Symbol Name ID |
Cacna1s
calcium channel, voltage-dependent, L type, alpha 1S subunit MGI:88294 |
Darker colors indicate more annotations |
Human Phenotypes | Fatigable weakness of respiratory muscles |
Respiratory paralysis |
Paralysis |
Periodic paralysis |
Periodic hypokalemic paresis |
Motor delay |
Disease(s) Associated with CACNA1S | ||||||
congenital myopathy 18 | ||||||
hypokalemic periodic paralysis |
Mouse Phenotypes | abnormal innervation pattern to muscle |
abnormal dorsal root ganglion morphology |
abnormal phrenic nerve morphology |
abnormal spinal cord ventral horn morphology |
|
Availability | Mouse Genotype | ||||
Cacna1smdg/Cacna1smdg |
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 08/02/2024 MGI 6.24 |
![]() |
|