Disease Clusters?
Groups of diseases that share a large number of curated genes with each other, computed via label propagation over the shared-gene similarity graph. See also Shared-Gene Disease Pairs for pairwise comparisons.
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Cluster 73
14
Diseases
30
Unique genes
0.418
Avg. similarity score
Spindle cell lipoma
Most-connected disease (13 links)
Disease
Searched: Myoepithelial tumor
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Myoepithelial tumor
Spindle cell lipoma
Keloid
Angiolipoma
Low grade fibromyxoid sarcoma with giant collagen rosettes
Parachordoma
Giant cell tumor of soft tissue
Amyotrophic lateral sclerosis type 6
Cutaneous fibrous histiocytoma
Epithelioid hemangioendothelioma
Myxoma
Ossifying fibroma
Congenital fibrosarcoma
Nodular fasciitis
Member diseases (most connected first ‐ the cluster's core)
| Disease ⇵ | Connections in cluster ⇵ | Significant partners ⇵ | Curated genes ⇵ |
|---|---|---|---|
| Spindle cell lipoma | 13 | 13 | 3 |
| Keloid | 11 | 11 | 4 |
| Angiolipoma | 8 | 8 | 3 |
| Low grade fibromyxoid sarcoma with giant collagen rosettes | 8 | 8 | 2 |
| Parachordoma | 8 | 8 | 2 |
| Giant cell tumor of soft tissue | 7 | 7 | 2 |
| Amyotrophic lateral sclerosis type 6 | 5 | 5 | 1 |
| Cutaneous fibrous histiocytoma | 5 | 5 | 9 |
| Epithelioid hemangioendothelioma | 5 | 5 | 6 |
| Myoepithelial tumor | 5 | 5 | 7 |
| Myxoma | 5 | 5 | 9 |
| Ossifying fibroma | 5 | 5 | 9 |
| Congenital fibrosarcoma | 4 | 4 | 7 |
| Nodular fasciitis | 3 | 3 | 9 |
Top shared genes (genes linked to 2+ member diseases)
| Gene ⇵ | Member diseases ⇵ | Linked diseases |
|---|---|---|
| FUS | 14 / 14 | Amyotrophic lateral sclerosis type 6, Angiolipoma, Congenital fibrosarcoma, Cutaneous fibrous histiocytoma and 10 more |
| CREB3L2 | 13 / 14 | Angiolipoma, Congenital fibrosarcoma, Cutaneous fibrous histiocytoma, Epithelioid hemangioendothelioma and 9 more |
| CREB3L1 | 9 / 14 | Angiolipoma, Congenital fibrosarcoma, Cutaneous fibrous histiocytoma, Keloid and 5 more |
| COL1A1 | 3 / 14 | Congenital fibrosarcoma, Cutaneous fibrous histiocytoma, Nodular fasciitis |
| EWSR1 | 3 / 14 | Cutaneous fibrous histiocytoma, Myoepithelial tumor, Myxoma |
| PDGFB | 3 / 14 | Congenital fibrosarcoma, Cutaneous fibrous histiocytoma, Nodular fasciitis |
| DDIT3 | 2 / 14 | Cutaneous fibrous histiocytoma, Myxoma |
| ETV6 | 2 / 14 | Congenital fibrosarcoma, Nodular fasciitis |
| NTRK3 | 2 / 14 | Congenital fibrosarcoma, Nodular fasciitis |
| TP53 | 2 / 14 | Keloid, Ossifying fibroma |
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 ⇵ |
|---|---|---|---|---|---|
| PI3K-Akt signaling pathway | KEGG | 13 / 361 | 14.4× | 9.96e-13 | 1.90e-10 ✓ sig. |
| Prostate cancer | KEGG | 9 / 98 | 36.8× | 1.37e-12 | 2.52e-10 ✓ sig. |
