FFCP PHASE1:Hg19::chr6:155504446..155504462,+
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Short description: | p5@TIAM2 |
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Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_5_at_TIAM2_5end |
Coexpression cluster: | C2849_Mast_plasma_splenic_migratory_Burkitt_CD14CD16_xeroderma |
Association with transcript: | 0bp_to_ENST00000543712_5end |
EntrezGene: | TIAM2 |
HGNC: | 11806 |
UniProt: | NA |
Genome view: | ZENBU |
View on UCSC genome browser
CAGE Expression
Sample | p5@TIAM2 |
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0.0
2.5
5.0
7.5
10.0
12.5
- 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 |
---|---|---|
hematopoietic cell | 2.05e-25 | 177 |
leukocyte | 2.14e-25 | 136 |
hematopoietic oligopotent progenitor cell | 1.71e-22 | 161 |
hematopoietic multipotent progenitor cell | 1.71e-22 | 161 |
hematopoietic stem cell | 2.49e-21 | 168 |
non-classical monocyte | 2.10e-18 | 3 |
CD14-low, CD16-positive monocyte | 2.10e-18 | 3 |
hematopoietic lineage restricted progenitor cell | 2.48e-18 | 120 |
classical monocyte | 3.12e-17 | 42 |
CD14-positive, CD16-negative classical monocyte | 3.12e-17 | 42 |
Showing 1 to 10 of 33 entries
Ontology term | p-value | n |
---|---|---|
hematopoietic system | 6.69e-19 | 98 |
blood island | 6.69e-19 | 98 |
hemolymphoid system | 8.92e-17 | 108 |
bone marrow | 8.32e-12 | 76 |
bone element | 9.51e-11 | 82 |
immune system | 1.01e-10 | 93 |
skeletal element | 1.48e-09 | 90 |
blood | 3.59e-09 | 15 |
haemolymphatic fluid | 3.59e-09 | 15 |
organism substance | 3.59e-09 | 15 |
Showing 1 to 10 of 12 entries
Ontology term | p-value | n |
---|---|---|
genetic disease | 4.31e-07 | 1 |
monogenic disease | 4.31e-07 | 1 |
xeroderma pigmentosum | 4.31e-07 | 1 |
Showing 1 to 3 of 3 entries