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Efnb3tm1Nwg
Targeted Allele Detail
Summary
Symbol: Efnb3tm1Nwg
Name: ephrin B3; targeted mutation 1, Nicholas W Gale
MGI ID: MGI:2388046
Synonyms: ephrin-B3-
Gene: Efnb3  Location: Chr11:69444918-69451031 bp, - strand  Genetic Position: Chr11, 42.8 cM
Alliance: Efnb3tm1Nwg page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:68814
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsThe coding region of exon 1 was deleted and replaced with a lacZ-PGK-neo cassette. Northern blot analysis of brain mRNA from homozygous mutant animals confirmed the absence of gene expression. However, the lacZ gene was not expressed as originally intended. (J:68814)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(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 Efnb3 Mutation:  11 strains or lines available
References
Original:  J:68814 Kullander K, et al., Ephrin-B3 is the midline barrier that prevents corticospinal tract axons from recrossing, allowing for unilateral motor control. Genes Dev. 2001 Apr 1;15(7):877-88
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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory