Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Biological process
- 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: NR2C2 ENSSHAG00000016078

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Description

nuclear receptor subfamily 2 group C member 2 [Source:HGNC Symbol;Acc:HGNC:7972]

Location

Primary_assembly 1: 54,133,589-54,241,490 reverse strand.

mSarHar1.11:LR735554.1

About this gene

This gene has 2 transcripts (splice variants), 224 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSHAT00000040829.1	NR2C2-201	2430	629aa	ENSSHAP00000045021.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A7N4PXG5	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,
ENSSHAT00000019096.2	NR2C2-202	2023	622aa	ENSSHAP00000018940.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3WU35	-

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Summary

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