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| Nomenclature |
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Symbol:
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Foxl2tm1Gpil
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Name:
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forkhead box L2;
targeted mutation 1, Giuseppe Pilia
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MGI ID: |
MGI:3044226 |
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Synonyms: |
Foxl2- |
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Gene:
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Foxl2
Location:
Chr9:98955607-98958126 bp, + strand
Genetic Position: Chr9,
51.41 cM, cytoband E4
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Mutation
origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:90371
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Parent Cell Line:
| Not Specified (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: The entire coding region, contained within one exon, was replaced with a neo cassette. Southern blot confirmed recombination in mutant ES cells. (J:90371)
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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 Foxl2 Mutation:
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2 strains or lines available |
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| References |
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Original: |
J:90371
Uda M et al.,
"Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development."
Hum Mol Genet 2004 Jun 1;13(11):1171-81
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All: |
6 reference(s)
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Analysis Tools
