Symbol Name ID |
Lmna
lamin A MGI:96794 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal lymphocyte physiology |
Splenomegaly |
Pancreatitis |
Acute pancreatitis |
Abnormality of complement system |
Cellulitis |
Disease(s) Associated with LMNA | ||||||
dilated cardiomyopathy 1A | ||||||
familial partial lipodystrophy type 2 |
Mouse Phenotypes | small thymus |
thymus atrophy |
increased susceptibility to otitis media |
abnormal peritoneal macrophage morphology |
small spleen |
keratoconjunctivitis sicca |
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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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