In(19Fgf8;Pitx3)1Fsp
Targeted Allele Detail

Summary

• Symbol: In(19Fgf8;Pitx3)1Fsp
• Name: inversion, Chr 19, Francois Spitz 1
• MGI ID: MGI:5501271
• Synonyms: In(19Fgf8-Pitx3)1Fsp, INV(F8-P3)
• Gene: In(19Fgf8;Pitx3)1Fsp Location: unknown Genetic Position: Chr19, Syntenic

Mutation origin

• Germline Transmission: Earliest citation of germline transmission: J:196292
• Parent Cell Line: Not Specified (ES Cell)
• Strain of Origin: 129P2/OlaHsd

Mutation description

• Allele Type: Targeted
• Mutations: Insertion, Inversion
• In(19Fgf8;Pitx3)1Fsp involves 24 genes/genome features (A013, D19Ertd132e, D19Ertd409e ...) View all
• Mutation details: STRING (sequential targeted recombination induced genomic rearrangement) between Fgf8^tm1.4Mrt and Pitx3^tm1Mli inverted the intervening sequence (Npm3, Gm15491, Mgea5, Kcnip2, 9130011E15Rik, Hps6, Ldb1, Pprc1, Nolc1 and Elovl3). (J:196292)

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 In(19Fgf8;Pitx3)1Fsp Mutation: 0 strains or lines available

References

• Original: J:196292 Marinic M, et al., An integrated holo-enhancer unit defines tissue and gene specificity of the Fgf8 regulatory landscape. Dev Cell. 2013 Mar 11;24(5):530-42
• All: 1 reference(s)