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Symbol Name ID |
Lmnb1
lamin B1 MGI:96795 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Bowel incontinence |
Pseudobulbar paralysis |
Depression |
Atypical behavior |
Personality changes |
Myalgia |
| Disease(s) Associated with LMNB1 | ||||||
| adult-onset autosomal dominant demyelinating leukodystrophy |
| Mouse Phenotypes | behavior/neurological phenotype |
increased susceptibility to pharmacologically induced seizures |
abnormal spatial learning |
abnormal spatial reference memory |
tremors |
impaired coordination |
straub tail |
seizures |
clonic seizures |
abnormal spike wave discharge |
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| Availability | Mouse Genotype | ||||||||||
| 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) |
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last database update 05/14/2024 MGI 6.23 |
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