Disease Clusters?
Groups of diseases that share a large number of curated genes with each other, computed via label propagation over the shared-gene similarity graph. See also Shared-Gene Disease Pairs for pairwise comparisons.
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Cluster 3
49
Diseases
797
Unique genes
0.111
Avg. similarity score
Arrhythmogenic right ventricular cardiomyopathy
Most-connected disease (20 links)
Disease
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Arrhythmogenic right ventricular cardiomyopathy
Left ventricular noncompaction cardiomyopathy
Wolff-parkinson-white syndrome
Conduction disorder of the heart
Long qt syndrome
Cardiomyopathy
Arrhythmogenic right ventricular dysplasia
Cardiac arrest
Catecholaminergic polymorphic ventricular tachycardia
Dilated cardiomyopathy
Left ventricular disease
Ventricular fibrillation
Brugada syndrome
Cardiac conduction disease
Hereditary bundle branch system defect
Hypertrophic cardiomyopathy
Sick sinus syndrome
Restrictive cardiomyopathy
Atrioventricular block
Cardiac arrhythmia
Paroxysmal familial ventricular fibrillation
Polymorphic catecholaminergic ventricular tachycardia
dilated cardiomyopathy 1BB
dilated cardiomyopathy 1CC
dilated cardiomyopathy 1JJ
Atrial flutter
Atrial tachyarrhythmia, infra-hisian cardiac conduction disease
Barth syndrome
Hereditary atrial fibrillation
Myofibrillar myopathy
dilated cardiomyopathy 1Z
familial isolated arrhythmogenic right ventricular dysplasia
intrinsic cardiomyopathy
Bronchial disease
cardiomyopathy, dilated, 2e
dilated cardiomyopathy 1HH
dilated cardiomyopathy 1I
dilated cardiomyopathy 1M
dilated cardiomyopathy 1Y
sick sinus syndrome 2, autosomal dominant
Vici syndrome
lissencephaly 10
5-oxoprolinase deficiency
Congenital right-sided heart lesions
FNIP1-associated syndrome
Hypertrophy
cardiomyopathy, dilated, 2h
hypokalemic alkalosis, familial, with specific renal tubulopathy
myofibrillar myopathy 8
Member diseases (most connected first ‐ the cluster's core)
Top shared genes (genes linked to 2+ member diseases ‐ top 100 shown, download for all)
| Gene ⇵ | Member diseases ⇵ | Linked diseases |
|---|---|---|
| SCN5A | 21 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Arrhythmogenic right ventricular dysplasia, Atrial flutter, Brugada syndrome and 17 more |
| TTN | 19 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Arrhythmogenic right ventricular dysplasia, Atrial flutter, Atrioventricular block and 15 more |
| DSP | 18 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Arrhythmogenic right ventricular dysplasia, Brugada syndrome, Cardiac arrest and 14 more |
| RYR2 | 17 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Arrhythmogenic right ventricular dysplasia, Brugada syndrome, Cardiac arrest and 13 more |
| MYH6 | 16 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Atrial flutter, Cardiac arrest, Cardiac arrhythmia and 12 more |
| PKP2 | 14 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Arrhythmogenic right ventricular dysplasia, Brugada syndrome, Cardiac arrhythmia and 10 more |
| TRPM4 | 14 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Atrioventricular block, Brugada syndrome, Cardiac arrest and 10 more |
| ANK2 | 13 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Brugada syndrome, Cardiac arrest, Cardiac arrhythmia and 9 more |
| LMNA | 13 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Atrioventricular block, Cardiac arrhythmia, Cardiac conduction disease and 9 more |
| DSG2 | 12 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Arrhythmogenic right ventricular dysplasia, Cardiac arrest, Cardiomyopathy and 8 more |
| HCN4 | 12 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Atrial flutter, Brugada syndrome, Cardiac arrest and 8 more |
| MYH7 | 12 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Arrhythmogenic right ventricular dysplasia, Cardiac arrhythmia, Cardiomyopathy and 8 more |
| CACNA1C | 11 / 49 | Brugada syndrome, Cardiac arrhythmia, Cardiomyopathy, Conduction disorder of the heart and 7 more |
