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Gulosfx
Spontaneous Allele Detail
Summary
Symbol: Gulosfx
Name: gulonolactone (L-) oxidase; spontaneous fracture
MGI ID: MGI:2157331
Gene: Gulo  Location: Chr14:66224235-66246656 bp, - strand  Genetic Position: Chr14, 34.36 cM
Alliance: Gulosfx page
Mutation
origin
Strain of Origin:  BALB/cBy-Rasa3scat
Mutation
description
Allele Type:    Spontaneous
Mutation:    Deletion
  Gulosfx involves 1 genes/genome features (Gulo) View all
    The mutation in the sfx mouse is a deletion that includes the entire Gulo gene. (J:95128)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Gulo Mutation:  27 strains or lines available
Notes

This spontaneous mutation appeared in a BALB/cBy-scat colony at The Jackson Laboratory. The scat and sfx mutations were separated from each other by backcrossing BALB/cBy-scat mice to BALB/cBy mice and observing F2 offspring for those that exhibited the sfx phenotype but not the scat phenotype.

References
Original:  J:66648 Beamer WG, et al., Spontaneous fracture (sfx): a mouse genetic model of defective peripubertal bone formation. Bone. 2000 Nov;27(5):619-26
All:  6 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)
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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory