| CACNA1G | 
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| Identifiers | 
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| Aliases | CACNA1G, Ca(V)T.1, Cav3.1, NBR13, SCA42, calcium voltage-gated channel subunit alpha1 G, SCA42ND | 
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| External IDs | OMIM: 604065; MGI: 1201678; HomoloGene: 22544; GeneCards: CACNA1G; OMA:CACNA1G - orthologs | 
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| | Gene location (Mouse) | 
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 |  |  | Chr. | Chromosome 11 (mouse) | 
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 |  |  | Band | 11|11 D | Start | 94,299,217 bp | 
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 | End | 94,365,024 bp | 
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| | RNA expression pattern | 
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 | Bgee | | Human | Mouse (ortholog) | 
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 | | Top expressed in |  | lateral nuclear group of thalamus
 right hemisphere of cerebellum
 right frontal lobe
 primary visual cortex
 cerebellar vermis
 endothelial cell
 prefrontal cortex
 orbitofrontal cortex
 dorsolateral prefrontal cortex
 testicle
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 | | Top expressed in |  | cerebellar cortex
 medial dorsal nucleus
 superior frontal gyrus
 lobe of cerebellum
 neural layer of retina
 cerebellar vermis
 medial geniculate nucleus
 primary visual cortex
 lumbar subsegment of spinal cord
 lateral geniculate nucleus
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 |  | More reference expression data | 
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 | BioGPS |  | 
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| Wikidata | 
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Calcium channel, voltage-dependent, T type, alpha 1G subunit, also known as CACNA1G or Cav3.1 is a protein which in humans is encoded by the CACNA1G gene. It is one of the primary targets in the pharmacology of absence seizure.