CSNK2A1, casein kinase 2 alpha 1, 1457

N. diseases: 87; N. variants: 11
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs869312840
rs869312840
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C4310739
Disease:
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
0.800 GeneticVariation UNIPROT De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features. 27048600 2016
dbSNP: rs869312845
rs869312845
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C4310739
Disease:
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
0.800 GeneticVariation UNIPROT De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features. 27048600 2016
dbSNP: rs869312848
rs869312848
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C4310739
Disease:
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
0.800 GeneticVariation UNIPROT De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features. 27048600 2016
dbSNP: rs869312849
rs869312849
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C4310739
Disease:
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
0.800 GeneticVariation UNIPROT De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features. 27048600 2016
dbSNP: rs869312840
rs869312840
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C4310739
Disease:
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
C 0.800 CausalMutation CLINVAR
dbSNP: rs869312845
rs869312845
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C4310739
Disease:
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
T 0.800 CausalMutation CLINVAR
dbSNP: rs869312848
rs869312848
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C4310739
Disease:
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
C 0.800 CausalMutation CLINVAR
dbSNP: rs869312849
rs869312849
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C4310739
Disease:
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
G 0.800 CausalMutation CLINVAR
dbSNP: rs869312845
rs869312845
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C0432072
Disease:
Dysmorphic features
T 0.700 GeneticVariation CLINVAR Okur-Chung neurodevelopmental syndrome: Eight additional cases with implications on phenotype and genotype expansion. 29240241 2018
dbSNP: rs869312845
rs869312845
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C0432072
Disease:
Dysmorphic features
T 0.700 GeneticVariation CLINVAR Prevalence and architecture of de novo mutations in developmental disorders. 28135719 2017
dbSNP: rs74448913
rs74448913
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C4505222
Disease:
Sleep Onset Latency
A 0.700 GeneticVariation GWASCAT Genome-wide association analysis of actigraphic sleep phenotypes in the LIFE Adult Study. 27126917 2016
dbSNP: rs869312845
rs869312845
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C0432072
Disease:
Dysmorphic features
T 0.700 GeneticVariation CLINVAR De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features. 27048600 2016
dbSNP: rs869312845
rs869312845
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C0432072
Disease:
Dysmorphic features
T 0.700 GeneticVariation CLINVAR Presynaptic CK2 promotes synapse organization and stability by targeting Ankyrin2. 24395637 2014
dbSNP: rs869312845
rs869312845
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C0432072
Disease:
Dysmorphic features
T 0.700 GeneticVariation CLINVAR Predominance of CK2α over CK2α' in the mammalian brain. 21761202 2011
dbSNP: rs6037828
rs6037828
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C0200695
Disease:
Fetal hemoglobin determination
0.700 GeneticVariation GWASDB Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. 18245381 2008
dbSNP: rs869312845
rs869312845
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C0432072
Disease:
Dysmorphic features
T 0.700 GeneticVariation CLINVAR The alpha catalytic subunit of protein kinase CK2 is required for mouse embryonic development. 17954558 2008
dbSNP: rs1057518092
rs1057518092
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C4310739
Disease:
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1555764992
rs1555764992
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C4310739
Disease:
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1568512728
rs1568512728
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C4310739
Disease:
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
G 0.700 CausalMutation CLINVAR
dbSNP: rs1568532361
rs1568532361
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C4310739
Disease:
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
C 0.700 CausalMutation CLINVAR
dbSNP: rs869312846
rs869312846
Entrez Id: 1457
Gene Symbol: CSNK2A1
CSNK2A1
CUI: C4310739
Disease:
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
G 0.700 CausalMutation CLINVAR