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Cluster 164

10 diseases · 30 shared-gene connections
10 Diseases
21 Unique genes
0.312 Avg. similarity score
B-cell lymphopenia Most-connected disease (8 links)
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Disease Searched: Radioulnar synostosis with amegakaryocytic thrombocytopenia 1 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
MECOM 9 / 10 B-cell lymphopenia, Digit abnormalities, Hyperpituitarism, Hypocellular bone marrow and 5 more
SYK 2 / 10 Hypogammaglobulinemia, Immunodeficiency 82 with systemic inflammation
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 ⇵
Antigen activates B Cell Receptor (BCR) leading to generation of second messengers Reactome 2 / 23 49.7× 7.21e-4 8.37e-3 ✓ sig.
Lysine degradation KEGG 2 / 63 18.2× 5.33e-3 3.65e-2 ✓ sig.
PKMTs methylate histone lysines Reactome 2 / 71 16.1× 6.73e-3 4.25e-2 ✓ sig.
Fc epsilon receptor (FCERI) signaling Reactome 1 / 6 95.3× 1.04e-2 5.63e-2
B cell receptor signaling pathway KEGG 2 / 91 12.6× 1.09e-2 5.79e-2
RUNX2 regulates bone development Reactome 1 / 7 81.7× 1.22e-2 6.20e-2
Hematopoietic cell lineage KEGG 2 / 100 11.4× 1.30e-2 6.44e-2
Conjugation of salicylate with glycine Reactome 1 / 8 71.5× 1.39e-2 6.72e-2
NF-kappa B signaling pathway KEGG 2 / 105 10.9× 1.43e-2 6.83e-2
Interleukin-2 signaling Reactome 1 / 12 47.7× 2.08e-2 8.54e-2
FCGR activation Reactome 1 / 12 47.7× 2.08e-2 8.54e-2
Osteoclast differentiation KEGG 2 / 142 8.1× 2.52e-2 9.61e-2
Role of LAT2/NTAL/LAB on calcium mobilization Reactome 1 / 15 38.1× 2.59e-2 9.76e-2
Role of phospholipids in phagocytosis Reactome 1 / 21 27.2× 3.61e-2 1.18e-1
Regulation of signaling by CBL Reactome 1 / 21 27.2× 3.61e-2 1.18e-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 ⇵
response to estrogen GO:0043627 3 / 49 54.5× 2.18e-5 9.63e-4 ✓ sig.
embryonic skeletal joint morphogenesis GO:0060272 2 / 11 162× 6.58e-5 2.22e-3 ✓ sig.
embryonic forelimb morphogenesis GO:0035115 2 / 33 53.9× 6.22e-4 1.08e-2 ✓ sig.
metanephros development GO:0001656 2 / 38 46.8× 8.25e-4 1.28e-2 ✓ sig.
daunorubicin transport GO:0043215 1 / 1 890× 1.12e-3 1.53e-2 ✓ sig.
terpenoid transport GO:0046865 1 / 1 890× 1.12e-3 1.53e-2 ✓ sig.
cellular response to nonylphenol GO:1904148 1 / 1 890× 1.12e-3 1.53e-2 ✓ sig.
positive regulation of establishment of Sertoli cell barrier GO:1904446 1 / 1 890× 1.12e-3 1.53e-2 ✓ sig.
cellular response to borneol GO:1905231 1 / 1 890× 1.12e-3 1.53e-2 ✓ sig.
response to codeine GO:1905233 1 / 1 890× 1.12e-3 1.53e-2 ✓ sig.
response to quercetin GO:1905235 1 / 1 890× 1.12e-3 1.53e-2 ✓ sig.
positive regulation of response to drug GO:2001025 1 / 1 890× 1.12e-3 1.53e-2 ✓ sig.
positive regulation of interleukin-1-mediated signaling pathway GO:2000661 1 / 1 890× 1.12e-3 1.53e-2 ✓ sig.
serotonin secretion GO:0001820 1 / 1 890× 1.12e-3 1.53e-2 ✓ sig.
positive regulation of interleukin-3 production GO:0032752 1 / 1 890× 1.12e-3 1.53e-2 ✓ sig.

