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

Symbol:	Meox2tm1Vpa
Name:	mesenchyme homeobox 2; targeted mutation 1, Vassilis Pachnis
MGI ID:	MGI:2674242
Synonyms:	Meox2tm1Pach, Mox2-
Gene:	Meox2  Location: Chr12:37158539-37229533 bp, + strand  Genetic Position: Chr12, 16.84 cM
Alliance:	Meox2tm1Vpa page

Germline Transmission:	Earliest citation of germline transmission: J:56172
Parent Cell Line:	Not Specified (ES Cell)
Strain of Origin:	129P2/OlaHsd

Allele Type:    Targeted (Null/knockout) Mutations:    Insertion, Intragenic deletion   Mutation details: A neo cassette inserted by homologous recombination replaced exon 1. Transcript was undetected by Northern blot analysis of RNA obtained from homozygous mutant heart, kidney, lung, and liver tissue. (J:56172)

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

In Mice Carrying this Mutation:	1 assay results
In Structures Affected by this Mutation:	3 anatomical structure(s)

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 Meox2 Mutation:	18 strains or lines available

Original:	J:56172 Mankoo BS, et al., Mox2 is a component of the genetic hierarchy controlling limb muscle development. Nature. 1999 Jul 1;400(6739):69-73
All:	10 reference(s)