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| Nomenclature |
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Symbol:
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Fezf2tm1.1Nses
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Name:
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Fez family zinc finger 2;
targeted mutation 1.1, Nenad Sestan
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MGI ID: |
MGI:5433045 |
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Synonyms: |
Fezf2fl |
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Gene:
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Fezf2
Location:
Chr14:12341892-12345865 bp, - strand
Genetic Position: Chr14,
6.36 cM
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Mutation origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:169221
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Parent Cell Line:
| W9.5/W95 (ES Cell) |
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Strain of Origin:
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129S1/Sv-Oca2+ Tyr+ Kitl+
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Mutation description |
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Allele
Type: | |
Targeted (Floxed/Frt) |
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Mutation: | |
Insertion |
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Mutation details: A loxP site was inserted upstream of exon 2. An FRT-flanked neo cassette with a 3' loxP site were inserted downstream of exon 2. Flp-mediated recombination removed the neo cassette and left exon 2 floxed. (J:169221)
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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 Fezf2 Mutation:
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5 strains or lines available |
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| References |
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Original: |
J:169221
Han W et al.,
"TBR1 directly represses Fezf2 to control the laminar origin and development of the corticospinal tract."
Proc Natl Acad Sci U S A 2011 Feb 15;108(7):3041-6
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All: |
2 reference(s)
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