×
Entrez Id:
3781
Gene Symbol:
KCNN2
KCNN2
Movement Disorders
0.100
GeneticVariation
CLINVAR
De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features.
27048600
2016
×
Entrez Id:
3781
Gene Symbol:
KCNN2
KCNN2
Movement Disorders
0.100
GeneticVariation
CLINVAR
UBE3A Regulates Synaptic Plasticity and Learning and Memory by Controlling SK2 Channel Endocytosis.
26166566
2015
×
Entrez Id:
3781
Gene Symbol:
KCNN2
KCNN2
Movement Disorders
0.100
GeneticVariation
CLINVAR
Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders.
25917818
2015
×
Entrez Id:
3781
Gene Symbol:
KCNN2
KCNN2
Movement Disorders
0.100
GeneticVariation
CLINVAR
Subcellular expression and neuroprotective effects of SK channels in human dopaminergic neurons.
24434522
2014
×
Entrez Id:
3781
Gene Symbol:
KCNN2
KCNN2
Movement Disorders
0.100
GeneticVariation
CLINVAR
Mitochondrial small conductance SK2 channels prevent glutamate-induced oxytosis and mitochondrial dysfunction.
23430260
2013
×
Entrez Id:
3781
Gene Symbol:
KCNN2
KCNN2
Movement Disorders
0.100
GeneticVariation
CLINVAR
Small-conductance Ca2+-activated K+ channels: form and function.
21942705
2012
×
Entrez Id:
3781
Gene Symbol:
KCNN2
KCNN2
Movement Disorders
0.100
GeneticVariation
CLINVAR
Patterns and rates of exonic de novo mutations in autism spectrum disorders.
22495311
2012
×
Entrez Id:
3781
Gene Symbol:
KCNN2
KCNN2
Movement Disorders
0.100
GeneticVariation
CLINVAR
Developmental profile of SK2 channel expression and function in CA1 neurons.
22072564
2012
×
Entrez Id:
3781
Gene Symbol:
KCNN2
KCNN2
Movement Disorders
0.100
GeneticVariation
CLINVAR
Targeting BK (big potassium) channels in epilepsy.
21923633
2011
×
Entrez Id:
3781
Gene Symbol:
KCNN2
KCNN2
Movement Disorders
0.100
GeneticVariation
CLINVAR
Altered expression and function of small-conductance (SK) Ca(2+)-activated K+ channels in pilocarpine-treated epileptic rats.
20553876
2010
×
Entrez Id:
3781
Gene Symbol:
KCNN2
KCNN2
Movement Disorders
0.100
GeneticVariation
CLINVAR
Selective activation of the SK1 subtype of human small-conductance Ca2+-activated K+ channels by 4-(2-methoxyphenylcarbamoyloxymethyl)-piperidine-1-carboxylic acid tert-butyl ester (GW542573X) is dependent on serine 293 in the S5 segment.
19515965
2009
×
Entrez Id:
3781
Gene Symbol:
KCNN2
KCNN2
Movement Disorders
0.100
GeneticVariation
CLINVAR
Behavioral effects of a deletion in Kcnn2, the gene encoding the SK2 subunit of small-conductance Ca2+-activated K+ channels.
18604572
2008
×
Entrez Id:
3781
Gene Symbol:
KCNN2
KCNN2
Movement Disorders
0.100
GeneticVariation
CLINVAR
K(+)-channel openers suppress epileptiform activities induced by 4-aminopyridine in cultured rat hippocampal neurons.
19075508
2008
×
Entrez Id:
3781
Gene Symbol:
KCNN2
KCNN2
Movement Disorders
0.100
GeneticVariation
CLINVAR
Organization and regulation of small conductance Ca2+-activated K+ channel multiprotein complexes.
17329434
2007
×
Entrez Id:
3781
Gene Symbol:
KCNN2
KCNN2
Movement Disorders
0.100
GeneticVariation
CLINVAR
Calcium-sensitive potassium channelopathy in human epilepsy and paroxysmal movement disorder.
15937479
2005
×
Entrez Id:
3781
Gene Symbol:
KCNN2
KCNN2
Movement Disorders
0.100
GeneticVariation
CLINVAR
Cerebellar ataxia and Purkinje cell dysfunction caused by Ca2+-activated K+ channel deficiency.
15194823
2004
×
Entrez Id:
3781
Gene Symbol:
KCNN2
KCNN2
Movement Disorders
0.100
GeneticVariation
CLINVAR
Overactive bladder and incontinence in the absence of the BK large conductance Ca2+-activated K+ channel.
15184377
2004
×
Entrez Id:
3781
Gene Symbol:
KCNN2
KCNN2
Movement Disorders
0.100
GeneticVariation
CLINVAR
Small conductance Ca2+-activated K+ channel knock-out mice reveal the identity of calcium-dependent afterhyperpolarization currents.
15190101
2004
×
Entrez Id:
3781
Gene Symbol:
KCNN2
KCNN2
Movement Disorders
0.100
GeneticVariation
CLINVAR
Comparative immunohistochemical distribution of three small-conductance Ca2+-activated potassium channel subunits, SK1, SK2, and SK3 in mouse brain.
15234350
2004
×
Entrez Id:
3781
Gene Symbol:
KCNN2
KCNN2
Movement Disorders
0.100
GeneticVariation
CLINVAR
On the cellular and network bases of epileptic seizures.
11181977
2001
×
Entrez Id:
3781
Gene Symbol:
KCNN2
KCNN2
Movement Disorders
0.100
GeneticVariation
CLINVAR
An apamin-sensitive Ca2+-activated K+ current in hippocampal pyramidal neurons.
10200319
1999