M1073b
Chemically induced Allele Detail

Summary

• Symbol: M1073b
• Name: mutant 1073b
• MGI ID: MGI:5515456
• Synonyms: line 1073
• Gene: M1073b Location: unknown Genetic Position: Chr13, Syntenic
• Alliance: M1073b page

Mutation origin

• Strain of Origin: mixed

Mutation description

• Allele Type: Chemically induced (ENU)
• Mutation: Undefined
• Mutation details: This mutation was identified in an ENU mutagenesis screen focused on the Del(13)36H deletion interval. (J:101156)
• Inheritance: Semidominant

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 2 strains available Cell Lines: 0 lines available
• Carrying any M1073b Mutation: 2 strains or lines available

Notes

This allele was induced by ENU treatment of a male mouse homozygous for Foxq1^sa on a mixed genetic background (mostly 101 and C3H, but derived from a linkage testing stock also homozygous for Wnt3a^vt (origin: C57BR) and Bloc1s5^mu (origin: t-allele stock)).

References

• Original: J:101156 Bogani D, et al., Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen. Proc Natl Acad Sci U S A. 2005 Aug 30;102(35):12477-82
• All: 1 reference(s)