FFCP PHASE2:Hg19::chr8:93074872..93074884,-
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| Short description: | p10@RUNX1T1 |
|---|---|
| Species: | Human (Homo sapiens) |
| DPI dataset: | Robust |
| TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
| DHS support(Yes/No): | Yes |
| Description: | CAGE_peak_10_at_RUNX1T1_5end |
| Coexpression cluster: | C4779_cerebellum_occipital_Hair_Fibroblast_heart_caudate_neuroectodermal |
| Association with transcript: | 306bp_to_ENST00000396218, NM_004349, uc003yfc.1_5end |
| EntrezGene: | RUNX1T1 |
| HGNC: | 1535 |
| UniProt: | Q06455 |
| Genome view: | ZENBU |
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CAGE Expression
| Sample | p10@RUNX1T1 |
|---|
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- Click each plot point to find sample in table
Ontology-based sample term enrichment analysis<b>Summary:</b>This analysis has been performed by utilizing wilcoxon rank sum test.When the number of associated cells/tissues are > n , randomly sampled n cells/tissues are used for P value calculation with rank sum test. this process are repeated several times, and the P values are averaged on the log space <br><b>Analyst:</b> Hideya Kawaji<br><br>link to source dataset<br>data
| Ontology term | p-value | n |
|---|---|---|
| skin fibroblast | 4.46e-16 | 23 |
| fibroblast | 7.54e-16 | 76 |
| outer root sheath cell | 5.24e-07 | 2 |
Showing 1 to 3 of 3 entries
| Ontology term | p-value | n |
|---|---|---|
| skin of body | 8.07e-13 | 41 |
| regional part of telencephalon | 1.85e-11 | 32 |
| cerebral hemisphere | 1.85e-11 | 32 |
| integument | 5.02e-11 | 46 |
| integumental system | 5.02e-11 | 46 |
| brain grey matter | 1.22e-10 | 34 |
| gray matter | 1.22e-10 | 34 |
| telencephalon | 1.22e-10 | 34 |
| regional part of forebrain | 6.25e-10 | 41 |
| forebrain | 6.25e-10 | 41 |
Showing 1 to 10 of 43 entries
| Ontology term | p-value | n |
|---|---|---|
| musculoskeletal system disease | 2.49e-10 | 5 |
| myotonic disease | 2.49e-10 | 5 |
| muscle tissue disease | 2.49e-10 | 5 |
| myopathy | 2.49e-10 | 5 |
| muscular disease | 2.49e-10 | 5 |
| myotonic dystrophy | 2.49e-10 | 5 |
Showing 1 to 6 of 6 entries
