FFCP PHASE1:Hg19::chr7:80275790..80275804,+: Difference between revisions
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{{FFCP | {{FFCP | ||
|DHSsupport=supported | |||
|DPIdataset=robust | |||
|EntrezGene=948 | |EntrezGene=948 | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=gencodeV16_protein_coding | |||
|HGNC=1663 | |HGNC=1663 | ||
|TSSclassifier=strong | |||
|UniProt=E7EU05,A4D1B1,P16671 | |UniProt=E7EU05,A4D1B1,P16671 | ||
|association_with_transcript=28bp_to_ENST00000419819,NM_001127444,uc003uhh.3_5end | |association_with_transcript=28bp_to_ENST00000419819,NM_001127444,uc003uhh.3_5end | ||
|cluster_id=chr7:80275790..80275804,+ | |||
|coexpression_cluster_id=C33 | |coexpression_cluster_id=C33 | ||
|description=CAGE_peak_22_at_CD36_5end | |description=CAGE_peak_22_at_CD36_5end | ||
Line 9: | Line 14: | ||
|ontology_enrichment_celltype=CL:0000764!2.80e-15!2;CL:0000765!2.80e-15!2;CL:0000050!2.80e-15!2;CL:0000038!2.80e-15!2;CL:0000558!2.80e-15!2;CL:0000547!2.80e-15!2;CL:0000549!2.80e-15!2;CL:0000550!2.80e-15!2;CL:0000552!2.80e-15!2 | |ontology_enrichment_celltype=CL:0000764!2.80e-15!2;CL:0000765!2.80e-15!2;CL:0000050!2.80e-15!2;CL:0000038!2.80e-15!2;CL:0000558!2.80e-15!2;CL:0000547!2.80e-15!2;CL:0000549!2.80e-15!2;CL:0000550!2.80e-15!2;CL:0000552!2.80e-15!2 | ||
|ontology_enrichment_celltype_v019=CL:0000764;3.99e-41;2!CL:0000558;3.99e-41;2 | |ontology_enrichment_celltype_v019=CL:0000764;3.99e-41;2!CL:0000558;3.99e-41;2 | ||
|ontology_enrichment_celltype_v019_2=CL:0000764,3.99e-41,2;CL:0000765,3.99e-41,2;CL:0000050,3.99e-41,2;CL:0000038,3.99e-41,2;CL:0000558,3.99e-41,2;CL:0000547,3.99e-41,2;CL:0000549,3.99e-41,2;CL:0000550,3.99e-41,2;CL:0000552,3.99e-41,2;CL:0000763,2.41e-11,108;CL:0000049,2.41e-11,108;CL:0002032,1.73e-07,161;CL:0000837,1.73e-07,161;CL:0000037,3.70e-07,168;CL:0000988,9.05e-07,177 | |||
|ontology_enrichment_development_v019= | |ontology_enrichment_development_v019= | ||
|ontology_enrichment_disease=DOID:8692!3.74e-13!31;DOID:1240!3.24e-10!39;DOID:8552!1.91e-08!1;DOID:1036!3.01e-08!8;DOID:2531!1.54e-07!51;DOID:0060083!1.54e-07!51 | |ontology_enrichment_disease=DOID:8692!3.74e-13!31;DOID:1240!3.24e-10!39;DOID:8552!1.91e-08!1;DOID:1036!3.01e-08!8;DOID:2531!1.54e-07!51;DOID:0060083!1.54e-07!51 | ||
|ontology_enrichment_disease_v019=DOID:8692;1.42e-21;31!DOID:8552;2.30e-21;1!DOID:1240;6.31e-13;39!DOID:2531;1.00e-09;51!DOID:0060083;1.00e-09;51 | |ontology_enrichment_disease_v019=DOID:8692;1.42e-21;31!DOID:8552;2.30e-21;1!DOID:1240;6.31e-13;39!DOID:2531;1.00e-09;51!DOID:0060083;1.00e-09;51 | ||
|ontology_enrichment_disease_v019_2=DOID:8692,6.77e-23,31;DOID:8552,2.30e-21,1;DOID:1240,3.29e-18,39;DOID:2531,6.37e-14,51;DOID:0060083,6.37e-14,51 | |||
|ontology_enrichment_uberon=UBERON:0001301!8.12e-08!1;UBERON:0001282!9.29e-08!1;UBERON:0009842!9.29e-08!1;UBERON:0003704!9.29e-08!1;UBERON:0001171!9.29e-08!1;UBERON:0001172!9.29e-08!1;UBERON:0002363!1.21e-07!1;UBERON:0007647!1.21e-07!1;UBERON:0010115!1.21e-07!1 | |ontology_enrichment_uberon=UBERON:0001301!8.12e-08!1;UBERON:0001282!9.29e-08!1;UBERON:0009842!9.29e-08!1;UBERON:0003704!9.29e-08!1;UBERON:0001171!9.29e-08!1;UBERON:0001172!9.29e-08!1;UBERON:0002363!1.21e-07!1;UBERON:0007647!1.21e-07!1;UBERON:0010115!1.21e-07!1 | ||
|ontology_enrichment_uberon_v019= | |ontology_enrichment_uberon_v019= | ||
|ontology_enrichment_uberon_v019_2= | |||
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|short_description=p22@CD36 | |short_description=p22@CD36 | ||
}} | }} |
Latest revision as of 16:59, 19 September 2015
Short description: | p22@CD36 |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_22_at_CD36_5end |
Coexpression cluster: | C33_Reticulocytes_liver_Whole_blood_chronic_acute_spleen |
Association with transcript: | 28bp_to_ENST00000419819, NM_001127444, uc003uhh.3_5end |
EntrezGene: | CD36 |
HGNC: | 1663 |
UniProt: | E7EU05A4D1B1P16671 |
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 | 3.99e-41 | 2 |
erythroblast | 3.99e-41 | 2 |
megakaryocyte-erythroid progenitor cell | 3.99e-41 | 2 |
erythroid progenitor cell | 3.99e-41 | 2 |
reticulocyte | 3.99e-41 | 2 |
proerythroblast | 3.99e-41 | 2 |
basophilic erythroblast | 3.99e-41 | 2 |
polychromatophilic erythroblast | 3.99e-41 | 2 |
orthochromatic erythroblast | 3.99e-41 | 2 |
myeloid cell | 2.41e-11 | 108 |
common myeloid progenitor | 2.41e-11 | 108 |
hematopoietic oligopotent progenitor cell | 1.73e-07 | 161 |
hematopoietic multipotent progenitor cell | 1.73e-07 | 161 |
hematopoietic stem cell | 3.70e-07 | 168 |
hematopoietic cell | 9.05e-07 | 177 |
Ontology term | p-value | n |
---|---|---|
myeloid leukemia | 6.77e-23 | 31 |
chronic myeloid leukemia | 2.30e-21 | 1 |
leukemia | 3.29e-18 | 39 |
hematologic cancer | 6.37e-14 | 51 |
immune system cancer | 6.37e-14 | 51 |