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Foxg1tm1M
Targeted Allele Detail
Summary
Symbol: Foxg1tm1M
Name: forkhead box G1; targeted mutation 1, Memorial Sloan Kettering Cancer Center
MGI ID: MGI:1857771
Synonyms: BF-1-, BF1-, BF1(-lacZ), Foxg1-, Foxg1lacZ
Gene: Foxg1  Location: Chr12:49429666-49433650 bp, + strand  Genetic Position: Chr12, 21.78 cM
Alliance: Foxg1tm1M page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:26720
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 detailsMost of the coding region was replaced with a lacZ and neomycin cassette. The lacZ sequence was fused in-frame following the first 13 codons of the gene. (J:26720)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 223 assay results
In Structures Affected by this Mutation: 18 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 Foxg1 Mutation:  28 strains or lines available
References
Original:  J:26720 Xuan S, et al., Winged helix transcription factor BF-1 is essential for the development of the cerebral hemispheres. Neuron. 1995 Jun;14(6):1141-52
All:  26 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
04/16/2024
MGI 6.23
The Jackson Laboratory