FFCP PHASE1:Hg19::chr13:30169807..30169839,-: Difference between revisions
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{{FFCP | 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25.3971340035222,4.4126697915703,22.6249485217561,8.44126408594265,4.75274240523338,4.6492130034174,21.4108164506649,3.10146929333517,6.31687302141056,4.79717548439659,22.3192423257072,14.4686897403434,7.22172300202514,2.19100916473955,5.96348068425903,4.15684791139209,5.36423311456828,6.4591915681369,1.74540276136151,3.1741610430924,5.95192029066802,2.31087814315709,1.29787968637137,12.9951417580131,5.35401302622108,7.72860856169766,23.5594196703978,9.08539177902906,7.1678021637179,7.77193371806363,3.86471360913021,6.16317499359211,3.31667775783512,3.30985586758065,4.90438158372256,4.28515976634733,5.36087951638851,4.15900585782248,11.4374499832226,2.80047496423926,4.44657815708082,10.2326871511572,5.81796611844978,8.75576689189638,2.51027718874367,3.99192427855216,23.4441413599607,18.9974675662334,7.7228912914776,21.9173493140072,4.69281884806909,2.93379466038879,4.06896178315738,0.665756774185513,5.63566622054873,6.09080135376143|short_description=p2@SLC7A1}} | ||
|DPIdataset=robustDPI | |||
|EntrezGene=6541 | |||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=gencodeV16_protein_coding | |||
|HGNC=11057 | |||
|TSSclassifier=S | |||
|UniProt=P30825 | |||
|association_with_transcript=0bp_to_NM_003045,uc001uso.2_5end | |||
|description=CAGE_peak_2_at_SLC7A1_5end | |||
|id=chr13:30169807..30169839,- | |||
|ontology_enrichment_celltype=CL:0000012!8.75e-19!682;CL:0000548!1.44e-18!679;CL:0000004!1.44e-18!679;CL:0000255!1.44e-18!679;CL:0000063!2.25e-12!578;CL:0000144!6.97e-12!625;CL:0002371!4.30e-11!591;CL:0000003!8.66e-10!722;CL:0000221!6.05e-07!71 | |||
|ontology_enrichment_celltype_v019= | |||
|ontology_enrichment_celltype_v019_2=CL:0002076,3.87e-07,42 | |||
|ontology_enrichment_development_v019= | |||
|ontology_enrichment_disease=DOID:162!2.62e-12!235;DOID:14566!1.31e-11!239;DOID:0050686!9.32e-09!137;DOID:0050687!9.39e-07!143 | |||
|ontology_enrichment_disease_v019= | |||
|ontology_enrichment_disease_v019_2=DOID:162,2.62e-12,235;DOID:14566,1.34e-11,239;DOID:0050686,9.34e-09,137;DOID:0050687,9.40e-07,143 | |||
|ontology_enrichment_uberon= | |||
|ontology_enrichment_uberon_v019= | |||
|ontology_enrichment_uberon_v019_2= | |||
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| |||
|short_description=p2@SLC7A1 | |||
}} |
Revision as of 01:57, 11 September 2013
Short description: | p2@SLC7A1 |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | NA |
TSS-like-by-RIKEN-classifier(Yes/No): | NA |
DHS support(Yes/No): | NA |
Description: | CAGE_peak_2_at_SLC7A1_5end |
Coexpression cluster: | NA |
Association with transcript: | 0bp_to_NM_003045, uc001uso.2_5end |
EntrezGene: | SLC7A1 |
HGNC: | 11057 |
UniProt: | P30825 |
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 |
---|---|---|
endo-epithelial cell | 3.87e-07 | 42 |
Ontology term | p-value | n |
---|---|---|
cancer | 2.62e-12 | 235 |
disease of cellular proliferation | 1.34e-11 | 239 |
organ system cancer | 9.34e-09 | 137 |
cell type cancer | 9.40e-07 | 143 |
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.