About   Help   FAQ
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
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Disease models
Loading...
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)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
03/19/2024
MGI 6.23
The Jackson Laboratory