|
Symbol Name ID |
Lmnb1
lamin B1 MGI:96795 |
| Darker colors indicate more annotations |
| Human Phenotypes | Flexion contracture |
Hypertonia |
Spasticity |
Spastic gait |
Functional motor deficit |
Muscle weakness |
| Disease(s) Associated with LMNB1 | ||||||
| adult-onset autosomal dominant demyelinating leukodystrophy |
| Mouse Phenotypes | thin diaphragm muscle |
muscle spasm |
|
| Availability | Mouse Genotype | ||
| Lmnb1tm1Yxz/Lmnb1tm1Yxz | |||
| Tg(Lmnb1)1Yfu/0 | |||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 05/14/2024 MGI 6.23 |
|
|
|
||
Analysis Tools