FFCP PHASE1:Hg19::chr5:159659030..159659074,+: Difference between revisions
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{{FFCP | {{FFCP | ||
| | |DHSsupport=supported | ||
| | |DPIdataset=robust | ||
|EntrezGene=2172 | |EntrezGene=2172 | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=gencodeV16_protein_coding | |||
|HGNC=3561 | |HGNC=3561 | ||
|TSSclassifier=strong | |||
|UniProt= | |UniProt= | ||
|association_with_transcript=0bp_to_ENST00000521362_5end | |||
|cluster_id=chr5:159659030..159659074,+ | |||
|coexpression_cluster_id=C356 | |||
|description=CAGE_peak_3_at_FABP6_5end | |||
|id=chr5:159659030..159659074,+ | |||
|ontology_enrichment_celltype=CL:0000945!7.61e-09!24;CL:0000826!7.61e-09!24;CL:0002166!4.94e-08!3 | |||
|ontology_enrichment_celltype_v019=CL:0000945;3.64e-12;24!CL:0002596;4.55e-07;2!CL:1000415;4.55e-07;2 | |||
|ontology_enrichment_celltype_v019_2=CL:0000945,3.08e-12,24;CL:0000826,3.08e-12,24;CL:0000838,8.99e-08,52;CL:0000542,1.28e-07,53;CL:0000051,1.28e-07,53;CL:1000415,4.17e-07,2;CL:0002596,4.69e-07,2 | |||
|ontology_enrichment_development_v019= | |||
|ontology_enrichment_disease=DOID:2394!1.44e-07!14 | |||
|ontology_enrichment_disease_v019=DOID:630;2.95e-13;1!DOID:0050177;2.95e-13;1!DOID:0050427;2.95e-13;1 | |||
|ontology_enrichment_disease_v019_2=DOID:630,2.95e-13,1;DOID:0050177,2.95e-13,1;DOID:0050427,2.95e-13,1 | |||
|ontology_enrichment_uberon= | |||
|ontology_enrichment_uberon_v019=UBERON:0005396;4.55e-07;2 | |||
|ontology_enrichment_uberon_v019_2=UBERON:0005396,4.69e-07,2 | |||
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| |phase1_expression=0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0.672325146451775,0,0,0.975865597581014,0,0,0,0,0,0,2.29240217243854,1.80621296789881,1.81034797021462,0,0,0,0.919421224478927,0,0,0,0.995184627411951,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0.132409180813219,0,0,0,2.1349799145941,0.24666754841716,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0.386521706326594,1.09098448236334,0,0.365921118388786,0.265059536642971,0,0,0,0.72995471815166,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0.590789906681404,0,0,0,0.548751427043128,0,0.100528972411631,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0.93733833986777,0.16798212819886,0.708875486211932,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0.301439377059586,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0.207970861530807,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0.308419387605311,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0.495854746082934,0.192190067365106,0,0.10115778085555,0,0,0,0,0.532306030317022,0,0.18532421910392,0.143124886741991,0,0,0,0,0,0,1.56989728039846,0,0,0,0.202182481573316,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0.30982349809975,0,0,0,0,0,0,0,0,0,0.0962221127255121,0,0,0,0,0,0.443430153536676,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0.0711418433484141,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,1.33732061132974,0,0,0,0,0,0,0,0,0,0,0,0,0,5.6619010512092,0.311039587661807,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0.113942055847001,0,0,0,0,0,0,0,0,0,0,0.19606253431774,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0.182454789215666,0.19566461893209,0,0,0,0,0,0.901940516486955,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0.794858446811959,0,0,1.68333522528221,0,0,0,0,0,0,0,0,0,0.104602846312333,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0.931406652723629,0,0,0.482259445395058,0.962776056180637,1.66176135211674,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0.170388021785422,0.113312091520126,0,0,0,0,0,0,0,0,0,0,0.197611631897944,0,0,0,0,0,0,0,0,0,0,0,0,0,0.138348634936231,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0.295710299979268,0.159296767163702,0.449803112163605,0.310525913752519,0,0,0,1.05180326298053,0.380805212168795,0,0,0.214821114084977,0,0.796191777397232,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0.256241518587947,0,0,0,0.194860308839388,0.265729680626726,0.490696182767533,0,0.737318726261158,0,0,0,0.172214979660816,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,7.86649767943728,0,0,0,0,0,0,0,0,0,0.548257766857182,0,0,0,0,0,0,0,0,0.691403925334676,0,0,0,0,0,0,0,0,0,17.0582797062711,64.4964778647518,0,2.21219056425817,0,0,0,0,0,0,0,0,0,0,0.22910686854405,0,0,0,0,0,0,0,0,0,0.233939463462106,0,0,0,0.109940516745429,0,0.0771741581079447,0,0,0,0,0,0,0,0,0,0,11.193409463592,0.357107877211315,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0,0.0918948995348449,0,0,0,0,0,0,0,0.387533459016037,0.620747142958579,0,0,0,0,0,0.0673520530145875,0,0,0,0,0,0,0,0,0,0,0,4.48795889224526 | ||
|short_description=p3@FABP6 | |||
}} | }} |
Latest revision as of 16:05, 16 September 2015
Short description: | p3@FABP6 |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_3_at_FABP6_5end |
Coexpression cluster: | C356_renal_Smooth_Chondrocyte_thyroid_serous_Small_mesenchymal |
Association with transcript: | 0bp_to_ENST00000521362_5end |
EntrezGene: | FABP6 |
HGNC: | 3561 |
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 |
---|---|---|
lymphocyte of B lineage | 3.08e-12 | 24 |
pro-B cell | 3.08e-12 | 24 |
lymphoid lineage restricted progenitor cell | 8.99e-08 | 52 |
lymphocyte | 1.28e-07 | 53 |
common lymphoid progenitor | 1.28e-07 | 53 |
epithelial cell of gall bladder | 4.17e-07 | 2 |
smooth muscle cell of the carotid artery | 4.69e-07 | 2 |
Ontology term | p-value | n |
---|---|---|
carotid artery segment | 4.69e-07 | 2 |
Ontology term | p-value | n |
---|---|---|
genetic disease | 2.95e-13 | 1 |
monogenic disease | 2.95e-13 | 1 |
xeroderma pigmentosum | 2.95e-13 | 1 |