Variant: rs869312845 

    present in Gene: CSNK2A1
    present in Chromosome: 20
    Position on Chromosome: 505191
    Alleles of this Variant: C/T

rs869312845 in CSNK2A1 gene and Dysmorphic features PMID 27048600 2016 De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features.

PMID 21761202 2011 Predominance of CK2α over CK2α' in the mammalian brain.

PMID 28135719 2017 Prevalence and architecture of de novo mutations in developmental disorders.

PMID 24395637 2014 Presynaptic CK2 promotes synapse organization and stability by targeting Ankyrin2.

PMID 29240241 2018 Okur-Chung neurodevelopmental syndrome: Eight additional cases with implications on phenotype and genotype expansion.

PMID 17954558 2008 The alpha catalytic subunit of protein kinase CK2 is required for mouse embryonic development.

rs869312845 in CSNK2A1 gene and OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME PMID 27048600 2016 De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features.