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Foxl1tm1Hfk
Targeted Allele Detail
Summary
Symbol: Foxl1tm1Hfk
Name: forkhead box L1; targeted mutation 1, Hiroshi Fukamachi
MGI ID: MGI:2180191
Synonyms: Fkh6-, Foxl1-
Gene: Foxl1  Location: Chr8:121854679-121857383 bp, + strand  Genetic Position: Chr8, 70.34 cM
Alliance: Foxl1tm1Hfk page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:76379
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutation:    Insertion
 
Mutation detailsThe gene was disrupted by insertion of a lacZ-polyA-neo cassette via homologous recombination. Absence of gene expression in homozygous mutant mice was confirmed via RNase protection assay. (J:76379)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 6 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 Foxl1 Mutation:  12 strains or lines available
References
Original:  J:76379 Fukamachi H, et al., Mesenchymal transcription factor Fkh6 is essential for the development and differentiation of parietal cells. Biochem Biophys Res Commun. 2001 Feb 2;280(4):1069-76
All:  4 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
12/10/2024
MGI 6.24
The Jackson Laboratory