Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Nfe2 ENSRNOG00000036837

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Description

nuclear factor, erythroid 2 [Source:RGD Symbol;Acc:1306888]

Gene Synonyms

LOC366998

Location

Primary_assembly 7: 136,261,236-136,268,585 reverse strand.

GRCr8:CM070397.1

About this gene

This gene has 2 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
ENSRNOT00000104324.2	Nfe2-202	1592	395aa	ENSRNOP00000088992.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ABT4	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,
ENSRNOT00000055281.5	Nfe2-201	1656	373aa	ENSRNOP00000052156.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6AYT2	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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