FFCP PHASE1:Hg19::chr1:181452460..181452471,+: Difference between revisions
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{{FFCP | {{FFCP | ||
|DHSsupport=supported | |||
|DPIdataset=robust | |||
|EntrezGene=777 | |EntrezGene=777 | ||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=gencodeV16_protein_coding | |||
|HGNC=1392 | |HGNC=1392 | ||
|TSSclassifier=strong | |||
|UniProt= | |UniProt= | ||
|association_with_transcript=13bp_to_ENST00000533229_5end | |association_with_transcript=13bp_to_ENST00000533229_5end | ||
|cluster_id=chr1:181452460..181452471,+ | |||
|coexpression_cluster_id=C35 | |||
|description=CAGE_peak_8_at_CACNA1E_5end | |description=CAGE_peak_8_at_CACNA1E_5end | ||
|id=chr1:181452460..181452471,+ | |id=chr1:181452460..181452471,+ | ||
|ontology_enrichment_celltype= | |ontology_enrichment_celltype= | ||
|ontology_enrichment_celltype_v019= | |||
|ontology_enrichment_celltype_v019_2= | |||
|ontology_enrichment_development_v019=UBERON:0010122;8.97e-41;2 | |||
|ontology_enrichment_disease= | |||
|ontology_enrichment_disease_v019=DOID:630;6.31e-21;1!DOID:0050177;6.31e-21;1!DOID:0050427;6.31e-21;1 | |||
|ontology_enrichment_disease_v019_2=DOID:630,4.22e-21,1;DOID:0050177,4.22e-21,1;DOID:0050427,4.22e-21,1 | |||
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|short_description=p8@CACNA1E | |short_description=p8@CACNA1E | ||
}} | }} |
Latest revision as of 00:28, 19 September 2015
Short description: | p8@CACNA1E |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | Robust |
TSS-like-by-RIKEN-classifier(Yes/No): | Yes |
DHS support(Yes/No): | Yes |
Description: | CAGE_peak_8_at_CACNA1E_5end |
Coexpression cluster: | C35_caudate_putamen_diencephalon_nucleus_globus_thalamus_insula |
Association with transcript: | 13bp_to_ENST00000533229_5end |
EntrezGene: | CACNA1E |
HGNC: | 1392 |
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 |
---|---|---|
genetic disease | 4.22e-21 | 1 |
monogenic disease | 4.22e-21 | 1 |
xeroderma pigmentosum | 4.22e-21 | 1 |