rs869312840
|
Entrez Id: |
1457 |
Gene Symbol: |
CSNK2A1 |
CSNK2A1
|
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
|
C |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs869312845
|
Entrez Id: |
1457 |
Gene Symbol: |
CSNK2A1 |
CSNK2A1
|
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
|
T |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs869312848
|
Entrez Id: |
1457 |
Gene Symbol: |
CSNK2A1 |
CSNK2A1
|
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
|
C |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs869312849
|
Entrez Id: |
1457 |
Gene Symbol: |
CSNK2A1 |
CSNK2A1
|
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
|
G |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs1057518092
|
Entrez Id: |
1457 |
Gene Symbol: |
CSNK2A1 |
CSNK2A1
|
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1555764992
|
Entrez Id: |
1457 |
Gene Symbol: |
CSNK2A1 |
CSNK2A1
|
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
|
T |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs1568512728
|
Entrez Id: |
1457 |
Gene Symbol: |
CSNK2A1 |
CSNK2A1
|
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs1568532361
|
Entrez Id: |
1457 |
Gene Symbol: |
CSNK2A1 |
CSNK2A1
|
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
|
C |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs869312846
|
Entrez Id: |
1457 |
Gene Symbol: |
CSNK2A1 |
CSNK2A1
|
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs869312845
|
Entrez Id: |
1457 |
Gene Symbol: |
CSNK2A1 |
CSNK2A1
|
Dysmorphic features
|
T |
0.700 |
GeneticVariation |
CLINVAR |
The alpha catalytic subunit of protein kinase CK2 is required for mouse embryonic development.
|
17954558 |
2008 |
rs6037828
|
Entrez Id: |
1457 |
Gene Symbol: |
CSNK2A1 |
CSNK2A1
|
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 |
rs869312845
|
Entrez Id: |
1457 |
Gene Symbol: |
CSNK2A1 |
CSNK2A1
|
Dysmorphic features
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Predominance of CK2α over CK2α' in the mammalian brain.
|
21761202 |
2011 |
rs869312845
|
Entrez Id: |
1457 |
Gene Symbol: |
CSNK2A1 |
CSNK2A1
|
Dysmorphic features
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Presynaptic CK2 promotes synapse organization and stability by targeting Ankyrin2.
|
24395637 |
2014 |
rs869312840
|
Entrez Id: |
1457 |
Gene Symbol: |
CSNK2A1 |
CSNK2A1
|
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
|
|
0.800 |
GeneticVariation |
UNIPROT |
De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features.
|
27048600 |
2016 |
rs869312845
|
Entrez Id: |
1457 |
Gene Symbol: |
CSNK2A1 |
CSNK2A1
|
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
|
|
0.800 |
GeneticVariation |
UNIPROT |
De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features.
|
27048600 |
2016 |
rs869312848
|
Entrez Id: |
1457 |
Gene Symbol: |
CSNK2A1 |
CSNK2A1
|
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
|
|
0.800 |
GeneticVariation |
UNIPROT |
De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features.
|
27048600 |
2016 |
rs869312849
|
Entrez Id: |
1457 |
Gene Symbol: |
CSNK2A1 |
CSNK2A1
|
OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME
|
|
0.800 |
GeneticVariation |
UNIPROT |
De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features.
|
27048600 |
2016 |
rs869312845
|
Entrez Id: |
1457 |
Gene Symbol: |
CSNK2A1 |
CSNK2A1
|
Dysmorphic features
|
T |
0.700 |
GeneticVariation |
CLINVAR |
De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features.
|
27048600 |
2016 |
rs74448913
|
Entrez Id: |
1457 |
Gene Symbol: |
CSNK2A1 |
CSNK2A1
|
Sleep Onset Latency
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association analysis of actigraphic sleep phenotypes in the LIFE Adult Study.
|
27126917 |
2016 |
rs869312845
|
Entrez Id: |
1457 |
Gene Symbol: |
CSNK2A1 |
CSNK2A1
|
Dysmorphic features
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Prevalence and architecture of de novo mutations in developmental disorders.
|
28135719 |
2017 |
rs869312845
|
Entrez Id: |
1457 |
Gene Symbol: |
CSNK2A1 |
CSNK2A1
|
Dysmorphic features
|
T |
0.700 |
GeneticVariation |
CLINVAR |
Okur-Chung neurodevelopmental syndrome: Eight additional cases with implications on phenotype and genotype expansion.
|
29240241 |
2018 |