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Cluster 371

5 diseases · 7 shared-gene connections
5 Diseases
10 Unique genes
0.175 Avg. similarity score
Carbohydrate metabolism disease 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)

Disease ⇵ Connections in cluster ⇵ Significant partners ⇵ Curated genes ⇵
Carbohydrate metabolism disease 4 4 10
Carbohydrate metabolism disorder 4 4 5
MPI-congenital disorder of glycosylation 2 2 1
Transaldolase deficiency 2 2 1
Triose phosphate isomerase deficiency 2 2 1

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

Gene ⇵ Member diseases ⇵ Linked diseases
MPI 3 / 5 Carbohydrate metabolism disease, Carbohydrate metabolism disorder, MPI-congenital disorder of glycosylation
TALDO1 3 / 5 Carbohydrate metabolism disease, Carbohydrate metabolism disorder, Transaldolase deficiency
TPI1 3 / 5 Carbohydrate metabolism disease, Carbohydrate metabolism disorder, Triose phosphate isomerase deficiency
ACAT1 2 / 5 Carbohydrate metabolism disease, Carbohydrate metabolism disorder
PRKAG3 2 / 5 Carbohydrate metabolism disease, Carbohydrate metabolism disorder
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 ⇵
Carbon metabolism KEGG 5 / 115 52.2× 1.79e-8 1.45e-6 ✓ sig.
Glycolysis / Gluconeogenesis KEGG 4 / 67 71.7× 1.81e-7 1.10e-5 ✓ sig.
Glycolysis Reactome 3 / 28 129× 1.35e-6 6.33e-5 ✓ sig.
Galactose metabolism KEGG 3 / 32 113× 2.04e-6 8.92e-5 ✓ sig.
Fructose and mannose metabolism KEGG 3 / 34 106× 2.45e-6 1.05e-4 ✓ sig.
Starch and sucrose metabolism KEGG 3 / 36 100× 2.93e-6 1.22e-4 ✓ sig.
Biosynthesis of nucleotide sugars KEGG 3 / 37 97.4× 3.18e-6 1.30e-4 ✓ sig.
Insulin signaling pathway KEGG 4 / 138 34.8× 3.32e-6 1.35e-4 ✓ sig.
Amino sugar and nucleotide sugar metabolism KEGG 3 / 38 94.8× 3.45e-6 1.40e-4 ✓ sig.
Neomycin, kanamycin and gentamicin biosynthesis KEGG 2 / 5 480× 6.23e-6 2.26e-4 ✓ sig.
Metabolic pathways KEGG 7 / 1,563 5.4× 5.23e-5 1.33e-3 ✓ sig.
Glucagon signaling pathway KEGG 3 / 107 33.7× 7.88e-5 1.85e-3 ✓ sig.
Gluconeogenesis Reactome 2 / 34 70.6× 3.45e-4 5.98e-3 ✓ sig.
Type II diabetes mellitus KEGG 2 / 47 51.1× 6.61e-4 9.91e-3 ✓ sig.
Carbohydrate digestion and absorption KEGG 2 / 48 50.0× 6.90e-4 1.02e-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 ⇵
glucose 6-phosphate metabolic process GO:0051156 3 / 11 510× 1.82e-8 2.87e-6 ✓ sig.
canonical glycolysis GO:0061621 3 / 22 255× 1.69e-7 1.88e-5 ✓ sig.
glyceraldehyde-3-phosphate metabolic process GO:0019682 2 / 3 1,246× 7.73e-7 6.73e-5 ✓ sig.
carbohydrate metabolic process GO:0005975 4 / 175 42.7× 1.49e-6 1.14e-4 ✓ sig.
glycolytic process GO:0006096 3 / 49 114× 2.01e-6 1.45e-4 ✓ sig.
hexose metabolic process GO:0019318 2 / 6 623× 3.86e-6 2.44e-4 ✓ sig.
GDP-mannose biosynthetic process GO:0009298 2 / 6 623× 3.86e-6 2.44e-4 ✓ sig.
glucose metabolic process GO:0006006 3 / 66 84.9× 4.96e-6 2.98e-4 ✓ sig.
fructose 6-phosphate metabolic process GO:0006002 2 / 13 287× 2.00e-5 8.99e-4 ✓ sig.
regulation of glycolytic process GO:0006110 2 / 13 287× 2.00e-5 8.99e-4 ✓ sig.
carbohydrate phosphorylation GO:0046835 2 / 24 156× 7.07e-5 2.34e-3 ✓ sig.
intracellular glucose homeostasis GO:0001678 2 / 27 138× 8.98e-5 2.79e-3 ✓ sig.
regulation of insulin secretion GO:0050796 2 / 46 81.2× 2.63e-4 6.14e-3 ✓ sig.
gluconeogenesis GO:0006094 2 / 56 66.7× 3.91e-4 8.07e-3 ✓ sig.
methylglyoxal biosynthetic process GO:0019242 1 / 1 1,869× 5.35e-4 9.98e-3 ✓ sig.

Pairs within this cluster, by significance

Disease A ⇵ Disease B ⇵ Similarity score ⇵ Shared genes ⇵ P-value ⇵ FDR q-value ⇵
Carbohydrate metabolism disease Carbohydrate metabolism disorder 0.455 5 3.50e-17 6.09e-16 ✓ sig.
Carbohydrate metabolism disorder Triose phosphate isomerase deficiency 0.167 1 3.25e-4 7.58e-4 ✓ sig.
Carbohydrate metabolism disorder MPI-congenital disorder of glycosylation 0.167 1 3.25e-4 7.58e-4 ✓ sig.
Carbohydrate metabolism disorder Transaldolase deficiency 0.167 1 3.25e-4 7.58e-4 ✓ sig.
Carbohydrate metabolism disease Triose phosphate isomerase deficiency 0.091 1 6.49e-4 1.22e-3 ✓ sig.
Carbohydrate metabolism disease MPI-congenital disorder of glycosylation 0.091 1 6.49e-4 1.22e-3 ✓ sig.
Carbohydrate metabolism disease Transaldolase deficiency 0.091 1 6.49e-4 1.22e-3 ✓ sig.