Swsap1^tm1.1Osb
Targeted Allele Detail

Summary

• Symbol: Swsap1^tm1.1Osb
• Name: SWIM type zinc finger 7 associated protein 1; targeted mutation 1.1, Research Institute for Microbial Diseases, Osaka University
• MGI ID: MGI:7546933
• Gene: Swsap1 Location: Chr9:21867051-21869560 bp, + strand Genetic Position: Chr9, 7.93 cM, cytoband A4
• Alliance: Swsap1^tm1.1Osb page

Mutation origin

• Germline Transmission: Earliest citation of germline transmission: J:273277
• Parent Cell Line: Not Specified (ES Cell)
• Strain of Origin: Not Specified

Mutation description

• Allele Type: Targeted (Null/knockout, Reporter)
• Mutations: Insertion, Intragenic deletion
• Mutation details: The targeting construct replaced exon 2 with a beta-geo cassette, loxP site, exon2, and loxP site. Cre-mediated recombination removed exon 2. (J:273277)

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 Swsap1 Mutation: 16 strains or lines available

References

• Original: J:273277 Matsuzaki K, et al., Human RAD51 paralogue SWSAP1 fosters RAD51 filament by regulating the anti-recombinase FIGNL1 AAA+ ATPase. Nat Commun. 2019 Mar 29;10(1):1407
• All: 2 reference(s)