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EntrezGene:381375

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Symbol:Dfnb59
Description:deafness, autosomal recessive 59 (human)
Synonyms:Gm1001, Pjvk
Species:Mouse (Mus musculus)
Xrefs:
EntrezGene:381375
MGI:2685847
Ensembl:ENSMUSG00000075267
Vega:OTTMUSG00000013131
Associated motifs:NA
Transcripton Factor?: No

TSS regions




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TSS expression






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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:381375
LocusTag:RP23-468L22.2
chromosome:2
map location:2 C3, 2, 2 C3;;2
type of gene:protein-coding
Symbol from
nomenclature authority:
Dfnb59
Full name from
nomenclature authority:
deafness, autosomal recessive 59 (human)
Nomenclature status:O
Other designations:autosomal recessive deafness type 59 protein homolog, pejvakin, autosomal recessive deafness type 59 protein homolog;;pejvakin
Modification date:18.11.2011