|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
GeneticVariation |
CLINVAR |
DDX3X mutations in two girls with a phenotype overlapping Toriello-Carey syndrome.
|
28371085 |
2017 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
CausalMutation |
CLINVAR |
DDX3X mutations in two girls with a phenotype overlapping Toriello-Carey syndrome.
|
28371085 |
2017 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
GeneticVariation |
CLINVAR |
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling.
|
26235985 |
2015 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
CausalMutation |
CLINVAR |
Large-scale discovery of novel genetic causes of developmental disorders.
|
25533962 |
2015 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
CausalMutation |
CLINVAR |
Cancer-associated mutants of RNA helicase DDX3X are defective in RNA-stimulated ATP hydrolysis.
|
25724843 |
2015 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
GeneticVariation |
CLINVAR |
Cancer-associated mutants of RNA helicase DDX3X are defective in RNA-stimulated ATP hydrolysis.
|
25724843 |
2015 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
CausalMutation |
CLINVAR |
De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum.
|
25326669 |
2015 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
CausalMutation |
CLINVAR |
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling.
|
26235985 |
2015 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
GeneticVariation |
CLINVAR |
Large-scale discovery of novel genetic causes of developmental disorders.
|
25533962 |
2015 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
GeneticVariation |
CLINVAR |
De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum.
|
25326669 |
2015 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
CausalMutation |
CLINVAR |
DDX3X regulates cell survival and cell cycle during mouse early embryonic development.
|
25050112 |
2014 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
GeneticVariation |
CLINVAR |
DDX3X regulates cell survival and cell cycle during mouse early embryonic development.
|
25050112 |
2014 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
GeneticVariation |
CLINVAR |
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
|
24267886 |
2013 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
CausalMutation |
CLINVAR |
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
|
24267886 |
2013 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
CausalMutation |
CLINVAR |
RNA helicase DDX3 is a regulatory subunit of casein kinase 1 in Wnt-β-catenin signaling.
|
23413191 |
2013 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
GeneticVariation |
CLINVAR |
RNA helicase DDX3 is a regulatory subunit of casein kinase 1 in Wnt-β-catenin signaling.
|
23413191 |
2013 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
CausalMutation |
CLINVAR |
Novel mutations target distinct subgroups of medulloblastoma.
|
22722829 |
2012 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
GeneticVariation |
CLINVAR |
Novel mutations target distinct subgroups of medulloblastoma.
|
22722829 |
2012 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
GeneticVariation |
CLINVAR |
Dosage compensation of the mammalian X chromosome influences the phenotypic variability of X-linked dominant male-lethal disorders.
|
18463129 |
2008 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
CausalMutation |
CLINVAR |
Dosage compensation of the mammalian X chromosome influences the phenotypic variability of X-linked dominant male-lethal disorders.
|
18463129 |
2008 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
CausalMutation |
CLINVAR |
The DDX3 subfamily of the DEAD box helicases: divergent roles as unveiled by studying different organisms and in vitro assays.
|
17979704 |
2007 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
GeneticVariation |
CLINVAR |
The DDX3 subfamily of the DEAD box helicases: divergent roles as unveiled by studying different organisms and in vitro assays.
|
17979704 |
2007 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
CausalMutation |
CLINVAR |
Divergent roles of the DEAD-box protein BS-PL10, the urochordate homologue of human DDX3 and DDX3Y proteins, in colony astogeny and ontogeny.
|
16518819 |
2006 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
GeneticVariation |
CLINVAR |
Divergent roles of the DEAD-box protein BS-PL10, the urochordate homologue of human DDX3 and DDX3Y proteins, in colony astogeny and ontogeny.
|
16518819 |
2006 |
|
| Entrez Id: |
1654 |
| Gene Symbol: |
DDX3X |
DDX3X
|
Movement Disorders
|
0.110 |
GeneticVariation |
CLINVAR |
Belle is a Drosophila DEAD-box protein required for viability and in the germ line.
|
15572142 |
2005 |