FFCP PHASE2:Hg19::chr2:201997681..201997696,+
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| Short description: | p31@CFLAR |
|---|---|
| Species: | Human (Homo sapiens) |
| DPI dataset: | Robust |
| TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
| DHS support(Yes/No): | Yes |
| Description: | CAGE_peak_31_at_CFLAR_5end |
| Coexpression cluster: | C80_immature_migratory_CD14_Dendritic_splenic_cord_Mast |
| Association with transcript: | 0bp_to_NM_001202518_5end |
| EntrezGene: | CFLAR |
| HGNC: | 1876 |
| UniProt: | B4E361O15519 |
| Genome view: | ZENBU |
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CAGE Expression
| Sample | p31@CFLAR |
|---|
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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 |
|---|---|---|
| conventional dendritic cell | 4.54e-38 | 8 |
| dendritic cell | 6.25e-31 | 10 |
| Langerhans cell | 1.69e-28 | 5 |
| immature conventional dendritic cell | 1.84e-22 | 5 |
| common dendritic progenitor | 1.84e-22 | 5 |
| myeloid cell | 3.87e-17 | 108 |
| common myeloid progenitor | 3.87e-17 | 108 |
| granulocyte monocyte progenitor cell | 1.10e-16 | 67 |
| macrophage dendritic cell progenitor | 3.35e-16 | 61 |
| leukocyte | 9.31e-13 | 136 |
Showing 1 to 10 of 35 entries
| Ontology term | p-value | n |
|---|---|---|
| immune system | 2.51e-16 | 93 |
| bone marrow | 2.50e-14 | 76 |
| hemolymphoid system | 1.66e-13 | 108 |
| bone element | 4.82e-13 | 82 |
| hematopoietic system | 6.03e-12 | 98 |
| blood island | 6.03e-12 | 98 |
| skeletal element | 1.35e-11 | 90 |
| skeletal system | 4.12e-10 | 100 |
| lateral plate mesoderm | 8.66e-10 | 203 |
| endothelial tube | 2.56e-09 | 9 |
Showing 1 to 10 of 15 entries
| Ontology term | p-value | n |
|---|---|---|
| genetic disease | 7.60e-07 | 1 |
| monogenic disease | 7.60e-07 | 1 |
| xeroderma pigmentosum | 7.60e-07 | 1 |
Showing 1 to 3 of 3 entries
