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Human (GRCh38.p13)
Description

nuclear receptor subfamily 1 group H member 2 [Source:HGNC Symbol;Acc:HGNC:7965]

Gene Synonyms

LXR-b, LXRb, NER, NER-I, RIP15, UNR

Location

Chromosome 19: 50,329,653-50,383,388 forward strand.

GRCh38:CM000681.2

About this gene

This gene has 14 transcripts (splice variants), 139 orthologues and 18 paralogues.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
NR1H2-214ENST00000652203.13592460aaENSP00000499121.1
 
Protein coding
CCDS42593P55055-1 -GENCODE basicAPPRIS P1
NR1H2-201ENST00000253727.102416460aaENSP00000253727.4
 
Protein coding
CCDS42593P55055-1 NM_007121.7TSL:1GENCODE basicAPPRIS P1MANE Select v0.91
NR1H2-204ENST00000593926.51828460aaENSP00000471194.1
 
Protein coding
CCDS42593P55055-1 -TSL:5GENCODE basicAPPRIS P1
NR1H2-202ENST00000411902.61466363aaENSP00000396151.2
 
Protein coding
CCDS58673P55055-2 -TSL:1GENCODE basic
NR1H2-210ENST00000598168.51915430aaENSP00000471294.1
 
Protein coding
-M0R0K3 -TSL:5GENCODE basic
NR1H2-211ENST00000599105.51830416aaENSP00000472526.1
 
Protein coding
-M0R2F9 -TSL:5GENCODE basic
NR1H2-207ENST00000597130.5894209aaENSP00000472138.1
 
Protein coding
-M0R1V8 -CDS 3' incompleteTSL:3
NR1H2-208ENST00000597157.1856228aaENSP00000469778.1
 
Protein coding
-M0QYE6 -CDS 3' incompleteTSL:1
NR1H2-209ENST00000597790.5718115aaENSP00000470518.1
 
Protein coding
-M0QZF5 -CDS 3' incompleteTSL:2
NR1H2-212ENST00000600355.550740aaENSP00000473099.1
 
Protein coding
-M0R3A7 -CDS 3' incompleteTSL:3
NR1H2-203ENST00000593532.52380176aaENSP00000472271.1
 
Nonsense mediated decay
-M0R229 -TSL:2
NR1H2-213ENST00000600978.1235No protein-
 
Processed transcript
---TSL:3
NR1H2-206ENST00000597085.1874No protein-
 
Retained intron
---TSL:3
NR1H2-205ENST00000595730.5713No protein-
 
Retained intron
---TSL:2

Gene-based displays