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

Configure this page

Share this page

Bookmark this page

.

Gene: NFE2 ENSSSCG00000000289

.

Description

nuclear factor, erythroid 2 [Source:VGNC Symbol;Acc:VGNC:90712]

Location

Primary_assembly 5: 19,494,677-19,501,810 reverse strand.

Sscrofa11.1:CM000816.5

About this gene

This gene has 1 transcript (splice variant), 188 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000047127.2	NFE2-201	1753	373aa	ENSSSCP00000035078.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1C7Q8 A0A8D2C781	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,

.

Summary

.

.