FFCP PHASE1:Hg19::chr19:695576..695587,-: Difference between revisions
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{{FFCP | {{FFCP | ||
|DHSsupport=supported | |||
|DPIdataset=robust | |||
|EntrezGene=400668 | |EntrezGene=400668 | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=gencodeV16_protein_coding | |||
|HGNC=31397 | |HGNC=31397 | ||
|TSSclassifier=strong | |||
|UniProt=Q6UWY2 | |UniProt=Q6UWY2 | ||
|association_with_transcript=-115bp_to_ENST00000329267,NM_214710,uc002lpl.1,uc010xfs.1_5end | |association_with_transcript=-115bp_to_ENST00000329267,NM_214710,uc002lpl.1,uc010xfs.1_5end | ||
|cluster_id=chr19:695576..695587,- | |||
|coexpression_cluster_id=C1829 | |coexpression_cluster_id=C1829 | ||
|description=CAGE_peak_4_at_PRSS57_5end | |description=CAGE_peak_4_at_PRSS57_5end | ||
Line 9: | Line 14: | ||
|ontology_enrichment_celltype=CL:0000763!5.87e-21!112;CL:0000049!5.87e-21!112;CL:0000037!4.37e-16!172;CL:0000566!4.37e-16!172;CL:0002032!2.03e-15!165;CL:0000837!2.03e-15!165;CL:0000988!6.64e-15!182;CL:0001024!3.73e-07!1 | |ontology_enrichment_celltype=CL:0000763!5.87e-21!112;CL:0000049!5.87e-21!112;CL:0000037!4.37e-16!172;CL:0000566!4.37e-16!172;CL:0002032!2.03e-15!165;CL:0000837!2.03e-15!165;CL:0000988!6.64e-15!182;CL:0001024!3.73e-07!1 | ||
|ontology_enrichment_celltype_v019=CL:0000763;2.57e-12;100!CL:0002032;2.79e-11;1!CL:0000557;2.79e-11;1!CL:0000037;3.76e-11;1!CL:0001024;3.76e-11;1 | |ontology_enrichment_celltype_v019=CL:0000763;2.57e-12;100!CL:0002032;2.79e-11;1!CL:0000557;2.79e-11;1!CL:0000037;3.76e-11;1!CL:0001024;3.76e-11;1 | ||
|ontology_enrichment_celltype_v019_2=CL:0000763,1.43e-22,108;CL:0000049,1.43e-22,108;CL:0000037,1.56e-15,168;CL:0000988,1.32e-14,177;CL:0002032,2.53e-14,161;CL:0000837,2.53e-14,161;CL:0001024,3.76e-11,1 | |||
|ontology_enrichment_development_v019=CL:0000049;3.30e-08;108 | |ontology_enrichment_development_v019=CL:0000049;3.30e-08;108 | ||
|ontology_enrichment_disease=DOID:8692!2.70e-67!31;DOID:1240!1.05e-63!39;DOID:2531!1.38e-47!51;DOID:0060083!1.38e-47!51;DOID:0050686!1.51e-14!137;DOID:1036!3.58e-11!8;DOID:8552!6.60e-07!1;DOID:225!7.82e-07!1;DOID:9119!9.25e-07!1 | |ontology_enrichment_disease=DOID:8692!2.70e-67!31;DOID:1240!1.05e-63!39;DOID:2531!1.38e-47!51;DOID:0060083!1.38e-47!51;DOID:0050686!1.51e-14!137;DOID:1036!3.58e-11!8;DOID:8552!6.60e-07!1;DOID:225!7.82e-07!1;DOID:9119!9.25e-07!1 | ||
|ontology_enrichment_disease_v019=DOID:8692;2.75e-72;31!DOID:1240;3.25e-43;39!DOID:2531;2.23e-29;51!DOID:0060083;2.23e-29;51!DOID:8552;9.97e-11;1!DOID:9119;1.54e-10;1!DOID:225;1.54e-10;1 | |ontology_enrichment_disease_v019=DOID:8692;2.75e-72;31!DOID:1240;3.25e-43;39!DOID:2531;2.23e-29;51!DOID:0060083;2.23e-29;51!DOID:8552;9.97e-11;1!DOID:9119;1.54e-10;1!DOID:225;1.54e-10;1 | ||
|ontology_enrichment_disease_v019_2=DOID:8692,1.92e-75,31;DOID:1240,1.66e-59,39;DOID:2531,5.78e-45,51;DOID:0060083,5.78e-45,51;DOID:0050686,4.54e-15,137;DOID:8552,9.97e-11,1;DOID:225,1.33e-10,1;DOID:9119,1.77e-10,1;DOID:162,9.98e-08,235;DOID:14566,1.64e-07,239 | |||
|ontology_enrichment_uberon=UBERON:0004177!3.44e-07!7 | |ontology_enrichment_uberon=UBERON:0004177!3.44e-07!7 | ||
|ontology_enrichment_uberon_v019= | |ontology_enrichment_uberon_v019= | ||
|ontology_enrichment_uberon_v019_2= | |||
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|short_description=p4@PRSS57 | |short_description=p4@PRSS57 | ||
}} | }} |
Latest revision as of 19:31, 24 September 2015
Short description: | p4@PRSS57 |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_4_at_PRSS57_5end |
Coexpression cluster: | C1829_acute_CD133_CD34_granulocyte_chronic_biphenotypic_myelodysplastic |
Association with transcript: | -115bp_to_ENST00000329267, NM_214710, uc002lpl.1, uc010xfs.1_5end |
EntrezGene: | PRSS57 |
HGNC: | 31397 |
UniProt: | Q6UWY2 |
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 |
---|---|---|
myeloid cell | 1.43e-22 | 108 |
common myeloid progenitor | 1.43e-22 | 108 |
hematopoietic stem cell | 1.56e-15 | 168 |
hematopoietic cell | 1.32e-14 | 177 |
hematopoietic oligopotent progenitor cell | 2.53e-14 | 161 |
hematopoietic multipotent progenitor cell | 2.53e-14 | 161 |
CD34-positive, CD38-negative hematopoietic stem cell | 3.76e-11 | 1 |
Ontology term | p-value | n |
---|---|---|
myeloid leukemia | 1.92e-75 | 31 |
leukemia | 1.66e-59 | 39 |
hematologic cancer | 5.78e-45 | 51 |
immune system cancer | 5.78e-45 | 51 |
organ system cancer | 4.54e-15 | 137 |
chronic myeloid leukemia | 9.97e-11 | 1 |
syndrome | 1.33e-10 | 1 |
acute myeloid leukemia | 1.77e-10 | 1 |
cancer | 9.98e-08 | 235 |
disease of cellular proliferation | 1.64e-07 | 239 |