Summary | Mutation origin | Mutation description | Phenotypes | Disease models | Tumor data | Find Mice (IMSR) | References

Symbol:	Msh2tm1Mak
Name:	mutS homolog 2; targeted mutation 1, Tak W Mak
MGI ID:	MGI:1857940
Synonyms:	MSH2-
Gene:	Msh2  Location: Chr17:87979960-88031141 bp, + strand  Genetic Position: Chr17, 57.87 cM
Alliance:	Msh2tm1Mak page

Germline Transmission:	Earliest citation of germline transmission: J:28397
Parent Cell Line:	E14 (ES Cell)
Strain of Origin:	129P2/OlaHsd

Allele Type:    Targeted (Null/knockout) Mutations:    Insertion, Intragenic deletion   Mutation details: A neomycin resistance cassette was inserted in an antisense orientation in an exon of the gene that corresponded to exon 11 of the human gene, resulting in the deletion of 68 bp (1959 - 2026). Western blots of protein extracts from tail fibroblasts of homozygous mutant mice showed no detectable protein expressed for the targeted gene. (J:28397)

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

List all tumor models in MMHCdb carrying Msh2tm1Mak

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 Msh2 Mutation:	95 strains or lines available

Original:	J:28397 Reitmair AH, et al., MSH2 deficient mice are viable and susceptible to lymphoid tumours. Nat Genet. 1995 Sep;11(1):64-70
All:	58 reference(s)