FFCP PHASE1:Hg19::chr5:180479777..180479800,+: Difference between revisions
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{{FFCP | {{FFCP | ||
|DHSsupport=supported | |||
|DPIdataset=robust | |||
|EntrezGene=153579 | |EntrezGene=153579 | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=gencodeV16_protein_coding | |||
|HGNC=24176 | |HGNC=24176 | ||
|TSSclassifier=strong | |||
|UniProt= | |UniProt= | ||
|association_with_transcript=0bp_to_ENST00000511589_5end | |association_with_transcript=0bp_to_ENST00000511589_5end | ||
|cluster_id=chr5:180479777..180479800,+ | |||
|description=CAGE_peak_5_at_BTNL9_5end | |description=CAGE_peak_5_at_BTNL9_5end | ||
|id=chr5:180479777..180479800,+ | |id=chr5:180479777..180479800,+ | ||
|ontology_enrichment_celltype=CL:0000945!2.48e-13!24;CL:0000826!2.48e-13!24;CL:0000236!2.06e-12!14 | |ontology_enrichment_celltype=CL:0000945!2.48e-13!24;CL:0000826!2.48e-13!24;CL:0000236!2.06e-12!14 | ||
|ontology_enrichment_celltype_v019=CL:0000236;8.70e-14;13!CL:0000945;7.98e-13;24!CL:0000946;6.22e-07;1!CL:0000785;6.22e-07;1!CL:0000819;6.22e-07;1!CL:0000786;6.22e-07;1 | |ontology_enrichment_celltype_v019=CL:0000236;8.70e-14;13!CL:0000945;7.98e-13;24!CL:0000946;6.22e-07;1!CL:0000785;6.22e-07;1!CL:0000819;6.22e-07;1!CL:0000786;6.22e-07;1 | ||
|ontology_enrichment_celltype_v019_2=CL:0000236,1.50e-17,14;CL:0000945,6.63e-13,24;CL:0000826,6.63e-13,24;CL:0000785,3.17e-12,2;CL:0000955,3.17e-12,2;CL:0000818,3.17e-12,2;CL:0000954,3.17e-12,2;CL:0000816,3.17e-12,2;CL:0000817,2.01e-08,3;CL:0000946,5.90e-07,1;CL:0000786,5.90e-07,1;CL:0000980,5.90e-07,1;CL:0000819,6.23e-07,1 | |||
|ontology_enrichment_development_v019=CL:0000954;3.34e-12;2!UBERON:0003056;1.23e-07;3!UBERON:0004872;3.00e-07;7 | |ontology_enrichment_development_v019=CL:0000954;3.34e-12;2!UBERON:0003056;1.23e-07;3!UBERON:0004872;3.00e-07;7 | ||
|ontology_enrichment_disease= | |ontology_enrichment_disease= | ||
|ontology_enrichment_disease_v019=DOID:114;1.62e-11;2!DOID:630;6.22e-07;1!DOID:0050177;6.22e-07;1!DOID:0060073;6.22e-07;1!DOID:8675;6.22e-07;1!DOID:0050427;6.22e-07;1 | |ontology_enrichment_disease_v019=DOID:114;1.62e-11;2!DOID:630;6.22e-07;1!DOID:0050177;6.22e-07;1!DOID:0060073;6.22e-07;1!DOID:8675;6.22e-07;1!DOID:0050427;6.22e-07;1 | ||
|ontology_enrichment_disease_v019_2=DOID:114,1.95e-11,2;DOID:0060073,6.23e-07,1;DOID:8675,6.23e-07,1;DOID:630,6.59e-07,1;DOID:0050177,6.59e-07,1;DOID:0050427,6.59e-07,1 | |||
