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Msx2tm1.1Yvla
Targeted Allele Detail
Summary
Symbol: Msx2tm1.1Yvla
Name: msh homeobox 2; targeted mutation 1.1, Yves Lallemand
MGI ID: MGI:3795775
Synonyms: Msx2GFP, Msx2Null-GFP
Gene: Msx2  Location: Chr13:53620917-53626816 bp, - strand  Genetic Position: Chr13, 27.84 cM
Alliance: Msx2tm1.1Yvla page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:136241
Parent Cell Line:  CK35 (ES Cell)
Strain of Origin:  129S2/SvPas
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutation:    Intragenic deletion
 
Mutation detailsThis allele was derived from Msx2tm1Yvla by germ line, cre-mediated excision of the entire coding region. Green fluorescent protein (GFP) is expressed under control of the endogenous regulatory sequences. (J:136241)
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: 1 strain available      Cell Lines: 0 lines available
Carrying any Msx2 Mutation:  23 strains or lines available
References
Original:  J:136241 Bensoussan V, et al., Generation of an Msx2-GFP conditional null allele. Genesis. 2008 May;46(5):276-82
All:  4 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
10/22/2024
MGI 6.24
The Jackson Laboratory