Human (GRCh37.p13)
Description

nuclear receptor subfamily 1, group H, member 4 [Source:HGNC Symbol;Acc:7967]

Gene Synonyms

BAR, FXR, HRR-1, HRR1, RIP14

Location

Chromosome 12: 100,867,486-100,958,191 forward strand.

GRCh37:CM000674.1

About this gene

This gene has 9 transcripts (splice variants), 18 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000548884.1NR1H4-0012884472aaENSP00000448506.1
 
Protein coding
CCDS9078B6ZGS9 Q96RI1 NM_005123.3GENCODE basic
ENST00000392986.3NR1H4-0031778476aaENSP00000376712.3
 
Protein coding
CCDS55873F1DAL1 Q96RI1 -GENCODE basic
ENST00000549996.1NR1H4-0021633425aaENSP00000448978.1
 
Protein coding
CCDS55874Q96RI1 NM_001206978.1GENCODE basic
ENST00000188403.7NR1H4-0051630482aaENSP00000188403.7
 
Protein coding
CCDS55875Q96RI1 NM_001206993.1GENCODE basic
ENST00000551379.1NR1H4-0061489486aaENSP00000447149.1
 
Protein coding
CCDS55876B7Z423 Q96RI1 -GENCODE basic
ENST00000546380.1NR1H4-00856545aaENSP00000446760.1
 
Protein coding
F8W1M1 -GENCODE basic
ENST00000551184.1NR1H4-00729434aaENSP00000446861.1
 
Protein coding
--CDS 5' incomplete
ENST00000321046.5NR1H4-0041779270aaENSP00000315442.5
 
Nonsense mediated decay
G8JLB0 --
ENST00000548621.1NR1H4-00949657aaENSP00000446584.1
 
Nonsense mediated decay
F8W656 --