Human (GRCh38.p14)
Description

nuclear receptor subfamily 3 group C member 2 [Source:HGNC Symbol;Acc:HGNC:7979]

Gene Synonyms

MLR, MR

Location

Chromosome 4: 148,078,762-148,444,698 reverse strand.

GRCh38:CM000666.2

About this gene

This gene has 9 transcripts (splice variants), 212 orthologues, 8 paralogues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000358102.8NR3C2-2035792984aaENSP00000350815.3
 
Protein coding
CCDS3772P08235-1 NM_000901.5MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P4TSL:1
ENST00000625323.2NR3C2-2095909988aaENSP00000486719.1
 
Protein coding
P08235-3 -GENCODE basicAPPRIS ALT1TSL:5
ENST00000344721.8NR3C2-2025712984aaENSP00000341390.4
 
Protein coding
CCDS3772P08235-1 -GENCODE basicAPPRIS P4TSL:5
ENST00000512865.5NR3C2-2083822867aaENSP00000423510.1
 
Protein coding
CCDS54811P08235-4 -GENCODE basicTSL:1
ENST00000511528.1NR3C2-2072967988aaENSP00000421481.1
 
Protein coding
P08235-3 -GENCODE basicAPPRIS ALT1TSL:5
ENST00000342437.8NR3C2-2013150706aaENSP00000343907.4
 
Nonsense mediated decay
P08235-2 -TSL:2
ENST00000503313.1NR3C2-205877No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000504753.1NR3C2-206438No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000503174.1NR3C2-204491No protein-
 
Retained intron
--TSL:3