FFCP PHASE1:Hg19::chr13:24044200..24044211,+: Difference between revisions
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{{FFCP | {{FFCP | ||
| | |DHSsupport=supported | ||
| | |DPIdataset=robust | ||
|EntrezGene= | |EntrezGene= | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=novel_noncoding | |||
|HGNC=42009 | |HGNC=42009 | ||
|TSSclassifier=strong | |||
|UniProt= | |UniProt= | ||
|association_with_transcript=14bp_to_ENST00000443778_5end | |||
|cluster_id=chr13:24044200..24044211,+ | |||
|description=CAGE_peak_2_at_LINC00327_5end | |||
|id=chr13:24044200..24044211,+ | |||
|ontology_enrichment_celltype=CL:0002620!1.16e-51!23;CL:0000057!3.18e-21!75;CL:0000055!1.20e-08!180;CL:0002551!7.16e-08!6 | |||
|ontology_enrichment_celltype_v019=CL:0002620;7.60e-79;23!CL:0000057;2.23e-09;73 | |||
|ontology_enrichment_celltype_v019_2=CL:0002620,5.28e-79,23;CL:0000057,2.30e-23,76 | |||
|ontology_enrichment_development_v019= | |||
|ontology_enrichment_disease=DOID:17!8.39e-25!5;DOID:450!8.39e-25!5;DOID:66!8.39e-25!5;DOID:423!8.39e-25!5;DOID:0080000!8.39e-25!5;DOID:11722!8.39e-25!5 | |||
|ontology_enrichment_disease_v019=DOID:17;9.74e-49;5!DOID:450;9.74e-49;5!DOID:66;9.74e-49;5!DOID:423;9.74e-49;5!DOID:0080000;9.74e-49;5!DOID:11722;9.74e-49;5!DOID:7;3.22e-09;39 | |||
|ontology_enrichment_disease_v019_2=DOID:17,8.65e-49,5;DOID:450,8.65e-49,5;DOID:66,8.65e-49,5;DOID:423,8.65e-49,5;DOID:0080000,8.65e-49,5;DOID:11722,8.65e-49,5;DOID:7,9.08e-10,39 | |||
|ontology_enrichment_uberon=UBERON:0002097!4.47e-40!40;UBERON:0002199!6.13e-39!45;UBERON:0002416!6.13e-39!45;UBERON:0003102!1.31e-19!95;UBERON:0003127!4.21e-10!2;UBERON:0002067!6.65e-09!9;UBERON:0004016!6.65e-09!9;UBERON:0010083!6.65e-09!9 | |||
|ontology_enrichment_uberon_v019=UBERON:0002097;5.32e-34;41!UBERON:0002199;7.21e-27;46!UBERON:0002416;7.21e-27;46!UBERON:0003102;1.43e-22;50!UBERON:0002067;1.02e-07;9 | |||
|ontology_enrichment_uberon_v019_2=UBERON:0002097,2.03e-52,41;UBERON:0002199,1.23e-46,46;UBERON:0002416,1.23e-46,46;UBERON:0003102,3.44e-21,99;UBERON:0002067,1.17e-07,9;UBERON:0004016,1.17e-07,9;UBERON:0010083,1.17e-07,9 | |||
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|short_description=p2@LINC00327 | |||
}} | }} |
Latest revision as of 20:48, 16 September 2015
Short description: | p2@LINC00327 |
---|---|
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_LINC00327_5end |
Coexpression cluster: | NA |
Association with transcript: | 14bp_to_ENST00000443778_5end |
EntrezGene: | NA |
HGNC: | 42009 |
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 |
---|---|---|
skin fibroblast | 5.28e-79 | 23 |
fibroblast | 2.30e-23 | 76 |
Ontology term | p-value | n |
---|---|---|
skin of body | 2.03e-52 | 41 |
integument | 1.23e-46 | 46 |
integumental system | 1.23e-46 | 46 |
surface structure | 3.44e-21 | 99 |
dermis | 1.17e-07 | 9 |
dermatome | 1.17e-07 | 9 |
future dermis | 1.17e-07 | 9 |
Ontology term | p-value | n |
---|---|---|
musculoskeletal system disease | 8.65e-49 | 5 |
myotonic disease | 8.65e-49 | 5 |
muscle tissue disease | 8.65e-49 | 5 |
myopathy | 8.65e-49 | 5 |
muscular disease | 8.65e-49 | 5 |
myotonic dystrophy | 8.65e-49 | 5 |
disease of anatomical entity | 9.08e-10 | 39 |