|ontology_enrichment_uberon=UBERON:0007023!4.96e-64!115;UBERON:0001049!8.92e-21!57;UBERON:0005068!8.92e-21!57;UBERON:0006241!8.92e-21!57;UBERON:0007135!8.92e-21!57;UBERON:0003075!1.60e-16!86;UBERON:0007284!1.60e-16!86;UBERON:0001017!5.08e-16!82;UBERON:0005743!6.63e-16!86;UBERON:0002616!7.66e-16!59;UBERON:0003080!2.76e-15!42;UBERON:0002346!2.86e-15!90;UBERON:0000955!3.13e-15!69;UBERON:0006238!3.13e-15!69;UBERON:0002020!1.80e-14!34;UBERON:0003528!1.80e-14!34;UBERON:0000073!2.16e-14!94;UBERON:0001016!2.16e-14!94;UBERON:0002780!2.50e-14!41;UBERON:0001890!2.50e-14!41;UBERON:0006240!2.50e-14!41;UBERON:0001893!6.36e-14!34;UBERON:0002791!3.45e-13!33;UBERON:0001869!3.74e-12!32;UBERON:0002619!2.02e-10!22;UBERON:0000153!1.94e-09!129;UBERON:0007811!1.94e-09!129;UBERON:0003056!2.17e-09!61;UBERON:0002298!2.49e-09!8;UBERON:0000956!9.06e-09!25;UBERON:0000203!9.06e-09!25;UBERON:0001950!2.53e-08!20;UBERON:0000033!4.58e-08!123;UBERON:0002308!8.03e-08!9;UBERON:0000125!8.03e-08!9;UBERON:0004121!7.14e-07!169;UBERON:0003076!9.45e-07!15;UBERON:0003057!9.45e-07!15 | |ontology_enrichment_uberon=UBERON:0007023!4.96e-64!115;UBERON:0001049!8.92e-21!57;UBERON:0005068!8.92e-21!57;UBERON:0006241!8.92e-21!57;UBERON:0007135!8.92e-21!57;UBERON:0003075!1.60e-16!86;UBERON:0007284!1.60e-16!86;UBERON:0001017!5.08e-16!82;UBERON:0005743!6.63e-16!86;UBERON:0002616!7.66e-16!59;UBERON:0003080!2.76e-15!42;UBERON:0002346!2.86e-15!90;UBERON:0000955!3.13e-15!69;UBERON:0006238!3.13e-15!69;UBERON:0002020!1.80e-14!34;UBERON:0003528!1.80e-14!34;UBERON:0000073!2.16e-14!94;UBERON:0001016!2.16e-14!94;UBERON:0002780!2.50e-14!41;UBERON:0001890!2.50e-14!41;UBERON:0006240!2.50e-14!41;UBERON:0001893!6.36e-14!34;UBERON:0002791!3.45e-13!33;UBERON:0001869!3.74e-12!32;UBERON:0002619!2.02e-10!22;UBERON:0000153!1.94e-09!129;UBERON:0007811!1.94e-09!129;UBERON:0003056!2.17e-09!61;UBERON:0002298!2.49e-09!8;UBERON:0000956!9.06e-09!25;UBERON:0000203!9.06e-09!25;UBERON:0001950!2.53e-08!20;UBERON:0000033!4.58e-08!123;UBERON:0002308!8.03e-08!9;UBERON:0000125!8.03e-08!9;UBERON:0004121!7.14e-07!169;UBERON:0003076!9.45e-07!15;UBERON:0003057!9.45e-07!15 | ||
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|short_description=p5@BTNL9 | |short_description=p5@BTNL9 | ||
}} | }} |
Latest revision as of 11:39, 17 September 2015
Short description: | p5@BTNL9 |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_5_at_BTNL9_5end |
Coexpression cluster: | NA |
Association with transcript: | 0bp_to_ENST00000511589_5end |
EntrezGene: | BTNL9 |
HGNC: | 24176 |
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 |
---|---|---|
B cell | 1.50e-17 | 14 |
lymphocyte of B lineage | 6.63e-13 | 24 |
pro-B cell | 6.63e-13 | 24 |
mature B cell | 3.17e-12 | 2 |
pre-B-II cell | 3.17e-12 | 2 |
transitional stage B cell | 3.17e-12 | 2 |
small pre-B-II cell | 3.17e-12 | 2 |
immature B cell | 3.17e-12 | 2 |
precursor B cell | 2.01e-08 | 3 |
antibody secreting cell | 5.90e-07 | 1 |
plasma cell | 5.90e-07 | 1 |
plasmablast | 5.90e-07 | 1 |
B-1 B cell | 6.23e-07 | 1 |
Ontology term | p-value | n |
---|---|---|
heart disease | 1.95e-11 | 2 |
lymphatic system cancer | 6.23e-07 | 1 |
lymphosarcoma | 6.23e-07 | 1 |
genetic disease | 6.59e-07 | 1 |
monogenic disease | 6.59e-07 | 1 |
xeroderma pigmentosum | 6.59e-07 | 1 |