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

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Gene: NR1H3 ENSBTAG00000010681

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Description

nuclear receptor subfamily 1 group H member 3 [Source:VGNC Symbol;Acc:VGNC:32231]

Location

Primary_assembly 15: 77,131,124-77,138,642 forward strand.

ARS-UCD2.0:CM008182.2

About this gene

This gene has 2 transcripts (splice variants), 390 orthologues and 18 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000014131.6	NR1H3-202	1734	456aa	ENSBTAP00000014131.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5E9B6	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, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,
ENSBTAT00000128824.2	NR1H3-201	1640	387aa	ENSBTAP00000089381.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SYP4	-

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Summary

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