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

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Gene: NR2C2 ENSSSCG00000011594

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Description

nuclear receptor subfamily 2 group C member 2 [Source:VGNC Symbol;Acc:VGNC:90876]

Location

Primary_assembly 13: 69,464,795-69,576,946 reverse strand.

Sscrofa11.1:CM000824.5

About this gene

This gene has 3 transcripts (splice variants), 224 orthologues and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000057618.3	NR2C2-201	7923	614aa	ENSSSCP00000040860.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D0JND0 A0A8D1Y473	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,
ENSSSCT00000012690.4	NR2C2-203	8009	596aa	ENSSSCP00000012357.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1UBA4 A0A8D0WYU5	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,
ENSSSCT00000067783.2	NR2C2-202	2579	583aa	ENSSSCP00000068932.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QXR1	-

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Summary

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