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EntrezGene:7957

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Revision as of 15:02, 10 February 2012 by Autoedit (talk | contribs) (Created page with "{{EntrezGene |tax_id=9606 |GeneID=7957 |Symbol=EPM2A |LocusTag=RP1-28C20.2 |Synonyms=EPM2;;MELF |dbXrefs=HGNC:3413;;MIM:607566;;Ensembl:ENSG00000112425;;HPRD:06345;;Vega...")
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Symbol:EPM2A
Description:epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
Synonyms:EPM2, MELF
Species:Human (Homo sapiens)
Xrefs:
EntrezGene:7957
HGNC:3413
MIM:607566
Ensembl:ENSG00000112425
HPRD:06345
Vega:OTTHUMG00000015747
Associated motifs:NA
Transcripton Factor?: No

TSS regions




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TSS expression






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  • Click each plot point to find sample in table

ENCODE TF ChIP-seq peak enrichment analysis Analyst: Erik Arner <br>Summary: For each TF and each co-expression cluster, the number of promoters with ENCODE TF ChIP signal was compared with the rest of promoters from the robust set using Fisher's exact test. Clusters with significant ChIP enrichment (q <= 0.05) after Benjamini-Hochberg correction were retained. <br><br><br>link to source dataset.<br>data


No analysis results for this cluster

Details<b>Summary:</b>It includes sequences from the international sequence collaboration, Swiss-Prot, and RefSeq. The RefSeq subset of this file is also available as gene2refseq.<br><br>links to source dataset.<br>human <br>mouse


GeneID:7957
LocusTag:RP1-28C20.2
chromosome:6
map location:6q24
type of gene:protein-coding
Symbol from
nomenclature authority:
EPM2A
Full name from
nomenclature authority:
epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
Nomenclature status:O
Other designations:LAFPTPase, epilepsy, progressive myoclonus type 2, Lafora disease (laforin), lafora PTPase, laforin, LAFPTPase;;epilepsy, progressive myoclonus type 2, Lafora disease (laforin);;lafora PTPase;;laforin
Modification date:12.01.2012