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

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Gene: NR3C2 ENSSHAG00000005709

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Description

nuclear receptor subfamily 3 group C member 2 [Source:HGNC Symbol;Acc:HGNC:7979]

Location

Primary_assembly 6: 72,720,497-73,077,991 reverse strand.

mSarHar1.11:LR735559.1

About this gene

This gene has 2 transcripts (splice variants), 211 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSHAT00000030096.1	NR3C2-201	6013	996aa	ENSSHAP00000033778.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A7N4P6L9	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,
ENSSHAT00000006618.2	NR3C2-202	4844	992aa	ENSSHAP00000006561.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3VTQ6	-

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Summary

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