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Cluster 638

5 diseases · 10 shared-gene connections
5 Diseases
2 Unique genes
0.433 Avg. similarity score
Immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosis 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
RAC2 5 / 5 Immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosis, Immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia, Immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia, Neutrophil immunodeficiency syndrome 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 ⇵
Thiamine metabolism KEGG 1 / 15 400× 2.50e-3 2.23e-2 ✓ sig.
PCP/CE pathway Reactome 1 / 18 334× 3.00e-3 2.54e-2 ✓ sig.
RHO GTPases Activate NADPH Oxidases Reactome 1 / 24 250× 3.99e-3 3.12e-2 ✓ sig.
Interconversion of nucleotide di- and triphosphates Reactome 1 / 29 207× 4.82e-3 3.57e-2 ✓ sig.
ROS and RNS production in phagocytes Reactome 1 / 34 177× 5.65e-3 3.96e-2 ✓ sig.
GPVI-mediated activation cascade Reactome 1 / 34 177× 5.65e-3 3.96e-2 ✓ sig.
VEGF signaling pathway KEGG 1 / 60 100× 9.97e-3 5.67e-2
Fc epsilon RI signaling pathway KEGG 1 / 69 87.0× 1.15e-2 6.18e-2
Viral myocarditis KEGG 1 / 70 85.8× 1.16e-2 6.22e-2
Constitutive Signaling by Aberrant PI3K in Cancer Reactome 1 / 75 80.1× 1.25e-2 6.50e-2
Pancreatic cancer KEGG 1 / 77 78.0× 1.28e-2 6.58e-2
Nucleotide metabolism KEGG 1 / 85 70.6× 1.41e-2 7.00e-2
Colorectal cancer KEGG 1 / 87 69.0× 1.44e-2 7.10e-2
B cell receptor signaling pathway KEGG 1 / 91 66.0× 1.51e-2 7.28e-2
Adherens junction KEGG 1 / 93 64.6× 1.54e-2 7.39e-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 ⇵
regulation of mast cell chemotaxis GO:0060753 1 / 1 9,344× 1.07e-4 3.25e-3 ✓ sig.
lymphocyte aggregation GO:0071593 1 / 3 3,115× 3.21e-4 7.04e-3 ✓ sig.
regulation of respiratory burst GO:0060263 1 / 4 2,336× 4.28e-4 8.53e-3 ✓ sig.
regulation of neutrophil migration GO:1902622 1 / 4 2,336× 4.28e-4 8.53e-3 ✓ sig.
mast cell proliferation GO:0070662 1 / 5 1,869× 5.35e-4 9.88e-3 ✓ sig.
erythrocyte enucleation GO:0043131 1 / 5 1,869× 5.35e-4 9.88e-3 ✓ sig.
ADP biosynthetic process GO:0006172 1 / 5 1,869× 5.35e-4 9.88e-3 ✓ sig.
positive regulation of mast cell proliferation GO:0070668 1 / 5 1,869× 5.35e-4 9.88e-3 ✓ sig.
regulation of hydrogen peroxide metabolic process GO:0010310 1 / 6 1,557× 6.42e-4 1.11e-2 ✓ sig.
nucleoside monophosphate metabolic process GO:0009123 1 / 6 1,557× 6.42e-4 1.11e-2 ✓ sig.
AMP metabolic process GO:0046033 1 / 7 1,335× 7.49e-4 1.23e-2 ✓ sig.
regulation of cell-substrate adhesion GO:0010810 1 / 8 1,168× 8.56e-4 1.33e-2 ✓ sig.
nucleobase-containing small molecule interconversion GO:0015949 1 / 8 1,168× 8.56e-4 1.33e-2 ✓ sig.
regulation of mast cell degranulation GO:0043304 1 / 8 1,168× 8.56e-4 1.33e-2 ✓ sig.
cortical cytoskeleton organization GO:0030865 1 / 10 934× 1.07e-3 1.51e-2 ✓ sig.

Pairs within this cluster, by significance

Disease A ⇵ Disease B ⇵ Similarity score ⇵ Shared genes ⇵ P-value ⇵ FDR q-value ⇵
Immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosis Immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia 0.500 1 6.46e-5 1.98e-4 ✓ sig.
Immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosis Immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia 0.500 1 6.46e-5 1.98e-4 ✓ sig.
Immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosis Neutrophil immunodeficiency syndrome 0.500 1 6.46e-5 1.98e-4 ✓ sig.
Immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia Immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia 0.500 1 6.46e-5 1.98e-4 ✓ sig.
Immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia Neutrophil immunodeficiency syndrome 0.500 1 6.46e-5 1.98e-4 ✓ sig.
Immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia Neutrophil immunodeficiency syndrome 0.500 1 6.46e-5 1.98e-4 ✓ sig.
Immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosis Reticular dysgenesis 0.333 1 1.29e-4 3.27e-4 ✓ sig.
Immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia Reticular dysgenesis 0.333 1 1.29e-4 3.27e-4 ✓ sig.
Immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia Reticular dysgenesis 0.333 1 1.29e-4 3.27e-4 ✓ sig.
Neutrophil immunodeficiency syndrome Reticular dysgenesis 0.333 1 1.29e-4 3.27e-4 ✓ sig.