MCL coexpression mm9:640
From FANTOM5_SSTAR
Phase1 CAGE Peaks
Short description | |
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Mm9::chr10:66648428..66648445,+ | p8@Jmjd1c |
Mm9::chr10:66648451..66648471,+ | p3@Jmjd1c |
Mm9::chr10:66648478..66648516,+ | p2@Jmjd1c |
Mm9::chr10:66648821..66648848,+ | p9@Jmjd1c |
Mm9::chr11:116704477..116704546,- | p2@Jmjd6 |
Mm9::chr13:112598892..112598909,- | p2@Map3k1 |
Mm9::chr15:100563143..100563171,- | p1@uc007xsd.1 |
Mm9::chr2:17985518..17985540,+ | p6@Mllt10 |
Mm9::chr4:102243124..102243149,+ | p3@Pde4b |
Mm9::chr5:77017688..77017767,+ | p1@Cep135 |
Mm9::chr9:72379740..72379757,+ | p7@Rfx7 |
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 ID | GO name | FDR corrected p-value |
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GO:0008632 | apoptotic program | 0.00530556953661704 |
GO:0051213 | dioxygenase activity | 0.00530556953661704 |
GO:0016702 | oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen | 0.00530556953661704 |
GO:0016701 | oxidoreductase activity, acting on single donors with incorporation of molecular oxygen | 0.00530556953661704 |
GO:0043010 | camera-type eye development | 0.00664349386223486 |
GO:0043654 | recognition of apoptotic cell | 0.00786563461192289 |
GO:0008545 | JUN kinase kinase activity | 0.00786563461192289 |
GO:0001654 | eye development | 0.00798859897006268 |
GO:0030838 | positive regulation of actin filament polymerization | 0.0183491254813308 |
GO:0007423 | sensory organ development | 0.0200150343694242 |
GO:0043277 | apoptotic cell clearance | 0.0200150343694242 |
GO:0004115 | 3',5'-cyclic-AMP phosphodiesterase activity | 0.0229313805203644 |
GO:0004708 | MAP kinase kinase activity | 0.0253981304505282 |
GO:0004712 | protein serine/threonine/tyrosine kinase activity | 0.028809073084668 |
GO:0042116 | macrophage activation | 0.028809073084668 |
GO:0060041 | retina development in camera-type eye | 0.028809073084668 |
GO:0048821 | erythrocyte development | 0.028809073084668 |
GO:0030833 | regulation of actin filament polymerization | 0.028809073084668 |
GO:0007257 | activation of JNK activity | 0.028809073084668 |
GO:0043507 | positive regulation of JNK activity | 0.028809073084668 |
GO:0006910 | phagocytosis, recognition | 0.028809073084668 |
GO:0043506 | regulation of JNK activity | 0.0374829797204489 |
GO:0004709 | MAP kinase kinase kinase activity | 0.0389321176228364 |
GO:0030041 | actin filament polymerization | 0.0389321176228364 |
GO:0008637 | apoptotic mitochondrial changes | 0.0417627181151422 |
GO:0004114 | 3',5'-cyclic-nucleotide phosphodiesterase activity | 0.049417168428541 |
GO:0033077 | T cell differentiation in the thymus | 0.049417168428541 |
GO:0004112 | cyclic-nucleotide phosphodiesterase activity | 0.049417168428541 |
GO:0002274 | myeloid leukocyte activation | 0.049417168428541 |
GO:0008064 | regulation of actin polymerization and/or depolymerization | 0.049417168428541 |
GO:0008270 | zinc ion binding | 0.049417168428541 |
GO:0032535 | regulation of cellular component size | 0.049417168428541 |
GO:0032956 | regulation of actin cytoskeleton organization and biogenesis | 0.049417168428541 |
GO:0030832 | regulation of actin filament length | 0.049417168428541 |
GO:0051493 | regulation of cytoskeleton organization and biogenesis | 0.049417168428541 |
GO:0033043 | regulation of organelle organization and biogenesis | 0.049417168428541 |
GO:0000187 | activation of MAPK activity | 0.049417168428541 |
GO:0030218 | erythrocyte differentiation | 0.049417168428541 |
GO:0006915 | apoptosis | 0.049417168428541 |
GO:0006909 | phagocytosis | 0.049417168428541 |
GO:0012501 | programmed cell death | 0.049417168428541 |
GO:0051258 | protein polymerization | 0.049417168428541 |
GO:0008154 | actin polymerization and/or depolymerization | 0.049417168428541 |
GO:0043406 | positive regulation of MAP kinase activity | 0.049417168428541 |
GO:0008219 | cell death | 0.049417168428541 |
GO:0016265 | death | 0.049417168428541 |
GO:0007254 | JNK cascade | 0.049417168428541 |
GO:0008037 | cell recognition | 0.049417168428541 |
GO:0007179 | transforming growth factor beta receptor signaling pathway | 0.049417168428541 |
GO:0031098 | stress-activated protein kinase signaling pathway | 0.049417168428541 |
GO:0004702 | receptor signaling protein serine/threonine kinase activity | 0.049417168428541 |
Relative expression of the co-expression cluster over median <br>Analyst:
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>
Ontology term | p-value | n |
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Ontology term | p-value | n |
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Ontology term | p-value | n |
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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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{{{tfbs_overrepresentation_jaspar}}} |