Del(19Poll-Fbxw4)4Fsp
Targeted Allele Detail

Summary

• Symbol: Del(19Poll-Fbxw4)4Fsp
• Name: deletion, Chr 19, Francois Spitz 4
• MGI ID: MGI:5501313
• Synonyms: Del4Fsp, DEL(P-F4)
• Gene: Del(19Poll-Fbxw4)4Fsp Location: Chr19:45540714-45648751 bp 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 (Null/knockout)
• Mutations: Insertion, Intergenic deletion, Intragenic deletion
• Del(19Poll-Fbxw4)4Fsp involves 3 genes/genome features (Poll, Dpcd, Fbxw4) View all
• Mutation details: Cre-mediated recombination between Poll^tm1Crey and Fbxw4^tm1.2Fsp deleted the intervening sequence (including Poll, Dpcd, Fbxw4 and Gm17018). This allele also deletes conserved elements CE58 to CE71. (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 Del(19Poll-Fbxw4)4Fsp 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)