Symbol Name ID |
Lmna
lamin A MGI:96794 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Hepatic steatosis |
Hepatomegaly |
Disease(s) Associated with LMNA | ||
familial partial lipodystrophy type 2 | ||
mandibuloacral dysplasia type A lipodystrophy |
Mouse Phenotypes | liver/biliary system phenotype |
decreased liver glycogen level |
increased liver triglyceride level |
hepatic steatosis |
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Availability | Mouse Genotype | ||||
LmnaGt(S7-1F1)Sor/LmnaGt(S7-1F1)Sor | |||||
Lmnaem1Fenz/Lmna+ | |||||
Lmnatm1Stw/Lmna+ | * |
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 04/30/2024 MGI 6.23 |
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