FFCP PHASE1:Hg19::chr10:44873515..44873537,-: Difference between revisions
From FANTOM5_SSTAR
(Created page with "{{FFCP
|id=chr10:44873515..44873537,-
|short_description=p@chr10:44873515..44873537,-
|description=CAGE_peak_at_chr10:44873515..44873537,-
|association_with_transcript=NA
...") |
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{{FFCP | {{FFCP | ||
| | |DHSsupport=supported | ||
| | |DPIdataset=robust | ||
|EntrezGene=NA | |EntrezGene=NA | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=no_gencodeV16_or_build2_transcript | |||
|HGNC=NA | |HGNC=NA | ||
|TSSclassifier=strong | |||
|UniProt=NA | |UniProt=NA | ||
|association_with_transcript=NA | |||
|cluster_id=chr10:44873515..44873537,- | |||
|coexpression_cluster_id=C873 | |||
|description=CAGE_peak_at_chr10:44873515..44873537,- | |||
|id=chr10:44873515..44873537,- | |||
|ontology_enrichment_celltype=CL:0000055!5.03e-15!180;CL:0000057!6.73e-13!75;CL:0002620!8.39e-09!23 | |||
|ontology_enrichment_celltype_v019=CL:0002620;4.59e-20;23!CL:0000135;1.40e-08;3!CL:0000388;1.40e-08;3 | |||
|ontology_enrichment_celltype_v019_2=CL:0002620,4.26e-20,23;CL:0000057,9.78e-19,76;CL:0000135,1.37e-08,3;CL:0000388,1.37e-08,3 | |||
|ontology_enrichment_development_v019= | |||
|ontology_enrichment_disease= | |||
|ontology_enrichment_disease_v019=DOID:17;7.35e-12;5!DOID:450;7.35e-12;5!DOID:66;7.35e-12;5!DOID:423;7.35e-12;5!DOID:0080000;7.35e-12;5!DOID:11722;7.35e-12;5 | |||
|ontology_enrichment_disease_v019_2=DOID:17,3.86e-12,5;DOID:450,3.86e-12,5;DOID:66,3.86e-12,5;DOID:423,3.86e-12,5;DOID:0080000,3.86e-12,5;DOID:11722,3.86e-12,5 | |||
|ontology_enrichment_uberon=UBERON:0002199!1.86e-07!45;UBERON:0002416!1.86e-07!45 | |||
|ontology_enrichment_uberon_v019=UBERON:0002199;3.44e-10;46!UBERON:0002416;3.44e-10;46!UBERON:0002097;4.17e-09;41!UBERON:0007846;1.40e-08;3!UBERON:0000043;1.40e-08;3!UBERON:0007845;1.40e-08;3!UBERON:0004905;2.32e-07;8!UBERON:0000982;2.32e-07;8!UBERON:0004770;2.32e-07;8!UBERON:0003102;4.07e-07;50 | |||
|ontology_enrichment_uberon_v019_2=UBERON:0002199,9.48e-14,46;UBERON:0002416,9.48e-14,46;UBERON:0002097,1.70e-12,41;UBERON:0007846,1.37e-08,3;UBERON:0000043,1.37e-08,3;UBERON:0007845,1.37e-08,3;UBERON:0003102,1.88e-08,99;UBERON:0004905,2.56e-07,8;UBERON:0000982,2.56e-07,8;UBERON:0004770,2.56e-07,8 | |||
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| ||
|short_description=p@chr10:44873515..44873537,- | |||
}} | }} |
Latest revision as of 13:46, 23 July 2015
Short description: | p@chr10:44873515..44873537, - |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_at_chr10:44873515..44873537, - |
Coexpression cluster: | C873_Cardiac_Synoviocyte_Fibroblast_tridermal_mesenchymal_tenocyte_liposarcoma |
Association with transcript: | NA |
EntrezGene: | NA |
HGNC: | NA |
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 | 4.26e-20 | 23 |
fibroblast | 9.78e-19 | 76 |
fibrocyte | 1.37e-08 | 3 |
tendon cell | 1.37e-08 | 3 |
Ontology term | p-value | n |
---|---|---|
integument | 9.48e-14 | 46 |
integumental system | 9.48e-14 | 46 |
skin of body | 1.70e-12 | 41 |
dense regular connective tissue | 1.37e-08 | 3 |
tendon | 1.37e-08 | 3 |
regular connective tissue | 1.37e-08 | 3 |
surface structure | 1.88e-08 | 99 |
articulation | 2.56e-07 | 8 |
skeletal joint | 2.56e-07 | 8 |
articular system | 2.56e-07 | 8 |
Ontology term | p-value | n |
---|---|---|
musculoskeletal system disease | 3.86e-12 | 5 |
myotonic disease | 3.86e-12 | 5 |
muscle tissue disease | 3.86e-12 | 5 |
myopathy | 3.86e-12 | 5 |
muscular disease | 3.86e-12 | 5 |
myotonic dystrophy | 3.86e-12 | 5 |