Human Disease and Mouse Model Detail
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Human Disease
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Lipodystrophy, Congenital Generalized, Type 1; CGL1
OMIM ID: 608594
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Synonyms
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Berardinelli-Seip Congenital Lipodystrophy, Type 1; BSCL1;
Brunzell Syndrome, Agpat2-Related;
Lipodystrophy, Berardinelli-Seip Congenital, Type 1
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View all models
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View ALL (1) mouse models for this human disease.
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Agpat2*
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AGPAT2*
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View 1 model
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1:1 Homology
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Mouse Models
Human Disease Modeled: Lipodystrophy, Congenital Generalized, Type 1; CGL1
Associated Mouse Gene:
Agpat2
Analysis Tools