| Human papillomavirus infection | KEGG | 12 / 333 | 14.4× | 9.37e-12 | 1.43e-9 ✓ sig. |
| Central carbon metabolism in cancer | KEGG | 7 / 71 | 39.5× | 3.41e-10 | 3.53e-8 ✓ sig. |
| Longevity regulating pathway | KEGG | 7 / 90 | 31.1× | 1.85e-9 | 1.62e-7 ✓ sig. |
| Melanogenesis | KEGG | 7 / 101 | 27.7× | 4.19e-9 | 3.40e-7 ✓ sig. |
| Growth hormone synthesis, secretion and action | KEGG | 7 / 122 | 23.0× | 1.57e-8 | 1.11e-6 ✓ sig. |
| Transcriptional misregulation in cancer | KEGG | 8 / 198 | 16.2× | 2.03e-8 | 1.38e-6 ✓ sig. |
| Melanoma | KEGG | 6 / 73 | 32.9× | 2.16e-8 | 1.46e-6 ✓ sig. |
| Relaxin signaling pathway | KEGG | 7 / 130 | 21.6× | 2.45e-8 | 1.63e-6 ✓ sig. |
| Human T-cell leukemia virus 1 infection | KEGG | 8 / 224 | 14.3× | 5.31e-8 | 3.21e-6 ✓ sig. |
| Human cytomegalovirus infection | KEGG | 8 / 226 | 14.2× | 5.69e-8 | 3.41e-6 ✓ sig. |
| Hepatitis B | KEGG | 7 / 163 | 17.2× | 1.17e-7 | 6.40e-6 ✓ sig. |
| Hepatocellular carcinoma | KEGG | 7 / 170 | 16.5× | 1.56e-7 | 8.24e-6 ✓ sig. |
| Endometrial cancer | KEGG | 5 / 59 | 33.9× | 3.12e-7 | 1.51e-5 ✓ 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 ⇵ |
|---|---|---|---|---|---|
| positive regulation of transcription by RNA polymerase II | GO:0045944 | 14 / 1,208 | 7.2× | 1.13e-9 | 2.57e-7 ✓ sig. |
| heart development | GO:0007507 | 7 / 273 | 16.0× | 2.01e-7 | 2.27e-5 ✓ sig. |
| negative regulation of cell population proliferation | GO:0008285 | 8 / 444 | 11.2× | 3.53e-7 | 3.63e-5 ✓ sig. |
| regulation of transcription by RNA polymerase II | GO:0006357 | 13 / 1,602 | 5.1× | 3.84e-7 | 3.89e-5 ✓ sig. |
| regulation of DNA-templated transcription | GO:0006355 | 12 / 1,454 | 5.1× | 1.08e-6 | 9.19e-5 ✓ sig. |
| cell surface receptor protein tyrosine kinase signaling pathway | GO:0007169 | 5 / 120 | 26.0× | 1.26e-6 | 1.04e-4 ✓ sig. |
| positive regulation of DNA-templated transcription | GO:0045893 | 9 / 778 | 7.2× | 2.33e-6 | 1.72e-4 ✓ sig. |
| cell migration | GO:0016477 | 6 / 303 | 12.3× | 7.40e-6 | 4.31e-4 ✓ sig. |
| negative regulation of gene expression | GO:0010629 | 6 / 339 | 11.0× | 1.40e-5 | 7.08e-4 ✓ sig. |
| positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction | GO:0051897 | 5 / 217 | 14.4× | 2.27e-5 | 1.02e-3 ✓ sig. |
| positive regulation of RNA polymerase II transcription preinitiation complex assembly | GO:0045899 | 2 / 5 | 249× | 2.48e-5 | 1.09e-3 ✓ sig. |
| response to purine-containing compound | GO:0014074 | 2 / 7 | 178× | 5.21e-5 | 1.90e-3 ✓ sig. |
| regulation of cell cycle | GO:0051726 | 5 / 262 | 11.9× | 5.58e-5 | 2.00e-3 ✓ sig. |
| positive chemotaxis | GO:0050918 | 3 / 51 | 36.6× | 7.38e-5 | 2.47e-3 ✓ sig. |
| visual learning | GO:0008542 | 3 / 54 | 34.6× | 8.76e-5 | 2.81e-3 ✓ sig. |