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

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Gene: NFE2L2 ENSBTAG00000019255

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Description

NFE2 like bZIP transcription factor 2 [Source:VGNC Symbol;Acc:VGNC:32036]

Location

Primary_assembly 2: 19,637,059-19,649,651 forward strand.

ARS-UCD2.0:CM008169.2

About this gene

This gene has 5 transcripts (splice variants), 212 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000135424.2	NFE2L2-201	2474	642aa	ENSBTAP00000085163.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SIL3	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSBTAT00000153341.1	NFE2L2-202	6511	593aa	ENSBTAP00000105234.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000081481.3	NFE2L2-203	2324	609aa	ENSBTAP00000059632.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LRK0	-
ENSBTAT00000025637.7	NFE2L2-204	2272	591aa	ENSBTAP00000025637.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MKR6	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSBTAT00000072818.3	NFE2L2-205	2180	561aa	ENSBTAP00000060452.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LTP2	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,

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Summary

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