Symbol Name ID |
Fbn1
fibrillin 1 MGI:95489 |
Darker colors indicate more annotations |
Human Phenotypes | Reduced subcutaneous adipose tissue |
Lipodystrophy |
Lipoatrophy |
Disease(s) Associated with FBN1 | |||
Marfan syndrome | |||
stiff skin syndrome |
Mouse Phenotypes | decreased subcutaneous adipose tissue amount |
decreased body fat mass |
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Availability | Mouse Genotype | ||
Fbn1tm3.2Lysa/Fbn1tm3.2Lysa | |||
Fbn1em1Chop/Fbn1+ | |||
Fbn1tm2.1Hcd/Fbn1+ | |||
Fbn1tm3.1Hcd/Fbn1+ | |||
Fbn1tm3.2Lysa/Fbn1+ |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/23/2024 MGI 6.23 |
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