NR3C2 gene homepage

General information
Gene symbol NR3C2
Gene name nuclear receptor subfamily 3, group C, member 2
Chromosome 4
Chromosomal band q31
Imprinted Unknown
Genomic reference NG_013350.1
Transcript reference NM_000901.4
Associated with diseases PHA-1A, Hypertension, early-onset, autosomal dominant, with severe exacerbation in pregnancy
Citation reference(s) -
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 28
Unique public DNA variants reported 25
Individuals with public variants 0
Hidden variants 6
Date created May 03, 2013

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
HGNC 7979
Entrez Gene 4306
PubMed articles NR3C2
OMIM - Gene 600983
OMIM - Diseases PHA-1A (pseudohypoaldosteronism type 1 autosomal dominant (PHA-1A))
Hypertension, early-onset, autosomal dominant, with severe exacerbation in pregnancy


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00014788 4 transcript variant 1 NM_000901.4 NP_000892.2 28


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