Del(3Lphn2-Prkacb)1Hgc
Targeted Allele Detail

Summary

• Symbol: Del(3Lphn2-Prkacb)1Hgc
• Name: deletion, Chr3, Human Genome Center 1; deletion, Chr 3, Human Genome Center 1
• MGI ID: MGI:3487278
• Synonyms: Del1Hgc, Del^MMU3
• Gene: Del(3Lphn2-Prkacb)1Hgc Location: Chr3:146435334-148694366 bp Genetic Position: Chr3, cytoband H3

Mutation origin

• Germline Transmission: Earliest citation of germline transmission: J:93237
• Parent Cell Line: ESVJ (ES Cell)
• Strain of Origin: 129X1/SvJ

Mutation description

• Allele Type: Targeted (Null/knockout)
• Mutations: Intergenic deletion, Intragenic deletion
• Del(3Lphn2-Prkacb)1Hgc involves 14 genes/genome features (Prkacb, Gm19104, Gm10288 ...) View all
• Mutation details: Cre-mediated recombination resulted in the deletion of a 1,511 kb segment extending distally from Lphn2 to Prkacb, with breakpoint coordinates 151,157 and 152,668 from NCBI mouse build 32. (J:93237)

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(3Lphn2-Prkacb)1Hgc Mutation: 0 strains or lines available

References

• Original: J:93237 Nobrega MA, et al., Megabase deletions of gene deserts result in viable mice. Nature. 2004 Oct 21;431(7011):988-93
• All: 1 reference(s)