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Cluster 318

7 diseases · 11 shared-gene connections
7 Diseases
7 Unique genes
0.258 Avg. similarity score
Muscular hypotonia Most-connected disease (5 links)
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Disease Searched: Central hypotonia 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
P4HTM 5 / 7 Abnormality of the eye, Central hypotonia, Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities, Hypoventilation and 1 more
MSL3 2 / 7 Basilicata-akhtar syndrome, Muscular hypotonia
NUDT2 2 / 7 Intellectual developmental disorder peripheral neuropathy, Muscular hypotonia
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 ⇵
Inhibition of replication initiation of damaged DNA by RB1/E2F1 Reactome 1 / 10 172× 5.82e-3 4.03e-2 ✓ sig.
ERKs are inactivated Reactome 1 / 13 132× 7.55e-3 4.77e-2 ✓ sig.
APC truncation mutants have impaired AXIN binding Reactome 1 / 14 123× 8.13e-3 5.01e-2
AXIN missense mutants destabilize the destruction complex Reactome 1 / 14 123× 8.13e-3 5.01e-2
Truncations of AMER1 destabilize the destruction complex Reactome 1 / 14 123× 8.13e-3 5.01e-2
ERK/MAPK targets Reactome 1 / 14 123× 8.13e-3 5.01e-2
Misspliced GSK3beta mutants stabilize beta-catenin Reactome 1 / 15 114× 8.71e-3 5.22e-2
S33 mutants of beta-catenin aren't phosphorylated Reactome 1 / 15 114× 8.71e-3 5.22e-2
S37 mutants of beta-catenin aren't phosphorylated Reactome 1 / 15 114× 8.71e-3 5.22e-2
S45 mutants of beta-catenin aren't phosphorylated Reactome 1 / 15 114× 8.71e-3 5.22e-2
T41 mutants of beta-catenin aren't phosphorylated Reactome 1 / 15 114× 8.71e-3 5.22e-2
Spry regulation of FGF signaling Reactome 1 / 16 107× 9.29e-3 5.43e-2
Beta-catenin phosphorylation cascade Reactome 1 / 17 101× 9.87e-3 5.65e-2
Platelet sensitization by LDL Reactome 1 / 17 101× 9.87e-3 5.65e-2
DARPP-32 events Reactome 1 / 19 90.3× 1.10e-2 6.03e-2

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

GO term ⇵ GO ID ⇵ Overlap genes ⇵ Fold enrichment ⇵ P-value ⇵ FDR q-value ⇵
AMP biosynthetic process GO:0006167 1 / 4 667× 1.50e-3 1.82e-2 ✓ sig.
negative regulation of glycolytic process through fructose-6-phosphate GO:1904539 1 / 4 667× 1.50e-3 1.82e-2 ✓ sig.
vascular endothelial cell response to oscillatory fluid shear stress GO:0097706 1 / 5 534× 1.87e-3 2.05e-2 ✓ sig.
regulation of erythrocyte differentiation GO:0045646 1 / 6 445× 2.25e-3 2.24e-2 ✓ sig.
positive regulation of focal adhesion disassembly GO:0120183 1 / 8 334× 2.99e-3 2.59e-2 ✓ sig.
peptidyl-threonine dephosphorylation GO:0035970 1 / 9 297× 3.37e-3 2.76e-2 ✓ sig.
positive regulation of keratinocyte migration GO:0051549 1 / 12 222× 4.49e-3 3.17e-2 ✓ sig.
dendritic spine development GO:0060996 1 / 15 178× 5.61e-3 3.51e-2 ✓ sig.
regulation of microtubule polymerization GO:0031113 1 / 16 167× 5.98e-3 3.62e-2 ✓ sig.
response to lead ion GO:0010288 1 / 17 157× 6.35e-3 3.73e-2 ✓ sig.
regulation of ARF protein signal transduction GO:0032012 1 / 19 141× 7.10e-3 3.94e-2 ✓ sig.
RNA polymerase II transcription initiation surveillance GO:0160240 1 / 20 133× 7.47e-3 4.04e-2 ✓ sig.
regulation of growth GO:0040008 1 / 23 116× 8.59e-3 4.32e-2 ✓ sig.
negative regulation of hippo signaling GO:0035331 1 / 25 107× 9.33e-3 4.50e-2 ✓ sig.
ATP biosynthetic process GO:0006754 1 / 26 103× 9.70e-3 4.58e-2 ✓ sig.

Pairs within this cluster, by significance