ADHDgene Database
  • Published Variant
  • Published Gene: 359
  • Published Region: 128
  • Pathway by PBA: 8
  • Study: 361

KEGG Pathway Report

Basic Info
ID hsa05412
Name Arrhythmogenic right ventricular cardiomyopathy (ARVC)
Description  Arrhythmogenic right ventricular cardiomyopathy (ARVC) is an inherited heart muscle disease that may result in arrhythmia, heart failure, and sudden death. The hallmark pathological findings are progressive myocyte loss and fibrofatty replacement, with a predilection for the right ventricle. A number of genetic studies have identified mutations in various components of the cardiac desmosome that have important roles in the pathogenesis of ARVC. Disruption of desmosomal function by defective proteins might lead to death of myocytes under mechanical stress. The myocardial injury may be accompanied by inflammation. Since regeneration of cardiac myocytes is limited, repair by fibrofatty replacement occurs. Several studies have implicated that desmosome dysfunction results in the delocalization and nuclear translocation of plakoglobin. As a result, competition between plakoglobin and beta-catenin will lead to the inhibition of Wnt/beta-catenin signaling, resulting in a shift from a myocyte fate towards an adipocyte fate of cells. The ryanodine receptor plays a crucial part in electromechanical coupling by control of release of calcium from the sarcoplasmic reticulum into the cytosol. Therefore, defects in this receptor could result in an imbalance of calcium homeostasis that might trigger cell death.
No. of Genes in ADHDgene  27
Source Pathway by Database Search

Pathway related genes in ADHDgene (count: 27)

Literature-origin genes (count: 4)

Approved Symbol Approved Name Location No. of Studies (significant/non-significant/trend)
CTNNA2 catenin (cadherin-associated protein), alpha 2 2p12-p11.1 2(1/1/0)
CACNA1C calcium channel, voltage-dependent, L type, alpha 1C subunit 12p13.3 1(0/1/0)
ITGA11 integrin, alpha 11 15q22.3-q23 1(0/0/1)
ITGA1 integrin, alpha 1 5q11.1 1(0/1/0)

Genes from other sources Help(count: 23)

Approved Symbol Approved Name Location Source
CACNG5 calcium channel, voltage-dependent, gamma subunit 5 17q24 Mapped by PBA pathway
CACNB4 calcium channel, voltage-dependent, beta 4 subunit 2q22-q23 Mapped by PBA pathway
CACNG1 calcium channel, voltage-dependent, gamma subunit 1 17q24 Mapped by PBA pathway
ACTN3 actinin, alpha 3 11q13-q14 Mapped by significant region
CACNG2 calcium channel, voltage-dependent, gamma subunit 2 22q13.1 Mapped by PBA pathway
CACNG4 calcium channel, voltage-dependent, gamma subunit 4 17q24 Mapped by PBA pathway
DES desmin 2q35 Mapped by significant region
GJA1 gap junction protein, alpha 1, 43kDa 6q22-q23 Mapped by significant region
CACNA1F calcium channel, voltage-dependent, L type, alpha 1F subunit Xp11.23 Mapped by LD-proxy; Mapped by PBA pathway; Mapped by literature SNP
CTNNA3 catenin (cadherin-associated protein), alpha 3 10q21 Mapped by CNV
CACNB1 calcium channel, voltage-dependent, beta 1 subunit 17q21-q22 Mapped by PBA pathway
CACNA2D1 calcium channel, voltage-dependent, alpha 2/delta subunit 1 7q21-q22 Mapped by PBA pathway
SGCD sarcoglycan, delta (35kDa dystrophin-associated glycoprotein) 5q33-q34 Mapped by CNV; Mapped by significant region
CACNB3 calcium channel, voltage-dependent, beta 3 subunit 12q13 Mapped by PBA pathway
CACNB2 calcium channel, voltage-dependent, beta 2 subunit 10p12 Mapped by PBA pathway
DSG2 desmoglein 2 18q12.1 Mapped by significant region
CACNA1D calcium channel, voltage-dependent, L type, alpha 1D subunit 3p14.3 Mapped by PBA pathway
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit 1q32 Mapped by PBA pathway
CDH2 cadherin 2, type 1, N-cadherin (neuronal) 18q12.1 Mapped by significant region
RYR2 ryanodine receptor 2 (cardiac) 1q43 Mapped by CNV; Mapped by PBA pathway
DSC2 desmocollin 2 18q12.1 Mapped by significant region
LAMA2 laminin, alpha 2 6q22-q23 Mapped by CNV; Mapped by significant region
ITGA2 integrin, alpha 2 (CD49B, alpha 2 subunit of VLA-2 receptor) 5q11.2 Mapped by LD-proxy