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Cluster 128

10 diseases · 18 shared-gene connections
10 Diseases
16 Unique genes
0.243 Avg. similarity score
Dacryocystitis Most-connected disease (6 links)
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Disease Searched: ectodermal dysplasia and immunodeficiency 2 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
IL1RN 7 / 10 Dacryocystitis, Dysthymic disorder, Exanthema, Interleukin 1 receptor antagonist deficiency and 3 more
IL1R1 2 / 10 Multifocal osteomyelitis, Recurrent multifocal osteomyelitis
LPIN2 2 / 10 Majeed syndrome, Multifocal osteomyelitis
NFKBIA 2 / 10 ectodermal dysplasia and immunodeficiency 2, Interleukin 1 receptor antagonist deficiency
NTRK2 2 / 10 Dysthymic disorder, Early-onset obesity-hyperphagia-severe developmental delay 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 ⇵
Alcoholic liver disease KEGG 4 / 144 20.9× 3.23e-5 8.99e-4 ✓ sig.
Interleukin-1 signaling Reactome 3 / 88 25.6× 1.99e-4 3.92e-3 ✓ sig.
NF-kappa B signaling pathway KEGG 3 / 105 21.4× 3.35e-4 5.94e-3 ✓ sig.
Defective MAOA causes Brunner syndrome (BRUNS) Reactome 1 / 1 751× 1.33e-3 1.73e-2 ✓ sig.
Serotonin clearance from the synaptic cleft Reactome 1 / 1 751× 1.33e-3 1.73e-2 ✓ sig.
Interleukin-10 signaling Reactome 2 / 47 31.9× 1.74e-3 2.10e-2 ✓ sig.
Alcoholism KEGG 3 / 188 12.0× 1.82e-3 2.18e-2 ✓ sig.
Enzymatic degradation of Dopamine by monoamine oxidase Reactome 1 / 2 375× 2.66e-3 2.88e-2 ✓ sig.
Metabolism of serotonin Reactome 1 / 2 375× 2.66e-3 2.88e-2 ✓ sig.
Transfer of LPS from LBP carrier to CD14 Reactome 1 / 2 375× 2.66e-3 2.88e-2 ✓ sig.
Biogenic amines are oxidatively deaminated to aldehydes by MAOA and MAOB Reactome 1 / 2 375× 2.66e-3 2.88e-2 ✓ sig.
Human T-cell leukemia virus 1 infection KEGG 3 / 224 10.1× 3.00e-3 3.11e-2 ✓ sig.
Human cytomegalovirus infection KEGG 3 / 226 10.0× 3.07e-3 3.17e-2 ✓ sig.
Coronavirus disease - COVID-19 KEGG 3 / 238 9.5× 3.56e-3 3.52e-2 ✓ sig.
Enzymatic degradation of dopamine by COMT Reactome 1 / 3 250× 3.99e-3 3.82e-2 ✓ 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 ⇵
interleukin-1-mediated signaling pathway GO:0070498 2 / 28 83.4× 2.56e-4 6.13e-3 ✓ sig.
acute-phase response GO:0006953 2 / 37 63.1× 4.50e-4 9.10e-3 ✓ sig.
lipopolysaccharide-mediated signaling pathway GO:0031663 2 / 38 61.5× 4.75e-4 9.45e-3 ✓ sig.
inflammatory response GO:0006954 4 / 467 10.0× 5.52e-4 1.04e-2 ✓ sig.
positive regulation of digestive system process GO:0060456 1 / 1 1,168× 8.56e-4 1.39e-2 ✓ sig.
positive regulation of interleukin-1-mediated signaling pathway GO:2000661 1 / 1 1,168× 8.56e-4 1.39e-2 ✓ sig.
positive regulation of serotonin secretion GO:0014064 1 / 1 1,168× 8.56e-4 1.39e-2 ✓ sig.
regulation of thalamus size GO:0090067 1 / 1 1,168× 8.56e-4 1.39e-2 ✓ sig.
long-term synaptic potentiation GO:0060291 2 / 71 32.9× 1.65e-3 2.08e-2 ✓ sig.
regulation of serotonin secretion GO:0014062 1 / 2 584× 1.71e-3 2.13e-2 ✓ sig.
lipopolysaccharide transport GO:0015920 1 / 2 584× 1.71e-3 2.13e-2 ✓ sig.
diterpenoid metabolic process GO:0016101 1 / 2 584× 1.71e-3 2.13e-2 ✓ sig.
negative regulation of circadian sleep/wake cycle, REM sleep GO:0042322 1 / 2 584× 1.71e-3 2.13e-2 ✓ sig.
positive regulation of respiratory burst involved in inflammatory response GO:0060265 1 / 2 584× 1.71e-3 2.13e-2 ✓ sig.
negative regulation of cerebellar granule cell precursor proliferation GO:0021941 1 / 2 584× 1.71e-3 2.13e-2 ✓ sig.

Pairs within this cluster, by significance

Disease A ⇵ Disease B ⇵ Similarity score ⇵ Shared genes ⇵ P-value ⇵ FDR q-value ⇵
Multifocal osteomyelitis Recurrent multifocal osteomyelitis 0.400 2 5.06e-8 3.72e-7 ✓ sig.
Dacryocystitis Sclerosis 0.500 1 6.49e-5 2.32e-4 ✓ sig.
Dacryocystitis Recurrent multifocal osteomyelitis 0.333 1 1.30e-4 3.91e-4 ✓ sig.
Dacryocystitis Interleukin 1 receptor antagonist deficiency 0.333 1 1.30e-4 3.91e-4 ✓ sig.
Recurrent multifocal osteomyelitis Sclerosis 0.333 1 1.30e-4 3.91e-4 ✓ sig.
ectodermal dysplasia and immunodeficiency 2 Interleukin 1 receptor antagonist deficiency 0.333 1 1.30e-4 3.91e-4 ✓ sig.
Interleukin 1 receptor antagonist deficiency Sclerosis 0.333 1 1.30e-4 3.91e-4 ✓ sig.
Interleukin 1 receptor antagonist deficiency Recurrent multifocal osteomyelitis 0.250 1 2.60e-4 6.48e-4 ✓ sig.
Dacryocystitis Multifocal osteomyelitis 0.200 1 2.60e-4 6.48e-4 ✓ sig.
Multifocal osteomyelitis Sclerosis 0.200 1 2.60e-4 6.48e-4 ✓ sig.
Majeed syndrome Multifocal osteomyelitis 0.200 1 2.60e-4 6.48e-4 ✓ sig.
Exanthema Sclerosis 0.143 1 3.90e-4 8.64e-4 ✓ sig.
Dacryocystitis Exanthema 0.143 1 3.90e-4 8.64e-4 ✓ sig.
Dysthymic disorder Sclerosis 0.125 1 4.55e-4 9.70e-4 ✓ sig.
Dacryocystitis Dysthymic disorder 0.125 1 4.55e-4 9.70e-4 ✓ sig.
Dysthymic disorder Early-onset obesity-hyperphagia-severe developmental delay syndrome 0.125 1 4.55e-4 9.70e-4 ✓ sig.
Interleukin 1 receptor antagonist deficiency Multifocal osteomyelitis 0.167 1 5.19e-4 1.06e-3 ✓ sig.
Exanthema Recurrent multifocal osteomyelitis 0.125 1 7.79e-4 1.40e-3 ✓ sig.