about
P688
Subunit composition and novel localization of K+ channels in spinal cordA missense mutation in the Kv1.1 voltage-gated potassium channel-encoding gene KCNA1 is linked to human autosomal dominant hypomagnesemiaEpisodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1Episodic ataxia results from voltage-dependent potassium channels with altered functionsHuman potassium channel genes: Molecular cloning and functional expressionFunctional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymiaNMR structure and functional characteristics of the hydrophilic N terminus of the potassium channel beta-subunit Kvbeta1.1
P921
Q24290543-C461853D-0976-49E3-9137-1832932E2A20Q24309111-16685CEE-70F5-40B4-92C0-03DB209BAE5DQ24312199-26EE7F0E-3061-4D64-B755-E2B16F9959DFQ24312207-7BB1E830-3755-4CD2-8E50-330308A745FCQ24317072-D294B31E-BE44-47A4-968B-7987AD673363Q24321507-21DB6DA9-DF13-4147-89B7-1CA11CF56514Q28910348-D5225479-C035-483B-9B62-5103D6830F53
P921
description
humanes Protein
@de
mammalian protein found in Homo sapiens
@en
menselijk eiwit
@nl
protein
@id
protein
@sv
proteinë
@sq
protèin
@ace
protéine humaine
@fr
بروتين بشري
@ar
name
Kv1.1
@pt
Potassium voltage-gated channel subfamily A member 1
@en
Potassium voltage-gated channel subfamily A member 1
@nl
type
label
Kv1.1
@pt
Potassium voltage-gated channel subfamily A member 1
@en
Potassium voltage-gated channel subfamily A member 1
@nl
altLabel
KCNA1
@en
potassium channel, voltage gated shaker related subfamily A, member 1
@en
potassium voltage-gated channel subfamily A member 1
@en
potassium voltage-gated channe ...... episodic ataxia with myokymia)
@en
voltage-gated K(+) channel HuKI
@en
voltage-gated potassium channel HBK1
@en
voltage-gated potassium channel subunit Kv1.1
@en
prefLabel
Kv1.1
@pt
Potassium voltage-gated channel subfamily A member 1
@en
Potassium voltage-gated channel subfamily A member 1
@nl
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ENSP00000371985
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1.A.1.2.12
8.B.31.1.1