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Cluster 69

14 diseases · 26 shared-gene connections
14 Diseases
14 Unique genes
0.261 Avg. similarity score
Central areolar choroidal dystrophy Most-connected disease (7 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
GUCY2D 6 / 14 Central areolar choroidal dystrophy, Choroidal dystrophy, Choroidal sclerosis, GUCY2D-related dominant retinopathy and 2 more
PRPH2 6 / 14 Central areolar choroidal dystrophy, Choroidal dystrophy, Choroidal sclerosis, Choroideremia and 2 more
CACNA2D4 2 / 14 CACNA2D4-related retinopathy, Retinal cone dystrophy
GUCA1A 2 / 14 Central areolar choroidal dystrophy, cone dystrophy 3
PRPF8 2 / 14 Choroideremia, PRPF8-related retinopathy
TOPORS 2 / 14 Choroideremia, TOPORS-related retinopathy
TTLL5 2 / 14 Central areolar choroidal dystrophy, TTLL5-related retinopathy
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 ⇵
Phototransduction KEGG 2 / 29 59.2× 5.03e-4 8.00e-3 ✓ sig.
Inactivation, recovery and regulation of the phototransduction cascade Reactome 2 / 33 52.0× 6.53e-4 9.80e-3 ✓ sig.
Purine metabolism KEGG 2 / 128 13.4× 9.43e-3 6.63e-2
SUMOylation of immune response proteins Reactome 1 / 11 78.0× 1.28e-2 7.89e-2
TP53 regulates transcription of several additional cell death genes whose specific roles in p53-dependent apoptosis remain uncertain Reactome 1 / 14 61.3× 1.62e-2 9.12e-2
The canonical retinoid cycle in rods (twilight vision) Reactome 1 / 20 42.9× 2.31e-2 1.12e-1
Phase 2 - plateau phase Reactome 1 / 25 34.3× 2.88e-2 1.26e-1
Endogenous sterols Reactome 1 / 25 34.3× 2.88e-2 1.26e-1
Carboxyterminal post-translational modifications of tubulin Reactome 1 / 27 31.8× 3.10e-2 1.31e-1
SUMOylation of SUMOylation proteins Reactome 1 / 34 25.2× 3.89e-2 1.49e-1
SUMOylation of transcription cofactors Reactome 1 / 41 20.9× 4.68e-2 1.65e-1
Voltage gated Potassium channels Reactome 1 / 43 20.0× 4.90e-2 1.70e-1
Phase 0 - rapid depolarisation Reactome 1 / 44 19.5× 5.01e-2 1.72e-1
mRNA Splicing - Minor Pathway Reactome 1 / 52 16.5× 5.90e-2 1.86e-1
RAB geranylgeranylation Reactome 1 / 65 13.2× 7.32e-2 2.09e-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 ⇵
visual perception GO:0007601 9 / 215 55.9× 5.69e-15 3.86e-12 ✓ sig.
detection of light stimulus involved in visual perception GO:0050908 5 / 24 278× 4.45e-12 1.76e-9 ✓ sig.
photoreceptor cell outer segment organization GO:0035845 3 / 15 267× 1.52e-7 1.72e-5 ✓ sig.
retina development in camera-type eye GO:0060041 3 / 85 47.1× 3.19e-5 1.28e-3 ✓ sig.
protein heterooligomerization GO:0051291 2 / 15 178× 5.44e-5 1.92e-3 ✓ sig.
protein homooligomerization GO:0051260 3 / 130 30.8× 1.13e-4 3.32e-3 ✓ sig.
response to low light intensity stimulus GO:0009645 1 / 1 1,335× 7.49e-4 1.25e-2 ✓ sig.
gamma-aminobutyric acid secretion, neurotransmission GO:0061534 1 / 2 667× 1.50e-3 1.91e-2 ✓ sig.
positive regulation of guanylate cyclase activity GO:0031284 1 / 2 667× 1.50e-3 1.91e-2 ✓ sig.
monoatomic ion transmembrane transport GO:0034220 3 / 404 9.9× 3.06e-3 2.85e-2 ✓ sig.
camera-type eye photoreceptor cell differentiation GO:0060219 1 / 5 267× 3.74e-3 3.18e-2 ✓ sig.
fatty acid omega-oxidation GO:0010430 1 / 6 222× 4.49e-3 3.47e-2 ✓ sig.
protein geranylgeranylation GO:0018344 1 / 6 222× 4.49e-3 3.47e-2 ✓ sig.
positive regulation of cGMP-mediated signaling GO:0010753 1 / 7 191× 5.23e-3 3.76e-2 ✓ sig.
protein localization to photoreceptor outer segment GO:1903546 1 / 7 191× 5.23e-3 3.76e-2 ✓ sig.

