pma
Spontaneous Allele Detail

Summary

• Symbol: pma
• Name: peroneal muscular atrophy
• MGI ID: MGI:1856996
• Gene: pma Location: unknown Genetic Position: Chr5, Syntenic
• Alliance: pma page

Mutation origin

• Strain of Origin: CF-1

Mutation description

• Allele Type: Spontaneous
• Inheritance: Recessive

Disease models

Expression

In Structures Affected by this Mutation:

5 anatomical structure(s)

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 pma Mutation: 0 strains or lines available

Notes

This mutation was found in the CF1 stock during the process of inbreeding.

References

• Original: J:6590 Esaki K, et al., [A new mutant in the mouse: peroneal muscular atrophy (author's transl)]. Jikken Dobutsu. 1981 Apr;30(2):151-5
• All: 7 reference(s)