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 | Death in infancy |
Miscarriage |
Sudden cardiac death |
Disease(s) Associated with LMNA | |||
autosomal dominant Emery-Dreifuss muscular dystrophy 2 | |||
congenital muscular dystrophy due to LMNA mutation | |||
dilated cardiomyopathy 1A | |||
Emery-Dreifuss muscular dystrophy | |||
Werner syndrome |
Mouse Phenotypes | mortality/aging |
decreased survivor rate |
premature death |
postnatal lethality, complete penetrance |
preweaning lethality, complete penetrance |
premature aging |
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Availability | Mouse Genotype | ||||||
LmnaDhe/LmnaDhe | |||||||
LmnaGt(S7-1F1)Sor/LmnaGt(S7-1F1)Sor | * | ||||||
Lmnatm1.1Bliu/Lmnatm1.1Bliu | |||||||
Lmnatm1.1Otin/Lmnatm1.1Otin | |||||||
Lmnatm1.2Yxz/Lmnatm1.2Yxz | |||||||
Lmnatm1b(EUCOMM)Wtsi/Lmnatm1b(EUCOMM)Wtsi | |||||||
Lmnatm1Gbon/Lmnatm1Gbon | |||||||
Lmnatm1Lgf/Lmnatm1Lgf | |||||||
Lmnatm1Stw/Lmnatm1Stw | |||||||
Lmnatm2.1Gbon/Lmnatm2.1Gbon | |||||||
Lmnatm2Stw/Lmnatm2Stw | |||||||
Lmnatm3Lgf/Lmnatm3Lgf | |||||||
Lmnatm3Stw/Lmnatm3Stw | |||||||
Lmnatm5Lgf/Lmnatm5Lgf | |||||||
Lmnatm7Lgf/Lmnatm7Lgf | * | ||||||
Lmnatm8Lgf/Lmnatm8Lgf | * | ||||||
Lmnatm9Lgf/Lmnatm9Lgf | * | ||||||
Lmnatm10Lgf/Lmnatm10Lgf | * | ||||||
Lmnatm11Lgf/Lmnatm11Lgf | |||||||
LmnaDhe/Lmna+ | |||||||
Lmnatm1.1Bliu/Lmna+ | |||||||
Lmnatm1.1Otin/Lmna+ | |||||||
Lmnatm1Lgf/Lmna+ | |||||||
Lmnatm1Lgf/Lmnatm1Stw | |||||||
Lmnatm2.1Gbon/Lmna+ | |||||||
Lmnatm3Lgf/Lmna+ | |||||||
Lmnatm4Lgf/Lmna+ | |||||||
Lmnatm11Lgf/Lmna+ | |||||||
Lmnatm4Stw/Lmnatm4Stw Tg(Zp3-cre)93Knw/0 (conditional) |
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Lmnatm1Bliu/Lmna+ Tg(Tek-cre)1Ywa/0 (conditional) |
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 04/16/2024 MGI 6.23 |
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