FFCP PHASE1:Hg19::chr3:69101461..69101494,-: Difference between revisions
From FANTOM5_SSTAR
m (moved FFCP PHASE1 hg19::chr3:69101461..69101494,- to FFCP PHASE1:Hg19::chr3:69101461..69101494,-: NSchange) |
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{{FFCP | {{FFCP | ||
| | |DHSsupport=supported | ||
| | |DPIdataset=robust | ||
|EntrezGene=7110 | |EntrezGene=7110 | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=gencodeV16_protein_coding | |||
|HGNC=11870 | |HGNC=11870 | ||
|TSSclassifier=strong | |||
|UniProt=E9PGE8,E7EWX9,P82094,Q6PII6 | |UniProt=E9PGE8,E7EWX9,P82094,Q6PII6 | ||
|association_with_transcript=0bp_to_ENST00000356248,ENST00000438636,ENST00000543976,NM_007114,uc003dnn.2,uc011bfx.1_5end | |||
|cluster_id=chr3:69101461..69101494,- | |||
|description=CAGE_peak_2_at_TMF1_5end | |||
|id=chr3:69101461..69101494,- | |||
|ontology_enrichment_celltype=CL:0000738!2.05e-09!140;CL:0002031!2.21e-07!124 | |||
|ontology_enrichment_celltype_v019= | |||
|ontology_enrichment_celltype_v019_2=CL:0000738,7.39e-10,136;CL:0002031,8.82e-08,120 | |||
|ontology_enrichment_development_v019= | |||
|ontology_enrichment_disease= | |||
|ontology_enrichment_disease_v019= | |||
|ontology_enrichment_disease_v019_2= | |||
|ontology_enrichment_uberon= | |||
|ontology_enrichment_uberon_v019= | |||
|ontology_enrichment_uberon_v019_2= | |||
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| ||
|short_description=p2@TMF1 | |||
}} | }} |
Latest revision as of 11:16, 19 September 2015
Short description: | p2@TMF1 |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_2_at_TMF1_5end |
Coexpression cluster: | NA |
Association with transcript: | 0bp_to_ENST00000356248, ENST00000438636, ENST00000543976, NM_007114, uc003dnn.2, uc011bfx.1_5end |
EntrezGene: | TMF1 |
HGNC: | 11870 |
UniProt: | E9PGE8E7EWX9P82094Q6PII6 |
Genome view: | ZENBU |
View on UCSC genome browser
CAGE Expression
- 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 |
---|---|---|
leukocyte | 7.39e-10 | 136 |
hematopoietic lineage restricted progenitor cell | 8.82e-08 | 120 |