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Symbol
Name
ID
Cacna1s
calcium channel, voltage-dependent, L type, alpha 1S subunit
MGI:88294
Phenotype annotations related to nervous system
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

Contributing Projects:
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
The Jackson Laboratory