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: NR1H4 ENSBTAG00000013596

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Description

nuclear receptor subfamily 1 group H member 4 [Source:VGNC Symbol;Acc:VGNC:32232]

Location

Primary_assembly 5: 64,396,457-64,478,362 forward strand.

ARS-UCD2.0:CM008172.2

About this gene

This gene has 4 transcripts (splice variants), 389 orthologues and 18 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000018079.6	NR1H4-204	2402	486aa	ENSBTAP00000018079.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MTT1	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,
ENSBTAT00000084441.3	NR1H4-201	5245	476aa	ENSBTAP00000064287.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M369	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,
ENSBTAT00000074644.3	NR1H4-202	5134	439aa	ENSBTAP00000068874.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MI96	-
ENSBTAT00000122153.2	NR1H4-203	5092	425aa	ENSBTAP00000090379.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9T1U7	-

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Summary

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