlteredExpression disease BEFREE Forced myocardin expression also endowed human MSFs with the ability to transmit an action potential and to repair an artificially created conduction block in cardiomyocyte cultures. 17579192 2007
Entrez Id: 4179
Gene Symbol: CD46
CD46
0.010 AlteredExpression disease BEFREE To examine fetal characteristics which might influence autoantibody-mediated diseases acquired in utero, such as heart block in neonatal lupus, the tissue expression of MCP was studied. 8528226 1995
Entrez Id: 822
Gene Symbol: CAPG
CAPG
0.010 AlteredExpression disease BEFREE To examine fetal characteristics which might influence autoantibody-mediated diseases acquired in utero, such as heart block in neonatal lupus, the tissue expression of MCP was studied. 8528226 1995
Entrez Id: 3762
Gene Symbol: KCNJ5
KCNJ5
0.300 Therapeutic disease CTD_human G protein-gated IKACh channels as therapeutic targets for treatment of sick sinus syndrome and heart block. 26831068 2016
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
0.330 Biomarker disease CTD_human Familial progressive sinoatrial and atrioventricular conduction disease of adult onset with sudden death, dilated cardiomyopathy, and brachydactyly. A new type of heart-hand syndrome? 15996213 2005
Entrez Id: 4000
Gene Symbol: LMNA
LMNA
0.330 Biomarker disease BEFREE The early diagnosis of LMNA-associated muscular dystrophy is important for preventing sudden arrest related to cardiac conduction block. 29057633 2017
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
0.320 Biomarker disease CTD_human Genetic variation in SCN10A influences cardiac conduction. 20062061 2010
Entrez Id: 776
Gene Symbol: CACNA1D
CACNA1D
0.300 Biomarker disease CTD_human G protein-gated IKACh channels as therapeutic targets for treatment of sick sinus syndrome and heart block. 26831068 2016
Entrez Id: 56244
Gene Symbol: BTNL2
BTNL2
0.100 Biomarker disease HPO
Entrez Id: 5264
Gene Symbol: PHYH
PHYH
0.100 Biomarker disease HPO
Entrez Id: 4540
Gene Symbol: ND5
ND5
0.100 Biomarker disease HPO
Entrez Id: 4513
Gene Symbol: COX2
COX2
0.100 Biomarker disease HPO
Entrez Id: 5191
Gene Symbol: PEX7
PEX7
0.100 Biomarker disease HPO
Entrez Id: 4564
Gene Symbol: TRNH
TRNH
0.100 Biomarker disease HPO
Entrez Id: 4535
Gene Symbol: ND1
ND1
0.100 Biomarker disease HPO
Entrez Id: 4572
Gene Symbol: TRNQ
TRNQ
0.100 Biomarker disease HPO
Entrez Id: 4558
Gene Symbol: TRNF
TRNF
0.100 Biomarker disease HPO
Entrez Id: 6023
Gene Symbol: RMRP
RMRP
0.100 Biomarker disease HPO
Entrez Id: 4538
Gene Symbol: ND4
ND4
0.100 Biomarker disease HPO
Entrez Id: 4514
Gene Symbol: COX3
COX3
0.100 Biomarker disease HPO
Entrez Id: 4574
Gene Symbol: TRNS1
TRNS1
0.100 Biomarker disease HPO
Entrez Id: 4541
Gene Symbol: ND6
ND6
0.100 Biomarker disease HPO