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: NR1H2 ENSCAFG00845018363

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Description

nuclear receptor subfamily 1 group H member 2 [Source:HGNC Symbol;Acc:HGNC:7965]

Location

Primary_assembly 1: 106,843,781-106,850,221 reverse strand.

ROS_Cfam_1.0:CM025100.1

About this gene

This gene has 2 transcripts (splice variants), 305 orthologues and 19 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSCAFT00845032512.1	NR1H2-201	2081	455aa	ENSCAFP00845025424.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8C0SEE4 A0A8I3NW80	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,
ENSCAFT00845032604.1	NR1H2-202	1790	358aa	ENSCAFP00845025499.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8C0SEX0 A0A8I3PDK1	-

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Summary

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