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 130
11
Diseases
23
Unique genes
0.286
Avg. similarity score
Bladder inflammatory myofibroblastic tumor
Most-connected disease (7 links)
Disease
Searched: Nemaline myopathy 1, autosomal dominant or recessive
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Nemaline myopathy 1, autosomal dominant or recessive
Bladder inflammatory myofibroblastic tumor
Congenital generalized hypercontractile muscle stiffness syndrome
Congenital myopathy 4a, autosomal dominant
Congenital myopathy 4b, autosomal recessive
Liver inflammatory myofibroblastic tumor
Cap myopathy
Inflammatory myofibroblastic tumor
Aica-ribosiduria
Microcephaly, developmental delay, and brittle hair and nails
Spastic paraplegia 57, autosomal recessive
Member diseases (most connected first ‐ the cluster's core)
| Disease ⇵ | Connections in cluster ⇵ | Significant partners ⇵ | Curated genes ⇵ |
|---|---|---|---|
| Bladder inflammatory myofibroblastic tumor | 7 | 7 | 5 |
| Congenital generalized hypercontractile muscle stiffness syndrome | 5 | 5 | 1 |
| Congenital myopathy 4a, autosomal dominant | 5 | 5 | 1 |
| Congenital myopathy 4b, autosomal recessive | 5 | 5 | 1 |
| Liver inflammatory myofibroblastic tumor | 5 | 5 | 9 |
| Nemaline myopathy 1, autosomal dominant or recessive | 5 | 5 | 1 |
| Cap myopathy | 4 | 4 | 3 |
| Inflammatory myofibroblastic tumor | 3 | 3 | 19 |
| Aica-ribosiduria | 2 | 2 | 1 |
| Microcephaly, developmental delay, and brittle hair and nails | 2 | 2 | 1 |
| Spastic paraplegia 57, autosomal recessive | 1 | 1 | 1 |
Top shared genes (genes linked to 2+ member diseases)
| Gene ⇵ | Member diseases ⇵ | Linked diseases |
|---|---|---|
| TPM3 | 8 / 11 | Bladder inflammatory myofibroblastic tumor, Cap myopathy, Congenital generalized hypercontractile muscle stiffness syndrome, Congenital myopathy 4a, autosomal dominant and 4 more |
| ALK | 3 / 11 | Bladder inflammatory myofibroblastic tumor, Inflammatory myofibroblastic tumor, Liver inflammatory myofibroblastic tumor |
| ATIC | 3 / 11 | Aica-ribosiduria, Bladder inflammatory myofibroblastic tumor, Liver inflammatory myofibroblastic tumor |
| CARS1 | 3 / 11 | Inflammatory myofibroblastic tumor, Liver inflammatory myofibroblastic tumor, Microcephaly, developmental delay, and brittle hair and nails |
| CLTC | 3 / 11 | Bladder inflammatory myofibroblastic tumor, Inflammatory myofibroblastic tumor, Liver inflammatory myofibroblastic tumor |
| TPM4 | 3 / 11 | Bladder inflammatory myofibroblastic tumor, Inflammatory myofibroblastic tumor, Liver inflammatory myofibroblastic tumor |
| NPM1 | 2 / 11 | Inflammatory myofibroblastic tumor, Liver inflammatory myofibroblastic tumor |
| RANBP2 | 2 / 11 | Inflammatory myofibroblastic tumor, Liver inflammatory myofibroblastic tumor |
| TFG | 2 / 11 | Liver inflammatory myofibroblastic tumor, Spastic paraplegia 57, autosomal recessive |
