FFCP PHASE1:Hg19::chr22:39493207..39493223,+
From FANTOM5_SSTAR
Jump to: navigation, search
| Short description: | p3@APOBEC3H |
|---|---|
| Species: | Human (Homo sapiens) |
| DPI dataset: | Robust |
| TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
| DHS support(Yes/No): | Yes |
| Description: | CAGE_peak_3_at_APOBEC3H_5end |
| Coexpression cluster: | C239_CD4_lymphangiectasia_CD8_NK_mycosis_Renal_hairy |
| Association with transcript: | -5bp_to_ENST00000348946, ENST00000421988, ENST00000442487, NM_001166002, NM_001166003, NM_001166004, NM_181773_5end |
| EntrezGene: | APOBEC3H |
| HGNC: | 24100 |
| UniProt: | E9PF38Q6NTF7B7TQM5B7TQM9B7TQM3 |
| Genome view: | ZENBU |
View on UCSC genome browser
Mouse over to see Genome browser image, Click image to go to Genome browser
CAGE Expression
| Sample | p3@APOBEC3H |
|---|
0
1
2
3
4
5
6
7
- 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 |
|---|---|---|
| lymphocyte | 2.41e-27 | 53 |
| common lymphoid progenitor | 2.41e-27 | 53 |
| lymphoid lineage restricted progenitor cell | 1.39e-24 | 52 |
| mature alpha-beta T cell | 2.07e-19 | 18 |
| alpha-beta T cell | 2.07e-19 | 18 |
| immature T cell | 2.07e-19 | 18 |
| mature T cell | 2.07e-19 | 18 |
| immature alpha-beta T cell | 2.07e-19 | 18 |
| CD8-positive, alpha-beta T cell | 2.25e-18 | 11 |
| T cell | 4.19e-17 | 25 |
Showing 1 to 10 of 49 entries
| Ontology term | p-value | n |
|---|---|---|
| thymus | 8.45e-07 | 4 |
| hemolymphoid system gland | 8.45e-07 | 4 |
| thymic region | 8.45e-07 | 4 |
| pharyngeal gland | 8.45e-07 | 4 |
| thymus primordium | 8.45e-07 | 4 |
Showing 1 to 5 of 5 entries
| Ontology term | p-value | n |
|---|---|---|
| genetic disease | 2.52e-07 | 1 |
| monogenic disease | 2.52e-07 | 1 |
| xeroderma pigmentosum | 2.52e-07 | 1 |
| acute leukemia | 5.14e-07 | 1 |
Showing 1 to 4 of 4 entries
