Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 7276
Gene Symbol: TTR
TTR
0.010 GeneticVariation disease BEFREE Patients with hereditary ATTR amyloidosis occasionally show electrophysiological demyelinating features without conduction block following severe axonal degeneration. 30688105 2019
Entrez Id: 79054
Gene Symbol: TRPM8
TRPM8
0.010 GeneticVariation disease BEFREE These results show that the ability of somatosensory TRP channels to promote the permeation of large cations also includes TRPM8, thereby suggesting that novel approaches to alter cold pain can also be employed via conduction block in TRPM8-positive sensory neurons. 28038937 2017
Entrez Id: 54795
Gene Symbol: TRPM4
TRPM4
0.040 Biomarker disease BEFREE Mutations in TRPM4 gene that encodes for transient receptor potential melastatin 4 have recently been reported to cause familial cases of PCCD and heart block. 29165759 2017
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 GeneticVariation disease BEFREE Aberrant Deactivation-Induced Gain of Function in TRPM4 Mutant Is Associated with Human Cardiac Conduction Block. 30021168 2018
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: 4578
Gene Symbol: TRNW
TRNW
0.100 Biomarker disease HPO
Entrez Id: 4575
Gene Symbol: TRNS2
TRNS2
0.100 Biomarker disease HPO
Entrez Id: 4574
Gene Symbol: TRNS1
TRNS1
0.100 Biomarker disease HPO
Entrez Id: 4572
Gene Symbol: TRNQ
TRNQ
0.100 Biomarker disease HPO
Entrez Id: 4567
Gene Symbol: TRNL1
TRNL1
0.100 Biomarker disease HPO
Entrez Id: 4564
Gene Symbol: TRNH
TRNH
0.100 Biomarker disease HPO
Entrez Id: 4558
Gene Symbol: TRNF
TRNF
0.100 Biomarker disease HPO
Entrez Id: 6737
Gene Symbol: TRIM21
TRIM21
0.020 Biomarker disease BEFREE In this study, we define the cellular mechanism leading to the disease and show that maternal autoantibodies directed to a specific epitope within the leucine zipper amino acid sequence 200-239 (p200) of the Ro52 protein correlate with prolongation of fetal atrioventricular (AV) time and heart block. 15630133 2005
Entrez Id: 6737
Gene Symbol: TRIM21
TRIM21
0.020 Biomarker disease BEFREE Isolated heart block in children, often associated with maternal autoimmune disease leading to anti-Ro/SS-A auto-antibody production, is an infrequent but potentially lethal disorder. 8195531 1994
Entrez Id: 7124
Gene Symbol: TNF
TNF
0.010 GeneticVariation disease LHGDN Cytokine polymorphisms and histologic expression in autopsy studies: contribution of TNF-alpha and TGF-beta 1 to the pathogenesis of autoimmune-associated congenital heart block. 12960355 2003
Entrez Id: 51284
Gene Symbol: TLR7
TLR7
0.010 Biomarker disease BEFREE Targeting downstream transcription factors and epigenetic modifications following Toll-like receptor 7/8 ligation to forestall tissue injury in anti-Ro60 associated heart block. 26432597 2016
Entrez Id: 7040
Gene Symbol: TGFB1
TGFB1
0.010 Biomarker disease LHGDN Cytokine polymorphisms and histologic expression in autopsy studies: contribution of TNF-alpha and TGF-beta 1 to the pathogenesis of autoimmune-associated congenital heart block. 12960355 2003
Entrez Id: 6625
Gene Symbol: SNRNP70
SNRNP70
0.010 Biomarker disease BEFREE While the true frequency of heart block associated with anti-U1RNP remains to be determined, this study might raise the consideration of echocardiographic surveillance in this setting. 31079145 2019
Entrez Id: 6535
Gene Symbol: SLC6A8
SLC6A8
0.010 Biomarker disease BEFREE We aimed to evaluate the feasibility of the heart block with electron compensation (HBE) technique, based on three-dimensional conformal radiotherapy (3D-CRT) in left-sided breast cancer patients with underlying cardiac or pulmonary disease. 28863179 2017
Entrez Id: 6331
Gene Symbol: SCN5A
SCN5A
0.010 GeneticVariation disease BEFREE We present clinical, genetic, and biophysical features of 2 new SCN5A mutations that result in atrioventricular (AV) conduction block. 11804990 2002
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
0.320 GeneticVariation disease BEFREE In addition, the A allele remained significant after adjusting for other covariates in a multivariate model (odds ratio = 6.30 [95% confidence interval: 2.24 to 19.09], P = 0.0005).The rs6795970 in the SCN10A gene, which is reported to carry a high risk of heart block, might be associated with cardiac conduction abnormalities in HCM patients. 26104176 2015
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
0.320 Biomarker disease CTD_human Genetic variation in SCN10A influences cardiac conduction. 20062061 2010
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
0.320 GeneticVariation disease BEFREE We have shown that the gene SCN10A encoding the sodium channel Na(v)1.8 is a susceptibility factor for heart block and serious ventricular arrhythmia. 21646736 2011
Entrez Id: 6738
Gene Symbol: RO60
RO60
0.020 Biomarker disease BEFREE Targeting downstream transcription factors and epigenetic modifications following Toll-like receptor 7/8 ligation to forestall tissue injury in anti-Ro60 associated heart block. 26432597 2016