Symbol Name ID |
Lmna
lamin A MGI:96794 |
Darker colors indicate more annotations |
Human Phenotypes | Pulmonary artery stenosis |
Pulmonary arterial hypertension |
Respiratory insufficiency due to muscle weakness |
Exertional dyspnea |
Respiratory distress |
Neoplasm of the lung |
Laryngomalacia |
Upper airway obstruction |
Respiratory insufficiency |
Disease(s) Associated with LMNA | |||||||||
autosomal dominant Emery-Dreifuss muscular dystrophy 2 | |||||||||
congenital muscular dystrophy due to LMNA mutation | |||||||||
Emery-Dreifuss muscular dystrophy | |||||||||
progeria | |||||||||
restrictive dermopathy 2 | |||||||||
Werner syndrome |
Mouse Phenotypes | pulmonary edema |
abnormal nasopharynx morphology |
tachypnea |
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Availability | Mouse Genotype | |||
Lmnatm1Gbon/Lmnatm1Gbon | ||||
LmnaDhe/Lmna+ | ||||
Lmnatm2.1Gbon/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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