Potassium inwardly rectifying channel subfamily J member 2
about
sameAs
P688
Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndromeInwardly rectifying potassium channels: their structure, function, and physiological rolesA novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 geneAlterations in conserved Kir channel-PIP2 interactions underlie channelopathiesDirect and specific activation of human inward rectifier K+ channels by membrane phosphatidylinositol 4,5-bisphosphateMolecular cloning and expression of a human heart inward rectifier potassium channel
P921
Potassium inwardly rectifying channel subfamily J member 2
description
Protein in Homo sapiens
@de
mammalian protein found in Homo sapiens
@en
protein
@id
protein
@sv
proteinë
@sq
proteïne in Kir2.1
@nl
protèin
@ace
protéine
@fr
بروتين في الإنسان العاقل
@ar
name
Kir2.1
@nl
Potassium inwardly rectifying channel subfamily J member 2
@en
type
label
Kir2.1
@nl
Potassium inwardly rectifying channel subfamily J member 2
@en
altLabel
IRK-1
@en
Inward rectifier K(+) channel Kir2.1
@en
KCNJ2
@en
Potassium channel, inwardly rectifying subfamily J member 2
@en
cardiac inward rectifier potassium channel
@en
hIRK1
@en
inward rectifier K+ channel KIR2.1
@en
inward rectifier potassium channel 2
@en
potassium channel, inwardly rectifying subfamily J, member 2
@en
potassium inwardly-rectifying channel, subfamily J, member 2
@en
prefLabel
Kir2.1
@nl
Potassium inwardly rectifying channel subfamily J member 2
@en
P680
P681
P682
P352
P637
P2888
P31
P352
P637
P680
P681
P682
P702
P703
P705
ENSP00000243457
ENSP00000441848