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Coexpression cluster:C227

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Full id: C227_chorionic_amniotic_Mesenchymal_Placental_gastric_diaphragm_tongue



Phase1 CAGE Peaks

Hg19::chr11:2016471..2016492,+p3@RPSA
Hg19::chr11:2016512..2016519,-p10@BC106079
Hg19::chr11:2016522..2016560,-p1@BC106079
Hg19::chr11:2016652..2016663,-p9@BC106079
Hg19::chr11:2016663..2016681,+p5@RPSA
Hg19::chr11:2016672..2016677,-p11@BC106079
Hg19::chr11:2016689..2016722,-p3@BC106079
Hg19::chr11:2016732..2016739,-p8@BC106079
Hg19::chr11:2016740..2016751,-p7@BC106079
Hg19::chr11:2016752..2016772,-p5@BC106079
Hg19::chr11:2016780..2016789,-p2@AF116709
Hg19::chr11:2016791..2016794,-p1@AF116709
Hg19::chr11:2016803..2016860,-p4@H19
Hg19::chr11:2016865..2016913,-p9@H19
Hg19::chr11:2016915..2016943,-p24@H19
Hg19::chr11:2016937..2016981,+p@chr11:2016937..2016981
+
Hg19::chr11:2016952..2016959,-p35@H19
Hg19::chr11:2016960..2016996,-p20@H19
Hg19::chr11:2017005..2017026,-p27@H19
Hg19::chr11:2017110..2017135,+p@chr11:2017110..2017135
+
Hg19::chr11:2017138..2017174,-p18@H19
Hg19::chr11:2017178..2017212,-p16@H19
Hg19::chr11:2017214..2017227,-p10@H19
Hg19::chr11:2017228..2017236,-p34@H19
Hg19::chr11:2017331..2017342,-p30@H19
Hg19::chr11:2017349..2017365,-p7@H19
Hg19::chr11:2017366..2017393,-p3@H19
Hg19::chr11:2017367..2017398,+p@chr11:2017367..2017398
+
Hg19::chr11:2017395..2017407,-p17@H19
Hg19::chr11:2017416..2017437,-p13@H19
Hg19::chr11:2017525..2017553,+p@chr11:2017525..2017553
+
Hg19::chr11:2017623..2017638,-p14@H19
Hg19::chr11:2017656..2017665,-p36@H19
Hg19::chr11:2017849..2017895,+p@chr11:2017849..2017895
+
Hg19::chr11:2017862..2017869,-p28@H19
Hg19::chr11:2017907..2017914,-p32@H19
Hg19::chr11:2017929..2017975,+p@chr11:2017929..2017975
+
Hg19::chr11:2018007..2018012,-p1@MIR675
Hg19::chr11:2018058..2018067,+p14@AF118081
Hg19::chr11:2018115..2018182,+p4@AF118081
Hg19::chr11:2018178..2018183,-p31@H19
Hg19::chr11:2018235..2018266,+p7@AF118081
Hg19::chr11:2018305..2018318,-p8@H19
Hg19::chr11:2018321..2018332,-p22@H19
Hg19::chr11:2018359..2018371,-p11@H19
Hg19::chr11:2018389..2018396,-p26@H19
Hg19::chr11:2018395..2018415,+p9@AF118081
Hg19::chr11:2018399..2018408,-p23@H19
Hg19::chr11:2018440..2018456,-p5@H19
Hg19::chr11:2018455..2018516,+p2@AF118081
Hg19::chr11:2018467..2018477,-p19@H19
Hg19::chr11:2018544..2018555,-p21@H19
Hg19::chr11:2018636..2018661,+p6@AF118081
Hg19::chr11:2018694..2018745,+p3@AF118081
Hg19::chr11:2018773..2018785,-p12@H19
Hg19::chr11:2018875..2018886,-p25@H19
Hg19::chr11:2018901..2018914,-p6@H19
Hg19::chr11:2018956..2018969,-p15@H19
Hg19::chr11:2018977..2019048,-p1@H19
Hg19::chr11:2150461..2150472,+p5@BC104421
Hg19::chr11:2160324..2160330,+p17@BC017277
Hg19::chr11:2160680..2160696,-p59@IGF2
Hg19::chr1:2066627..2066640,+p19@PRKCZ


Enriched pathways on this co-expression cluster<b>Summary:</b><br>Canonical pathway gene sets were compiled from Reactome, Wikipathways and KEGG. For the major signaling pathways, the transcriptionally-regulated genes (downstream targets) were obtained from Netpath. Combined, the canonical pathways and downstream targets totaled 489 human gene sets. The corresponding M. musculus gene sets were inferred by homology using the HomoloGene database. Enrichment for each of the canonical 489 pathways and gene sets included in the co-expression cluster was assessed by the hypergeometric probability. The resulting P values were also then adjusted by the Benjamini-Hochberg method for multiple comparisons.<br><b>Analyst: </b>Emmanuel Dimont<br><br>link to source dataset<br>data


p.valueFDRnGenesnPathwayName
1.2723518646306e-050.008053987303111713312Diabetes pathways (Reactome):REACT_15380



