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

Symbol:	Fbxo11Mutt
Name:	F-box protein 11; Mutt
MGI ID:	MGI:3690632
Gene:	Fbxo11  Location: Chr17:88298287-88372719 bp, - strand  Genetic Position: Chr17, 57.87 cM
Alliance:	Fbxo11Mutt page

Strain of Origin:

(C3H/HeN x BALB/c)F1

Allele Type:    Chemically induced (ENU) (Hypomorph) Mutation:    Nucleotide substitutions     This is a hypomorphic allele caused by a serine to leucine mutation at position 244 in exon 7. (J:114851)

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

In Structures Affected by this Mutation:

2 anatomical structure(s)

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 Fbxo11 Mutation:	51 strains or lines available

Original:	J:114851 Hardisty-Hughes RE, et al., A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse. Hum Mol Genet. 2006 Nov 15;15(22):3273-9
All:	1 reference(s)