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Q-type calcium channel

From Wikipedia, the free encyclopedia
Family of transport proteins

calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
Identifiers
SymbolCACNA1A
Alt. symbolsCACNL1A4, SCA6, MHP1, MHP
IUPHAR532
NCBI gene773
HGNC1388
OMIM601011
RefSeqNM_000068
UniProtO00555
Other data
LocusChr. 19p13
Search for
StructuresSwiss-model
DomainsInterPro

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]

References

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  1. ^Indelicato E, Unterberger I, Nachbauer W, Eigentler A, Amprosi M, Zeiner F, et al. (July 2021)."The electrophysiological footprint of CACNA1A disorders".Journal of Neurology.268 (7):2493–2505.doi:10.1007/s00415-021-10415-x.PMC 8217028.PMID 33544220.

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Ligand-gated
Voltage-gated
Constitutively active
Proton-gated
Voltage-gated
Calcium-activated
Inward-rectifier
Tandem pore domain
Voltage-gated
Miscellaneous
Cl:Chloride channel
H+:Proton channel
M+:CNG cation channel
M+:TRP cation channel
H2O (+solutes):Porin
Cytoplasm:Gap junction
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Ion channel class
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