Personal tools

EntrezGene:140775

From FANTOM5_SSTAR

Jump to: navigation, search

Symbol:SMCR8
Description:Smith-Magenis syndrome chromosome region, candidate 8
Synonyms:NA
Species:Human (Homo sapiens)
Xrefs:
EntrezGene:140775
HGNC:17921
Ensembl:ENSG00000176994
HPRD:18075
Vega:OTTHUMG00000059394
Associated motifs:NA
Transcripton Factor?: No

TSS regions




View on UCSC genome browser


Mouse over to see Genome browser image, Click image to go to Genome browser


TSS expression






0
25
50
75
100
125
150





  • 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:140775
LocusTag:-
chromosome:17
map location:17p11.2
type of gene:protein-coding
Symbol from
nomenclature authority:
SMCR8
Full name from
nomenclature authority:
Smith-Magenis syndrome chromosome region, candidate 8
Nomenclature status:O
Other designations:Smith-Magenis syndrome chromosomal region candidate gene 8 protein
Modification date:08.01.2012