Dbf
Spontaneous Allele Detail

Summary

• Symbol: Dbf
• Name: doublefoot
• MGI ID: MGI:1857644
• Gene: Dbf Location: Chr1:59938031-82944074 bp Genetic Position: Chr1, Syntenic
• Alliance: Dbf page

Mutation origin

• Strain of Origin: (C3H/HeH x 101/H)F1

Mutation description

• Allele Type: Spontaneous
• Mutation: Intergenic deletion
• Dbf involves 24 genes/genome features (Slc23a3, Cnppd1, Retreg2 ...) View all
• Mutation details: This is a 595,992bp deletion on Chromosome 1. Using Build 37 (mm9), the centromeric break point is at 75,098,488 bp and the telomeric breakpoint is at 75,694,480 bp. (J:135300)
• Inheritance: Dominant

Disease models

Expression

In Mice Carrying this Mutation:	108 assay results
In Structures Affected by this Mutation:	28 anatomical structure(s)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 2 strains available Cell Lines: 0 lines available
• Carrying any Dbf Mutation: 2 strains or lines available

References

• Original: J:14233 Lyon MF, et al., Doublefoot, a new mutation affecting limb development. Mouse News Lett. 1989;83:158
• All: 10 reference(s)