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| Nomenclature |
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Symbol:
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Foxc2tm1Blh
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Name:
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forkhead box C2;
targeted mutation 1, Brigid L Hogan
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MGI ID: |
MGI:1857865 |
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Synonyms: |
Foxc2-, mfh1tm1 |
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Gene:
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Foxc2
Location:
Chr8:121116171-121118892 bp, + strand
Genetic Position: Chr8,
70.33 cM
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Mutation
origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:39636
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Parent Cell Line:
| TL1/TL-1 (ES Cell) |
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Strain of Origin:
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129S6/SvEvTac
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Mutation
description |
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Allele
Type: | |
Targeted (knock-out) |
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Mutations: | |
Insertion, Intragenic deletion |
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Mutation details: A PGK-neomyin selection cassette replaced all of the coding sequences of the gene. In situ hybridization experiments on sections of homozygous embryos confirmed that no detectable transcript was expressed from this allele. (J:39636)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available |
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Carrying any Foxc2 Mutation:
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0 strains or lines available |
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| References |
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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
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All: |
12 reference(s)
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Analysis Tools
