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: NR2C2 ENSOCUG00000006975

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Description

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

Location

Chromosome 9: 10,502,766-10,567,683 forward strand.

OryCun2.0:CM000798.1

About this gene

This gene has 3 transcripts (splice variants), 223 orthologues and 7 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSOCUT00000055225.1	NR2C2-203	2899	632aa	ENSOCUP00000048892.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSOCUT00000006977.4	NR2C2-201	2139	629aa	ENSOCUP00000006035.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G1SS47	-
ENSOCUT00000064035.1	NR2C2-202	1990	592aa	ENSOCUP00000044127.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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