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Eomestm1Whk
Targeted Allele Detail
Summary
Symbol: Eomestm1Whk
Name: eomesodermin; targeted mutation 1, William H Klein
MGI ID: MGI:3774146
Synonyms: Eomesflox, Tbr2flox
Gene: Eomes  Location: Chr9:118307259-118315176 bp, + strand  Genetic Position: Chr9, 70.21 cM, cytoband F3
Alliance: Eomestm1Whk page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:130570
Parent Cell Line:  R1 (ES Cell)
Strain of Origin:  (129X1/SvJ x 129S1/Sv)F1-Kitl+
Mutation
description
Allele Type:    Targeted (Conditional ready, No functional change)
Mutation:    Insertion
 
Mutation detailsA neo cassette flanked by frt sites with a 3' loxP site was inserted into intron 3 and an additional loxP site was inserted into intron 2 resulting in a floxed exon 3. The neo cassette was removed by germ-line, flp-mediated recombination. (J:130570)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
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 Eomes Mutation:  41 strains or lines available
References
Original:  J:130570 Mao CA, et al., Eomesodermin, a target gene of Pou4f2, is required for retinal ganglion cell and optic nerve development in the mouse. Development. 2008 Jan;135(2):271-80
All:  12 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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory