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Cluster 126

10 diseases · 20 shared-gene connections
10 Diseases
16 Unique genes
0.261 Avg. similarity score
Pseudoxanthoma elasticum Most-connected disease (9 links)
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Disease Searched: inherited pseudoxanthoma elasticum 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
ENPP1 6 / 10 arterial calcification, generalized, of infancy, 1, Cole disease, Coronary medial sclerosis of infancy, Crystal arthropathy and 2 more
XYLT1 3 / 10 Desbuquois dysplasia, Graft versus host disease, Pseudoxanthoma elasticum
ABCC2 2 / 10 Dubin-johnson syndrome, Pseudoxanthoma elasticum
ABCC6 2 / 10 inherited pseudoxanthoma elasticum, Pseudoxanthoma elasticum
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 ⇵
ABC transporters KEGG 3 / 45 50.0× 2.66e-5 7.39e-4 ✓ sig.
Heme degradation Reactome 2 / 14 107× 1.50e-4 3.02e-3 ✓ sig.
Glycosaminoglycan biosynthesis - chondroitin sulfate / dermatan sulfate KEGG 2 / 21 71.5× 3.44e-4 5.88e-3 ✓ sig.
Glycosaminoglycan biosynthesis - heparan sulfate / heparin KEGG 2 / 24 62.6× 4.51e-4 7.28e-3 ✓ sig.
A tetrasaccharide linker sequence is required for GAG synthesis Reactome 2 / 26 57.7× 5.31e-4 8.25e-3 ✓ sig.
Antifolate resistance KEGG 2 / 30 50.0× 7.08e-4 1.03e-2 ✓ sig.
Folate transport and metabolism KEGG 2 / 31 48.4× 7.57e-4 1.08e-2 ✓ sig.
Defective ABCC2 causes Dubin-Johnson syndrome Reactome 1 / 1 751× 1.33e-3 1.67e-2 ✓ sig.
Defective ABCC6 causes pseudoxanthoma elasticum (PXE) Reactome 1 / 1 751× 1.33e-3 1.67e-2 ✓ sig.
Pyrimidine metabolism KEGG 2 / 58 25.9× 2.63e-3 2.79e-2 ✓ sig.
ABC-family proteins mediated transport Reactome 2 / 81 18.5× 5.07e-3 4.42e-2 ✓ sig.
Nucleotide metabolism KEGG 2 / 85 17.7× 5.57e-3 4.71e-2 ✓ sig.
Bile secretion KEGG 2 / 90 16.7× 6.22e-3 5.08e-2
Vitamin B2 (riboflavin) metabolism Reactome 1 / 7 107× 9.29e-3 6.61e-2
Riboflavin metabolism KEGG 1 / 8 93.8× 1.06e-2 7.20e-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 ⇵
proteoglycan biosynthetic process GO:0030166 4 / 21 222× 2.13e-9 4.36e-7 ✓ sig.
phosphate ion homeostasis GO:0055062 3 / 15 234× 2.33e-7 2.45e-5 ✓ sig.
inorganic diphosphate transport GO:0030505 2 / 4 584× 4.12e-6 2.59e-4 ✓ sig.
carboxylic acid transport GO:0046942 2 / 5 467× 6.86e-6 3.90e-4 ✓ sig.
xenobiotic transport across blood-brain barrier GO:1990962 2 / 6 389× 1.03e-5 5.37e-4 ✓ sig.
leukotriene transport GO:0071716 2 / 7 334× 1.44e-5 6.99e-4 ✓ sig.
intracellular phosphate ion homeostasis GO:0030643 2 / 10 234× 3.08e-5 1.25e-3 ✓ sig.
glycosaminoglycan metabolic process GO:0030203 2 / 12 195× 4.51e-5 1.67e-3 ✓ sig.
transepithelial transport GO:0070633 2 / 13 180× 5.33e-5 1.90e-3 ✓ sig.
glycosaminoglycan biosynthetic process GO:0006024 2 / 20 117× 1.29e-4 3.69e-3 ✓ sig.
glycoprotein biosynthetic process GO:0009101 2 / 21 111× 1.43e-4 3.96e-3 ✓ sig.
chondroitin sulfate proteoglycan biosynthetic process GO:0050650 2 / 26 89.8× 2.21e-4 5.40e-3 ✓ sig.
heparan sulfate proteoglycan biosynthetic process GO:0015012 2 / 30 77.9× 2.95e-4 6.67e-3 ✓ sig.
ATP metabolic process GO:0046034 2 / 36 64.9× 4.26e-4 8.64e-3 ✓ sig.
monoatomic anion transmembrane transport GO:0098656 2 / 40 58.4× 5.26e-4 1.00e-2 ✓ sig.

