Summary | Mutation origin | Mutation description | Expression | Phenotypes | Disease models | Find Mice (IMSR) | References

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

Strain of Origin:

(C3H/HeH x 101/H)F1

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

View phenotypes and curated references for all genotypes (concatenated display).

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

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

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