about
P688
Spinocerebellar ataxia-13 Kv3.3 potassium channels: arginine-to-histidine mutations affect both functional and protein expression on the cell surfaceFrequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13)KCNC3(R420H), a K(+) channel mutation causative in spinocerebellar ataxia 13 displays aberrant intracellular traffickingFunctional analysis helps to define KCNC3 mutational spectrum in Dutch ataxia casesKCNC3: phenotype, mutations, channel biophysics-a study of 260 familial ataxia patients
P921
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in Potassium voltage-gated channel subfamily C member 3
@nl
protèin
@ace
protéine
@fr
بروتين في الإنسان العاقل
@ar
name
Potassium voltage-gated channel subfamily C member 3
@en
Potassium voltage-gated channel subfamily C member 3
@nl
type
label
Potassium voltage-gated channel subfamily C member 3
@en
Potassium voltage-gated channel subfamily C member 3
@nl
altLabel
KCNC3
@en
KSHIIID
@en
Shaw-related voltage-gated potassium channel protein 3
@en
potassium channel, voltage gated Shaw related subfamily C, member 3
@en
potassium voltage-gated channel subfamily C member 3
@en
potassium voltage-gated channel, Shaw-related subfamily, member 3
@en
voltage-gated potassium channel protein KV3.3
@en
voltage-gated potassium channel subunit Kv3.3
@en
prefLabel
Potassium voltage-gated channel subfamily C member 3
@en
Potassium voltage-gated channel subfamily C member 3
@nl
P361
P527
P680
P681
P682
P705
P352
P31
P352
P361
P527
P637
NP_001359234
P680
P681
P682
P702
P703
P705
ENSP00000366158
ENSP00000432438
ENSP00000434241
ENSP00000499301
P7260
1.A.1.2.13