# Calcium voltage-gated channel subunit alpha1 S

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21111803](https://www.wikidata.org/wiki/Q21111803)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Cav1.1)  
**Source**: https://4ort.xyz/entity/calcium-voltage-gated-channel-subunit-alpha1-s


## References

1. UniProt
2. IUPHAR/BPS Guide to PHARMACOLOGY
3. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL2074972)
4. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL460291)
5. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL1200382)
6. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL1697)
7. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL1200402)
8. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q13698)
9. Q20641742
10. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q13698&geneProductId=UniProtKB:Q13698)
11. [Gating of the L-type Ca channel in human skeletal myotubes: an activation defect caused by the hypokalemic periodic paralysis mutation R528H](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q13698&geneProductId=UniProtKB:Q13698)
12. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q13698)
13. [A proteome-scale map of the human interactome network](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q13698)
14. [Gating of the L-type Ca channel in human skeletal myotubes: an activation defect caused by the hypokalemic periodic paralysis mutation R528H](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q13698)
15. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q13698)
16. [Triad proteins and intracellular Ca2+ transients during development of human skeletal muscle cells in aneural and innervated cultures](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q13698)
17. [Abnormal distribution of calcium-handling proteins: a novel distinctive marker in core myopathies](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q13698&geneProductId=UniProtKB:Q13698)
18. [Abnormal distribution of calcium-handling proteins: a novel distinctive marker in core myopathies](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q13698)
19. [Hypokalaemic periodic paralysis due to the CACNA1S R1239H mutation in a large African family](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q13698)
20. Ensembl Release 99
21. Transporter Classification database