FFCP PHASE1:Hg19::chr2:176973557..176973561,+: Difference between revisions
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{{FFCP | {{FFCP | ||
| | |DHSsupport=supported | ||
| | |DPIdataset=robust | ||
|EntrezGene=3236 | |EntrezGene=3236 | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=gencodeV16_protein_coding | |||
|HGNC=5133 | |HGNC=5133 | ||
|TSSclassifier=strong | |||
|UniProt= | |UniProt= | ||
|association_with_transcript=39bp_to_ENST00000490088_5end | |||
|cluster_id=chr2:176973557..176973561,+ | |||
|description=CAGE_peak_10_at_HOXD10_5end | |||
|id=chr2:176973557..176973561,+ | |||
|ontology_enrichment_celltype=CL:0002553!1.41e-08!1 | |||
|ontology_enrichment_celltype_v019= | |||
|ontology_enrichment_celltype_v019_2= | |||
|ontology_enrichment_development_v019=UBERON:0003918;2.87e-11;10!UBERON:0007687;2.87e-11;10 | |||
|ontology_enrichment_disease= | |||
|ontology_enrichment_disease_v019=DOID:17;4.66e-21;5!DOID:450;4.66e-21;5!DOID:66;4.66e-21;5!DOID:423;4.66e-21;5!DOID:0080000;4.66e-21;5!DOID:11722;4.66e-21;5 | |||
|ontology_enrichment_disease_v019_2=DOID:17,4.21e-21,5;DOID:450,4.21e-21,5;DOID:66,4.21e-21,5;DOID:423,4.21e-21,5;DOID:0080000,4.21e-21,5;DOID:11722,4.21e-21,5 | |||
|ontology_enrichment_uberon=UBERON:0006834!3.10e-08!1 | |||
|ontology_enrichment_uberon_v019= | |||
|ontology_enrichment_uberon_v019_2= | |||
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|short_description=p10@HOXD10 | |||
}} | }} |
Latest revision as of 08:56, 18 September 2015
Short description: | p10@HOXD10 |
---|---|
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_HOXD10_5end |
Coexpression cluster: | NA |
Association with transcript: | 39bp_to_ENST00000490088_5end |
EntrezGene: | HOXD10 |
HGNC: | 5133 |
UniProt: | NA |
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 |
---|---|---|
musculoskeletal system disease | 4.21e-21 | 5 |
myotonic disease | 4.21e-21 | 5 |
muscle tissue disease | 4.21e-21 | 5 |
myopathy | 4.21e-21 | 5 |
muscular disease | 4.21e-21 | 5 |
myotonic dystrophy | 4.21e-21 | 5 |