FFCP PHASE1:Hg19::chr3:44155786..44155788,+: Difference between revisions
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|id=chr3:44155786..44155788,+
|short_description=p1@MIR138-1
|description=CAGE_peak_1_at_MIR138-1_5end
|association_with_transcript=82bp_to_NR_029700,uc011azu.1_5en...") |
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{{FFCP | {{FFCP | ||
| | |DHSsupport=supported | ||
| | |DPIdataset=robust | ||
|EntrezGene=406929 | |EntrezGene=406929 | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=no_gencodeV16_or_build2_transcript | |||
|HGNC=31524 | |HGNC=31524 | ||
|TSSclassifier=strong | |||
|UniProt= | |UniProt= | ||
|association_with_transcript=82bp_to_NR_029700,uc011azu.1_5end | |||
|cluster_id=chr3:44155786..44155788,+ | |||
|description=CAGE_peak_1_at_MIR138-1_5end | |||
|id=chr3:44155786..44155788,+ | |||
|ontology_enrichment_celltype=CL:0000057!9.58e-07!75 | |||
|ontology_enrichment_celltype_v019= | |||
|ontology_enrichment_celltype_v019_2= | |||
|ontology_enrichment_development_v019=UBERON:0005425;1.54e-15;1 | |||
|ontology_enrichment_disease= | |||
|ontology_enrichment_disease_v019=DOID:17;2.51e-12;5!DOID:450;2.51e-12;5!DOID:66;2.51e-12;5!DOID:423;2.51e-12;5!DOID:0080000;2.51e-12;5!DOID:11722;2.51e-12;5 | |||
|ontology_enrichment_disease_v019_2=DOID:17,2.00e-12,5;DOID:450,2.00e-12,5;DOID:66,2.00e-12,5;DOID:423,2.00e-12,5;DOID:0080000,2.00e-12,5;DOID:11722,2.00e-12,5 | |||
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|ontology_enrichment_uberon_v019=UBERON:0000941;1.54e-15;1!UBERON:0001785;1.54e-15;1!UBERON:0002464;1.54e-15;1!UBERON:0004904;1.54e-15;1!UBERON:0001021;1.54e-15;1!UBERON:0003714;2.00e-08;2!UBERON:0005162;2.00e-08;2!UBERON:0000122;2.00e-08;2 | |||
|ontology_enrichment_uberon_v019_2=UBERON:0000941,9.99e-16,1;UBERON:0001785,9.99e-16,1;UBERON:0002464,9.99e-16,1;UBERON:0004904,9.99e-16,1;UBERON:0001021,9.99e-16,1;UBERON:0003902,9.99e-16,1;UBERON:0005425,9.99e-16,1;UBERON:0003714,1.61e-08,2;UBERON:0005162,1.61e-08,2;UBERON:0000122,1.61e-08,2 | |||
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| ||
|short_description=p1@MIR138-1 | |||
}} | }} |
Latest revision as of 07:43, 18 September 2015
Short description: | p1@MIR138-1 |
---|---|
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_MIR138-1_5end |
Coexpression cluster: | NA |
Association with transcript: | 82bp_to_NR_029700, uc011azu.1_5end |
EntrezGene: | MIR138-1 |
HGNC: | 31524 |
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 |
---|---|---|
cranial nerve II | 9.99e-16 | 1 |
cranial nerve | 9.99e-16 | 1 |
nerve trunk | 9.99e-16 | 1 |
nerve connecting eye with brain | 9.99e-16 | 1 |
nerve | 9.99e-16 | 1 |
retinal neural layer | 9.99e-16 | 1 |
presumptive neural retina | 9.99e-16 | 1 |
neural tissue | 1.61e-08 | 2 |
multi cell component structure | 1.61e-08 | 2 |
neuron projection bundle | 1.61e-08 | 2 |
Ontology term | p-value | n |
---|---|---|
musculoskeletal system disease | 2.00e-12 | 5 |
myotonic disease | 2.00e-12 | 5 |
muscle tissue disease | 2.00e-12 | 5 |
myopathy | 2.00e-12 | 5 |
muscular disease | 2.00e-12 | 5 |
myotonic dystrophy | 2.00e-12 | 5 |