FFCP PHASE1:Hg19::chr11:63330814..63330827,-: Difference between revisions
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{{FFCP | {{FFCP | ||
|DHSsupport=supported | |||
|DPIdataset=robust | |||
|EntrezGene=54979 | |EntrezGene=54979 | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=gencodeV16_protein_coding | |||
|HGNC=17824 | |HGNC=17824 | ||
|TSSclassifier=strong | |||
|UniProt=Q9NWW9 | |UniProt=Q9NWW9 | ||
|association_with_transcript=27bp_to_ENST00000255695,NM_017878,uc001nxg.1_5end | |association_with_transcript=27bp_to_ENST00000255695,NM_017878,uc001nxg.1_5end | ||
|cluster_id=chr11:63330814..63330827,- | |||
|coexpression_cluster_id=C68 | |||
|description=CAGE_peak_2_at_HRASLS2_5end | |description=CAGE_peak_2_at_HRASLS2_5end | ||
|id=chr11:63330814..63330827,- | |id=chr11:63330814..63330827,- | ||
|ontology_enrichment_celltype=CL:0000945!1.58e-23!24;CL:0000826!1.58e-23!24;CL:0000236!3.21e-14!14;CL:0000838!1.59e-10!52;CL:0000542!3.17e-10!53;CL:0000051!3.17e-10!53 | |ontology_enrichment_celltype=CL:0000945!1.58e-23!24;CL:0000826!1.58e-23!24;CL:0000236!3.21e-14!14;CL:0000838!1.59e-10!52;CL:0000542!3.17e-10!53;CL:0000051!3.17e-10!53 | ||
|ontology_enrichment_celltype_v019=CL:0000236;5.83e-29;13!CL:0000945;1.58e-23;24!CL:0002097;9.04e-13;2!CL:0000542;6.00e-09;53!CL:0000174;8.35e-09;3 | |||
|ontology_enrichment_celltype_v019_2=CL:0000236,8.57e-27,14;CL:0000945,1.85e-23,24;CL:0000826,1.85e-23,24;CL:0002097,1.08e-12,2;CL:0000838,6.08e-12,52;CL:0000542,1.12e-11,53;CL:0000051,1.12e-11,53;CL:0000174,9.40e-09,3 | |||
|ontology_enrichment_development_v019=CL:0000051;6.00e-09;53 | |||
|ontology_enrichment_disease= | |ontology_enrichment_disease= | ||
|ontology_enrichment_disease_v019=DOID:630;1.54e-07;1!DOID:0050177;1.54e-07;1!DOID:0050427;1.54e-07;1!DOID:2355;5.03e-07;1 | |||
|ontology_enrichment_disease_v019_2=DOID:630,1.44e-07,1;DOID:0050177,1.44e-07,1;DOID:0050427,1.44e-07,1;DOID:2355,7.40e-07,1 | |||
|ontology_enrichment_uberon=UBERON:0001737!2.70e-13!9;UBERON:0001557!3.24e-08!19;UBERON:0004921!2.02e-07!129;UBERON:0004185!2.02e-07!129;UBERON:0008947!7.26e-07!38;UBERON:0003258!7.26e-07!38 | |||
|ontology_enrichment_uberon_v019=UBERON:0002369;8.35e-09;3!UBERON:0001235;8.35e-09;3!UBERON:0006858;8.35e-09;3!UBERON:0005409;9.77e-09;22 | |||
|ontology_enrichment_uberon_v019_2=UBERON:0002369,9.40e-09,3;UBERON:0001235,9.40e-09,3;UBERON:0006858,9.40e-09,3;UBERON:0005409,1.14e-07,25 | |||
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| ||
|short_description=p2@HRASLS2 | |short_description=p2@HRASLS2 | ||
}} | }} |
Latest revision as of 23:11, 18 September 2015
Short description: | p2@HRASLS2 |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_2_at_HRASLS2_5end |
Coexpression cluster: | C68_amniotic_chorionic_Placental_salivary_placenta_tongue_mesothelioma |
Association with transcript: | 27bp_to_ENST00000255695, NM_017878, uc001nxg.1_5end |
EntrezGene: | HRASLS2 |
HGNC: | 17824 |
UniProt: | Q9NWW9 |
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 | 8.57e-27 | 14 |
lymphocyte of B lineage | 1.85e-23 | 24 |
pro-B cell | 1.85e-23 | 24 |
cortical cell of adrenal gland | 1.08e-12 | 2 |
lymphoid lineage restricted progenitor cell | 6.08e-12 | 52 |
lymphocyte | 1.12e-11 | 53 |
common lymphoid progenitor | 1.12e-11 | 53 |
steroid hormone secreting cell | 9.40e-09 | 3 |
Ontology term | p-value | n |
---|---|---|
adrenal gland | 9.40e-09 | 3 |
adrenal cortex | 9.40e-09 | 3 |
adrenal/interrenal gland | 9.40e-09 | 3 |
gastrointestinal system | 1.14e-07 | 25 |
Ontology term | p-value | n |
---|---|---|
genetic disease | 1.44e-07 | 1 |
monogenic disease | 1.44e-07 | 1 |
xeroderma pigmentosum | 1.44e-07 | 1 |
anemia | 7.40e-07 | 1 |