View gene NR1H3

General information
Gene symbol NR1H3
Gene name nuclear receptor subfamily 1, group H, member 3
Chromosome 11
Chromosomal band p11.2
Gene Alias
Imprinted Unknown
Genomic reference NG_030392.1
Transcript reference NM_005693.3
Study Type Both
Expression Status[Source: Literature] Associated with UPREGULATION in Vitiligo Kumar et al.(2012);Kumar et al.(2009); Agrawal et al.(2016)
Expression Summary[Source: Literature] Sample : Skin;Blood;Saliva || Population : NA;INDIAN || Gene name used in study : LXR-ALPHA
Total number of public variants reported 2
Unique public DNA variants reported 2
Individuals with public variants 0
Hidden variants 0
Curators (1) IGIB
Date created September 03, 2015
Date last updated September 03, 2015
Version NR1H3:150903

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Gene Expression Meta-Analysis
HGNC 7966
Entrez Gene 10062
PubMed articles NR1H3
OMIM - Gene 602423

Active transcripts




NCBI ID     

NCBI Protein ID     

00378 11 transcript variant 1 NM_005693.3 NP_005684.2 2