FFCP PHASE1:Hg19::chr19:37862054..37862110,+: Difference between revisions
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{{FFCP | 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| ||
|DPIdataset=robustDPI | |||
|EntrezGene=84503 | |||
|GencodeV16b_All_Build2_RSEM10_CPAT_consensus=gencodeV16_protein_coding | |||
|HGNC=29385 | |||
|TSSclassifier=S | |||
|UniProt=Q8NB42,Q0P6G1,Q96JJ8 | |||
|association_with_transcript=0bp_to_ENST00000317566,ENST00000356178,ENST00000483919,NM_032453,uc002oge.2,uc002ogf.3,uc010efk.1,uc010xtq.1_5end | |||
|description=CAGE_peak_1_at_ZNF527_5end | |||
|id=chr19:37862054..37862110,+ | |||
|ontology_enrichment_celltype=CL:0000542!1.46e-07!53;CL:0000051!1.46e-07!53;CL:0000838!2.73e-07!52 | |||
|ontology_enrichment_celltype_v019= | |||
|ontology_enrichment_celltype_v019_2=CL:0000542,4.36e-07,53;CL:0000051,4.36e-07,53;CL:0000838,8.11e-07,52 | |||
|ontology_enrichment_development_v019=UBERON:0006601;3.35e-08;82 | |||
|ontology_enrichment_disease= | |||
|ontology_enrichment_disease_v019= | |||
|ontology_enrichment_disease_v019_2= | |||
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|ontology_enrichment_uberon_v019=UBERON:0002780;1.32e-12;41!UBERON:0001890;1.32e-12;41!UBERON:0000073;4.83e-12;53!UBERON:0002616;4.83e-12;53!UBERON:0001893;2.49e-11;34!UBERON:0001869;5.66e-11;32!UBERON:0002791;6.41e-11;32!UBERON:0003528;7.77e-11;34!UBERON:0002020;7.77e-11;34!UBERON:0002619;2.14e-09;22!UBERON:0001016;3.21e-09;83!UBERON:0007023;4.99e-09;114!UBERON:0000956;1.13e-08;25!UBERON:0000203;1.13e-08;25!UBERON:0000955;1.39e-08;68!UBERON:0001017;1.62e-08;75!UBERON:0001950;2.23e-08;20 | |||
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| |||
|short_description=p1@ZNF527 | |||
}} |
Revision as of 20:23, 11 September 2013
Short description: | p1@ZNF527 |
---|---|
Species: | Human (Homo sapiens) |
DPI dataset: | NA |
TSS-like-by-RIKEN-classifier(Yes/No): | NA |
DHS support(Yes/No): | NA |
Description: | CAGE_peak_1_at_ZNF527_5end |
Coexpression cluster: | NA |
Association with transcript: | 0bp_to_ENST00000317566, ENST00000356178, ENST00000483919, NM_032453, uc002oge.2, uc002ogf.3, uc010efk.1, uc010xtq.1_5end |
EntrezGene: | ZNF527 |
HGNC: | 29385 |
UniProt: | Q8NB42Q0P6G1Q96JJ8 |
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 |
---|---|---|
lymphocyte | 4.36e-07 | 53 |
common lymphoid progenitor | 4.36e-07 | 53 |
lymphoid lineage restricted progenitor cell | 8.11e-07 | 52 |
Ontology term | p-value | n |
---|---|---|
adult organism | 3.80e-29 | 114 |
nervous system | 1.74e-21 | 89 |
neural tube | 2.72e-20 | 56 |
neural rod | 2.72e-20 | 56 |
future spinal cord | 2.72e-20 | 56 |
neural keel | 2.72e-20 | 56 |
central nervous system | 1.50e-19 | 81 |
regional part of nervous system | 4.50e-19 | 53 |
regional part of brain | 4.50e-19 | 53 |
brain | 3.38e-17 | 68 |
future brain | 3.38e-17 | 68 |
regional part of forebrain | 5.08e-17 | 41 |
forebrain | 5.08e-17 | 41 |
anterior neural tube | 5.08e-17 | 41 |
future forebrain | 5.08e-17 | 41 |
neural plate | 1.72e-14 | 82 |
presumptive neural plate | 1.72e-14 | 82 |
neurectoderm | 5.04e-14 | 86 |
telencephalon | 2.70e-13 | 34 |
brain grey matter | 1.79e-12 | 34 |
gray matter | 1.79e-12 | 34 |
cerebral hemisphere | 2.51e-12 | 32 |
regional part of telencephalon | 3.59e-12 | 32 |
pre-chordal neural plate | 2.69e-11 | 61 |
regional part of cerebral cortex | 5.43e-10 | 22 |
ectoderm-derived structure | 9.25e-10 | 171 |
ectoderm | 9.25e-10 | 171 |
presumptive ectoderm | 9.25e-10 | 171 |
structure with developmental contribution from neural crest | 1.74e-09 | 132 |
neocortex | 5.77e-09 | 20 |
ecto-epithelium | 7.36e-09 | 104 |
cerebral cortex | 8.50e-09 | 25 |
pallium | 8.50e-09 | 25 |
Property "DHS support" (as page type) with input value "{{{DHSsupport}}}" contains invalid characters or is incomplete and therefore can cause unexpected results during a query or annotation process.