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Cluster 458

6 diseases · 7 shared-gene connections
6 Diseases
17 Unique genes
0.205 Avg. similarity score
Genetic peripheral neuropathy Most-connected disease (4 links)
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Disease Pinned (dragged)
Node size = connections within this cluster · edge thickness = similarity strength · hover an edge for its details · click a node to select it and show its pairs below (double-click or Ctrl/⌘-click opens the disease page) · drag a node to pin it in place · scroll/pinch to zoom.

Member diseases (most connected first ‐ the cluster's core)

Top shared genes (genes linked to 2+ member diseases)

Gene ⇵ Member diseases ⇵ Linked diseases
TRPA1 4 / 6 Benign fasciculation-cramp syndrome, Bronchial hyperreactivity, Cramp-fasciculation syndrome, Genetic peripheral neuropathy
ARHGEF10 2 / 6 Genetic peripheral neuropathy, Slowed nerve conduction velocity
HSPB1 2 / 6 Charcot-Marie-Tooth disease axonal type 2F, Genetic peripheral neuropathy
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 ⇵
Cytokine-cytokine receptor interaction KEGG 7 / 298 16.6× 8.48e-8 4.83e-6 ✓ sig.
Interleukin-10 signaling Reactome 4 / 47 60.1× 4.72e-7 2.17e-5 ✓ sig.
Chemokine receptors bind chemokines Reactome 3 / 59 35.9× 7.29e-5 1.48e-3 ✓ sig.
IL-17 signaling pathway KEGG 3 / 94 22.5× 2.92e-4 4.41e-3 ✓ sig.
Rheumatoid arthritis KEGG 3 / 95 22.3× 3.01e-4 4.52e-3 ✓ sig.
Viral protein interaction with cytokine and cytokine receptor KEGG 3 / 100 21.2× 3.50e-4 5.07e-3 ✓ sig.
NF-kappa B signaling pathway KEGG 3 / 105 20.2× 4.04e-4 5.66e-3 ✓ sig.
Interleukin-4 and Interleukin-13 signaling Reactome 3 / 108 19.6× 4.39e-4 6.03e-3 ✓ sig.
TNF signaling pathway KEGG 3 / 119 17.8× 5.83e-4 7.52e-3 ✓ sig.
COX reactions Reactome 1 / 1 706× 1.42e-3 1.47e-2 ✓ sig.
Malaria KEGG 2 / 50 28.3× 2.22e-3 2.06e-2 ✓ sig.
Chemokine signaling pathway KEGG 3 / 193 11.0× 2.35e-3 2.15e-2 ✓ sig.
TRKA activation by NGF Reactome 1 / 2 353× 2.83e-3 2.44e-2 ✓ sig.
NFG and proNGF binds to p75NTR Reactome 1 / 2 353× 2.83e-3 2.44e-2 ✓ sig.
Lipid and atherosclerosis KEGG 3 / 216 9.8× 3.24e-3 2.69e-2 ✓ 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 ⇵
antimicrobial humoral immune response mediated by antimicrobial peptide GO:0061844 6 / 124 53.2× 8.81e-10 2.08e-7 ✓ sig.
sensory perception of pain GO:0019233 4 / 44 99.9× 6.22e-8 8.53e-6 ✓ sig.
inflammatory response GO:0006954 7 / 467 16.5× 9.11e-8 1.17e-5 ✓ sig.
antifungal humoral response GO:0019732 3 / 13 254× 1.78e-7 2.05e-5 ✓ sig.
immune response GO:0006955 7 / 543 14.2× 2.54e-7 2.77e-5 ✓ sig.
response to yeast GO:0001878 3 / 16 206× 3.48e-7 3.60e-5 ✓ sig.
antibacterial humoral response GO:0019731 3 / 65 50.7× 2.64e-5 1.13e-3 ✓ sig.
regulation of blood pressure GO:0008217 3 / 83 39.7× 5.49e-5 1.98e-3 ✓ sig.
cellular response to oxygen-containing compound GO:1901701 2 / 16 137× 9.28e-5 2.92e-3 ✓ sig.
killing of cells of another organism GO:0031640 3 / 104 31.7× 1.08e-4 3.26e-3 ✓ sig.
defense response to Gram-negative bacterium GO:0050829 3 / 106 31.1× 1.14e-4 3.40e-3 ✓ sig.
response to pain GO:0048265 2 / 19 116× 1.32e-4 3.77e-3 ✓ sig.
eosinophil chemotaxis GO:0048245 2 / 20 110× 1.47e-4 4.07e-3 ✓ sig.
positive regulation of macrophage activation GO:0043032 2 / 21 105× 1.62e-4 4.37e-3 ✓ sig.
defense response to Gram-positive bacterium GO:0050830 3 / 135 24.4× 2.33e-4 5.65e-3 ✓ sig.

Pairs within this cluster, by significance

Disease A ⇵ Disease B ⇵ Similarity score ⇵ Shared genes ⇵ P-value ⇵ FDR q-value ⇵
Benign fasciculation-cramp syndrome Cramp-fasciculation syndrome 0.500 1 6.46e-5 1.98e-4 ✓ sig.
Benign fasciculation-cramp syndrome Genetic peripheral neuropathy 0.200 1 2.58e-4 5.38e-4 ✓ sig.
Charcot-Marie-Tooth disease axonal type 2F Genetic peripheral neuropathy 0.200 1 2.58e-4 5.38e-4 ✓ sig.
Cramp-fasciculation syndrome Genetic peripheral neuropathy 0.200 1 2.58e-4 5.38e-4 ✓ sig.
Genetic peripheral neuropathy Slowed nerve conduction velocity 0.200 1 2.58e-4 5.38e-4 ✓ sig.
Benign fasciculation-cramp syndrome Bronchial hyperreactivity 0.067 1 9.04e-4 1.41e-3 ✓ sig.
Bronchial hyperreactivity Cramp-fasciculation syndrome 0.067 1 9.04e-4 1.41e-3 ✓ sig.