Nxnl1^tm1.2Tlev
Targeted Allele Detail

Summary

• Symbol: Nxnl1^tm1.2Tlev
• Name: nucleoredoxin-like 1; targeted mutation 1.2, Thierry Leveillard
• MGI ID: MGI:5432155
• Gene: Nxnl1 Location: Chr8:72013199-72019245 bp, - strand Genetic Position: Chr8, 34.43 cM
• Alliance: Nxnl1^tm1.2Tlev page

Mutation origin

• Germline Transmission: Earliest citation of germline transmission: J:186370
• Parent Cell Line: Not Specified (ES Cell)
• Strain of Origin: BALB/c

Mutation description

• Allele Type: Targeted (Null/knockout)
• Mutations: Insertion, Intragenic deletion
• Mutation details: A loxP site was inserted upstream of exon 1. An FRT flanked neo cassette with a 5' losP site was inserted downstream of exon 1. FLP mediated recombination removed the neo cassette. Cre mediated recombination removed exon 1. Western blot analysis confirmed the abscence of protein expression in the retina. (J:186370)

Expression

In Mice Carrying this Mutation:	1 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation:	3 anatomical structure(s)

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 Nxnl1 Mutation: 11 strains or lines available

References

• Original: J:186370 Cronin T, et al., The disruption of the rod-derived cone viability gene leads to photoreceptor dysfunction and susceptibility to oxidative stress. Cell Death Differ. 2010 Jul;17(7):1199-210
• All: 3 reference(s)