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

Symbol:	Fcgr1tm1(EGFP/Cre/ERT2)Wtsi
Name:	Fc receptor, IgG, high affinity I; targeted mutation 1, Wellcome Trust Sanger Institute
MGI ID:	MGI:5660015
Synonyms:	Fcgr1tm1(EGFP_CreERT2)Wtsi
Gene:	Fcgr1  Location: Chr3:96190225-96201285 bp, - strand  Genetic Position: Chr3, 41.72 cM
Alliance:	Fcgr1tm1(EGFP/Cre/ERT2)Wtsi page

Mutant Cell Line:	CEPD0073_1_E03
Germline Transmission:	Earliest citation of germline transmission: J:204812
Parent Cell Line:	JM8.N4 (ES Cell)
Strain of Origin:	C57BL/6N
Project Collection:	EUCOMMTOOLS

Allele Type:    Targeted (Inducible, Null/knockout, Recombinase, Reporter) Inducer:    tamoxifen Mutations:    Insertion, Intragenic deletion   Fcgr1tm1(EGFP/Cre/ERT2)Wtsi expression driven by 1 gene Knock-in expression driven by: Organism Driver Gene Note mouse Fcgr1 (MGI:95498)   Mutation details: According the the allele molecular image presented by the International Knockout Mouse Consortium, this allele has one FRT site, an engrailed 2 splice acceptor sequence, an EGFP and cre/ERT2 expression cassette, a Rox flanked puromycin resistance cassette and a single loxP site replacing a genomic fragment containing exons 3-5. (J:157065)

Activity:	Tissue activity of this recombinase allele
Driver:	Fcgr1 (mouse) Summary of all recombinase alleles driven by Fcgr1. Alliance mouse Fcgr1 gene page

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 2 strains available      Cell Lines: 0 lines available
Carrying any Fcgr1 Mutation:	34 strains or lines available

Original:	J:157065 Helmholtz Zentrum Muenchen GmbH, Alleles produced for the EUCOMM and EUCOMMTools projects by the Helmholtz Zentrum Muenchen GmbH (Hmgu). MGI Direct Data Submission. 2010-2015;
All:	2 reference(s)