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Cluster 341

6 diseases · 9 shared-gene connections
6 Diseases
39 Unique genes
0.159 Avg. similarity score
Intellectual developmental disorder expressive speech dysmorphic 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
SETBP1 5 / 6 Bundle branch block, Coronary aneurysm, Intellectual developmental disorder expressive speech dysmorphic, Intellectual developmental disorder speech dysmorphic and 1 more
DOCK2 2 / 6 Coronary aneurysm, Dock2 deficiency
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 ⇵
Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane Reactome 2 / 18 34.2× 1.52e-3 1.87e-2 ✓ sig.
Defective MAN1B1 causes MRT15 Reactome 1 / 1 308× 3.25e-3 3.26e-2 ✓ sig.
Regulation of gap junction activity Reactome 1 / 3 103× 9.71e-3 6.74e-2
Assembly and cell surface presentation of NMDA receptors Reactome 1 / 6 51.3× 1.93e-2 1.01e-1
Nef and signal transduction Reactome 1 / 8 38.5× 2.57e-2 1.18e-1
Ca2+ activated K+ channels Reactome 1 / 9 34.2× 2.89e-2 1.26e-1
Gap junction KEGG 2 / 89 6.9× 3.37e-2 1.38e-1
Formation of annular gap junctions Reactome 1 / 11 28.0× 3.52e-2 1.41e-1
Gap junction degradation Reactome 1 / 12 25.7× 3.83e-2 1.48e-1
mRNA decay by 5' to 3' exoribonuclease Reactome 1 / 14 22.0× 4.45e-2 1.61e-1
Calcium signaling pathway KEGG 3 / 254 3.6× 4.89e-2 1.69e-1
Gap junction assembly Reactome 1 / 18 17.1× 5.69e-2 1.84e-1
Cilium Assembly Reactome 1 / 19 16.2× 6.00e-2 1.88e-1
ER Quality Control Compartment (ERQC) Reactome 1 / 21 14.7× 6.61e-2 1.98e-1
Carboxyterminal post-translational modifications of tubulin Reactome 1 / 27 11.4× 8.42e-2 2.26e-1

Enriched GO Terms (Biological Process, a second line of biological evidence)

GO term ⇵ GO ID ⇵ Overlap genes ⇵ Fold enrichment ⇵ P-value ⇵ FDR q-value ⇵
nervous system development GO:0007399 7 / 631 5.3× 2.90e-4 6.56e-3 ✓ sig.
cerebral cortex radially oriented cell migration GO:0021799 2 / 13 73.7× 3.26e-4 7.11e-3 ✓ sig.
prepulse inhibition GO:0060134 2 / 14 68.5× 3.80e-4 7.90e-3 ✓ sig.
cochlea morphogenesis GO:0090103 2 / 28 34.2× 1.55e-3 1.95e-2 ✓ sig.
brain development GO:0007420 4 / 244 7.9× 1.63e-3 2.01e-2 ✓ sig.
regulation of granulocyte chemotaxis GO:0071622 1 / 1 479× 2.09e-3 2.31e-2 ✓ sig.
regulation of systemic arterial blood pressure by baroreceptor feedback GO:0003025 1 / 1 479× 2.09e-3 2.31e-2 ✓ sig.
glossopharyngeal nerve development GO:0021563 1 / 1 479× 2.09e-3 2.31e-2 ✓ sig.
vagus nerve development GO:0021564 1 / 1 479× 2.09e-3 2.31e-2 ✓ sig.
microtubule-based transport GO:0099111 1 / 1 479× 2.09e-3 2.31e-2 ✓ sig.
protein alpha-1,2-demannosylation GO:0036508 1 / 1 479× 2.09e-3 2.31e-2 ✓ sig.
viral RNA genome packaging GO:0019074 1 / 2 240× 4.17e-3 3.34e-2 ✓ sig.
negative regulation of endothelial cell-matrix adhesion via fibronectin GO:1904905 1 / 2 240× 4.17e-3 3.34e-2 ✓ sig.
negative regulation of gonadotropin secretion GO:0032277 1 / 2 240× 4.17e-3 3.34e-2 ✓ sig.
positive regulation of morphogenesis of an epithelium GO:1905332 1 / 2 240× 4.17e-3 3.34e-2 ✓ sig.

Pairs within this cluster, by significance