Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Cellular component
- GO: Molecular function
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

Configure this page

Share this page

Bookmark this page

.

Gene: NR1H2 ENSMICG00000002174

.

Description

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

Location

Chromosome 22: 20,236,961-20,244,739 forward strand.

Mmur_3.0:CM007682.1

About this gene

This gene has 2 transcripts (splice variants), 304 orthologues and 18 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSMICT00000049426.2	NR1H2-201	3346	458aa	ENSMICP00000037381.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8C5W5K0	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical,
ENSMICT00000002178.3	NR1H2-202	1086	361aa	ENSMICP00000001993.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8C5UM14	-

.

Summary

.

.