About   Help   FAQ
Foxp2tm2.2Woen
Targeted Allele Detail
Nomenclature
Symbol: Foxp2tm2.2Woen
Name: forkhead box P2; targeted mutation 2.2, Wolfgang Enard
MGI ID: MGI:3851108
Synonyms: Foxp2ko
Gene: Foxp2  Location: Chr6:14901388-15441201 bp, + strand  Genetic Position: Chr6, 6.49 cM, cytoband A2
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:150425
Parent Cell Line:  Bruce 4 (ES Cell)
Strain of Origin:  B6.Cg-Thy1a
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsGerm line, cre mediated recombination removed exon 7. The absence of protein expression was confirmed by western blot analysis on embryo extracts. (J:150425)
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
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 Foxp2 Mutation:  31 strains or lines available
References
Original:  J:150425 Enard W, et al., A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice. Cell. 2009 May 29;137(5):961-71
All:  3 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
08/15/2017
MGI 6.10
The Jackson Laboratory