Gene

nfe2l2a

ID
ZDB-GENE-030723-2
Name
nfe2 like bZIP transcription factor 2a
Symbol
nfe2l2a Nomenclature History
Previous Names
  • nfe2l2
  • Nrf2 (1)
  • Nrf2a (1)
  • wu:fc15g09 (1)
  • wu:fj67e03 (1)
Type
protein_coding_gene
Location
Chr: 9 Mapping Details/Browsers
Description
Enables protein heterodimerization activity and transcription cis-regulatory region binding activity. Contributes to DNA-binding transcription factor activity. Acts upstream of or within several processes, including cellular response to prostaglandin stimulus; larval feeding behavior; and positive regulation of DNA-templated transcription. Located in cytoplasm and nucleus. Part of transcription regulator complex. Is expressed in several structures, including digestive system; female organism; heart; pleuroperitoneal region; and sensory system. Human ortholog(s) of this gene implicated in Alzheimer's disease; cataract; hepatocellular carcinoma; macular degeneration; and tuberculosis. Orthologous to human NFE2L2 (NFE2 like bZIP transcription factor 2).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
39 figures from 36 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
10 figures from 5 publications
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Allele Type Localization Consequence Mutagen Supplier
dw213Allele with one deletionUnknownInframe DeletionCRISPR
dw214aAllele with one deletionUnknownInframe DeletionCRISPR
fh318Allele with one point mutationUnknownMissenseENU
fh319Allele with one point mutationUnknownUnknownENU
ihb247Allele with one delinsExon 2UnknownCRISPR
ihb256Allele with one deletionExon 4UnknownCRISPR
it321Allele with one delinsExon 2UnknownCRISPR
la026758TgTransgenic insertionUnknownUnknownDNA
la026760TgTransgenic insertionUnknownUnknownDNA
nfe2l2a_unrecoveredAllele with one point mutationUnknownUnknownENU
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Sequence Targeting Reagents
Human Disease
Associated With nfe2l2a Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Immunodeficiency, developmental delay, and hypohomocysteinemia 617744
Associated With nfe2l2a Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR004826 Basic leucine zipper domain, Maf-type
Domain IPR004827 Basic-leucine zipper domain
Family IPR047167 Nuclear Factor Erythroid-derived 2-like
Homologous_superfamily IPR008917 Transcription factor, Skn-1-like, DNA-binding domain superfamily
Homologous_superfamily IPR046347 Basic-leucine zipper domain superfamily
Domain Details Per Protein
Protein Additional Resources Length Basic-leucine zipper domain Basic leucine zipper domain, Maf-type Basic-leucine zipper domain superfamily Nuclear Factor Erythroid-derived 2-like Transcription factor, Skn-1-like, DNA-binding domain superfamily
UniProtKB:Q8JIM1 InterPro 586
UniProtKB:A0A8M2BJQ0 InterPro 585
Transcripts
Genome Browsers
Genome Build: GRCz11Chromosome: 9
Type Name Annotation Method Has Havana Data Length (nt) Analysis
mRNA nfe2l2a-201 (1) Ensembl 4,739 nt
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
No data available
Marker Relationships
Relationship Marker Type Marker Accession Numbers Citations
Contained inBACCH211-230E14ZFIN Curated Data
EncodesESTfc15g09
EncodesESTfj67e03
EncodescDNAMGC:56001ZFIN Curated Data
EncodescDNAMGC:174016ZFIN Curated Data
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Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Species Symbol Chromosome Accession # Evidence
HumanNFE2L22
Amino acid sequence comparison (5)
Conserved genome location (synteny) (3)
Phylogenetic tree (1)
MouseNfe2l22
Amino acid sequence comparison (2)
Phylogenetic tree (1)
Citations
1 - 10 of 231
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