FFCP PHASE1:Hg19::chr17:57918343..57918368,+: Difference between revisions
From FANTOM5_SSTAR
m (moved FFCP PHASE1 hg19::chr17:57918343..57918368,+ to FFCP PHASE1:Hg19::chr17:57918343..57918368,+: NSchange) |
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{{FFCP | {{FFCP | ||
| | |DHSsupport=supported | ||
| | |DPIdataset=robust | ||
|EntrezGene=406991 | |EntrezGene=406991 | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=no_gencodeV16_or_build2_transcript | |||
|HGNC=31586 | |HGNC=31586 | ||
|TSSclassifier=strong | |||
|UniProt= | |UniProt= | ||
|association_with_transcript=-258bp_to_NR_029493_5end | |||
|cluster_id=chr17:57918343..57918368,+ | |||
|coexpression_cluster_id=C3662 | |||
|description=CAGE_peak_6_at_MIR21_5end | |||
|id=chr17:57918343..57918368,+ | |||
|ontology_enrichment_celltype=CL:0000557!8.21e-07!71 | |||
|ontology_enrichment_celltype_v019= | |||
|ontology_enrichment_celltype_v019_2=CL:0000839,6.34e-07,66;CL:0000557,8.65e-07,67 | |||
|ontology_enrichment_development_v019= | |||
|ontology_enrichment_disease=DOID:162!3.57e-11!235;DOID:14566!8.64e-11!239;DOID:0050687!9.25e-11!143;DOID:305!7.14e-08!106 | |||
|ontology_enrichment_disease_v019=DOID:3350;1.27e-09;2 | |||
|ontology_enrichment_disease_v019_2=DOID:3350,6.88e-10,2 | |||
|ontology_enrichment_uberon= | |||
|ontology_enrichment_uberon_v019= | |||
|ontology_enrichment_uberon_v019_2= | |||
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| ||
|short_description=p6@MIR21 | |||
}} | }} |
Latest revision as of 13:44, 16 September 2015
Short description: | p6@MIR21 |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_6_at_MIR21_5end |
Coexpression cluster: | C3662_breast_tridermal_rectal_bronchioalveolar_acute_stomach_embryonic |
Association with transcript: | -258bp_to_NR_029493_5end |
EntrezGene: | MIR21 |
HGNC: | 31586 |
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 |
---|---|---|
myeloid lineage restricted progenitor cell | 6.34e-07 | 66 |
granulocyte monocyte progenitor cell | 8.65e-07 | 67 |
Ontology term | p-value | n |
---|---|---|
mesenchymal cell neoplasm | 6.88e-10 | 2 |