Pairs within this cluster, by significance

Disease A ⇵ Disease B ⇵ Similarity score ⇵ Shared genes ⇵ P-value ⇵ FDR q-value ⇵
Choroidal dystrophy Choroidal sclerosis 0.667 2 8.44e-9 7.20e-8 ✓ sig.
Central areolar choroidal dystrophy Choroidal dystrophy 0.333 2 8.44e-8 6.27e-7 ✓ sig.
Central areolar choroidal dystrophy Choroidal sclerosis 0.333 2 8.44e-8 6.27e-7 ✓ sig.
GUCY2D-related dominant retinopathy GUCY2D-related recessive retinopathy 0.500 1 6.49e-5 2.34e-4 ✓ sig.
Choroidal dystrophy PRPH2-related retinopathy 0.333 1 1.30e-4 3.90e-4 ✓ sig.
Choroidal dystrophy GUCY2D-related dominant retinopathy 0.333 1 1.30e-4 3.90e-4 ✓ sig.
Choroidal dystrophy GUCY2D-related recessive retinopathy 0.333 1 1.30e-4 3.90e-4 ✓ sig.
Choroidal sclerosis PRPH2-related retinopathy 0.333 1 1.30e-4 3.90e-4 ✓ sig.
Choroidal sclerosis GUCY2D-related dominant retinopathy 0.333 1 1.30e-4 3.90e-4 ✓ sig.
Choroidal sclerosis GUCY2D-related recessive retinopathy 0.333 1 1.30e-4 3.90e-4 ✓ sig.
PRPH2-related retinopathy Retinitis pigmentosa, digenic 0.333 1 1.30e-4 3.90e-4 ✓ sig.
Choroidal sclerosis Retinitis pigmentosa, digenic 0.250 1 2.60e-4 6.40e-4 ✓ sig.
Choroidal dystrophy Retinitis pigmentosa, digenic 0.250 1 2.60e-4 6.40e-4 ✓ sig.
CACNA2D4-related retinopathy Retinal cone dystrophy 0.167 1 3.25e-4 7.58e-4 ✓ sig.
GUCY2D-related recessive retinopathy Retinal cone dystrophy 0.167 1 3.25e-4 7.58e-4 ✓ sig.
GUCY2D-related dominant retinopathy Retinal cone dystrophy 0.167 1 3.25e-4 7.58e-4 ✓ sig.
Central areolar choroidal dystrophy GUCY2D-related recessive retinopathy 0.167 1 3.25e-4 7.58e-4 ✓ sig.
Central areolar choroidal dystrophy TTLL5-related retinopathy 0.167 1 3.25e-4 7.58e-4 ✓ sig.
Central areolar choroidal dystrophy cone dystrophy 3 0.167 1 3.25e-4 7.58e-4 ✓ sig.
Choroideremia TOPORS-related retinopathy 0.167 1 3.25e-4 7.58e-4 ✓ sig.
Choroideremia PRPF8-related retinopathy 0.167 1 3.25e-4 7.58e-4 ✓ sig.
Choroideremia PRPH2-related retinopathy 0.167 1 3.25e-4 7.58e-4 ✓ sig.
Central areolar choroidal dystrophy GUCY2D-related dominant retinopathy 0.167 1 3.25e-4 7.58e-4 ✓ sig.
Central areolar choroidal dystrophy PRPH2-related retinopathy 0.167 1 3.25e-4 7.58e-4 ✓ sig.
Choroidal sclerosis Choroideremia 0.143 1 6.49e-4 1.22e-3 ✓ sig.
Choroidal dystrophy Choroideremia 0.143 1 6.49e-4 1.22e-3 ✓ sig.