| JUP | 11 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Arrhythmogenic right ventricular dysplasia, Cardiomyopathy, Conduction disorder of the heart and 7 more |
| MYBPC3 | 11 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Brugada syndrome, Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia and 7 more |
| CASQ2 | 10 / 49 | Atrial flutter, Cardiac arrhythmia, Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia and 6 more |
| KCNH2 | 10 / 49 | Atrial flutter, Brugada syndrome, Cardiac arrhythmia, Cardiomyopathy and 6 more |
| FLNC | 9 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Cardiac arrhythmia, Cardiomyopathy, Conduction disorder of the heart and 5 more |
| KCNJ2 | 9 / 49 | Brugada syndrome, Cardiac arrhythmia, Catecholaminergic polymorphic ventricular tachycardia, Hereditary atrial fibrillation and 5 more |
| LDB3 | 9 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Arrhythmogenic right ventricular dysplasia, Cardiomyopathy, Dilated cardiomyopathy and 5 more |
| RBM20 | 9 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Conduction disorder of the heart, Dilated cardiomyopathy and 5 more |
| SCN1B | 9 / 49 | Brugada syndrome, Cardiac arrhythmia, Cardiac conduction disease, Cardiomyopathy and 5 more |
| ABCC9 | 8 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Brugada syndrome, Cardiomyopathy, Dilated cardiomyopathy and 4 more |
| ACTC1 | 8 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy and 4 more |
| BAG3 | 8 / 49 | Arrhythmogenic right ventricular dysplasia, Atrioventricular block, Cardiomyopathy, Dilated cardiomyopathy and 4 more |
| CACNB2 | 8 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Brugada syndrome, Cardiac arrest, Cardiac conduction disease and 4 more |
| CEP85L | 8 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Atrial flutter, Cardiac arrest, Cardiac arrhythmia and 4 more |
| DSC2 | 8 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Arrhythmogenic right ventricular dysplasia, Cardiomyopathy, Dilated cardiomyopathy and 4 more |
| LAMA4 | 8 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Brugada syndrome, Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia and 4 more |
| NEXN | 8 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Dilated cardiomyopathy, dilated cardiomyopathy 1CC and 4 more |
| NKX2-5 | 8 / 49 | Atrial flutter, Atrioventricular block, Dilated cardiomyopathy, Hereditary atrial fibrillation and 4 more |
| TNNT2 | 8 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy and 4 more |
| ACTN2 | 7 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy and 3 more |
| AKAP9 | 7 / 49 | Brugada syndrome, Cardiac arrest, Dilated cardiomyopathy, Hypertrophic cardiomyopathy and 3 more |
| DMD | 7 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Conduction disorder of the heart, Dilated cardiomyopathy and 3 more |
| JPH2 | 7 / 49 | Cardiomyopathy, cardiomyopathy, dilated, 2e, Dilated cardiomyopathy, Hypertrophic cardiomyopathy and 3 more |
| KCNQ1 | 7 / 49 | Brugada syndrome, Cardiac arrhythmia, Conduction disorder of the heart, Hereditary atrial fibrillation and 3 more |
| PLN | 7 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Cardiac arrest, Cardiac arrhythmia, Cardiomyopathy and 3 more |
| SCN10A | 7 / 49 | Atrial flutter, Atrioventricular block, Brugada syndrome, Cardiac arrhythmia and 3 more |
| TBX5 | 7 / 49 | Atrial flutter, Atrioventricular block, Brugada syndrome, Cardiac arrhythmia and 3 more |
| TMEM43 | 7 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Arrhythmogenic right ventricular dysplasia, Cardiomyopathy, Dilated cardiomyopathy and 3 more |
| TNNI3 | 7 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy and 3 more |
| TPM1 | 7 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Dilated cardiomyopathy, dilated cardiomyopathy 1Y and 3 more |
| AGT | 6 / 49 | Cardiac arrhythmia, Cardiomyopathy, Hypertrophic cardiomyopathy, Hypertrophy and 2 more |
| CTNNA3 | 6 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Arrhythmogenic right ventricular dysplasia, Cardiomyopathy, Dilated cardiomyopathy and 2 more |
| DES | 6 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Atrioventricular block, Dilated cardiomyopathy, dilated cardiomyopathy 1I and 2 more |
