Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
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: NR1D2 ENSSHAG00000001369

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Description

nuclear receptor subfamily 1 group D member 2 [Source:HGNC Symbol;Acc:HGNC:7963]

Location

Primary_assembly 5: 260,672,568-260,717,034 forward strand.

mSarHar1.11:LR735558.1

About this gene

This gene has 2 transcripts (splice variants), 472 orthologues and 20 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSHAT00000050933.1	NR1D2-202	2461	576aa	ENSSHAP00000040362.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A7N4V598	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,
ENSSHAT00000001552.2	NR1D2-201	4869	573aa	ENSSHAP00000001536.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3VED2	-

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Summary

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