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Coexpression cluster:C722

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Full id: C722_Mast_Natural_CD8_CD4_CD19_mature_Basophils



Phase1 CAGE Peaks

Hg19::chr10:3934617..3934629,-p@chr10:3934617..3934629
-
Hg19::chr11:9594422..9594446,+p@chr11:9594422..9594446
+
Hg19::chr14:50101898..50101922,-p3@DNAAF2
Hg19::chr19:14529156..14529170,+p@chr19:14529156..14529170
+
Hg19::chr1:59249645..59249656,-p4@JUN
Hg19::chr1:59249688..59249703,-p3@JUN
Hg19::chr1:59249707..59249727,-p1@JUN
Hg19::chr1:59249732..59249749,-p2@JUN
Hg19::chr6:170122964..170122975,+p@chr6:170122964..170122975
+
Hg19::chr6:31830554..31830563,-p4@NEU1
Hg19::chr9:123346608..123346621,+p@chr9:123346608..123346621
+


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
2.38818258532104e-050.01511719576508222140Regulation of toll-like receptor signaling pathway (Wikipathways):WP1449



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:0035026leading edge cell differentiation0.00284936345388452
GO:0043202lysosomal lumen0.00284936345388452
GO:0031953negative regulation of protein amino acid autophosphorylation0.00284936345388452
GO:0031952regulation of protein amino acid autophosphorylation0.00284936345388452
GO:0005775vacuolar lumen0.00284936345388452
GO:0016997alpha-sialidase activity0.00508792435269485
GO:0004308exo-alpha-sialidase activity0.00508792435269485
GO:0001933negative regulation of protein amino acid phosphorylation0.00569822364226741
GO:0045763negative regulation of amino acid metabolic process0.00569822364226741
GO:0033239negative regulation of amine metabolic process0.00569822364226741
GO:0031974membrane-enclosed lumen0.0082293520490518
GO:0043233organelle lumen0.0082293520490518
GO:0030855epithelial cell differentiation0.0181924770505665
GO:0046777protein amino acid autophosphorylation0.0181924770505665
GO:0001932regulation of protein amino acid phosphorylation0.0181924770505665
GO:0033238regulation of amine metabolic process0.0181924770505665
GO:0006521regulation of amino acid metabolic process0.0181924770505665
GO:0016540protein autoprocessing0.0181924770505665
GO:0005765lysosomal membrane0.0191069383036046
GO:0005774vacuolar membrane0.0196412195283527
GO:0002009morphogenesis of an epithelium0.0196412195283527
GO:0042325regulation of phosphorylation0.0196412195283527
GO:0044437vacuolar part0.0196412195283527
GO:0051174regulation of phosphorus metabolic process0.0196412195283527
GO:0019220regulation of phosphate metabolic process0.0196412195283527
GO:0016485protein processing0.02608187441823
GO:0000228nuclear chromosome0.02608187441823
GO:0045944positive regulation of transcription from RNA polymerase II promoter0.0352913285426469
GO:0004553hydrolase activity, hydrolyzing O-glycosyl compounds0.0462804105238576
GO:0005764lysosome0.0462804105238576
GO:0000323lytic vacuole0.0462804105238576
GO:0005667transcription factor complex0.0465692044661635
GO:0016798hydrolase activity, acting on glycosyl bonds0.0465692044661635
GO:0045893positive regulation of transcription, DNA-dependent0.0465692044661635
GO:0005773vacuole0.0472603152259916
GO:0044446intracellular organelle part0.0483224709928153
GO:0044422organelle part0.0483224709928153



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><br><br>



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)

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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


No analysis results for this cluster

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


This analysis result is provided for C0 - C305 clusters.