Pairs within this cluster, by significance

Disease A ⇵ Disease B ⇵ Similarity score ⇵ Shared genes ⇵ P-value ⇵ FDR q-value ⇵
arterial calcification, generalized, of infancy, 1 Coronary medial sclerosis of infancy 0.500 1 6.49e-5 2.33e-4 ✓ sig.
arterial calcification, generalized, of infancy, 1 hypopigmentation-punctate palmoplantar keratoderma syndrome 0.500 1 6.49e-5 2.33e-4 ✓ sig.
arterial calcification, generalized, of infancy, 1 Cole disease 0.500 1 6.49e-5 2.33e-4 ✓ sig.
Cole disease Coronary medial sclerosis of infancy 0.500 1 6.49e-5 2.33e-4 ✓ sig.
Cole disease hypopigmentation-punctate palmoplantar keratoderma syndrome 0.500 1 6.49e-5 2.33e-4 ✓ sig.
Coronary medial sclerosis of infancy hypopigmentation-punctate palmoplantar keratoderma syndrome 0.500 1 6.49e-5 2.33e-4 ✓ sig.
Coronary medial sclerosis of infancy Crystal arthropathy 0.200 1 2.60e-4 6.51e-4 ✓ sig.
Crystal arthropathy hypopigmentation-punctate palmoplantar keratoderma syndrome 0.200 1 2.60e-4 6.51e-4 ✓ sig.
Cole disease Crystal arthropathy 0.200 1 2.60e-4 6.51e-4 ✓ sig.
arterial calcification, generalized, of infancy, 1 Crystal arthropathy 0.200 1 2.60e-4 6.51e-4 ✓ sig.
Cole disease Pseudoxanthoma elasticum 0.167 1 3.25e-4 7.70e-4 ✓ sig.
arterial calcification, generalized, of infancy, 1 Pseudoxanthoma elasticum 0.167 1 3.25e-4 7.70e-4 ✓ sig.
Coronary medial sclerosis of infancy Pseudoxanthoma elasticum 0.167 1 3.25e-4 7.70e-4 ✓ sig.
Dubin-johnson syndrome Pseudoxanthoma elasticum 0.167 1 3.25e-4 7.70e-4 ✓ sig.
hypopigmentation-punctate palmoplantar keratoderma syndrome Pseudoxanthoma elasticum 0.167 1 3.25e-4 7.70e-4 ✓ sig.
inherited pseudoxanthoma elasticum Pseudoxanthoma elasticum 0.167 1 3.25e-4 7.70e-4 ✓ sig.
Desbuquois dysplasia Pseudoxanthoma elasticum 0.125 1 9.74e-4 1.66e-3 ✓ sig.
Crystal arthropathy Pseudoxanthoma elasticum 0.111 1 1.30e-3 2.06e-3 ✓ sig.
Desbuquois dysplasia Graft versus host disease 0.100 1 1.36e-3 2.15e-3 ✓ sig.
Graft versus host disease Pseudoxanthoma elasticum 0.083 1 2.27e-3 3.19e-3 ✓ sig.