| DPP6 | 6 / 49 | Cardiac arrest, Dilated cardiomyopathy, Long qt syndrome, Paroxysmal familial ventricular fibrillation and 2 more |
| DTNA | 6 / 49 | Cardiac arrhythmia, Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy and 2 more |
| KCNE1 | 6 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Dilated cardiomyopathy, Hereditary atrial fibrillation and 2 more |
| KCNE2 | 6 / 49 | Cardiac arrhythmia, Cardiomyopathy, Dilated cardiomyopathy, Hereditary atrial fibrillation and 2 more |
| MYL3 | 6 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy and 2 more |
| MYPN | 6 / 49 | Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy, Left ventricular disease and 2 more |
| NEBL | 6 / 49 | Cardiac arrest, Cardiac arrhythmia, Cardiomyopathy, Dilated cardiomyopathy and 2 more |
| PITX2 | 6 / 49 | Atrial flutter, Cardiac arrhythmia, Dilated cardiomyopathy, Hereditary atrial fibrillation and 2 more |
| PRDM16 | 6 / 49 | Cardiomyopathy, Dilated cardiomyopathy, Left ventricular disease, Left ventricular noncompaction cardiomyopathy and 2 more |
| PRKAG2 | 6 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy and 2 more |
| SNTA1 | 6 / 49 | Brugada syndrome, Dilated cardiomyopathy, Long qt syndrome, Sick sinus syndrome and 2 more |
| SYNE2 | 6 / 49 | Atrial flutter, Cardiac arrhythmia, Dilated cardiomyopathy, Left ventricular disease and 2 more |
| VCL | 6 / 49 | Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy, Long qt syndrome and 2 more |
| ANKRD1 | 5 / 49 | Brugada syndrome, Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy and 1 more |
| CALM3 | 5 / 49 | Cardiac arrhythmia, Cardiomyopathy, Catecholaminergic polymorphic ventricular tachycardia, Long qt syndrome and 1 more |
| CDKN1A | 5 / 49 | Atrial flutter, Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy and 1 more |
| KCNJ5 | 5 / 49 | Atrial flutter, Hereditary atrial fibrillation, Hypertrophic cardiomyopathy, Long qt syndrome and 1 more |
| KCNJ8 | 5 / 49 | Brugada syndrome, Cardiac arrest, Cardiac arrhythmia, Long qt syndrome and 1 more |
| MYH7B | 5 / 49 | Brugada syndrome, Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy and 1 more |
| MYL2 | 5 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy and 1 more |
| MYOM1 | 5 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Cardiac arrest, Cardiomyopathy, Dilated cardiomyopathy and 1 more |
| RAF1 | 5 / 49 | Cardiac arrhythmia, Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy and 1 more |
| TAFAZZIN | 5 / 49 | Barth syndrome, Cardiomyopathy, Dilated cardiomyopathy, Left ventricular disease and 1 more |
| TCAP | 5 / 49 | Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy, Left ventricular noncompaction cardiomyopathy and 1 more |
| TGFB3 | 5 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Arrhythmogenic right ventricular dysplasia, Brugada syndrome, Hypertrophic cardiomyopathy and 1 more |
| TNNC1 | 5 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Dilated cardiomyopathy, dilated cardiomyopathy 1Z and 1 more |
| TNNI3K | 5 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Atrial tachyarrhythmia, infra-hisian cardiac conduction disease, Bronchial disease, Cardiac conduction disease and 1 more |
| TRDN | 5 / 49 | Cardiac arrhythmia, Catecholaminergic polymorphic ventricular tachycardia, Hypertrophic cardiomyopathy, Long qt syndrome and 1 more |
| ACTA1 | 4 / 49 | Dilated cardiomyopathy, Hypertrophy, Left ventricular disease, Restrictive cardiomyopathy |
| C2ORF49 | 4 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Dilated cardiomyopathy, Left ventricular noncompaction cardiomyopathy |
| CACNA2D1 | 4 / 49 | Brugada syndrome, Cardiac arrest, Long qt syndrome, Ventricular fibrillation |
| CALM1 | 4 / 49 | Cardiac arrhythmia, Catecholaminergic polymorphic ventricular tachycardia, Long qt syndrome, Polymorphic catecholaminergic ventricular tachycardia |
| CALM2 | 4 / 49 | Cardiac arrhythmia, Catecholaminergic polymorphic ventricular tachycardia, Long qt syndrome, Polymorphic catecholaminergic ventricular tachycardia |
