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

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Gene: NR1H2 ENSGGOG00000005607

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Description

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

Location

Chromosome 19: 49,689,997-49,696,646 forward strand.

gorGor4:FR853090.2

About this gene

This gene has 2 transcripts (splice variants), 304 orthologues and 18 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSGGOT00000005633.3	NR1H2-201	2089	461aa	ENSGGOP00000005489.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3QS62	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,
ENSGGOT00000048928.1	NR1H2-202	1095	364aa	ENSGGOP00000045812.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I2ZFG7	-

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Summary

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