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

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Gene: NFE2 ENSBTAG00000001562

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Description

nuclear factor, erythroid 2 [Source:VGNC Symbol;Acc:VGNC:32034]

Location

Primary_assembly 5: 25,769,886-25,777,479 forward strand.

ARS-UCD1.3:CM008172.2

About this gene

This gene has 4 transcripts (splice variants), 187 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000134390.1	NFE2-201	2033	520aa	ENSBTAP00000086726.1	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,
ENSBTAT00000066479.2	NFE2-204	1757	428aa	ENSBTAP00000059395.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5EAD3	-
ENSBTAT00000002043.3	NFE2-203	1691	406aa	ENSBTAP00000002043.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5EAD3	-
ENSBTAT00000047424.2	NFE2-202	1491	374aa	ENSBTAP00000044631.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q5EAD3	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,

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Summary

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