AHR

Information AHR

Description

The protein encoded by this gene is a ligand-activated helix-loop-helix transcription factor involved in the regulation of biological responses to planar aromatic hydrocarbons. This receptor has been shown to regulate xenobiotic-metabolizing enzymes such as cytochrome P450. Before ligand binding, the encoded protein is sequestered in the cytoplasm; upon ligand binding, this protein moves to the nucleus and stimulates transcription of target genes. [provided by RefSeq, Sep 2015]

Full Name

aryl hydrocarbon receptor

Source NCBI

ReMap Statistics

Datasets
8
Biotypes
3
Peaks
567,764
Non-redundant peaks
462,961

TF Classification

Super Class
Basic domains
Class
Basic helix-loop-helix factors (bHLH)
Familly
PAS domain factors
Sub Familly
Ahr-like factors

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000106546
UniProt
P35869
Genevisible
P35869
RefSeq
NM_001621
Aliases
RP85; bHLHe76
All peaks AHR
Download BED file
Non redundant peaks AHR
Download BED file
SEQUENCES AHR
Download FASTA file
DOWNLOAD All ReMap
Got to catalogue

Datasets Table for AHR

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
AHR Hep-G2 ENCODE Homo sapiens ENCSR412ZDC 211,391
AHR GM01310 3MC GEO Homo sapiens GSE116632 25,821
AHR GM01310 DMSO GEO Homo sapiens GSE116632 27,145
AHR MCF-7 GEO Homo sapiens GSE41820 194,004
AHR MCF-7 DMSO_1d GEO Homo sapiens GSE90550 9,903
AHR MCF-7 DMSO_45min GEO Homo sapiens GSE90550 29,405
AHR MCF-7 TCDD_1d GEO Homo sapiens GSE90550 10,714
AHR MCF-7 TCDD_45min GEO Homo sapiens GSE90550 59,381
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.