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Fbxo32tm1Glas
Targeted Allele Detail
Summary
Symbol: Fbxo32tm1Glas
Name: F-box protein 32; targeted mutation 1, David J Glass
MGI ID: MGI:2676047
Synonyms: MAFbx -
Gene: Fbxo32  Location: Chr15:58039275-58078288 bp, - strand  Genetic Position: Chr15, 24.43 cM, cytoband D2
Alliance: Fbxo32tm1Glas page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:77660
Parent Cell Line:  CJ7 (ES Cell)
Strain of Origin:  129S1/Sv-Oca2+ Tyr+ Kitl+
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsAn in-frame lacZ gene and neomycin selection cassette replaced approximately 35 kb of gene sequences, including exons 1-7 and most of exon 8. Northern blot analysis on RNA derived from muscle of homozygous mice confirmed that no wild-type transcript is expressed from this allele. Beta-galactosidase is expressed from this allele under the control of the endogenous promoter. (J:77660)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
Find Mice (IMSR)
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 Fbxo32 Mutation:  17 strains or lines available
References
Original:  J:77660 Bodine SC, et al., Identification of ubiquitin ligases required for skeletal muscle atrophy. Science. 2001 Nov 23;294(5547):1704-8
All:  8 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
11/05/2024
MGI 6.24
The Jackson Laboratory