FFCP PHASE1:Hg19::chr3:74663803..74663825,-: Difference between revisions
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{{FFCP | {{FFCP | ||
|DHSsupport=supported | |||
|DPIdataset=robust | |||
|EntrezGene=NA | |EntrezGene=NA | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=novel_coding | |||
|HGNC=NA | |HGNC=NA | ||
|TSSclassifier=strong | |||
|UniProt=NA | |UniProt=NA | ||
|association_with_transcript=NA | |association_with_transcript=NA | ||
|cluster_id=chr3:74663803..74663825,- | |||
|coexpression_cluster_id=C2752 | |||
|description=CAGE_peak_at_chr3:74663803..74663825,- | |description=CAGE_peak_at_chr3:74663803..74663825,- | ||
|id=chr3:74663803..74663825,- | |id=chr3:74663803..74663825,- | ||
|ontology_enrichment_celltype=CL:0000055!1.51e-13!180;CL:0000057!3.98e-11!75;CL:0000359!1.48e-10!32;CL:0002620!1.98e-08!23;CL:0000192!2.06e-08!42;CL:0000514!2.06e-08!42;CL:0000393!3.10e-08!60;CL:0000211!3.10e-08!60;CL:0000680!3.17e-08!57;CL:0000056!3.17e-08!57;CL:0000355!3.17e-08!57;CL:0000187!9.76e-08!54;CL:0000183!4.74e-07!59 | |ontology_enrichment_celltype=CL:0000055!1.51e-13!180;CL:0000057!3.98e-11!75;CL:0000359!1.48e-10!32;CL:0002620!1.98e-08!23;CL:0000192!2.06e-08!42;CL:0000514!2.06e-08!42;CL:0000393!3.10e-08!60;CL:0000211!3.10e-08!60;CL:0000680!3.17e-08!57;CL:0000056!3.17e-08!57;CL:0000355!3.17e-08!57;CL:0000187!9.76e-08!54;CL:0000183!4.74e-07!59 | ||
|ontology_enrichment_celltype_v019=CL:0000359;3.34e-11;32!CL:0002620;2.76e-09;23 | |||
|ontology_enrichment_celltype_v019_2=CL:0000359,6.15e-12,32;CL:0002620,2.63e-09,23;CL:0000192,6.59e-08,43;CL:0000514,6.59e-08,43;CL:0000057,3.51e-07,76 | |||
|ontology_enrichment_development_v019=UBERON:0006601;7.67e-08;82 | |||
|ontology_enrichment_disease= | |ontology_enrichment_disease= | ||
|ontology_enrichment_disease_v019=DOID:17;4.68e-07;5!DOID:450;4.68e-07;5!DOID:66;4.68e-07;5!DOID:423;4.68e-07;5!DOID:0080000;4.68e-07;5!DOID:11722;4.68e-07;5 | |||
|ontology_enrichment_disease_v019_2=DOID:17,4.67e-07,5;DOID:450,4.67e-07,5;DOID:66,4.67e-07,5;DOID:423,4.67e-07,5;DOID:0080000,4.67e-07,5;DOID:11722,4.67e-07,5 | |||
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| ||
|short_description=p@chr3:74663803..74663825,- | |short_description=p@chr3:74663803..74663825,- | ||
}} | }} |
Latest revision as of 23:37, 29 July 2015
Short description: | p@chr3:74663803..74663825, - |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_at_chr3:74663803..74663825, - |
Coexpression cluster: | C2752_pineal_duodenum_occipital_Fibroblast_lung_amygdala_insula |
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 |
---|---|---|
vascular associated smooth muscle cell | 6.15e-12 | 32 |
skin fibroblast | 2.63e-09 | 23 |
smooth muscle cell | 6.59e-08 | 43 |
smooth muscle myoblast | 6.59e-08 | 43 |
fibroblast | 3.51e-07 | 76 |
Ontology term | p-value | n |
---|---|---|
musculoskeletal system disease | 4.67e-07 | 5 |
myotonic disease | 4.67e-07 | 5 |
muscle tissue disease | 4.67e-07 | 5 |
myopathy | 4.67e-07 | 5 |
muscular disease | 4.67e-07 | 5 |
myotonic dystrophy | 4.67e-07 | 5 |