BMI1

Information BMI1

Description

This gene encodes a ring finger protein that is major component of the polycomb group complex 1 (PRC1). This complex functions through chromatin remodeling as an essential epigenetic repressor of multiple regulatory genes involved in embryonic development and self-renewal in somatic stem cells. This protein also plays a central role in DNA damage repair. This gene is an oncogene and aberrant expression is associated with numerous cancers and is associated with resistance to certain chemotherapies. A pseudogene of this gene is found on chromosome X. Read-through transcription also exists between this gene and the upstream COMM domain containing 3 (COMMD3) gene. [provided by RefSeq, Sep 2015]

Full Name

BMI1 proto-oncogene, polycomb ring finger

Source NCBI

ReMap Statistics

Datasets
5
Biotypes
5
Peaks
38,030
Non-redundant peaks
32,868

TF Classification

Super Class
Unknown
Class
Unknown
Familly
Unknown
Sub Familly
Unknown

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000168283
UniProt
P35226
Genevisible
P35226
RefSeq
NM_005180
Aliases
FLVI2/BMI1; PCGF4; RNF51; flvi-2/bmi-1
All peaks BMI1
Download BED file
Non redundant peaks BMI1
Download BED file
SEQUENCES BMI1
Download FASTA file
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Datasets Table for BMI1

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
BMI1 GM12878 ENCODE Homo sapiens ENCSR469WII 12,987
BMI1 K-562 ENCODE Homo sapiens ENCSR782WRO 10,383
BMI1 MCF-7 ENCODE Homo sapiens ENCSR966YYJ 14,461
BMI1 HEK293T GEO Homo sapiens GSE34774 55
BMI1 LNCaP-C4-2 GEO Homo sapiens GSE97831 144
Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks

ReMap is a database of transcriptional regulators peaks derived from curated ChIP-seq, ChIP-exo, DAP-seq experiments in Human and Thaliana.

You are using the 2020 ReMap (3rd) release.
The ReMap catalogues (2020, 2018, 2015) are under CC BY-NC 4.0 international license, while ReMapEnrich, remap-pipeline under GNU GPLv3 licence.

Inserm TAGC
AMU AMU-MESO

This work was granted access to the HPC resources of Aix-Marseille Université financed by the project Equip@Meso (ANR-10-EQPX-29-01) of the program "Investissements d’Avenir" supervised by the Agence Nationale de la Recherche.