Fndc5^tm1.1Jkche
Targeted Allele Detail

Summary

• Symbol: Fndc5^tm1.1Jkche
• Name: fibronectin type III domain containing 5; targeted mutation 1.1, Jake J Chen
• MGI ID: MGI:6822321
• Synonyms: FNDC5/irisin^flox
• Gene: Fndc5 Location: Chr4:129030672-129038386 bp, + strand Genetic Position: Chr4, 62.93 cM
• Alliance: Fndc5^tm1.1Jkche page

Mutation origin

• Germline Transmission: Earliest citation of germline transmission: J:314278
• Parent Cell Line: Not Specified (ES Cell)
• Strain of Origin: Not Specified

Mutation description

• Allele Type: Targeted (Conditional ready)
• Mutation: Insertion
• Mutation details: Using homologous recombination in ES cells, the targeting vector inserted a loxP upstream of the exon 2 of the Fndc5 gene and FRT flanked Neo selection cassette and the second loxP sequences in the intron downstream of the exon 2. The neo cassette was removed by Flp recombinase, leaving the exon 2 flanked by loxP sites. Cre mediated removal of exon 2 will result in a 75 aa (28 aa Nterminal sequence of irisin and 47 aa frameshifted nonsense aa) truncation. (J:314278)

Expression

In Mice Carrying this Mutation:

10 assay results

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 Fndc5 Mutation: 18 strains or lines available

References

• Original: J:314278 Zhu X, et al., Irisin deficiency disturbs bone metabolism. J Cell Physiol. 2021 Jan;236(1):664-676
• All: 2 reference(s)