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Human Disease and Mouse Model Detail
Human Disease Lipodystrophy, Familial Partial, Type 2; FPLD2
OMIM ID: 151660
Human Phenotype Ontology associations
Synonyms FPL2; Lipoatrophic Diabetes; Lipodystrophy, Familial Partial; Lipodystrophy, Familial Partial, Dunnigan Type; Lipodystrophy, Familial, of Limbs and Lower Trunk; Lipodystrophy, Reverse Partial
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

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     ZMPSTE24 Zmpste24* View 1 model HomoloGene and HGNC
     LMNA* Lmna View 2 models HomoloGene and HGNC
Transgenes and
other genome features
Transgenes and other genome features developed in mice to model this disease.

     Transgenes and Other Genome Features Mouse Models
  Tg(Fabp4-LMNA*R482Q)11ACdl View 1 model
  Tg(Fabp4-LMNA*R482Q)17CCdl View 1 model
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
MGI 6.07
The Jackson Laboratory