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

Symbol:	Fgf20tm2.1(cre/EGFP)Dor
Name:	fibroblast growth factor 20; targeted mutation 2.1, David M Ornitz
MGI ID:	MGI:5751785
Synonyms:	Fgf20Cre, Fgf20-Gfp-Cre
Gene:	Fgf20  Location: Chr8:40732206-40740060 bp, - strand  Genetic Position: Chr8, 23.89 cM, cytoband B1.2
Alliance:	Fgf20tm2.1(cre/EGFP)Dor page

Germline Transmission:	Earliest citation of germline transmission: J:229246
Parent Cell Line:	Not Specified (ES Cell)
Strain of Origin:	Not Specified

Allele Type:    Targeted (Recombinase, Reporter) Mutations:    Insertion, Intragenic deletion   Fgf20tm2.1(cre/EGFP)Dor expression driven by 1 gene Knock-in expression driven by: Organism Driver Gene Note mouse Fgf20 (MGI:1891346)   Mutation details: A cre recombinase gene, EGFP reporter gene and FRT-flanked neomycin resistance cassette replaced exon 1. Flp-mediated recombination removed the selection cassette. (J:229246)

Activity:	Tissue activity of this recombinase allele
Driver:	Fgf20 (mouse) Summary of all recombinase alleles driven by Fgf20. Alliance mouse Fgf20 gene page

In Mice Carrying this Mutation:

1 RNA-Seq or microarray experiment(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 Fgf20 Mutation:	14 strains or lines available

Original:	J:229246 Huh SH, et al., Cochlear progenitor number is controlled through mesenchymal FGF receptor signaling. Elife. 2015;4
All:	8 reference(s)