FFCP PHASE1:Hg19::chr6:10585672..10585677,+: Difference between revisions
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{{FFCP | {{FFCP | ||
|DHSsupport=supported | |||
|DPIdataset=robust | |||
|EntrezGene=2651 | |EntrezGene=2651 | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=gencodeV16_protein_coding | |||
|HGNC=4204 | |HGNC=4204 | ||
|TSSclassifier=strong | |||
|UniProt=Q8NFS9 | |UniProt=Q8NFS9 | ||
|association_with_transcript=-301bp_to_ENST00000265012_5end | |association_with_transcript=-301bp_to_ENST00000265012_5end | ||
|cluster_id=chr6:10585672..10585677,+ | |||
|coexpression_cluster_id=C33 | |coexpression_cluster_id=C33 | ||
|description=CAGE_peak_42_at_GCNT2_5end | |description=CAGE_peak_42_at_GCNT2_5end | ||
Line 9: | Line 14: | ||
|ontology_enrichment_celltype=CL:0000764!1.05e-79!2;CL:0000765!1.05e-79!2;CL:0000050!1.05e-79!2;CL:0000038!1.05e-79!2;CL:0000558!1.05e-79!2;CL:0000547!1.05e-79!2;CL:0000549!1.05e-79!2;CL:0000550!1.05e-79!2;CL:0000552!1.05e-79!2 | |ontology_enrichment_celltype=CL:0000764!1.05e-79!2;CL:0000765!1.05e-79!2;CL:0000050!1.05e-79!2;CL:0000038!1.05e-79!2;CL:0000558!1.05e-79!2;CL:0000547!1.05e-79!2;CL:0000549!1.05e-79!2;CL:0000550!1.05e-79!2;CL:0000552!1.05e-79!2 | ||
|ontology_enrichment_celltype_v019=CL:0000764;3.29e-195;2!CL:0000558;3.29e-195;2 | |ontology_enrichment_celltype_v019=CL:0000764;3.29e-195;2!CL:0000558;3.29e-195;2 | ||
|ontology_enrichment_celltype_v019_2=CL:0000764,3.29e-195,2;CL:0000765,3.29e-195,2;CL:0000050,3.29e-195,2;CL:0000038,3.29e-195,2;CL:0000558,3.29e-195,2;CL:0000547,3.29e-195,2;CL:0000549,3.29e-195,2;CL:0000550,3.29e-195,2;CL:0000552,3.29e-195,2;CL:0000839,3.65e-07,66 | |||
|ontology_enrichment_development_v019= | |ontology_enrichment_development_v019= | ||
|ontology_enrichment_disease= | |ontology_enrichment_disease= | ||
|ontology_enrichment_disease_v019= | |ontology_enrichment_disease_v019= | ||
|ontology_enrichment_disease_v019_2= | |||
|ontology_enrichment_uberon=UBERON:0001872!2.97e-09!5 | |ontology_enrichment_uberon=UBERON:0001872!2.97e-09!5 | ||
|ontology_enrichment_uberon_v019= | |ontology_enrichment_uberon_v019= | ||
|ontology_enrichment_uberon_v019_2= | |||
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|short_description=p42@GCNT2 | |short_description=p42@GCNT2 | ||
}} | }} |
Latest revision as of 14:19, 19 September 2015
Short description: | p42@GCNT2 |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_42_at_GCNT2_5end |
Coexpression cluster: | C33_Reticulocytes_liver_Whole_blood_chronic_acute_spleen |
Association with transcript: | -301bp_to_ENST00000265012_5end |
EntrezGene: | GCNT2 |
HGNC: | 4204 |
UniProt: | Q8NFS9 |
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 |
---|---|---|
erythroid lineage cell | 3.29e-195 | 2 |
erythroblast | 3.29e-195 | 2 |
megakaryocyte-erythroid progenitor cell | 3.29e-195 | 2 |
erythroid progenitor cell | 3.29e-195 | 2 |
reticulocyte | 3.29e-195 | 2 |
proerythroblast | 3.29e-195 | 2 |
basophilic erythroblast | 3.29e-195 | 2 |
polychromatophilic erythroblast | 3.29e-195 | 2 |
orthochromatic erythroblast | 3.29e-195 | 2 |
myeloid lineage restricted progenitor cell | 3.65e-07 | 66 |