FFCP PHASE1:Hg19::chr3:142838563..142838574,+: Difference between revisions
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|ontology_enrichment_celltype= | |ontology_enrichment_celltype= | ||
|ontology_enrichment_celltype_v019=CL:0000764;3.56e-16;2!CL:0000558;3.56e-16;2!CL:0002195;1.33e-15;2!CL:0002571;1.33e-15;2!CL:0000875;1.03e-10;3!CL:0002396;1.03e-10;3 | |ontology_enrichment_celltype_v019=CL:0000764;3.56e-16;2!CL:0000558;3.56e-16;2!CL:0002195;1.33e-15;2!CL:0002571;1.33e-15;2!CL:0000875;1.03e-10;3!CL:0002396;1.03e-10;3 | ||
|ontology_enrichment_celltype_v019_2=CL:0000764,1.87e-16,2;CL:0000765,1.87e-16,2;CL:0000050,1.87e-16,2;CL:0000038,1.87e-16,2;CL:0000558,1.87e-16,2;CL:0000547,1.87e-16,2;CL:0000549,1.87e-16,2;CL:0000550,1.87e-16,2;CL:0000552,1.87e-16,2;CL:0002195,1.43e-15,2;CL:0002571,1.43e-15,2;CL:0000875,1.08e-10,3;CL:0002396,1.08e-10,3 | |||
|ontology_enrichment_development_v019= | |ontology_enrichment_development_v019= | ||
|ontology_enrichment_disease= | |ontology_enrichment_disease= | ||
|ontology_enrichment_disease_v019= | |ontology_enrichment_disease_v019= | ||
|ontology_enrichment_disease_v019_2= | |||
|ontology_enrichment_uberon= | |ontology_enrichment_uberon= | ||
|ontology_enrichment_uberon_v019=UBERON:0002067;5.39e-08;9 | |ontology_enrichment_uberon_v019=UBERON:0002067;5.39e-08;9 | ||
|ontology_enrichment_uberon_v019_2=UBERON:0002067,4.90e-08,9;UBERON:0004016,4.90e-08,9;UBERON:0010083,4.90e-08,9 | |||
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| ||
|short_description=p5@CHST2 | |short_description=p5@CHST2 | ||
}} | }} |
Revision as of 13:04, 18 November 2012
Short description: | p5@CHST2 |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | NA |
TSS-like-by-RIKEN-classifier(Yes/No): | NA |
DHS support(Yes/No): | NA |
Description: | CAGE_peak_5_at_CHST2_5end |
Coexpression cluster: | NA |
Association with transcript: | -43bp_to_NM_004267_5end |
EntrezGene: | CHST2 |
HGNC: | 1970 |
UniProt: | Q9Y4C5 |
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 | 1.87e-16 | 2 |
erythroblast | 1.87e-16 | 2 |
megakaryocyte-erythroid progenitor cell | 1.87e-16 | 2 |
erythroid progenitor cell | 1.87e-16 | 2 |
reticulocyte | 1.87e-16 | 2 |
proerythroblast | 1.87e-16 | 2 |
basophilic erythroblast | 1.87e-16 | 2 |
polychromatophilic erythroblast | 1.87e-16 | 2 |
orthochromatic erythroblast | 1.87e-16 | 2 |
hepatic stem cell | 1.43e-15 | 2 |
hepatic mesenchymal stem cell | 1.43e-15 | 2 |
non-classical monocyte | 1.08e-10 | 3 |
CD14-low, CD16-positive monocyte | 1.08e-10 | 3 |
Ontology term | p-value | n |
---|---|---|
dermis | 4.90e-08 | 9 |
dermatome | 4.90e-08 | 9 |
future dermis | 4.90e-08 | 9 |
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Property "TSS like by RIKEN classifier" (as page type) with input value "{{{TSSclassifier}}}" contains invalid characters or is incomplete and therefore can cause unexpected results during a query or annotation process.
Property "DHS support" (as page type) with input value "{{{DHSsupport}}}" contains invalid characters or is incomplete and therefore can cause unexpected results during a query or annotation process.