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Conduction disorder of the heart
Conduction disorder of the heart
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Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
CONDUCTION DISORDER OF THE HEART
C0264886
CACNA1C
Causal
—
Disgenet
MAPK signaling pathway
Calcium signaling pathway
cGMP-PKG signaling pathway
cAMP signaling pathway
Cardiac muscle contraction
Adrenergic signaling in cardiomyocytes
Vascular smooth muscle contraction
Circadian entrainment
Long-term potentiation
Retrograde endocannabinoid signaling
Glutamatergic synapse
Cholinergic synapse
Serotonergic synapse
GABAergic synapse
Dopaminergic synapse
Taste transduction
Insulin secretion
GnRH signaling pathway
Oxytocin signaling pathway
Renin secretion
Aldosterone synthesis and secretion
Cortisol synthesis and secretion
GnRH secretion
Type II diabetes mellitus
Cushing syndrome
Growth hormone synthesis, secretion and action
Alzheimer disease
Prion disease
Pathways of neurodegeneration - multiple diseases
Amphetamine addiction
Chemical carcinogenesis - receptor activation
Hypertrophic cardiomyopathy
Arrhythmogenic right ventricular cardiomyopathy
Dilated cardiomyopathy
Regulation of insulin secretion
Phase 0 - rapid depolarisation
Phase 2 - plateau phase
+34 more
FLNC
Causal
—
Disgenet
Cytoskeleton in muscle cells
Cell-extracellular matrix interactions
RYR2
Causal
—
Disgenet
Calcium signaling pathway
cAMP signaling pathway
Cardiac muscle contraction
Adrenergic signaling in cardiomyocytes
Apelin signaling pathway
Circadian entrainment
Insulin secretion
Oxytocin signaling pathway
Pancreatic secretion
Prion disease
Pathways of neurodegeneration - multiple diseases
Hypertrophic cardiomyopathy
Arrhythmogenic right ventricular cardiomyopathy
Dilated cardiomyopathy
Diabetic cardiomyopathy
Stimuli-sensing channels
Ion homeostasis
+14 more
All
24
Causal
3
Unknown
21
Select all
Clear
ClinVar
0
Orphanet
0
Disgenet
3
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
0
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Ventricular fibrillation
13 shared genes
DSG2, JUP, PKP2, RBM20, TRPM4, DSP, CACNA1C, MYH6, KCNH2, RYR2, SCN5A, TTN +1 more
Related via 13 shared genes including DSG2, JUP, PKP2.
Catecholaminergic polymorphic ventricular tachycardia
9 shared genes
DSG2, PKP2, TRPM4, DSP, CASQ2, KCNH2, RYR2, SCN5A, ANK2
Related via 9 shared genes including DSG2, PKP2, TRPM4.
Wolff-parkinson-white syndrome
15 shared genes
JUP, RBM20, TRPM4, DSP, CACNA1C, MYH6, CASQ2, FLNC, KCNH2, KCNQ1, RYR2, SCN5A +3 more
Related via 15 shared genes including JUP, RBM20, TRPM4.
Arrhythmogenic right ventricular cardiomyopathy
14 shared genes
DMD, DSG2, JUP, PKP2, RBM20, TRPM4, DSP, MYH6, FLNC, RYR2, SCN5A, MYH7 +2 more
Related via 14 shared genes including DMD, DSG2, JUP.
Arrhythmogenic right ventricular dysplasia
7 shared genes
DSG2, JUP, PKP2, DSP, RYR2, SCN5A, MYH7
Related via 7 shared genes including DSG2, JUP, PKP2.
1
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