NR1H3

Information NR1H3

Description

The protein encoded by this gene belongs to the NR1 subfamily of the nuclear receptor superfamily. The NR1 family members are key regulators of macrophage function, controlling transcriptional programs involved in lipid homeostasis and inflammation. This protein is highly expressed in visceral organs, including liver, kidney and intestine. It forms a heterodimer with retinoid X receptor (RXR), and regulates expression of target genes containing retinoid response elements. Studies in mice lacking this gene suggest that it may play an important role in the regulation of cholesterol homeostasis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]

Full Name

nuclear receptor subfamily 1 group H member 3

Source NCBI

ReMap Statistics

Datasets
3
Biotypes
2
Peaks
1,902
Non-redundant peaks
1,799

TF Classification

Super Class
Zinc-coordinating DNA-binding domains
Class
Nuclear receptors with C4 zinc fingers
Familly
Thyroid hormone receptor-related factors (NR1)
Sub Familly
LXR (NR1H)

Source TFClass

External IDs

JASPAR
Ensembl
ENSG00000025434
UniProt
Q13133
Genevisible
Q13133
RefSeq
NM_001130101
Aliases
LXR-a; LXRA; LXRa; RLD-1
All peaks NR1H3
Download BED file
Non redundant peaks NR1H3
Download BED file
SEQUENCES NR1H3
Download FASTA file
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Datasets Table for NR1H3

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
NR1H3 SGBS GEO Homo sapiens GSE41629 1,254
NR1H3 THP-1 GEO Homo sapiens GSE28319 331
NR1H3 THP-1 T09 GEO Homo sapiens GSE28319 317
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.