| 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.