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Cluster 311

6 diseases · 8 shared-gene connections
6 Diseases
5 Unique genes
0.283 Avg. similarity score
Micropenis 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)

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

Gene ⇵ Member diseases ⇵ Linked diseases
FIG4 4 / 6 amyotrophic lateral sclerosis type 11, Bilateral parasagittal parieto-occipital polymicrogyria, Micropenis, Yunis-varon syndrome
ANOS1 2 / 6 hypogonadotropic hypogonadism 1 with or without anosmia, Micropenis
VAC14 2 / 6 Childhood-onset basal ganglia degeneration syndrome, Yunis-varon 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 ⇵
Synthesis of PIPs at the late endosome membrane Reactome 2 / 10 480× 6.23e-6 2.26e-4 ✓ sig.
Synthesis of PIPs at the early endosome membrane Reactome 2 / 15 320× 1.45e-5 4.57e-4 ✓ sig.
Synthesis of PIPs at the Golgi membrane Reactome 2 / 18 267× 2.12e-5 6.27e-4 ✓ sig.
Androgen biosynthesis Reactome 1 / 11 218× 4.57e-3 4.13e-2 ✓ sig.
FGFR1c ligand binding and activation Reactome 1 / 12 200× 4.99e-3 4.37e-2 ✓ sig.
BBSome-mediated cargo-targeting to cilium Reactome 1 / 23 104× 9.54e-3 6.67e-2
Negative regulation of FGFR1 signaling Reactome 1 / 26 92.4× 1.08e-2 7.19e-2
Steroid hormone biosynthesis KEGG 1 / 63 38.1× 2.60e-2 1.19e-1
Inositol phosphate metabolism KEGG 1 / 73 32.9× 3.00e-2 1.29e-1
Prostate cancer KEGG 1 / 98 24.5× 4.01e-2 1.52e-1
Viral carcinogenesis KEGG 1 / 205 11.7× 8.25e-2 2.23e-1
Human T-cell leukemia virus 1 infection KEGG 1 / 224 10.7× 8.99e-2 2.33e-1
Metabolic pathways KEGG 2 / 1,563 3.1× 1.29e-1 2.85e-1
Amyotrophic lateral sclerosis KEGG 1 / 368 6.5× 1.44e-1 3.03e-1
Pathways of neurodegeneration - multiple diseases KEGG 1 / 480 5.0× 1.85e-1 3.48e-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 ⇵
phosphatidylinositol biosynthetic process GO:0006661 2 / 44 170× 5.39e-5 1.90e-3 ✓ sig.
phthalate metabolic process GO:0018963 1 / 1 3,737× 2.68e-4 6.20e-3 ✓ sig.
biphenyl metabolic process GO:0018879 1 / 2 1,869× 5.35e-4 9.98e-3 ✓ sig.
dibenzo-p-dioxin metabolic process GO:0018894 1 / 3 1,246× 8.03e-4 1.30e-2 ✓ sig.
response to biphenyl GO:1904614 1 / 3 1,246× 8.03e-4 1.30e-2 ✓ sig.
response to follicle-stimulating hormone GO:0032354 1 / 4 934× 1.07e-3 1.57e-2 ✓ sig.
receptor localization to non-motile cilium GO:0097500 1 / 5 747× 1.34e-3 1.79e-2 ✓ sig.
testosterone biosynthetic process GO:0061370 1 / 6 623× 1.60e-3 1.98e-2 ✓ sig.
steroid catabolic process GO:0006706 1 / 7 534× 1.87e-3 2.19e-2 ✓ sig.
myelin assembly GO:0032288 1 / 7 534× 1.87e-3 2.19e-2 ✓ sig.
female genitalia development GO:0030540 1 / 7 534× 1.87e-3 2.19e-2 ✓ sig.
androgen biosynthetic process GO:0006702 1 / 9 415× 2.41e-3 2.50e-2 ✓ sig.
negative regulation of myelination GO:0031642 1 / 9 415× 2.41e-3 2.50e-2 ✓ sig.
leukocyte homeostasis GO:0001776 1 / 9 415× 2.41e-3 2.50e-2 ✓ sig.
myeloid cell homeostasis GO:0002262 1 / 11 340× 2.94e-3 2.79e-2 ✓ sig.

Pairs within this cluster, by significance

Disease A ⇵ Disease B ⇵ Similarity score ⇵ Shared genes ⇵ P-value ⇵ FDR q-value ⇵
amyotrophic lateral sclerosis type 11 Bilateral parasagittal parieto-occipital polymicrogyria 0.500 1 6.49e-5 2.34e-4 ✓ sig.
amyotrophic lateral sclerosis type 11 Yunis-varon syndrome 0.333 1 1.30e-4 3.90e-4 ✓ sig.
Bilateral parasagittal parieto-occipital polymicrogyria Yunis-varon syndrome 0.333 1 1.30e-4 3.90e-4 ✓ sig.
Childhood-onset basal ganglia degeneration syndrome Yunis-varon syndrome 0.333 1 1.30e-4 3.90e-4 ✓ sig.
amyotrophic lateral sclerosis type 11 Micropenis 0.200 1 2.60e-4 6.40e-4 ✓ sig.
Bilateral parasagittal parieto-occipital polymicrogyria Micropenis 0.200 1 2.60e-4 6.40e-4 ✓ sig.
hypogonadotropic hypogonadism 1 with or without anosmia Micropenis 0.200 1 2.60e-4 6.40e-4 ✓ sig.
Micropenis Yunis-varon syndrome 0.167 1 5.19e-4 1.04e-3 ✓ sig.