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Efnb1tm2.2Sor
Targeted Allele Detail
Summary
Symbol: Efnb1tm2.2Sor
Name: ephrin B1; targeted mutation 2.2, Philippe Soriano
MGI ID: MGI:3850114
Synonyms: Ephrin-B16F
Gene: Efnb1  Location: ChrX:98179736-98192597 bp, + strand  Genetic Position: ChrX, 43.22 cM, cytoband D
Alliance: Efnb1tm2.2Sor page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:150043
Parent Cell Line:  AK7.1 (ES Cell)
Strain of Origin:  129S4/SvJaeSor
Mutation
description
Allele Type:    Targeted
Mutations:    Insertion, Nucleotide substitutions
 
Mutation detailsGerm line, cre mediated recombination removed the wild-type exon 5 allowing for expression of the modified exon 5 in which all 6 intracellular tyrosines are replaced with phenylalanine. The protein product is predicted to lack the capacity for intracellular signalling. (J:150043)
Phenotypes
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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 Efnb1 Mutation:  15 strains or lines available
References
Original:  J:150043 Bush JO, et al., Ephrin-B1 regulates axon guidance by reverse signaling through a PDZ-dependent mechanism. Genes Dev. 2009 Jul 1;23(13):1586-99
All:  2 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
10/29/2024
MGI 6.24
The Jackson Laboratory