FFCP PHASE1:Hg19::chr10:119303078..119303169,+: Difference between revisions
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{{FFCP | {{FFCP | ||
|DHSsupport=supported | |||
|DPIdataset=robust | |||
|EntrezGene=2018 | |EntrezGene=2018 | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=gencodeV16_protein_coding | |||
|HGNC=3341 | |HGNC=3341 | ||
|TSSclassifier=strong | |||
|UniProt= | |UniProt= | ||
|association_with_transcript=0bp_to_ENST00000442245_5end | |association_with_transcript=0bp_to_ENST00000442245_5end | ||
|cluster_id=chr10:119303078..119303169,+ | |||
|coexpression_cluster_id=C1298 | |||
|description=CAGE_peak_2_at_EMX2_5end | |description=CAGE_peak_2_at_EMX2_5end | ||
|id=chr10:119303078..119303169,+ | |id=chr10:119303078..119303169,+ | ||
|ontology_enrichment_celltype=CL:0002620!3.75e-14!23;CL:0000057!5.79e-10!75;CL:0002334!7.15e-07!12;CL:0000136!9.26e-07!15 | |ontology_enrichment_celltype=CL:0002620!3.75e-14!23;CL:0000057!5.79e-10!75;CL:0002334!7.15e-07!12;CL:0000136!9.26e-07!15 | ||
|ontology_enrichment_celltype_v019=CL:0002620;2.66e-18;23!CL:1000507;1.91e-08;10!CL:1000494;1.91e-08;10!CL:0000136;5.38e-07;13 | |||
|ontology_enrichment_celltype_v019_2=CL:0002620,1.53e-18,23;CL:0000057,2.19e-09,76;CL:0000136,8.94e-09,15;CL:1000507,2.31e-08,10;CL:1000494,2.31e-08,10 | |||
|ontology_enrichment_development_v019= | |||
|ontology_enrichment_disease= | |ontology_enrichment_disease= | ||
|ontology_enrichment_disease_v019=DOID:17;3.95e-07;5!DOID:450;3.95e-07;5!DOID:66;3.95e-07;5!DOID:423;3.95e-07;5!DOID:0080000;3.95e-07;5!DOID:11722;3.95e-07;5 | |||
|ontology_enrichment_disease_v019_2=DOID:17,3.88e-07,5;DOID:450,3.88e-07,5;DOID:66,3.88e-07,5;DOID:423,3.88e-07,5;DOID:0080000,3.88e-07,5;DOID:11722,3.88e-07,5 | |||
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|ontology_enrichment_uberon_v019=UBERON:0001893;1.95e-17;34!UBERON:0003528;4.79e-17;34!UBERON:0002020;4.79e-17;34!UBERON:0002791;6.94e-17;32!UBERON:0001869;9.02e-17;32!UBERON:0002780;3.71e-16;41!UBERON:0001890;3.71e-16;41!UBERON:0000956;5.18e-14;25!UBERON:0000203;5.18e-14;25!UBERON:0000073;8.96e-13;53!UBERON:0002616;8.96e-13;53!UBERON:0002199;5.40e-12;46!UBERON:0002416;5.40e-12;46!UBERON:0002619;1.00e-11;22!UBERON:0002097;1.30e-10;41!UBERON:0001950;2.90e-10;20!UBERON:0001013;1.60e-09;14!UBERON:0003102;1.75e-09;50!UBERON:0001017;3.98e-09;75!UBERON:0004211;1.91e-08;10!UBERON:0009773;1.91e-08;10!UBERON:0001231;1.91e-08;10!UBERON:0004810;1.91e-08;10!UBERON:0000955;2.77e-08;68!UBERON:0002420;8.46e-08;9!UBERON:0007245;8.46e-08;9!UBERON:0010009;8.46e-08;9!UBERON:0010011;8.46e-08;9!UBERON:0000454;8.46e-08;9!UBERON:0001016;1.07e-07;83!UBERON:0000125;1.55e-07;9!UBERON:0002308;1.55e-07;9!UBERON:0000489;7.04e-07;29 | |||
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| ||
|short_description=p2@EMX2 | |short_description=p2@EMX2 | ||
}} | }} |
Latest revision as of 15:54, 16 September 2015
Short description: | p2@EMX2 |
---|---|
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_EMX2_5end |
Coexpression cluster: | C1298_ductus_seminal_Fibroblast_kidney_uterus_epididymis_mesenchymal |
Association with transcript: | 0bp_to_ENST00000442245_5end |
EntrezGene: | EMX2 |
HGNC: | 3341 |
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 |
---|---|---|
skin fibroblast | 1.53e-18 | 23 |
fibroblast | 2.19e-09 | 76 |
fat cell | 8.94e-09 | 15 |
kidney tubule cell | 2.31e-08 | 10 |
nephron tubule epithelial cell | 2.31e-08 | 10 |
Ontology term | p-value | n |
---|---|---|
musculoskeletal system disease | 3.88e-07 | 5 |
myotonic disease | 3.88e-07 | 5 |
muscle tissue disease | 3.88e-07 | 5 |
myopathy | 3.88e-07 | 5 |
muscular disease | 3.88e-07 | 5 |
myotonic dystrophy | 3.88e-07 | 5 |