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Msx2tm1Rilm
Targeted Allele Detail
Nomenclature
Symbol: Msx2tm1Rilm
Name: msh homeobox 2; targeted mutation 1, Richard Maas
MGI ID: MGI:1926381
Synonyms: Msx2-
Gene: Msx2  Location: Chr13:53467877-53473074 bp, - strand  Genetic Position: Chr13, 27.84 cM
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:61509
Parent Cell Line:  J1 (ES Cell)
Strain of Origin:  129S4/SvJae
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Insertion
 
Mutation details
Inheritance:    Recessive
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Disease models
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Expression
In Mice Carrying this Mutation: 16 assay results
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:  10 strains or lines available
References
Original:  J:61509 Satokata I, et al., Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation. Nat Genet. 2000 Apr;24(4):391-5
All:  27 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
07/15/2014
MGI 5.18
The Jackson Laboratory