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

Configure this page

Share this page

Bookmark this page

.

Gene: NR2F2 ENSSSCG00000002254

.

Description

nuclear receptor subfamily 2 group F member 2 [Source:VGNC Symbol;Acc:VGNC:90881]

Location

Primary_assembly 7: 83,076,124-83,090,535 reverse strand.

Sscrofa11.1:CM000818.5

About this gene

This gene has 3 transcripts (splice variants), 229 orthologues and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000002510.5	NR2F2-202	4028	414aa	ENSSSCP00000002448.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1ULS2 F6Q4U7	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, 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,
ENSSSCT00000058785.3	NR2F2-203	2593	281aa	ENSSSCP00000048884.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1UL52 B5A7P0	-
ENSSSCT00000093090.1	NR2F2-201	1598	298aa	ENSSSCP00000075861.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8W4F963	-

.

Summary

.

.