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 ⇵ |
|---|---|---|---|---|---|
| Longevity regulating pathway | KEGG | 6 / 90 | 34.8× | 1.36e-8 | 9.77e-7 ✓ sig. |
| Prostate cancer | KEGG | 6 / 98 | 32.0× | 2.28e-8 | 1.54e-6 ✓ sig. |
| Pathways in cancer | KEGG | 9 / 533 | 8.8× | 2.92e-7 | 1.43e-5 ✓ sig. |
| Thyroid cancer | KEGG | 4 / 37 | 56.5× | 6.47e-7 | 2.86e-5 ✓ sig. |
| PI3K-Akt signaling pathway | KEGG | 7 / 361 | 10.1× | 3.38e-6 | 1.18e-4 ✓ sig. |
| Breast cancer | KEGG | 5 / 148 | 17.6× | 7.47e-6 | 2.29e-4 ✓ sig. |
| Adrenergic signaling in cardiomyocytes | KEGG | 5 / 154 | 17.0× | 9.07e-6 | 2.69e-4 ✓ sig. |
| Central carbon metabolism in cancer | KEGG | 4 / 71 | 29.4× | 9.12e-6 | 2.70e-4 ✓ sig. |
| Non-small cell lung cancer | KEGG | 4 / 73 | 28.6× | 1.02e-5 | 2.96e-4 ✓ sig. |
| Hepatitis B | KEGG | 5 / 163 | 16.0× | 1.20e-5 | 3.38e-4 ✓ sig. |
| Human papillomavirus infection | KEGG | 6 / 333 | 9.4× | 2.94e-5 | 7.13e-4 ✓ sig. |
| Transcriptional misregulation in cancer | KEGG | 5 / 198 | 13.2× | 3.06e-5 | 7.36e-4 ✓ sig. |
| Smooth Muscle Contraction | Reactome | 3 / 34 | 46.1× | 3.53e-5 | 8.29e-4 ✓ sig. |
| Viral carcinogenesis | KEGG | 5 / 205 | 12.7× | 3.61e-5 | 8.43e-4 ✓ sig. |
| Melanogenesis | KEGG | 4 / 101 | 20.7× | 3.69e-5 | 8.57e-4 ✓ 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 ⇵ |
|---|---|---|---|---|---|
| regulation of cell population proliferation | GO:0042127 | 5 / 201 | 20.2× | 3.94e-6 | 2.61e-4 ✓ sig. |
| regulation of DNA damage response, signal transduction by p53 class mediator | GO:0043516 | 2 / 7 | 232× | 3.03e-5 | 1.26e-3 ✓ sig. |
| energy homeostasis | GO:0097009 | 3 / 64 | 38.1× | 6.46e-5 | 2.24e-3 ✓ sig. |
| muscle contraction | GO:0006936 | 3 / 85 | 28.7× | 1.51e-4 | 4.16e-3 ✓ sig. |
| glial cell proliferation | GO:0014009 | 2 / 18 | 90.3× | 2.19e-4 | 5.40e-3 ✓ sig. |
| regulation of gluconeogenesis | GO:0006111 | 2 / 19 | 85.5× | 2.45e-4 | 5.86e-3 ✓ sig. |
| vascular endothelial growth factor signaling pathway | GO:0038084 | 2 / 19 | 85.5× | 2.45e-4 | 5.86e-3 ✓ sig. |
| positive regulation of cellular senescence | GO:2000774 | 2 / 20 | 81.2× | 2.72e-4 | 6.31e-3 ✓ sig. |
| regulation of mitotic spindle organization | GO:0060236 | 2 / 20 | 81.2× | 2.72e-4 | 6.31e-3 ✓ sig. |
| positive regulation of DNA-templated transcription | GO:0045893 | 6 / 778 | 6.3× | 2.81e-4 | 6.46e-3 ✓ sig. |
| protein autophosphorylation | GO:0046777 | 3 / 113 | 21.6× | 3.49e-4 | 7.48e-3 ✓ sig. |
| negative regulation of apoptotic process | GO:0043066 | 5 / 524 | 7.8× | 3.77e-4 | 7.84e-3 ✓ sig. |
| cell surface receptor protein tyrosine kinase signaling pathway | GO:0007169 | 3 / 120 | 20.3× | 4.16e-4 | 8.43e-3 ✓ sig. |
| positive regulation of transcription by RNA polymerase II | GO:0045944 | 7 / 1,208 | 4.7× | 4.54e-4 | 8.90e-3 ✓ sig. |
| osteoblast differentiation | GO:0001649 | 3 / 137 | 17.8× | 6.13e-4 | 1.09e-2 ✓ sig. |