NR1H2

Information NR1H2

Description

The liver X receptors, LXRA (NR1H3; MIM 602423) and LXRB, form a subfamily of the nuclear receptor superfamily and are key regulators of macrophage function, controlling transcriptional programs involved in lipid homeostasis and inflammation. The inducible LXRA is highly expressed in liver, adrenal gland, intestine, adipose tissue, macrophages, lung, and kidney, whereas LXRB is ubiquitously expressed. Ligand-activated LXRs form obligate heterodimers with retinoid X receptors (RXRs; see MIM 180245) and regulate expression of target genes containing LXR response elements (summary by Korf et al., 2009 [PubMed 19436111]).[supplied by OMIM, Jan 2010]

Full Name

nuclear receptor subfamily 1 group H member 2

Source NCBI

ReMap Statistics

Datasets
2
Biotypes
1
Peaks
53,627
Non-redundant peaks
41,353

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
MA0115
Ensembl
ENSG00000131408
UniProt
P55055
Genevisible
P55055
RefSeq
NM_001256647
Aliases
LXR-b; LXRB; LXRb; NER; NER-I; RIP15; UNR
All peaks NR1H2
Download BED file
Non redundant peaks NR1H2
Download BED file
SEQUENCES NR1H2
Download FASTA file
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Datasets Table for NR1H2

Target name Target modification Ecotype/Strain Biotype Biotype modification Source Species Experiment Peaks
NR1H2 HT29 GW3965_2H GEO Homo sapiens GSE77039 15,625
NR1H2 HT29 GW3965_48H GEO Homo sapiens GSE77039 38,002
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.