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Cluster 241

7 diseases · 7 shared-gene connections
7 Diseases
62 Unique genes
0.079 Avg. similarity score
Polyneuropathy 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)

Disease ⇵ Connections in cluster ⇵ Significant partners ⇵ Curated genes ⇵
Polyneuropathy 4 4 24
Cerebellar atrophy 3 3 30
Dysarthria 3 3 22
Congenital cataract microcephaly intellectual disability syndrome 1 1 1
Congenital cerebellar hypoplasia 1 1 1
Sterol carrier protein 2 deficiency 1 1 1
Troyer syndrome 1 1 1

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

Gene ⇵ Member diseases ⇵ Linked diseases
BIVM-ERCC5 3 / 7 Cerebellar atrophy, Dysarthria, Polyneuropathy
ERCC5 3 / 7 Cerebellar atrophy, Dysarthria, Polyneuropathy
PNPLA6 3 / 7 Cerebellar atrophy, Dysarthria, Polyneuropathy
SMC1A 3 / 7 Cerebellar atrophy, Dysarthria, Polyneuropathy
CACNA1A 2 / 7 Cerebellar atrophy, Dysarthria
DNMT1 2 / 7 Cerebellar atrophy, Dysarthria
DYNC1H1 2 / 7 Cerebellar atrophy, Polyneuropathy
HARS1 2 / 7 Cerebellar atrophy, Dysarthria
MED25 2 / 7 Congenital cataract microcephaly intellectual disability syndrome, Polyneuropathy
OXR1 2 / 7 Cerebellar atrophy, Congenital cerebellar hypoplasia
SCP2 2 / 7 Polyneuropathy, Sterol carrier protein 2 deficiency
SPART 2 / 7 Dysarthria, Troyer syndrome
SPG7 2 / 7 Dysarthria, Polyneuropathy
TBC1D24 2 / 7 Cerebellar atrophy, Dysarthria
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 ⇵
Adenylate cyclase activating pathway Reactome 2 / 10 38.7× 1.15e-3 1.51e-2 ✓ sig.
Adenylate cyclase inhibitory pathway Reactome 2 / 14 27.7× 2.29e-3 2.52e-2 ✓ sig.
Parkinson disease KEGG 6 / 268 4.3× 2.52e-3 2.71e-2 ✓ sig.
Retrograde endocannabinoid signaling KEGG 4 / 149 5.2× 7.27e-3 5.61e-2
SUMOylation of DNA damage response and repair proteins Reactome 3 / 77 7.5× 7.31e-3 5.62e-2
Phagosome KEGG 4 / 155 5.0× 8.34e-3 6.12e-2
Respiratory electron transport Reactome 3 / 83 7.0× 8.98e-3 6.42e-2
Amyotrophic lateral sclerosis KEGG 6 / 368 3.2× 1.15e-2 7.48e-2
Morphine addiction KEGG 3 / 91 6.4× 1.15e-2 7.49e-2
Detoxification of Reactive Oxygen Species Reactome 2 / 34 11.4× 1.32e-2 8.07e-2
FCGR3A-mediated IL10 synthesis Reactome 2 / 35 11.1× 1.40e-2 8.35e-2
Glycerophospholipid catabolism Reactome 1 / 3 64.6× 1.54e-2 8.85e-2
Selenocysteine synthesis Reactome 1 / 3 64.6× 1.54e-2 8.85e-2
Glycogen storage disease type IV (GBE1) Reactome 1 / 3 64.6× 1.54e-2 8.85e-2
Breakdown of the nuclear lamina Reactome 1 / 3 64.6× 1.54e-2 8.85e-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 ⇵
response to hyperoxia GO:0055093 3 / 14 64.6× 1.23e-5 6.14e-4 ✓ sig.
bile acid metabolic process GO:0008206 3 / 17 53.2× 2.29e-5 9.96e-4 ✓ sig.
nuclear pore localization GO:0051664 2 / 5 121× 1.08e-4 3.19e-3 ✓ sig.
negative regulation of cellular response to oxidative stress GO:1900408 2 / 5 121× 1.08e-4 3.19e-3 ✓ sig.
adult walking behavior GO:0007628 3 / 34 26.6× 1.93e-4 4.94e-3 ✓ sig.
response to axon injury GO:0048678 3 / 37 24.4× 2.49e-4 5.91e-3 ✓ sig.
DNA repair GO:0006281 7 / 420 5.0× 4.67e-4 9.14e-3 ✓ sig.
adenylate cyclase-activating dopamine receptor signaling pathway GO:0007191 2 / 11 54.8× 5.84e-4 1.07e-2 ✓ sig.
intracellular cholesterol transport GO:0032367 2 / 13 46.4× 8.25e-4 1.33e-2 ✓ sig.
cerebellar Purkinje cell differentiation GO:0021702 2 / 14 43.1× 9.61e-4 1.47e-2 ✓ sig.
base-excision repair, gap-filling GO:0006287 2 / 14 43.1× 9.61e-4 1.47e-2 ✓ sig.
removal of superoxide radicals GO:0019430 2 / 15 40.2× 1.11e-3 1.61e-2 ✓ sig.
proton motive force-driven mitochondrial ATP synthesis GO:0042776 3 / 64 14.1× 1.25e-3 1.74e-2 ✓ sig.
sterol transport GO:0015918 2 / 17 35.5× 1.43e-3 1.87e-2 ✓ sig.
aerobic respiration GO:0009060 3 / 68 13.3× 1.49e-3 1.91e-2 ✓ sig.

Pairs within this cluster, by significance

Disease A ⇵ Disease B ⇵ Similarity score ⇵ Shared genes ⇵ P-value ⇵ FDR q-value ⇵
Cerebellar atrophy Dysarthria 0.178 8 2.35e-17 4.12e-16 ✓ sig.
Dysarthria Polyneuropathy 0.119 5 1.53e-10 1.58e-9 ✓ sig.
Cerebellar atrophy Polyneuropathy 0.100 5 8.19e-10 7.89e-9 ✓ sig.
Dysarthria Troyer syndrome 0.043 1 1.43e-3 2.21e-3 ✓ sig.
Congenital cataract microcephaly intellectual disability syndrome Polyneuropathy 0.040 1 1.56e-3 2.36e-3 ✓ sig.
Polyneuropathy Sterol carrier protein 2 deficiency 0.040 1 1.56e-3 2.36e-3 ✓ sig.
Cerebellar atrophy Congenital cerebellar hypoplasia 0.032 1 1.95e-3 2.81e-3 ✓ sig.