Summary | Mutation origin | Mutation description | Expression | Phenotypes | Disease models | Find Mice (IMSR) | References

Symbol:	Foxl2tm1Gpil
Name:	forkhead box L2; targeted mutation 1, Giuseppe Pilia
MGI ID:	MGI:3044226
Synonyms:	Foxl2-
Gene:	Foxl2  Location: Chr9:98837660-98840179 bp, + strand  Genetic Position: Chr9, 51.41 cM, cytoband E4
Alliance:	Foxl2tm1Gpil page

Germline Transmission:	Earliest citation of germline transmission: J:90371
Parent Cell Line:	Not Specified (ES Cell)
Strain of Origin:	129S6/SvEvTac

Allele Type:    Targeted (Null/knockout) Mutations:    Insertion, Intragenic deletion   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)

View phenotypes and curated references for all genotypes (concatenated display).

In Mice Carrying this Mutation:	30 assay results 3 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation:	5 anatomical structure(s)

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 Foxl2 Mutation:	15 strains or lines available

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
All:	15 reference(s)