Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: NR1H3 ENSPTRG00000003560

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Description

nuclear receptor subfamily 1 group H member 3 [Source:VGNC Symbol;Acc:VGNC:3089]

Location

Chromosome 11: 47,498,421-47,518,571 forward strand.

Pan_tro_3.0:CM000325.3

About this gene

This gene has 3 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
ENSPTRT00000105073.1	NR1H3-201	1699	453aa	ENSPTRP00000079039.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3SPS8 A0A6D2W0D7	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,
ENSPTRT00000006697.5	NR1H3-202	1996	447aa	ENSPTRP00000006182.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2XX46 K7AUZ1	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,
ENSPTRT00000082307.1	NR1H3-203	1164	387aa	ENSPTRP00000072725.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2J8LGZ6 A0A6D2WH08	-

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Summary

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