| CALR3 | 4 / 49 | Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy, Restrictive cardiomyopathy |
| CAV3 | 4 / 49 | Brugada syndrome, Cardiomyopathy, Hypertrophic cardiomyopathy, Long qt syndrome |
| COL1A1 | 4 / 49 | Dilated cardiomyopathy, Hypertrophic cardiomyopathy, Hypertrophy, Left ventricular disease |
| CRYAB | 4 / 49 | Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy, Myofibrillar myopathy |
| CSRP3 | 4 / 49 | Cardiomyopathy, Dilated cardiomyopathy, dilated cardiomyopathy 1M, Hypertrophic cardiomyopathy |
| EDN1 | 4 / 49 | Cardiac arrhythmia, Cardiomyopathy, Hypertrophy, Left ventricular disease |
| FHL2 | 4 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Dilated cardiomyopathy, Left ventricular noncompaction cardiomyopathy |
| FPGT-TNNI3K | 4 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Bronchial disease, Cardiac conduction disease, Dilated cardiomyopathy |
| GAA | 4 / 49 | Cardiomyopathy, Hypertrophic cardiomyopathy, Hypertrophy, Left ventricular disease |
| GJA5 | 4 / 49 | Atrial flutter, Hereditary atrial fibrillation, Hypertrophic cardiomyopathy, Wolff-parkinson-white syndrome |
| GPD1L | 4 / 49 | Brugada syndrome, Dilated cardiomyopathy, Long qt syndrome, Wolff-parkinson-white syndrome |
| INS | 4 / 49 | Cardiac arrest, Cardiomyopathy, Hypertrophic cardiomyopathy, Ventricular fibrillation |
| MAPT | 4 / 49 | Atrial flutter, Cardiac arrhythmia, Cardiomyopathy, Dilated cardiomyopathy |
| MYC | 4 / 49 | Cardiomyopathy, Hypertrophic cardiomyopathy, Hypertrophy, Left ventricular disease |
| MYLK2 | 4 / 49 | Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy, Left ventricular noncompaction cardiomyopathy |
| NPPA | 4 / 49 | Dilated cardiomyopathy, Hereditary atrial fibrillation, Hypertrophy, Left ventricular disease |
| OBSCN | 4 / 49 | Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Dilated cardiomyopathy, Hypertrophic cardiomyopathy |
| POMC | 4 / 49 | Cardiomyopathy, Hypertrophic cardiomyopathy, Long qt syndrome, Sick sinus syndrome |
| SCN3B | 4 / 49 | Brugada syndrome, Cardiac arrhythmia, Hereditary atrial fibrillation, Long qt syndrome |
| SCN4B | 4 / 49 | Catecholaminergic polymorphic ventricular tachycardia, Dilated cardiomyopathy, Hereditary atrial fibrillation, Long qt syndrome |
| SLC25A4 | 4 / 49 | Dilated cardiomyopathy, Hypertrophic cardiomyopathy, Left ventricular disease, Restrictive cardiomyopathy |
What do these columns mean?
- Connections in cluster
- How many other members this disease has a shared-gene link to (the node size in the network above). The most-connected diseases are the cluster's core.
- Significant partners
- How many of those links are statistically significant (FDR q < 0.05).
- Curated genes
- Distinct curated genes linked to that disease in GeDiPNet.
- Member diseases (Top shared genes)
- How many of this cluster's diseases are linked to the gene, out of the cluster's total. Genes shared by many members are the most direct explanation of why they group together.
- Overlap genes (x / y)
- x = genes shared between this cluster and the pathway/GO term; y = that pathway/GO term's total gene count. A higher x relative to y (and to the cluster's own size) means a tighter biological match.
- Cluster gene count
- Total distinct genes across every disease in this cluster -- the "n" used in the significance test below.
- Fold enrichment
- Observed overlap divided by the overlap expected by chance, given the cluster's gene count, the pathway/term's size and the gene universe tested. 5× means five times more shared genes than random. Tells strong hits apart when q-values are all vanishingly small.
- P-value / FDR q-value
- Is this pathway/GO term's overlap with the cluster more than chance? Upper-tail hypergeometric test, Benjamini-Hochberg corrected across every tested pathway/term (prefer the q-value -- it accounts for testing many at once).
- Shared genes (Pairs within this cluster)
- Number of curated genes the two diseases in that row have in common.
- Similarity score (Pairs within this cluster)
- Jaccard-based gene overlap between the two specific diseases in that row -- same metric as the main Shared-Gene Disease Pairs page.
