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

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Gene: NR1H3 ENSSSCG00000013241

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Description

nuclear receptor subfamily 1 group H member 3 [Source:VGNC Symbol;Acc:VGNC:90871]

Location

Primary_assembly 2: 15,315,282-15,334,820 reverse strand.

Sscrofa11.1:CM000813.5

About this gene

This gene has 4 transcripts (splice variants), 391 orthologues and 18 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000014461.5	NR1H3-201	1730	470aa	ENSSSCP00000014069.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D0SCS9 F6Q6I2	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,
ENSSSCT00000041989.3	NR1H3-204	2716	400aa	ENSSSCP00000040913.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A480WYK6	-
ENSSSCT00000040674.3	NR1H3-202	1750	447aa	ENSSSCP00000055296.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1VT52 Q4TU03	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,
ENSSSCT00000103000.1	NR1H3-203	1570	387aa	ENSSSCP00000080842.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1VS07 A0A8W4FNT8	-

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Summary

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