|
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 | Decreased fetal movement |
Feeding difficulties |
Back pain |
Low back pain |
Vocal cord paralysis |
Abnormality of the voice |
Arthralgia |
Hip pain |
Myalgia |
| Disease(s) Associated with LMNA | |||||||||
| congenital muscular dystrophy due to LMNA mutation | |||||||||
| Emery-Dreifuss muscular dystrophy | |||||||||
| familial partial lipodystrophy type 2 | |||||||||
| mandibuloacral dysplasia type A lipodystrophy | |||||||||
| progeria | |||||||||
| restrictive dermopathy 2 | |||||||||
| Werner syndrome |
| Mouse Phenotypes | behavior/neurological phenotype |
abnormal behavior |
abnormal suckling behavior |
poor grooming |
impaired coordination |
decreased grip strength |
hunched posture |
abnormal gait |
decreased locomotor activity |
bradykinesia |
impaired exercise endurance |
|
| Availability | Mouse Genotype | |||||||||||
| LmnaGt(S7-1F1)Sor/LmnaGt(S7-1F1)Sor | ||||||||||||
| Lmnatm1.1Otin/Lmnatm1.1Otin | ||||||||||||
| Lmnatm1.1Vde/Lmnatm1.1Vde | * | |||||||||||
| Lmnatm1Gbon/Lmnatm1Gbon | ||||||||||||
| Lmnatm1Stw/Lmnatm1Stw | ||||||||||||
| Lmnatm2.1Gbon/Lmnatm2.1Gbon | ||||||||||||
| Lmnatm2Stw/Lmnatm2Stw | ||||||||||||
| Lmnatm3Stw/Lmnatm3Stw | ||||||||||||
| Lmnatm9Lgf/Lmnatm9Lgf | * | |||||||||||
| Lmnatm10Lgf/Lmnatm10Lgf | * | |||||||||||
| Lmnatm1Lgf/Lmna+ | * | |||||||||||
| Lmnatm4Stw/Lmnatm4Stw Tg(Zp3-cre)93Knw/0 (conditional) |
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| Lmnatm1Bliu/Lmna+ Tg(Tek-cre)1Ywa/0 (conditional) |
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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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