| calcium channel, voltage-dependent, P/Q type, alpha 1A subunit | |||||||
|---|---|---|---|---|---|---|---|
| Identifiers | |||||||
| Symbol | CACNA1A | ||||||
| Alt. symbols | CACNL1A4, SCA6, MHP1, MHP | ||||||
| IUPHAR | 532 | ||||||
| NCBI gene | 773 | ||||||
| HGNC | 1388 | ||||||
| OMIM | 601011 | ||||||
| RefSeq | NM_000068 | ||||||
| UniProt | O00555 | ||||||
| Other data | |||||||
| Locus | Chr. 19p13 | ||||||
| |||||||
TheQ-type calcium channel is a type ofvoltage-dependent calcium channel. Like the others of this class, the α1 subunit is the one that determines most of the channel's properties.
They are poorly understood, but likeR-type calcium channels, they appear to be present incerebellar granule cells. They have a high threshold of activation and relatively slow kinetics.
Mutations in the CACNA1Agene that encodes this protein are responsible forfamilial hemiplegic migraine type 1 (FHM1),episodic ataxia type 2 (EA2) andspinocerebellar ataxia type 6 (SCA6).[1]
This article related tomedical imaging is astub. You can help Wikipedia byexpanding it. |