Pedm32
Chemically induced Allele Detail

Summary

• Symbol: Pedm32
• Name: Pedm32, Harwell; Pedm/32, Harwell
• MGI ID: MGI:5499196
• Gene: Pedm32 Location: unknown
• Alliance: Pedm32 page

Mutation origin

• Strain of Origin: C57BL/6J
• Project Collection: Harwell ENU Mutagenesis

Mutation description

• Allele Type: Chemically induced (ENU)
• Mutation: Undefined
• Mutation details: This phenotypic mutant was discovered among the G1 progeny of an ENU-treated male mouse and was shown to be heritable.
• Inheritance: Dominant

Find Mice (IMSR)

• 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 Pedm32 Mutation: 0 strains or lines available

Notes

This stock is progeny from a recessive pedigree generated from an ENU mutagenised C57BL/6J mouse which was subsequently bred with C3H females to produce a G3 recessive population of mice. Twenty male mice in this pedigree were phenotyped and two were identified as having albuminuria at 16 & 24 weeks of age. There was no associated detection of glucose in the urine. Further investigation of this line is needed to identify the underlying genetic defect and also to refine the phenotypic profile.

References

• Original: J:169366 MouseBook^TM, Information obtained from MouseBook^TM, Medical Research Council Mammalian Genetics Unit, Harwell, UK. Unpublished. 2005-2013
• All: 1 reference(s)