FFCP PHASE1:Hg19::chr19:7765061..7765070,-: Difference between revisions
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{{FFCP | {{FFCP | ||
| | |DHSsupport=supported | ||
| | |DPIdataset=robust | ||
|EntrezGene=2208 | |EntrezGene=2208 | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=gencodeV16_protein_coding | |||
|HGNC=3612 | |HGNC=3612 | ||
|TSSclassifier=strong | |||
|UniProt= | |UniProt= | ||
|association_with_transcript=-92bp_to_uc010xjs.1_5end | |||
|cluster_id=chr19:7765061..7765070,- | |||
|coexpression_cluster_id=C36 | |||
|description=CAGE_peak_10_at_FCER2_5end | |||
|id=chr19:7765061..7765070,- | |||
|ontology_enrichment_celltype=CL:0000945!7.56e-69!24;CL:0000826!7.56e-69!24;CL:0000838!4.90e-31!52;CL:0000542!2.01e-30!53;CL:0000051!2.01e-30!53;CL:0000236!7.30e-21!14;CL:0002087!7.32e-15!119;CL:0002031!3.38e-14!124;CL:0000946!2.62e-13!1;CL:0000786!2.62e-13!1;CL:0000980!2.62e-13!1;CL:0000738!2.18e-12!140;CL:0002032!2.99e-10!165;CL:0000837!2.99e-10!165;CL:0000037!9.19e-10!172;CL:0000566!9.19e-10!172;CL:0000988!3.95e-09!182;CL:0000785!2.74e-07!2;CL:0000955!2.74e-07!2;CL:0000818!2.74e-07!2;CL:0000954!2.74e-07!2;CL:0000816!2.74e-07!2 | |||
|ontology_enrichment_celltype_v019=CL:0000945;1.93e-42;24!CL:0000946;2.73e-29;1!CL:0000786;2.73e-29;1!CL:0000542;5.67e-09;53 | |||
|ontology_enrichment_celltype_v019_2=CL:0000945,1.86e-42,24;CL:0000826,1.86e-42,24;CL:0000946,2.37e-29,1;CL:0000786,2.37e-29,1;CL:0000980,2.37e-29,1;CL:0000838,7.83e-20,52;CL:0000542,1.82e-19,53;CL:0000051,1.82e-19,53;CL:0000785,2.05e-15,2;CL:0000955,2.05e-15,2;CL:0000818,2.05e-15,2;CL:0000954,2.05e-15,2;CL:0000816,2.05e-15,2;CL:0000817,9.90e-11,3;CL:0002087,5.00e-09,115;CL:0002031,1.16e-08,120;CL:0000738,1.15e-07,136 | |||
|ontology_enrichment_development_v019=CL:0000954;2.21e-15;2!CL:0000051;5.67e-09;53 | |||
|ontology_enrichment_disease=DOID:630!2.32e-13!1;DOID:0050177!2.32e-13!1;DOID:0050427!2.32e-13!1;DOID:2355!4.77e-13!1;DOID:0060058!4.02e-11!10;DOID:74!3.70e-07!2 | |||
|ontology_enrichment_disease_v019=DOID:630;1.54e-29;1!DOID:0050177;1.54e-29;1!DOID:0050427;1.54e-29;1 | |||
|ontology_enrichment_disease_v019_2=DOID:630,1.78e-29,1;DOID:0050177,1.78e-29,1;DOID:0050427,1.78e-29,1 | |||
|ontology_enrichment_uberon=UBERON:0002106!1.88e-16!3;UBERON:0004854!1.88e-16!3;UBERON:0009034!1.88e-16!3;UBERON:0002095!1.88e-16!3;UBERON:0004782!1.88e-16!3;UBERON:0003281!1.88e-16!3;UBERON:0009664!1.88e-16!3;UBERON:0002296!1.88e-16!3;UBERON:0005602!1.88e-16!3;UBERON:0001179!1.88e-16!3;UBERON:0006293!1.88e-16!3;UBERON:0001154!9.73e-13!1;UBERON:0001153!9.73e-13!1;UBERON:0004177!1.43e-07!7;UBERON:0000945!9.94e-07!8;UBERON:0010039!9.94e-07!8 | |||
|ontology_enrichment_uberon_v019=UBERON:0002106;1.04e-10;3!UBERON:0004177;6.21e-07;5!UBERON:0005057;6.21e-07;5 | |||
|ontology_enrichment_uberon_v019_2=UBERON:0002106,1.09e-10,3;UBERON:0004854,1.09e-10,3;UBERON:0009034,1.09e-10,3;UBERON:0002095,1.09e-10,3;UBERON:0004782,1.09e-10,3;UBERON:0003281,1.09e-10,3;UBERON:0009664,1.09e-10,3;UBERON:0002296,1.09e-10,3;UBERON:0005602,1.09e-10,3;UBERON:0001179,1.09e-10,3;UBERON:0006293,1.09e-10,3 | |||
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|short_description=p10@FCER2 | |||
}} | }} |
Latest revision as of 21:41, 24 September 2015
Short description: | p10@FCER2 |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_10_at_FCER2_5end |
Coexpression cluster: | C36_B_b_splenic_plasma_xeroderma_adrenal_Burkitt |
Association with transcript: | -92bp_to_uc010xjs.1_5end |
EntrezGene: | FCER2 |
HGNC: | 3612 |
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 |
---|---|---|
lymphocyte of B lineage | 1.86e-42 | 24 |
pro-B cell | 1.86e-42 | 24 |
antibody secreting cell | 2.37e-29 | 1 |
plasma cell | 2.37e-29 | 1 |
plasmablast | 2.37e-29 | 1 |
lymphoid lineage restricted progenitor cell | 7.83e-20 | 52 |
lymphocyte | 1.82e-19 | 53 |
common lymphoid progenitor | 1.82e-19 | 53 |
mature B cell | 2.05e-15 | 2 |
pre-B-II cell | 2.05e-15 | 2 |
transitional stage B cell | 2.05e-15 | 2 |
small pre-B-II cell | 2.05e-15 | 2 |
immature B cell | 2.05e-15 | 2 |
precursor B cell | 9.90e-11 | 3 |
nongranular leukocyte | 5.00e-09 | 115 |
hematopoietic lineage restricted progenitor cell | 1.16e-08 | 120 |
leukocyte | 1.15e-07 | 136 |
Ontology term | p-value | n |
---|---|---|
spleen | 1.09e-10 | 3 |
gastrointestinal system mesentery | 1.09e-10 | 3 |
stomach region | 1.09e-10 | 3 |
mesentery | 1.09e-10 | 3 |
gastrointestinal system serosa | 1.09e-10 | 3 |
mesentery of stomach | 1.09e-10 | 3 |
gut mesentery | 1.09e-10 | 3 |
dorsal mesentery | 1.09e-10 | 3 |
dorsal mesogastrium | 1.09e-10 | 3 |
peritoneal cavity | 1.09e-10 | 3 |
spleen primordium | 1.09e-10 | 3 |
Ontology term | p-value | n |
---|---|---|
genetic disease | 1.78e-29 | 1 |
monogenic disease | 1.78e-29 | 1 |
xeroderma pigmentosum | 1.78e-29 | 1 |