Symbol Name ID |
Lmna
lamin A MGI:96794 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal lymphocyte physiology |
Intracranial hemorrhage |
Elevated hemoglobin A1c |
Splenomegaly |
Disease(s) Associated with LMNA | ||||
dilated cardiomyopathy 1A | ||||
familial partial lipodystrophy type 2 | ||||
progeria | ||||
Werner syndrome |
Mouse Phenotypes | small thymus |
thymus atrophy |
abnormal peritoneal macrophage morphology |
small spleen |
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Availability | Mouse Genotype | ||||
Lmnatm1.1Otin/Lmnatm1.1Otin | |||||
Lmnatm1Stw/Lmnatm1Stw | |||||
LmnaDhe/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 05/14/2024 MGI 6.23 |
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