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

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Gene: NR1H2 ENSMMUG00000023418

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Description

nuclear receptor subfamily 1 group H member 2 [Source:VGNC Symbol;Acc:VGNC:75504]

Location

Primary_assembly 19: 50,275,760-50,290,922 forward strand.

Mmul_10:CM014354.1

About this gene

This gene has 2 transcripts (splice variants), 304 orthologues and 19 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSMMUT00000032951.4	NR1H2-202	2305	461aa	ENSMMUP00000030833.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8J8XDQ9 F7F982	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,
ENSMMUT00000038404.3	NR1H2-201	1919	461aa	ENSMMUP00000031505.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8J8XDQ9 F7F982	-

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Summary

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