FFCP PHASE1:Hg19::chr12:120315104..120315145,-: Difference between revisions
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{{FFCP | {{FFCP | ||
|DHSsupport=supported | |||
|DPIdataset=robust | |||
|EntrezGene=11113 | |EntrezGene=11113 | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=gencodeV16_protein_coding | |||
|HGNC=1985 | |HGNC=1985 | ||
|TSSclassifier=strong | |||
|UniProt=Q2M5E1,O14578 | |UniProt=Q2M5E1,O14578 | ||
|association_with_transcript=-9bp_to_ENST00000392521,NM_001206999,NM_007174_5end | |association_with_transcript=-9bp_to_ENST00000392521,NM_001206999,NM_007174_5end | ||
|cluster_id=chr12:120315104..120315145,- | |||
|coexpression_cluster_id=C109 | |||
|description=CAGE_peak_1_at_CIT_5end | |description=CAGE_peak_1_at_CIT_5end | ||
|id=chr12:120315104..120315145,- | |id=chr12:120315104..120315145,- | ||
|ontology_enrichment_celltype=CL:0000066!2.18e-14!254;CL:0000548!3.67e-13!679;CL:0000004!3.67e-13!679;CL:0000255!3.67e-13!679;CL:0000012!8.69e-13!682;CL:0000055!3.15e-08!180;CL:0000333!6.03e-08!41;CL:0000003!1.92e-07!722;CL:0002321!6.62e-07!248 | |ontology_enrichment_celltype=CL:0000066!2.18e-14!254;CL:0000548!3.67e-13!679;CL:0000004!3.67e-13!679;CL:0000255!3.67e-13!679;CL:0000012!8.69e-13!682;CL:0000055!3.15e-08!180;CL:0000333!6.03e-08!41;CL:0000003!1.92e-07!722;CL:0002321!6.62e-07!248 | ||
|ontology_enrichment_celltype_v019= | |||
|ontology_enrichment_celltype_v019_2=CL:0000066,2.31e-13,253;CL:0000333,8.93e-08,41;CL:0000095,7.80e-07,17;CL:0000123,7.80e-07,17 | |||
|ontology_enrichment_development_v019= | |||
|ontology_enrichment_disease=DOID:162!7.17e-48!235;DOID:14566!2.76e-47!239;DOID:0050687!4.19e-26!143;DOID:0050686!8.91e-25!137;DOID:305!2.90e-19!106;DOID:2531!5.20e-18!51;DOID:0060083!5.20e-18!51;DOID:1240!4.14e-14!39;DOID:8692!7.79e-11!31;DOID:7!6.43e-07!39 | |||
|ontology_enrichment_disease_v019=DOID:2531;1.27e-11;51!DOID:0060083;1.27e-11;51!DOID:1240;1.54e-11;39!DOID:8692;4.78e-11;31!DOID:162;4.15e-07;235!DOID:0050687;4.79e-07;143!DOID:305;7.02e-07;106!DOID:14566;8.10e-07;239 | |||
|ontology_enrichment_disease_v019_2=DOID:162,5.71e-48,235;DOID:14566,1.46e-47,239;DOID:0050687,3.01e-26,143;DOID:0050686,2.65e-24,137;DOID:305,2.92e-19,106;DOID:2531,6.13e-19,51;DOID:0060083,6.13e-19,51;DOID:1240,8.12e-15,39;DOID:8692,2.34e-11,31;DOID:7,4.84e-07,39 | |||
|ontology_enrichment_uberon= | |||
|ontology_enrichment_uberon_v019= | |||
|ontology_enrichment_uberon_v019_2= | |||
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| ||
|short_description=p1@CIT | |short_description=p1@CIT | ||
}} | }} |
Latest revision as of 19:04, 16 September 2015
Short description: | p1@CIT |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_1_at_CIT_5end |
Coexpression cluster: | C109_Reticulocytes_non_acute_Hodgkin_Burkitt_retinoblastoma_lymphoma |
Association with transcript: | -9bp_to_ENST00000392521, NM_001206999, NM_007174_5end |
EntrezGene: | CIT |
HGNC: | 1985 |
UniProt: | Q2M5E1O14578 |
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 |
---|---|---|
epithelial cell | 2.31e-13 | 253 |
migratory neural crest cell | 8.93e-08 | 41 |
neuron associated cell | 7.80e-07 | 17 |
neuron associated cell (sensu Vertebrata) | 7.80e-07 | 17 |
Ontology term | p-value | n |
---|---|---|
cancer | 5.71e-48 | 235 |
disease of cellular proliferation | 1.46e-47 | 239 |
cell type cancer | 3.01e-26 | 143 |
organ system cancer | 2.65e-24 | 137 |
carcinoma | 2.92e-19 | 106 |
hematologic cancer | 6.13e-19 | 51 |
immune system cancer | 6.13e-19 | 51 |
leukemia | 8.12e-15 | 39 |
myeloid leukemia | 2.34e-11 | 31 |
disease of anatomical entity | 4.84e-07 | 39 |