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Human Disease and Mouse Model Detail
Human Disease Lipodystrophy, Familial Partial, Type 3; FPLD3
OMIM ID: 604367
Synonyms Lipodystrophy, Familial Partial; Lipodystrophy, Familial Partial, Associated with PPARG Mutations
View all models View ALL (3) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Pparg* PPARG* View 3 models 1:1 Homology
     Ppp1r3a PPP1R3A*   1:1 Homology
References Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/09/2014
MGI 5.20
The Jackson Laboratory