Enriched Pathways (why this cluster is grouped, biologically)
| Pathway ⇵ | Source ⇵ | Overlap genes ⇵ | Fold enrichment ⇵ | P-value ⇵ | FDR q-value ⇵ |
|---|---|---|---|---|---|
| Cytoskeleton in muscle cells | KEGG | 74 / 232 | 4.8× | 9.53e-32 | 3.09e-28 ✓ sig. |
| Hypertrophic cardiomyopathy | KEGG | 39 / 99 | 5.9× | 5.61e-21 | 5.21e-18 ✓ sig. |
| Dilated cardiomyopathy | KEGG | 37 / 105 | 5.3× | 4.80e-18 | 2.80e-15 ✓ sig. |
| Adrenergic signaling in cardiomyocytes | KEGG | 45 / 154 | 4.4× | 5.17e-18 | 2.96e-15 ✓ sig. |
| Proteoglycans in cancer | KEGG | 48 / 204 | 3.5× | 5.19e-15 | 1.74e-12 ✓ sig. |
| Oxytocin signaling pathway | KEGG | 41 / 154 | 4.0× | 5.76e-15 | 1.92e-12 ✓ sig. |
| Striated Muscle Contraction | Reactome | 20 / 36 | 8.4× | 5.78e-15 | 1.92e-12 ✓ sig. |
| Arrhythmogenic right ventricular cardiomyopathy | KEGG | 30 / 86 | 5.3× | 9.69e-15 | 3.04e-12 ✓ sig. |
| cGMP-PKG signaling pathway | KEGG | 42 / 166 | 3.8× | 1.86e-14 | 5.47e-12 ✓ sig. |
| Phase 0 - rapid depolarisation | Reactome | 19 / 44 | 6.5× | 9.72e-12 | 1.75e-9 ✓ sig. |
| Calcium signaling pathway | KEGG | 48 / 254 | 2.8× | 2.82e-11 | 4.57e-9 ✓ sig. |
| Lipid and atherosclerosis | KEGG | 43 / 216 | 3.0× | 5.42e-11 | 8.25e-9 ✓ sig. |
| Cardiac muscle contraction | KEGG | 25 / 87 | 4.3× | 2.04e-10 | 2.74e-8 ✓ sig. |
| Renin secretion | KEGG | 22 / 69 | 4.8× | 2.70e-10 | 3.53e-8 ✓ sig. |
| Glioma | KEGG | 23 / 76 | 4.6× | 3.45e-10 | 4.40e-8 ✓ sig. |
Enriched GO Terms (Biological Process, a second line of biological evidence)
| GO term ⇵ | GO ID ⇵ | Overlap genes ⇵ | Fold enrichment ⇵ | P-value ⇵ | FDR q-value ⇵ |
|---|---|---|---|---|---|
| regulation of heart rate by cardiac conduction | GO:0086091 | 35 / 43 | 19.1× | 5.66e-41 | 6.60e-37 ✓ sig. |
| cardiac muscle contraction | GO:0060048 | 35 / 43 | 19.1× | 5.66e-41 | 6.60e-37 ✓ sig. |
| sarcomere organization | GO:0045214 | 27 / 43 | 14.7× | 9.20e-27 | 3.39e-23 ✓ sig. |
| heart development | GO:0007507 | 60 / 273 | 5.2× | 2.30e-26 | 8.22e-23 ✓ sig. |
| ventricular cardiac muscle cell action potential | GO:0086005 | 16 / 17 | 22.1× | 1.69e-21 | 3.31e-18 ✓ sig. |
| muscle contraction | GO:0006936 | 30 / 85 | 8.3× | 4.17e-20 | 7.01e-17 ✓ sig. |
| regulation of ventricular cardiac muscle cell membrane repolarization | GO:0060307 | 16 / 21 | 17.9× | 1.73e-18 | 2.23e-15 ✓ sig. |
| regulation of heart rate | GO:0002027 | 20 / 39 | 12.0× | 1.01e-17 | 1.17e-14 ✓ sig. |
| membrane repolarization during ventricular cardiac muscle cell action potential | GO:0098915 | 12 / 13 | 21.6× | 4.18e-16 | 3.53e-13 ✓ sig. |
| regulation of ventricular cardiac muscle cell action potential | GO:0098911 | 11 / 11 | 23.4× | 7.95e-16 | 6.33e-13 ✓ sig. |
| cardiac muscle cell action potential involved in contraction | GO:0086002 | 15 / 24 | 14.7× | 2.26e-15 | 1.67e-12 ✓ sig. |
| vasodilation | GO:0042311 | 19 / 50 | 8.9× | 6.58e-14 | 3.72e-11 ✓ sig. |
| regulation of cardiac muscle contraction | GO:0055117 | 14 / 24 | 13.7× | 7.77e-14 | 4.36e-11 ✓ sig. |
| cardiac muscle cell development | GO:0055013 | 14 / 25 | 13.1× | 1.70e-13 | 8.98e-11 ✓ sig. |
| positive regulation of gene expression | GO:0010628 | 61 / 504 | 2.8× | 1.76e-13 | 9.29e-11 ✓ sig. |