|
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 | Eclampsia |
Delayed menarche |
Hypogonadism |
Female hypogonadism |
Hypergonadotropic hypogonadism |
Labial pseudohypertrophy |
Abnormal testis morphology |
Aplasia/Hypoplasia of the testes |
Hypoplastic male external genitalia |
Polycystic ovaries |
Ovarian neoplasm |
Secondary amenorrhea |
Dysmenorrhea |
Decreased fertility |
| Disease(s) Associated with LMNA | ||||||||||||||
| dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome | ||||||||||||||
| familial partial lipodystrophy type 2 | ||||||||||||||
| progeria | ||||||||||||||
| Werner syndrome |
| Mouse Phenotypes | reproductive system phenotype |
azoospermia |
oligozoospermia |
abnormal meiosis |
abnormal chromosomal synapsis |
abnormal female meiosis |
arrest of male meiosis |
small seminiferous tubules |
small testis |
penis prolapse |
abnormal reproductive system morphology |
small gonad |
female infertility |
reduced female fertility |
infertility |
male infertility |
reduced male fertility |
|
| Availability | Mouse Genotype | |||||||||||||||||
| Lmnatm1.1Otin/Lmnatm1.1Otin | ||||||||||||||||||
| Lmnatm1Rben/Lmnatm1Rben | * | |||||||||||||||||
| Lmnatm1Stw/Lmnatm1Stw | ||||||||||||||||||
| Lmnatm2Stw/Lmnatm2Stw | ||||||||||||||||||
| Lmnatm7Lgf/Lmnatm7Lgf | * | |||||||||||||||||
| 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 04/30/2024 MGI 6.23 |
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