Enriched Gene Ontology terms on this co-expression cluster<b>Summary:</b> Results for GOStat analysis on co-expressed clusters. Each cluster with promoters mapping to at least two different genes was analysed with GOStat (PMID: 14962934) with default parameter. <br><b>Analyst:</b> Erik Arner<br><br>link to source dataset<br>data


GO IDGO nameFDR corrected p-value
GO:0005055laminin receptor activity0.0172190497820848
GO:0004700atypical protein kinase C activity0.0172190497820848
GO:0006349genetic imprinting0.0229553539426068
GO:0018445prothoracicotrophic hormone activity0.0229553539426068
GO:0005159insulin-like growth factor receptor binding0.0245899540279904
GO:0004697protein kinase C activity0.0245899540279904
GO:0001565phorbol ester receptor activity0.0245899540279904
GO:0008286insulin receptor signaling pathway0.0389942395441504
GO:0005184neuropeptide hormone activity0.0389942395441504
GO:0005843cytosolic small ribosomal subunit (sensu Eukaryota)0.0389942395441504
GO:0007165signal transduction0.0409608036317618
GO:0007154cell communication0.0474708623037988
GO:0008305integrin complex0.0482976234877922
GO:0019992diacylglycerol binding0.0482976234877922
GO:0040029regulation of gene expression, epigenetic0.0496531872163847



Enriched sample ontology terms on this co-expression cluster<b>Summary:</b>To summarize promoter activities (expression profile of a TSS region) across ~1000 samples, we performed enrichment analysis based on FANTOM5 Sample Ontology (FF ontology). The question here is “in which type of samples the promoter is more active”. To answer this question, we compared expressions (TPMs) in the samples associated with a sample ontology term and the rest of the samples by using the Mann-Whitney rank sum test. To summarize ontologies enriched in this co-expression cluster, we ran the same analysis on an averaged expression profile of all promoters that make up. <b>Analyst:</b> Hideya Kawaji <br><br>links to source dataset<br><br><br>uberon_data<br><br>


Uber Anatomy
Ontology termp-valuen
multi-tissue structure2.61e-14347
endoderm-derived structure2.84e-13169
endoderm2.84e-13169
presumptive endoderm2.84e-13169
mesenchyme4.09e-13238
entire embryonic mesenchyme4.09e-13238
subdivision of digestive tract9.27e-13129
endodermal part of digestive tract9.27e-13129
mixed endoderm/mesoderm-derived structure2.51e-11130
digestive system1.13e-10155
digestive tract1.13e-10155
primitive gut1.13e-10155
multi-cellular organism2.52e-10659
organ part3.13e-10219
foregut1.22e-0998
extraembryonic membrane3.10e-0914
membranous layer3.10e-0914
organ component layer9.61e-0957
organ segment3.81e-0897
trunk3.91e-08216
compound organ5.69e-0869
embryo6.28e-08612
extraembryonic structure9.22e-0824
upper respiratory tract1.16e-0719
immaterial anatomical entity1.80e-07126
larynx2.01e-079
subdivision of trunk2.25e-07113
abdominal segment of trunk3.29e-0761
abdomen3.29e-0761
trunk region element3.89e-07107
primordium4.68e-07168
organism subdivision8.58e-07365


Overrepresented TFBS (DNA) motifs on this co-expression cluster<b>Summary:</b>The values shown are the p-values for overrepresentation of the motif in this coexpression cluster. So a small p-value means a strong overrepresentation. <b>Analyst:</b> Michiel de Hoon <br><br>link to source data <br> Novel motifs <br>data <br><br> Jaspar motifs <br>data


Novel motifs



JASPAR motifs

Motifs-log10(p-value)

{{{tfbs_overrepresentation_jaspar}}}



ENCODE TF ChIP-seq peak enrichment analysis<b>Summary:</b> For each TF and each co-expression cluster, the number of promoters with ENCODE TF ChIP signal was compared with the rest of promoters from the robust set using Fisher's exact test. Clusters with significant ChIP enrichment (q <= 0.05) after Benjamini-Hochberg correction were retained. <br><b>Analyst:</b> Erik Arner<br><br>link to source dataset<br><br>data


(#promoters = Number of promoters in this coexpression cluster that have ChIP signal of the TF)

TF#promotersEnrichmentp-valueq-value
EGR1#1958231.821081256835450.001803058739523370.0109089127387951



Relative expression of the co-expression cluster<b>Summary:</b>Co-expression clusters are compared against FANTOM5 samples to obtain relative expression. <br><b>Analyst:</b>NA<br><br>link to data source<br> data


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