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Foxc2tm1Blh
Targeted Allele Detail
Nomenclature
Symbol: Foxc2tm1Blh
Name: forkhead box C2; targeted mutation 1, Brigid L Hogan
MGI ID: MGI:1857865
Synonyms: Foxc2-, mfh1tm1
Gene: Foxc2  Location: Chr8:121116171-121118895 bp, + strand  Genetic Position: Chr8, 70.33 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:39636
Parent Cell Line:  TL1/TL-1 (ES Cell)
Strain of Origin:  129S6/SvEvTac
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation details
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 11 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 Foxc2 Mutation:  0 strains or lines available
References
Original:  J:39636 Winnier GE, et al., The winged helix transcription factor MFH1 is required for proliferation and patterning of paraxial mesoderm in the mouse embryo. Genes Dev. 1997 Apr 1;11(7):926-40
All:  12 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
11/18/2014
MGI 5.20
The Jackson Laboratory