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Foxj1tm1Slb
Targeted Allele Detail
Nomenclature
Symbol: Foxj1tm1Slb
Name: forkhead box J1; targeted mutation 1, Steven L Brody
MGI ID: MGI:2158221
Synonyms: FoxJ1-, Foxj1lacZ, HFH-4 -
Gene: Foxj1  Location: Chr11:116330704-116335399 bp, - strand  Genetic Position: Chr11, 81.16 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:73616
Parent Cell Line:  RW-4 (ES Cell)
Strain of Origin:  129X1/SvJ
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutation:    Insertion
 
Mutation details
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Disease models
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Expression
In Mice Carrying this Mutation: 6 assay results
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 Foxj1 Mutation:  3 strains or lines available
Notes
Phenotypic Similarity to Human Syndrome: Kartagener Syndrome or Primary Ciliary Dyskinesia (J:73616)

References
Original:  J:73616 Brody SL, et al., Ciliogenesis and left-right axis defects in forkhead factor HFH-4-null mice. Am J Respir Cell Mol Biol. 2000 Jul;23(1):45-51
All:  10 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
07/15/2014
MGI 5.18
The Jackson Laboratory