FFCP PHASE1:Hg19::chr9:21994694..21994706,+: Difference between revisions
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{{FFCP | {{FFCP | ||
|DHSsupport=supported | |||
|DPIdataset=robust | |||
|EntrezGene=100048912 | |EntrezGene=100048912 | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=gencodeV16_ncRNA | |||
|HGNC=34341 | |HGNC=34341 | ||
|TSSclassifier=strong | |||
|UniProt= | |UniProt= | ||
|association_with_transcript=-83bp_to_ENST00000428597,NR_003529,uc003zpm.2,uc010miw.1,uc010mix.1_5end | |association_with_transcript=-83bp_to_ENST00000428597,NR_003529,uc003zpm.2,uc010miw.1,uc010mix.1_5end | ||
|cluster_id=chr9:21994694..21994706,+ | |||
|description=CAGE_peak_7_at_CDKN2B-AS_5end | |description=CAGE_peak_7_at_CDKN2B-AS_5end | ||
|id=chr9:21994694..21994706,+ | |id=chr9:21994694..21994706,+ | ||
|ontology_enrichment_celltype= | |ontology_enrichment_celltype= | ||
|ontology_enrichment_celltype_v019=CL:0000764;6.10e-23;2!CL:0000558;6.10e-23;2!CL:0002545;8.28e-07;2 | |ontology_enrichment_celltype_v019=CL:0000764;6.10e-23;2!CL:0000558;6.10e-23;2!CL:0002545;8.28e-07;2 | ||
|ontology_enrichment_celltype_v019_2=CL:0000764,4.89e-23,2;CL:0000765,4.89e-23,2;CL:0000050,4.89e-23,2;CL:0000038,4.89e-23,2;CL:0000558,4.89e-23,2;CL:0000547,4.89e-23,2;CL:0000549,4.89e-23,2;CL:0000550,4.89e-23,2;CL:0000552,4.89e-23,2 | |||
|ontology_enrichment_development_v019= | |ontology_enrichment_development_v019= | ||
|ontology_enrichment_disease= | |ontology_enrichment_disease= | ||
|ontology_enrichment_disease_v019=DOID:225;2.32e-12;1!DOID:154;4.55e-07;2!DOID:4236;4.55e-07;2!DOID:74;8.28e-07;2!DOID:3193;8.28e-07;2!DOID:962;8.28e-07;2 | |ontology_enrichment_disease_v019=DOID:225;2.32e-12;1!DOID:154;4.55e-07;2!DOID:4236;4.55e-07;2!DOID:74;8.28e-07;2!DOID:3193;8.28e-07;2!DOID:962;8.28e-07;2 | ||
|ontology_enrichment_disease_v019_2=DOID:225,2.75e-12,1;DOID:154,4.56e-07,2;DOID:4236,4.56e-07,2;DOID:74,9.02e-07,2 | |||
|ontology_enrichment_uberon= | |ontology_enrichment_uberon= | ||
|ontology_enrichment_uberon_v019=UBERON:0003714;8.28e-07;2!UBERON:0005800;8.28e-07;2!UBERON:0001515;8.28e-07;2 | |ontology_enrichment_uberon_v019=UBERON:0003714;8.28e-07;2!UBERON:0005800;8.28e-07;2!UBERON:0001515;8.28e-07;2 | ||
|ontology_enrichment_uberon_v019_2= | |||
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| ||
|short_description=p7@CDKN2B-AS | |short_description=p7@CDKN2B-AS | ||
}} | }} |
Latest revision as of 23:23, 16 September 2015
Short description: | p7@CDKN2B-AS |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_7_at_CDKN2B-AS_5end |
Coexpression cluster: | NA |
Association with transcript: | -83bp_to_ENST00000428597, NR_003529, uc003zpm.2, uc010miw.1, uc010mix.1_5end |
EntrezGene: | CDKN2B-AS |
HGNC: | 34341 |
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 |
---|---|---|
erythroid lineage cell | 4.89e-23 | 2 |
erythroblast | 4.89e-23 | 2 |
megakaryocyte-erythroid progenitor cell | 4.89e-23 | 2 |
erythroid progenitor cell | 4.89e-23 | 2 |
reticulocyte | 4.89e-23 | 2 |
proerythroblast | 4.89e-23 | 2 |
basophilic erythroblast | 4.89e-23 | 2 |
polychromatophilic erythroblast | 4.89e-23 | 2 |
orthochromatic erythroblast | 4.89e-23 | 2 |
Ontology term | p-value | n |
---|---|---|
syndrome | 2.75e-12 | 1 |
mixed cell type cancer | 4.56e-07 | 2 |
carcinosarcoma | 4.56e-07 | 2 |
hematopoietic system disease | 9.02e-07 | 2 |