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| Nomenclature |
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Symbol:
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Foxc2tm1Miu
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Name:
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forkhead box C2;
targeted mutation 1, Naoyuki Miura
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MGI ID: |
MGI:1857740 |
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Synonyms: |
Mfh1-, MFH-1- |
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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:55316
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Parent Cell Line:
| E14.1 (ES Cell) |
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Strain of Origin:
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129P2/OlaHsd
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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 neomycin resistance cassette replaced a genomic fragment containing the entire coding region of the gene. RT-PCR analysis on RNA derived from E11.5 homozygous embryos confirmed that no detectable transcript was produced from this allele. (J:55316)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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Disease models
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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:55316
Iida K et al.,
"Essential roles of the winged helix transcription factor MFH-1 in aortic arch patterning and skeletogenesis."
Development 1997 Nov;124(22):4627-38
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All: |
11 reference(s)
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