About   Help   FAQ
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
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Disease models
Loading...
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)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory