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Cluster 266

7 diseases · 11 shared-gene connections
7 Diseases
9 Unique genes
0.253 Avg. similarity score
Blast crisis Most-connected disease (5 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 ⇵
Blast crisis 5 5 2
Hyper-immunoglobulin m syndrome 4 4 4
Hyper-immunoglobulin syndrome 4 4 2
hyper-IgM syndrome type 2 3 3 1
Chromosome 22q11.2 microdeletion syndrome 2 2 3
Myelogenous leukemia 2 2 3
hyper-IgM syndrome type 3 2 2 1

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

Gene ⇵ Member diseases ⇵ Linked diseases
AICDA 4 / 7 Blast crisis, hyper-IgM syndrome type 2, Hyper-immunoglobulin m syndrome, Hyper-immunoglobulin syndrome
BCR 3 / 7 Blast crisis, Chromosome 22q11.2 microdeletion syndrome, Myelogenous leukemia
CD40 3 / 7 hyper-IgM syndrome type 3, Hyper-immunoglobulin m syndrome, Hyper-immunoglobulin syndrome
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 ⇵
Primary immunodeficiency KEGG 4 / 38 140× 1.06e-8 9.18e-7 ✓ sig.
Chronic myeloid leukemia KEGG 4 / 77 69.3× 1.92e-7 1.16e-5 ✓ sig.
Intestinal immune network for IgA production KEGG 3 / 50 80.1× 5.60e-6 2.08e-4 ✓ sig.
Viral myocarditis KEGG 3 / 70 57.2× 1.55e-5 4.85e-4 ✓ sig.
ErbB signaling pathway KEGG 3 / 86 46.6× 2.89e-5 8.08e-4 ✓ sig.
Frs2-mediated activation Reactome 2 / 12 222× 3.28e-5 9.00e-4 ✓ sig.
Toxoplasmosis KEGG 3 / 112 35.7× 6.37e-5 1.55e-3 ✓ sig.
TNF receptor superfamily (TNFSF) members mediating non-canonical NF-kB pathway Reactome 2 / 18 148× 7.59e-5 1.79e-3 ✓ sig.
Neurotrophin signaling pathway KEGG 3 / 120 33.4× 7.82e-5 1.83e-3 ✓ sig.
Asthma KEGG 2 / 32 83.4× 2.45e-4 4.58e-3 ✓ sig.
RHO GTPases Activate WASPs and WAVEs Reactome 2 / 36 74.1× 3.10e-4 5.51e-3 ✓ sig.
Allograft rejection KEGG 2 / 39 68.4× 3.65e-4 6.25e-3 ✓ sig.
Pathways in cancer KEGG 4 / 533 10.0× 4.04e-4 6.76e-3 ✓ sig.
Lipid and atherosclerosis KEGG 3 / 216 18.5× 4.45e-4 7.28e-3 ✓ sig.
Malaria KEGG 2 / 50 53.4× 6.00e-4 9.19e-3 ✓ sig.

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

GO term ⇵ GO ID ⇵ Overlap genes ⇵ Fold enrichment ⇵ P-value ⇵ FDR q-value ⇵
isotype switching GO:0045190 3 / 19 328× 7.46e-8 9.43e-6 ✓ sig.
B cell proliferation GO:0042100 3 / 38 164× 6.46e-7 5.80e-5 ✓ sig.
cellular response to lipopolysaccharide GO:0071222 4 / 187 44.4× 1.18e-6 9.44e-5 ✓ sig.
thymus development GO:0048538 3 / 50 125× 1.50e-6 1.14e-4 ✓ sig.
regulation of immunoglobulin production GO:0002637 2 / 9 461× 7.41e-6 4.11e-4 ✓ sig.
CD40 signaling pathway GO:0023035 2 / 10 415× 9.26e-6 4.92e-4 ✓ sig.
Bergmann glial cell differentiation GO:0060020 2 / 11 378× 1.13e-5 5.73e-4 ✓ sig.
somatic hypermutation of immunoglobulin genes GO:0016446 2 / 14 297× 1.87e-5 8.50e-4 ✓ sig.
T cell receptor signaling pathway GO:0050852 3 / 121 51.5× 2.16e-5 9.55e-4 ✓ sig.
regulation of gene expression GO:0010468 4 / 402 20.7× 2.44e-5 1.04e-3 ✓ sig.
intracellular signal transduction GO:0035556 4 / 471 17.6× 4.54e-5 1.68e-3 ✓ sig.
positive regulation of macromolecule biosynthetic process GO:0010557 2 / 29 143× 8.32e-5 2.64e-3 ✓ sig.
positive regulation of endothelial cell apoptotic process GO:2000353 2 / 29 143× 8.32e-5 2.64e-3 ✓ sig.
positive regulation of canonical NF-kappaB signal transduction GO:0043123 3 / 232 26.8× 1.50e-4 4.10e-3 ✓ sig.
positive regulation of interleukin-12 production GO:0032735 2 / 43 96.6× 1.84e-4 4.77e-3 ✓ sig.

Pairs within this cluster, by significance

Disease A ⇵ Disease B ⇵ Similarity score ⇵ Shared genes ⇵ P-value ⇵ FDR q-value ⇵
Hyper-immunoglobulin m syndrome Hyper-immunoglobulin syndrome 0.400 2 5.06e-8 3.92e-7 ✓ sig.
Blast crisis hyper-IgM syndrome type 2 0.333 1 1.30e-4 3.90e-4 ✓ sig.
hyper-IgM syndrome type 2 Hyper-immunoglobulin syndrome 0.333 1 1.30e-4 3.90e-4 ✓ sig.
hyper-IgM syndrome type 3 Hyper-immunoglobulin syndrome 0.333 1 1.30e-4 3.90e-4 ✓ sig.
Blast crisis Hyper-immunoglobulin syndrome 0.250 1 2.60e-4 6.40e-4 ✓ sig.
hyper-IgM syndrome type 2 Hyper-immunoglobulin m syndrome 0.200 1 2.60e-4 6.40e-4 ✓ sig.
hyper-IgM syndrome type 3 Hyper-immunoglobulin m syndrome 0.200 1 2.60e-4 6.40e-4 ✓ sig.
Blast crisis Myelogenous leukemia 0.200 1 3.90e-4 8.52e-4 ✓ sig.
Blast crisis Chromosome 22q11.2 microdeletion syndrome 0.200 1 3.90e-4 8.52e-4 ✓ sig.
Blast crisis Hyper-immunoglobulin m syndrome 0.167 1 5.19e-4 1.04e-3 ✓ sig.
Chromosome 22q11.2 microdeletion syndrome Myelogenous leukemia 0.167 1 5.84e-4 1.14e-3 ✓ sig.