Pairs within this cluster, by significance

Disease A ⇵ Disease B ⇵ Similarity score ⇵ Shared genes ⇵ P-value ⇵ FDR q-value ⇵
B-cell lymphopenia Hypocellular bone marrow 0.500 1 6.46e-5 1.98e-4 ✓ sig.
B-cell lymphopenia Digit abnormalities 0.500 1 6.46e-5 1.98e-4 ✓ sig.
B-cell lymphopenia Radioulnar synostosis with amegakaryocytic thrombocytopenia 2 0.500 1 6.46e-5 1.98e-4 ✓ sig.
B-cell lymphopenia MECOM-associated syndrome 0.500 1 6.46e-5 1.98e-4 ✓ sig.
Digit abnormalities MECOM-associated syndrome 0.500 1 6.46e-5 1.98e-4 ✓ sig.
Digit abnormalities Hypocellular bone marrow 0.500 1 6.46e-5 1.98e-4 ✓ sig.
Digit abnormalities Radioulnar synostosis with amegakaryocytic thrombocytopenia 2 0.500 1 6.46e-5 1.98e-4 ✓ sig.
MECOM-associated syndrome Radioulnar synostosis with amegakaryocytic thrombocytopenia 2 0.500 1 6.46e-5 1.98e-4 ✓ sig.
Hypocellular bone marrow Radioulnar synostosis with amegakaryocytic thrombocytopenia 2 0.500 1 6.46e-5 1.98e-4 ✓ sig.
Hypocellular bone marrow MECOM-associated syndrome 0.500 1 6.46e-5 1.98e-4 ✓ sig.
Radioulnar synostosis with amegakaryocytic thrombocytopenia 1 Radioulnar synostosis with amegakaryocytic thrombocytopenia 2 0.333 1 1.29e-4 3.27e-4 ✓ sig.
MECOM-associated syndrome Radioulnar synostosis with amegakaryocytic thrombocytopenia 1 0.333 1 1.29e-4 3.27e-4 ✓ sig.
Hypocellular bone marrow Radioulnar synostosis with amegakaryocytic thrombocytopenia 1 0.333 1 1.29e-4 3.27e-4 ✓ sig.
B-cell lymphopenia Radioulnar synostosis with amegakaryocytic thrombocytopenia 1 0.333 1 1.29e-4 3.27e-4 ✓ sig.
Digit abnormalities Radioulnar synostosis with amegakaryocytic thrombocytopenia 1 0.333 1 1.29e-4 3.27e-4 ✓ sig.
Radioulnar synostosis Radioulnar synostosis with amegakaryocytic thrombocytopenia 2 0.250 1 1.94e-4 4.41e-4 ✓ sig.
B-cell lymphopenia Radioulnar synostosis 0.250 1 1.94e-4 4.41e-4 ✓ sig.
Digit abnormalities Radioulnar synostosis 0.250 1 1.94e-4 4.41e-4 ✓ sig.
Hypocellular bone marrow Radioulnar synostosis 0.250 1 1.94e-4 4.41e-4 ✓ sig.
MECOM-associated syndrome Radioulnar synostosis 0.250 1 1.94e-4 4.41e-4 ✓ sig.
Hypogammaglobulinemia Immunodeficiency 82 with systemic inflammation 0.200 1 2.58e-4 5.38e-4 ✓ sig.
Hypogammaglobulinemia Radioulnar synostosis with amegakaryocytic thrombocytopenia 2 0.200 1 2.58e-4 5.38e-4 ✓ sig.
B-cell lymphopenia Hypogammaglobulinemia 0.200 1 2.58e-4 5.38e-4 ✓ sig.
Digit abnormalities Hypogammaglobulinemia 0.200 1 2.58e-4 5.38e-4 ✓ sig.
Hypocellular bone marrow Hypogammaglobulinemia 0.200 1 2.58e-4 5.38e-4 ✓ sig.
Hypogammaglobulinemia MECOM-associated syndrome 0.200 1 2.58e-4 5.38e-4 ✓ sig.
B-cell lymphopenia Hyperpituitarism 0.063 1 9.68e-4 1.50e-3 ✓ sig.
Hyperpituitarism MECOM-associated syndrome 0.063 1 9.68e-4 1.50e-3 ✓ sig.
Hyperpituitarism Hypocellular bone marrow 0.063 1 9.68e-4 1.50e-3 ✓ sig.
Digit abnormalities Hyperpituitarism 0.063 1 9.68e-4 1.50e-3 ✓ sig.