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Nfe2l2tm2Mym
Targeted Allele Detail
Summary
Symbol: Nfe2l2tm2Mym
Name: nuclear factor, erythroid derived 2, like 2; targeted mutation 2, Masayuki Yamamoto
MGI ID: MGI:7645688
Synonyms: Nrf2L30F
Gene: Nfe2l2  Location: Chr2:75505857-75534985 bp, - strand  Genetic Position: Chr2, 44.75 cM
Alliance: Nfe2l2tm2Mym page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:347771
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Targeted (Conditional ready, Humanized sequence, Null/knockout, Reporter)
Mutations:    Insertion, Single point mutation
 
Mutation detailsLeucine codon 30 (CTT) in exon 2 was changed to phenylalanine (TTT) (p.L30F) and a loxP site flanked beta-galactosidase and neomycin resistance fusion gene cassette was inserted into intron 1. The mutation is the equivalent of the same human mutation associated with esophageal squamous cell carcinoma (ESCC). This allele is a reporter knockout allele and only after Cre-mediated removal of the beta-geo cassette will it express the mutated transcript and peptide. (J:347771)
Tumor Data
List all tumor models in MMHCdb carrying Nfe2l2tm2Mym
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Nfe2l2 Mutation:  94 strains or lines available
References
Original:  J:347771 Takahashi J, et al., Differential squamous cell fates elicited by NRF2 gain of function versus KEAP1 loss of function. Cell Rep. 2024 Apr 23;43(4):114104
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
12/30/2025
MGI 6.24
The Jackson Laboratory