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Ephb3tm1.1Meg
Targeted Allele Detail
Summary
Symbol: Ephb3tm1.1Meg
Name: Eph receptor B3; targeted mutation 1.1, Michael E Greenberg
MGI ID: MGI:5505688
Synonyms: EphB3T706A
Gene: Ephb3  Location: Chr16:21023530-21042054 bp, + strand  Genetic Position: Chr16, 12.62 cM, cytoband B1-B4
Alliance: Ephb3tm1.1Meg page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:197489
Parent Cell Line:  J1 (ES Cell)
Strain of Origin:  129S4/SvJae
Mutation
description
Allele Type:    Targeted
Mutation:    Single point mutation
 
Mutation detailsA point mtuation (A to G) in exon 11 results in the amino acid substitution of threonine with alanine at position 706 (p.T706A) in the encoded protein. This mutation creates a PP1 analog-sensitive protein. Cre-mediated recombination removed the loxP site flanked neomycin resistance gene cassette inserted into intron 9. (J:197489)
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 Ephb3 Mutation:  52 strains or lines available
References
Original:  J:197489 Soskis MJ, et al., A chemical genetic approach reveals distinct EphB signaling mechanisms during brain development. Nat Neurosci. 2012 Dec;15(12):1645-54
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
04/16/2024
MGI 6.23
The Jackson Laboratory