Gene: CSNK2A1 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs869312845
rs869312845
CSNK2A1
T 0.700 GeneticVariation CLINVAR Okur-Chung neurodevelopmental syndrome: Eight additional cases with implications on phenotype and genotype expansion. 29240241

2018
dbSNP: rs869312845
rs869312845
CSNK2A1
T 0.700 GeneticVariation CLINVAR Prevalence and architecture of de novo mutations in developmental disorders. 28135719

2017
dbSNP: rs869312845
rs869312845
CSNK2A1
T 0.700 GeneticVariation CLINVAR De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features. 27048600

2016
dbSNP: rs869312845
rs869312845
CSNK2A1
T 0.700 GeneticVariation CLINVAR Presynaptic CK2 promotes synapse organization and stability by targeting Ankyrin2. 24395637

2014
dbSNP: rs869312845
rs869312845
CSNK2A1
T 0.700 GeneticVariation CLINVAR Predominance of CK2α over CK2α' in the mammalian brain. 21761202

2011
dbSNP: rs869312845
rs869312845
CSNK2A1
T 0.700 GeneticVariation CLINVAR The alpha catalytic subunit of protein kinase CK2 is required for mouse embryonic development. 17954558

2008