FFCP PHASE1:Hg19::chr17:1936721..1936751,+: Difference between revisions
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m (moved FFCP PHASE1 hg19::chr17:1936721..1936751,+ to FFCP PHASE1:Hg19::chr17:1936721..1936751,+: NSchange) |
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{{FFCP | {{FFCP | ||
| | |DHSsupport=supported | ||
| | |DPIdataset=robust | ||
|EntrezGene=1801 | |EntrezGene=1801 | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=gencodeV16_protein_coding | |||
|HGNC=3003 | |HGNC=3003 | ||
|TSSclassifier=strong | |||
|UniProt=B4DNK0 | |UniProt=B4DNK0 | ||
|association_with_transcript=34bp_to_AK297947_5end | |||
|cluster_id=chr17:1936721..1936751,+ | |||
|description=CAGE_peak_3_at_DPH1_5end | |||
|id=chr17:1936721..1936751,+ | |||
|ontology_enrichment_celltype=CL:0002620!5.66e-26!23;CL:0000057!2.49e-16!75;CL:0000062!1.11e-13!11;CL:0000375!1.11e-13!11;CL:0000335!1.11e-13!11;CL:0000055!1.11e-11!180;CL:0002579!3.19e-08!3;CL:0000035!7.47e-07!20 | |||
|ontology_enrichment_celltype_v019=CL:0002620;3.21e-40;23!CL:0000138;2.91e-07;6 | |||
|ontology_enrichment_celltype_v019_2=CL:0002620,2.41e-40,23;CL:0000057,2.91e-16,76;CL:0000058,2.78e-07,6;CL:0000138,2.78e-07,6 | |||
|ontology_enrichment_development_v019= | |||
|ontology_enrichment_disease=DOID:17!1.66e-13!5;DOID:450!1.66e-13!5;DOID:66!1.66e-13!5;DOID:423!1.66e-13!5;DOID:0080000!1.66e-13!5;DOID:11722!1.66e-13!5 | |||
|ontology_enrichment_disease_v019=DOID:17;1.35e-17;5!DOID:450;1.35e-17;5!DOID:66;1.35e-17;5!DOID:423;1.35e-17;5!DOID:0080000;1.35e-17;5!DOID:11722;1.35e-17;5 | |||
|ontology_enrichment_disease_v019_2=DOID:17,9.91e-18,5;DOID:450,9.91e-18,5;DOID:66,9.91e-18,5;DOID:423,9.91e-18,5;DOID:0080000,9.91e-18,5;DOID:11722,9.91e-18,5 | |||
|ontology_enrichment_uberon=UBERON:0002097!6.49e-17!40;UBERON:0002199!1.77e-14!45;UBERON:0002416!1.77e-14!45;UBERON:0003102!1.93e-13!95;UBERON:0003688!8.37e-07!6;UBERON:0002358!8.37e-07!6;UBERON:0003684!8.37e-07!6;UBERON:0001178!8.37e-07!6 | |||
|ontology_enrichment_uberon_v019=UBERON:0002097;2.93e-19;41!UBERON:0002199;5.87e-15;46!UBERON:0002416;5.87e-15;46!UBERON:0003102;1.57e-13;50 | |||
|ontology_enrichment_uberon_v019_2=UBERON:0002097,1.29e-26,41;UBERON:0002199,1.51e-23,46;UBERON:0002416,1.51e-23,46;UBERON:0003102,3.09e-14,99 | |||
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| ||
|short_description=p3@DPH1 | |||
}} | }} |
Latest revision as of 00:16, 19 September 2015
Short description: | p3@DPH1 |
---|---|
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_DPH1_5end |
Coexpression cluster: | NA |
Association with transcript: | 34bp_to_AK297947_5end |
EntrezGene: | DPH1 |
HGNC: | 3003 |
UniProt: | B4DNK0 |
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 |
---|---|---|
skin fibroblast | 2.41e-40 | 23 |
fibroblast | 2.91e-16 | 76 |
chondroblast | 2.78e-07 | 6 |
chondrocyte | 2.78e-07 | 6 |
Ontology term | p-value | n |
---|---|---|
skin of body | 1.29e-26 | 41 |
integument | 1.51e-23 | 46 |
integumental system | 1.51e-23 | 46 |
surface structure | 3.09e-14 | 99 |
Ontology term | p-value | n |
---|---|---|
musculoskeletal system disease | 9.91e-18 | 5 |
myotonic disease | 9.91e-18 | 5 |
muscle tissue disease | 9.91e-18 | 5 |
myopathy | 9.91e-18 | 5 |
muscular disease | 9.91e-18 | 5 |
myotonic dystrophy | 9.91e-18 | 5 |