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Fgf20tm2.1(cre/EGFP)Dor
Targeted Allele Detail
Summary
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
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:229246
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Targeted (Recombinase, Reporter)
Mutations:    Insertion, Intragenic deletion
 
Fgf20tm2.1(cre/EGFP)Dor expression driven by 1 gene
 
Mutation detailsA cre recombinase gene, EGFP reporter gene and FRT-flanked neomycin resistance cassette replaced exon 1. Flp-mediated recombination removed the selection cassette. (J:229246)
Recombinase
activity
Activity:
 Tissue activity of this recombinase allele
Driver: Fgf20 (mouse)
Summary of all recombinase alleles driven by Fgf20.
 

Expression
In Mice Carrying this Mutation: 1 RNA-Seq or microarray experiment(s)
Find Mice (IMSR)
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:  16 strains or lines available
References
Original:  J:229246 Huh SH, et al., Cochlear progenitor number is controlled through mesenchymal FGF receptor signaling. Elife. 2015;4
All:  10 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Funding Information
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory