FFCP PHASE1:Hg19::chr1:28052518..28052545,+: Difference between revisions
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{{FFCP | {{FFCP | ||
|DHSsupport=supported | |||
|DPIdataset=robust | |||
|EntrezGene=199870 | |EntrezGene=199870 | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=gencodeV16_protein_coding | |||
|HGNC=28530 | |HGNC=28530 | ||
|TSSclassifier=strong | |||
|UniProt=E9PQL1 | |UniProt=E9PQL1 | ||
|association_with_transcript=0bp_to_ENST00000234549,ENST00000373949,ENST00000530324_5end | |association_with_transcript=0bp_to_ENST00000234549,ENST00000373949,ENST00000530324_5end | ||
|cluster_id=chr1:28052518..28052545,+ | |||
|description=CAGE_peak_2_at_FAM76A_5end | |description=CAGE_peak_2_at_FAM76A_5end | ||
|id=chr1:28052518..28052545,+ | |id=chr1:28052518..28052545,+ | ||
|ontology_enrichment_celltype=CL:0000738!3.37e-18!140;CL:0002031!7.41e-16!124;CL:0002087!9.35e-15!119;CL:0000037!2.44e-12!172;CL:0000566!2.44e-12!172;CL:0000988!6.81e-11!182;CL:0002032!1.76e-10!165;CL:0000837!1.76e-10!165;CL:0000542!1.98e-10!53;CL:0000051!1.98e-10!53;CL:0000838!5.25e-10!52;CL:0000557!4.23e-07!71 | |ontology_enrichment_celltype=CL:0000738!3.37e-18!140;CL:0002031!7.41e-16!124;CL:0002087!9.35e-15!119;CL:0000037!2.44e-12!172;CL:0000566!2.44e-12!172;CL:0000988!6.81e-11!182;CL:0002032!1.76e-10!165;CL:0000837!1.76e-10!165;CL:0000542!1.98e-10!53;CL:0000051!1.98e-10!53;CL:0000838!5.25e-10!52;CL:0000557!4.23e-07!71 | ||
|ontology_enrichment_celltype_v019=CL:0000542;4.65e-07;53 | |ontology_enrichment_celltype_v019=CL:0000542;4.65e-07;53 | ||
|ontology_enrichment_celltype_v019_2=CL:0000738,5.40e-18,136;CL:0002031,1.28e-15,120;CL:0002087,1.60e-14,115;CL:0000037,4.28e-12,168;CL:0000988,7.64e-11,177;CL:0000542,1.97e-10,53;CL:0000051,1.97e-10,53;CL:0002032,3.02e-10,161;CL:0000837,3.02e-10,161;CL:0000838,5.22e-10,52;CL:0000557,6.99e-07,67 | |||
|ontology_enrichment_development_v019=CL:0000051;4.65e-07;53 | |ontology_enrichment_development_v019=CL:0000051;4.65e-07;53 | ||
|ontology_enrichment_disease= | |ontology_enrichment_disease= | ||
|ontology_enrichment_disease_v019= | |ontology_enrichment_disease_v019= | ||
|ontology_enrichment_disease_v019_2= | |||
|ontology_enrichment_uberon=UBERON:0002390!6.81e-07!102;UBERON:0003061!6.81e-07!102 | |ontology_enrichment_uberon=UBERON:0002390!6.81e-07!102;UBERON:0003061!6.81e-07!102 | ||
|ontology_enrichment_uberon_v019= | |ontology_enrichment_uberon_v019= | ||
|ontology_enrichment_uberon_v019_2= | |||
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| ||
|short_description=p2@FAM76A | |short_description=p2@FAM76A | ||
}} | }} |
Latest revision as of 09:00, 17 September 2015
Short description: | p2@FAM76A |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_2_at_FAM76A_5end |
Coexpression cluster: | NA |
Association with transcript: | 0bp_to_ENST00000234549, ENST00000373949, ENST00000530324_5end |
EntrezGene: | FAM76A |
HGNC: | 28530 |
UniProt: | E9PQL1 |
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 |
---|---|---|
leukocyte | 5.40e-18 | 136 |
hematopoietic lineage restricted progenitor cell | 1.28e-15 | 120 |
nongranular leukocyte | 1.60e-14 | 115 |
hematopoietic stem cell | 4.28e-12 | 168 |
hematopoietic cell | 7.64e-11 | 177 |
lymphocyte | 1.97e-10 | 53 |
common lymphoid progenitor | 1.97e-10 | 53 |
hematopoietic oligopotent progenitor cell | 3.02e-10 | 161 |
hematopoietic multipotent progenitor cell | 3.02e-10 | 161 |
lymphoid lineage restricted progenitor cell | 5.22e-10 | 52 |
granulocyte monocyte progenitor cell | 6.99e-07 | 67 |