Summary | Mutation origin | Mutation description | Recombinase activity | Find Mice (IMSR) | References

Symbol:	Foxl2em1(cre)Gaof
Name:	forkhead box L2; endonuclease-mediated mutation 1, Fei Gao
MGI ID:	MGI:6739811
Synonyms:	Foxl2-Cre
Gene:	Foxl2  Location: Chr9:98837660-98840179 bp, + strand  Genetic Position: Chr9, 51.41 cM, cytoband E4
Alliance:	Foxl2em1(cre)Gaof page

Strain of Origin:

Not Specified

Allele Type:    Endonuclease-mediated (Recombinase) Mutation:    Insertion   Foxl2em1(cre)Gaof expression driven by 1 gene Knock-in expression driven by: Organism Driver Gene Note mouse Foxl2 (MGI:1349428)   Mutation details: A Cre-P2A expression cassette was knocked into the Foxg1 gene start codon site via CRISPR/Cas9 mediated recombination. (J:292639)

Activity:	Tissue activity of this recombinase allele
Driver:	Foxl2 (mouse) Summary of all recombinase alleles driven by Foxl2. Comparative matrix view of recombinase activities Alliance mouse Foxl2 gene page

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:292639 Cen C, et al., Inactivation of Wt1 causes pre-granulosa cell to steroidogenic cell transformation and defect of ovary development. Biol Reprod. 2020 Jun 23;103(1):60-69
All:	3 reference(s)