Human Disease and Mouse Model Detail

Human Disease

Lipodystrophy, Familial Partial, Type 3; FPLD3
OMIM ID: 604367

Synonyms

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

Mouse Models

Human Disease Modeled: Lipodystrophy, Familial Partial, Type 3; FPLD3
Associated Mouse Gene: Pparg

Allelic Composition	Genetic Background	Reference	Phenotypes
Ppargtm2Yba/Pparg⁺	involves: 129S1/SvImJ * C57BL/6	J:125992	View
Ppargtm3Yba/Pparg⁺	involves: 129S1/SvImJ * C57BL/6	J:125992	View
Lepob/Lepob Ppargtm1Avp/Pparg⁺	involves: 129S2/SvPas * C57BL/6	J:116568	View

NOT Models
No similarity to the expected human disease phenotype was found.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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