FFCP PHASE1:Hg19::chr14:106371329..106371353,-: Difference between revisions
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|ontology_enrichment_celltype_v019=CL:0000236;2.80e-84;13!CL:0000945;1.59e-53;24!CL:0000542;7.98e-18;53 | |ontology_enrichment_celltype_v019=CL:0000236;2.80e-84;13!CL:0000945;1.59e-53;24!CL:0000542;7.98e-18;53 | ||
|ontology_enrichment_celltype_v019_2=CL:0000236,3.61e-78,14;CL:0000945,1.55e-53,24;CL:0000826,1.55e-53,24;CL:0000838,1.03e-23,52;CL:0000542,3.14e-23,53;CL:0000051,3.14e-23,53;CL:0002087,1.50e-09,115;CL:0002031,4.49e-09,120;CL:0000738,8.79e-08,136 | |||
|ontology_enrichment_development_v019=CL:0000051;7.98e-18;53!UBERON:0001045;2.39e-10;1 | |ontology_enrichment_development_v019=CL:0000051;7.98e-18;53!UBERON:0001045;2.39e-10;1 | ||
|ontology_enrichment_disease= | |ontology_enrichment_disease= | ||
|ontology_enrichment_disease_v019=DOID:630;1.43e-10;1!DOID:0050177;1.43e-10;1!DOID:0050427;1.43e-10;1 | |ontology_enrichment_disease_v019=DOID:630;1.43e-10;1!DOID:0050177;1.43e-10;1!DOID:0050427;1.43e-10;1 | ||
|ontology_enrichment_disease_v019_2=DOID:630,1.43e-10,1;DOID:0050177,1.43e-10,1;DOID:0050427,1.43e-10,1 | |||
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|ontology_enrichment_uberon_v019_2=UBERON:0000178,1.11e-14,15;UBERON:0000179,1.11e-14,15;UBERON:0000463,1.11e-14,15;UBERON:0001154,2.50e-10,1;UBERON:0001153,2.50e-10,1;UBERON:0001045,2.50e-10,1;UBERON:0000029,2.74e-10,1;UBERON:0002372,3.96e-10,1;UBERON:0001961,3.96e-10,1;UBERON:0001744,3.96e-10,1;UBERON:0001735,3.96e-10,1 | |||
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| ||
|short_description=p1@IGHD | |short_description=p1@IGHD | ||
}} | }} |
Revision as of 15:23, 18 November 2012
Short description: | p1@IGHD |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | NA |
TSS-like-by-RIKEN-classifier(Yes/No): | NA |
DHS support(Yes/No): | NA |
Description: | CAGE_peak_1_at_IGHD_5end |
Coexpression cluster: | C47_CD19_Burkitt_acute_xeroderma_tonsil_lymphoma_appendix |
Association with transcript: | 49bp_to_AK090461_5end |
EntrezGene: | IGHD |
HGNC: | 5480 |
UniProt: | Q8NF20 |
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 |
---|---|---|
B cell | 3.61e-78 | 14 |
lymphocyte of B lineage | 1.55e-53 | 24 |
pro-B cell | 1.55e-53 | 24 |
lymphoid lineage restricted progenitor cell | 1.03e-23 | 52 |
lymphocyte | 3.14e-23 | 53 |
common lymphoid progenitor | 3.14e-23 | 53 |
nongranular leukocyte | 1.50e-09 | 115 |
hematopoietic lineage restricted progenitor cell | 4.49e-09 | 120 |
leukocyte | 8.79e-08 | 136 |
Ontology term | p-value | n |
---|---|---|
blood | 1.11e-14 | 15 |
haemolymphatic fluid | 1.11e-14 | 15 |
organism substance | 1.11e-14 | 15 |
vermiform appendix | 2.50e-10 | 1 |
caecum | 2.50e-10 | 1 |
midgut | 2.50e-10 | 1 |
lymph node | 2.74e-10 | 1 |
tonsil | 3.96e-10 | 1 |
mucosa-associated lymphoid tissue | 3.96e-10 | 1 |
lymphoid tissue | 3.96e-10 | 1 |
tonsillar ring | 3.96e-10 | 1 |
Ontology term | p-value | n |
---|---|---|
genetic disease | 1.43e-10 | 1 |
monogenic disease | 1.43e-10 | 1 |
xeroderma pigmentosum | 1.43e-10 | 1 |
Property "Dpi dataset" (as page type) with input value "{{{DPIdataset}}}" contains invalid characters or is incomplete and therefore can cause unexpected results during a query or annotation process.
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.