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Cluster 618

5 diseases · 10 shared-gene connections
5 Diseases
3 Unique genes
0.375 Avg. similarity score
Combined psap deficiency 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 ⇵
Combined psap deficiency 4 4 1
Combined saposin deficiency 4 4 2
Gaucher disease due to saposin C deficiency 4 4 1
Krabbe disease 4 4 2
Krabbe disease due to saposin A deficiency 4 4 1

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

Gene ⇵ Member diseases ⇵ Linked diseases
PSAP 5 / 5 Combined psap deficiency, Combined saposin deficiency, Gaucher disease due to saposin C deficiency, Krabbe disease and 1 more
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 ⇵
Glycosphingolipid metabolism Reactome 2 / 46 174× 4.30e-5 9.70e-4 ✓ sig.
Sphingolipid metabolism KEGG 2 / 54 148× 5.94e-5 1.25e-3 ✓ sig.
Lysosome KEGG 2 / 133 60.2× 3.63e-4 5.21e-3 ✓ sig.
Peptide ligand-binding receptors Reactome 1 / 106 37.8× 2.62e-2 1.00e-1
Platelet degranulation Reactome 1 / 123 32.5× 3.04e-2 1.09e-1
G alpha (i) signalling events Reactome 1 / 249 16.1× 6.09e-2 1.62e-1
Neutrophil degranulation Reactome 1 / 480 8.3× 1.15e-1 2.35e-1
Metabolic pathways KEGG 1 / 1,563 2.6× 3.42e-1 4.72e-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 ⇵
sphingolipid metabolic process GO:0006665 2 / 59 211× 2.93e-5 1.23e-3 ✓ sig.
positive regulation of beta-galactosidase activity GO:1903771 1 / 1 6,229× 1.61e-4 4.34e-3 ✓ sig.
ganglioside GM1 transport to membrane GO:1905572 1 / 1 6,229× 1.61e-4 4.34e-3 ✓ sig.
galactosylceramide catabolic process GO:0006683 1 / 2 3,115× 3.21e-4 7.04e-3 ✓ sig.
epithelial cell differentiation involved in prostate gland development GO:0060742 1 / 5 1,246× 8.03e-4 1.28e-2 ✓ sig.
equilibrioception GO:0050957 1 / 6 1,038× 9.63e-4 1.42e-2 ✓ sig.
prostate gland growth GO:0060736 1 / 8 779× 1.28e-3 1.67e-2 ✓ sig.
glycosphingolipid catabolic process GO:0046479 1 / 12 519× 1.93e-3 2.07e-2 ✓ sig.
sensory perception of light stimulus GO:0050953 1 / 13 479× 2.09e-3 2.17e-2 ✓ sig.
cell-cell adhesion via plasma-membrane adhesion molecules GO:0098742 1 / 18 346× 2.89e-3 2.55e-2 ✓ sig.
inner ear auditory receptor cell differentiation GO:0042491 1 / 19 328× 3.05e-3 2.62e-2 ✓ sig.
auditory receptor cell stereocilium organization GO:0060088 1 / 19 328× 3.05e-3 2.62e-2 ✓ sig.
inner ear receptor cell stereocilium organization GO:0060122 1 / 25 249× 4.01e-3 3.01e-2 ✓ sig.
lysosomal transport GO:0007041 1 / 26 240× 4.17e-3 3.06e-2 ✓ sig.
cochlea development GO:0090102 1 / 35 178× 5.61e-3 3.51e-2 ✓ sig.

Pairs within this cluster, by significance

Disease A ⇵ Disease B ⇵ Similarity score ⇵ Shared genes ⇵ P-value ⇵ FDR q-value ⇵
Combined psap deficiency Gaucher disease due to saposin C deficiency 0.500 1 6.46e-5 1.98e-4 ✓ sig.
Combined psap deficiency Krabbe disease due to saposin A deficiency 0.500 1 6.46e-5 1.98e-4 ✓ sig.
Gaucher disease due to saposin C deficiency Krabbe disease due to saposin A deficiency 0.500 1 6.46e-5 1.98e-4 ✓ sig.
Combined psap deficiency Combined saposin deficiency 0.333 1 1.29e-4 3.27e-4 ✓ sig.
Combined psap deficiency Krabbe disease 0.333 1 1.29e-4 3.27e-4 ✓ sig.
Combined saposin deficiency Gaucher disease due to saposin C deficiency 0.333 1 1.29e-4 3.27e-4 ✓ sig.
Combined saposin deficiency Krabbe disease due to saposin A deficiency 0.333 1 1.29e-4 3.27e-4 ✓ sig.
Gaucher disease due to saposin C deficiency Krabbe disease 0.333 1 1.29e-4 3.27e-4 ✓ sig.
Krabbe disease Krabbe disease due to saposin A deficiency 0.333 1 1.29e-4 3.27e-4 ✓ sig.
Combined saposin deficiency Krabbe disease 0.250 1 2.58e-4 5.38e-4 ✓ sig.