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Symbol
Name
ID
Cacna1s
calcium channel, voltage-dependent, L type, alpha 1S subunit
MGI:88294
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Scoliosis
Disease(s) Associated with CACNA1S
congenital myopathy 18

Mouse Phenotypes
enlarged interparietal bone
enlarged occipital bone
abnormal mandible morphology
small mandibular condyloid process
small mandibular coronoid process
short mandible
micrognathia
absent deltoid tuberosity
small clavicle
decreased diameter of long bones
small scapula
abnormal sternum morphology
abnormal sternebra morphology
sternebra fusion
short sternum
abnormal axial skeleton morphology
abnormal rib morphology
long ribs
thin ribs
thoracic vertebral fusion
abnormal vertebral column morphology
abnormal spine curvature
kyphosis
abnormal cervical vertebrae morphology
cervical vertebral fusion
abnormal cartilage morphology
abnormal joint 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
04/16/2024
MGI 6.23
The Jackson Laboratory