Human (GRCh38.p14)
Description

nuclear receptor subfamily 5 group A member 2 [Source:HGNC Symbol;Acc:HGNC:7984]

Gene Synonyms

B1F2, FTF, FTZ-F1, FTZ-F1BETA, HB1F, HB1F-2, LRH-1, LRH1

Location

Chromosome 1: 200,027,614-200,177,420 forward strand.

GRCh38:CM000663.2

About this gene

This gene has 6 transcripts (splice variants), 228 orthologues and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000367362.8NR5A2-2034969541aaENSP00000356331.3
 
Protein coding
CCDS1401O00482-1 NM_205860.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS ALT1TSL:1
ENST00000544748.5NR5A2-2064775469aaENSP00000439116.1
 
Protein coding
CCDS60383O00482-4 -GENCODE basicAPPRIS P4TSL:2
ENST00000236914.7NR5A2-2013115495aaENSP00000236914.3
 
Protein coding
CCDS1400O00482-2 -GENCODE basicAPPRIS ALT1TSL:1
ENST00000367357.3NR5A2-2021793377aaENSP00000356326.3
 
Protein coding
H0Y328 -TSL:1CDS 5' incomplete
ENST00000447034.1NR5A2-20421371aaENSP00000414888.1
 
Protein coding
H0Y7S7 -TSL:1CDS 5' and 3' incomplete
ENST00000474307.1NR5A2-2051713113aaENSP00000436776.1
 
Nonsense mediated decay
E9PQH2 -TSL:1