FFCP PHASE1:Hg19::chr6:105405020..105405033,+: Difference between revisions
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{{FFCP | {{FFCP | ||
|DHSsupport=supported | |||
|DPIdataset=robust | |||
|EntrezGene=389421 | |EntrezGene=389421 | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=gencodeV16_protein_coding | |||
|HGNC=32207 | |HGNC=32207 | ||
|TSSclassifier=strong | |||
|UniProt=Q6ZN17 | |UniProt=Q6ZN17 | ||
|association_with_transcript=97bp_to_ENST00000345080,NM_001004317,uc003pqv.1_5end | |association_with_transcript=97bp_to_ENST00000345080,NM_001004317,uc003pqv.1_5end | ||
|cluster_id=chr6:105405020..105405033,+ | |||
|coexpression_cluster_id=C1967 | |||
|description=CAGE_peak_7_at_LIN28B_5end | |description=CAGE_peak_7_at_LIN28B_5end | ||
|id=chr6:105405020..105405033,+ | |id=chr6:105405020..105405033,+ | ||
|ontology_enrichment_celltype=CL:0002322!1.47e-15!5;CL:0000333!4.13e-09!41;CL:0000133!4.60e-09!59;CL:0002319!1.48e-07!25;CL:0000242!4.79e-07!2;CL:0000221!5.52e-07!71 | |ontology_enrichment_celltype=CL:0002322!1.47e-15!5;CL:0000333!4.13e-09!41;CL:0000133!4.60e-09!59;CL:0002319!1.48e-07!25;CL:0000242!4.79e-07!2;CL:0000221!5.52e-07!71 | ||
|ontology_enrichment_celltype_v019= | |||
|ontology_enrichment_celltype_v019_2= | |||
|ontology_enrichment_development_v019=UBERON:0003918;1.75e-13;10!UBERON:0007687;1.75e-13;10!UBERON:0003104;8.08e-12;31 | |||
|ontology_enrichment_disease=DOID:14566!7.28e-15!239;DOID:3095!8.40e-15!22;DOID:2994!8.40e-15!22;DOID:162!1.89e-14!235;DOID:171!2.14e-14!10;DOID:169!9.10e-13!6;DOID:1036!1.61e-09!8;DOID:1240!1.30e-08!39;DOID:2531!1.92e-08!51;DOID:0060083!1.92e-08!51;DOID:0050687!4.66e-08!143;DOID:8692!1.10e-07!31;DOID:74!2.13e-07!2 | |||
|ontology_enrichment_disease_v019=DOID:9119;6.93e-16;1!DOID:2355;1.07e-15;1!DOID:74;1.67e-08;2 | |||
|ontology_enrichment_disease_v019_2=DOID:9119,7.46e-16,1;DOID:2355,1.16e-15,1;DOID:74,1.73e-08,2 | |||
|ontology_enrichment_uberon=UBERON:0000013!2.67e-10!5;UBERON:0002410!2.67e-10!5;UBERON:0000010!1.86e-08!8 | |||
|ontology_enrichment_uberon_v019= | |||
|ontology_enrichment_uberon_v019_2= | |||
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| ||
|short_description=p7@LIN28B | |short_description=p7@LIN28B | ||
}} | }} |
Latest revision as of 13:54, 19 September 2015
Short description: | p7@LIN28B |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_7_at_LIN28B_5end |
Coexpression cluster: | C1967_anaplastic_embryonic_hepatoblastoma_chronic_hepatocellular_Wilms_hereditary |
Association with transcript: | 97bp_to_ENST00000345080, NM_001004317, uc003pqv.1_5end |
EntrezGene: | LIN28B |
HGNC: | 32207 |
UniProt: | Q6ZN17 |
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 |
---|---|---|
acute myeloid leukemia | 7.46e-16 | 1 |
anemia | 1.16e-15 | 1 |
hematopoietic system disease | 1.73e-08 | 2 |