Gene: NR1I2 (nuclear receptor subfamily 1, group I, member 2)  Homo sapiens

Symbol: NR1I2
Name: nuclear receptor subfamily 1, group I, member 2
Description: This gene product belongs to the nuclear receptor superfamily, members of which are transcription factors characterized by a ligand-binding domain and a DNA-binding domain. The encoded protein is a transcriptional regulator of the cytochrome P450 gene CYP3A4, binding to the response element of the CYP3A4 promoter as a heterodimer with the 9-cis retinoic acid receptor RXR. It is activated by a range of compounds that induce CYP3A4, including dexamethasone and rifampicin. Several alternatively spliced transcripts encoding different isoforms, some of which use non-AUG (CUG) translation initiation codon, have been described for this gene. Additional transcript variants exist, however, they have not been fully characterized. [provided by RefSeq, Jul 2008]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: BXR; nuclear receptor subfamily 1 group I member 2; nuclear receptor subfamily 1, group 1, member 2; ONR1; orphan nuclear receptor PAR1; orphan nuclear receptor PXR; OTTHUMP00000215173; OTTHUMP00000215174; OTTHUMP00000215175; PAR; PAR1; PAR2; PARq; pregnane X nuclear receptor variant 2; pregnane X receptor; PRR; PXR; SAR; steroid and xenobiotic receptor; SXR
Orthologs: Mus musculus : Nr1i2 (nuclear receptor subfamily 1, group I, member 2)  MGI
Rattus norvegicus : Nr1i2 (nuclear receptor subfamily 1, group I, member 2)
Latest Assembly: Human Genome Assembly GRCh37
Position:
MapChrPositionStrandSource
Human Alternate Assembly CHM1_13119,466,468 - 119,504,552+NCBI
Human Genome Assembly HuRef3116,874,950 - 116,913,074+NCBI
Human Genome Assembly GRCh373119,499,331 - 119,537,332+NCBI
Human Genome Assembly Build 363120,982,021 - 121,020,022+NCBI
Human Cytogenetic Map3q12-q13.3 NCBI
Human Genome Assembly3120,982,020 - 121,020,021 NCBI
Model

Launch Genome Browser (GBrowse) : build 36 (hg18) build 37 (hg19)


Gene-Chemical Interaction Annotations
Gene Ontology Annotations
References - curated
References - uncurated
RGD Disease Portals

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Human Genome Assembly GRCh37)

Sequence

Nucleotide Sequences
Protein Sequences
Promoters

Additional Information

External Database Links
Nomenclature History
 
More on NR1I2
Entrez Gene
Ensembl Gene
Genome Browser: (hg18) (hg19)
HGNC Report
NCBI Map Viewer
Vista
Vista + UCSC

RGD Object Information
RGD ID: 69105
Created: 2001-11-08
Species: Homo sapiens
Last Modified: 2013-03-06
Status: ACTIVE