Summary | Mutation origin | Mutation description | Expression | Phenotypes | Find Mice (IMSR) | References

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

Germline Transmission:	Earliest citation of germline transmission: J:136241
Parent Cell Line:	CK35 (ES Cell)
Strain of Origin:	129S2/SvPas

Allele Type:    Targeted (Null/knockout, Reporter) Mutation:    Intragenic deletion   Mutation details: This 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)

View phenotypes and curated references for all genotypes (concatenated display).

In Structures Affected by this Mutation:

1 anatomical structure(s)

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

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)