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MCL coexpression mm9:655

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Phase1 CAGE Peaks

 Short description
Mm9::chr11:55854487..55854525,-p1@Nmur2
Mm9::chr11:57886520..57886533,-p1@ENSMUST00000137124
Mm9::chr11:57886538..57886549,-p2@ENSMUST00000137124
Mm9::chr12:105247210..105247245,-p@chr12:105247210..105247245
-
Mm9::chr15:101361561..101361569,-p@chr15:101361561..101361569
-
Mm9::chr17:14398060..14398061,+p@chr17:14398060..14398061
+
Mm9::chr2:155140315..155140326,-p@chr2:155140315..155140326
-
Mm9::chr3:92169070..92169078,+p3@Sprr2f
Mm9::chr3:92169100..92169115,+p1@Sprr2f
Mm9::chr3:92169958..92169968,+p@chr3:92169958..92169968
+
Mm9::chr7:148248944..148248945,-p@chr7:148248944..148248945
-


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


GO IDGO nameFDR corrected p-value
GO:0001607neuromedin U receptor activity0.00657408166816525
GO:0042924neuromedin U binding0.00657408166816525
GO:0001533cornified envelope0.0244772157503047
GO:0007566embryo implantation0.0244772157503047
GO:0030216keratinocyte differentiation0.0244772157503047
GO:0031424keratinization0.0244772157503047
GO:0009913epidermal cell differentiation0.0244772157503047
GO:0042923neuropeptide binding0.0244772157503047
GO:0008188neuropeptide receptor activity0.0244772157503047
GO:0042698menstrual cycle0.0244772157503047
GO:0007565female pregnancy0.0244772157503047
GO:0048730epidermis morphogenesis0.0268096031911463
GO:0032504multicellular organism reproduction0.0303963336594432
GO:0048609reproductive process in a multicellular organism0.0303963336594432
GO:0048729tissue morphogenesis0.0303963336594432
GO:0007218neuropeptide signaling pathway0.0303963336594432
GO:0030594neurotransmitter receptor activity0.0303963336594432
GO:0042165neurotransmitter binding0.0303963336594432
GO:0008544epidermis development0.0303963336594432
GO:0007398ectoderm development0.0303963336594432
GO:0001653peptide receptor activity0.0303963336594432
GO:0008528peptide receptor activity, G-protein coupled0.0303963336594432
GO:0042277peptide binding0.0370275566252879



Relative expression of the co-expression cluster over median <br>Analyst:



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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>cell_data<br>uberon_data<br>disease_data<br>


Cell Type
Ontology termp-valuen

Uber Anatomy
Ontology termp-valuen

Disease
Ontology termp-valuen


TFBS overrepresentation<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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