fm
Spontaneous Allele Detail

Summary

• Symbol: fm
• Name: foam cell reticulosis
• MGI ID: MGI:1856873
• Gene: fm Location: unknown
• Alliance: fm page

Mutation origin

• Strain of Origin: CBA/H

Mutation description

• Allele Type: Spontaneous
• Inheritance: Recessive

Disease models

Expression

In Structures Affected by this Mutation:

9 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 fm Mutation: 0 strains or lines available

Notes

The disease resembles a group of lipid storage diseases in human and is most similar to Niemann-Pick disease, type C (J:5696).

References

• Original: J:29163 Hulse EV, et al., Foam-cell reticulosis, fm. Mouse News Lett. 1965;32:38
• All: 6 reference(s)