×
Entrez Id:
1654
Gene Symbol:
DDX3X
DDX3X
0.110
GeneticVariation
group
BEFREE
The phenotypes associated with DDX3X variants are heterogeneous and include brain and behavioral abnormalities, microcephaly, hypotonia, and movement disorders and/or spasticity.
30734472
2019
×
Entrez Id:
1654
Gene Symbol:
DDX3X
DDX3X
0.110
GeneticVariation
group
CLINVAR
DDX3X mutations in two girls with a phenotype overlapping Toriello-Carey syndrome.
28371085
2017
×
Entrez Id:
1654
Gene Symbol:
DDX3X
DDX3X
0.110
CausalMutation
group
CLINVAR
DDX3X mutations in two girls with a phenotype overlapping Toriello-Carey syndrome.
28371085
2017
×
Entrez Id:
1654
Gene Symbol:
DDX3X
DDX3X
0.110
GeneticVariation
group
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
0.110
CausalMutation
group
CLINVAR
Large-scale discovery of novel genetic causes of developmental disorders.
25533962
2015
×
Entrez Id:
1654
Gene Symbol:
DDX3X
DDX3X
0.110
CausalMutation
group
CLINVAR
Cancer-associated mutants of RNA helicase DDX3X are defective in RNA-stimulated ATP hydrolysis.
25724843
2015
×
Entrez Id:
1654
Gene Symbol:
DDX3X
DDX3X
0.110
GeneticVariation
group
CLINVAR
Cancer-associated mutants of RNA helicase DDX3X are defective in RNA-stimulated ATP hydrolysis.
25724843
2015
×
Entrez Id:
1654
Gene Symbol:
DDX3X
DDX3X
0.110
CausalMutation
group
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
0.110
CausalMutation
group
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
0.110
GeneticVariation
group
CLINVAR
Large-scale discovery of novel genetic causes of developmental disorders.
25533962
2015
×
Entrez Id:
1654
Gene Symbol:
DDX3X
DDX3X
0.110
GeneticVariation
group
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
0.110
CausalMutation
group
CLINVAR
DDX3X regulates cell survival and cell cycle during mouse early embryonic development.
25050112
2014
×
Entrez Id:
1654
Gene Symbol:
DDX3X
DDX3X
0.110
GeneticVariation
group
CLINVAR
DDX3X regulates cell survival and cell cycle during mouse early embryonic development.
25050112
2014
×
Entrez Id:
1654
Gene Symbol:
DDX3X
DDX3X
0.110
GeneticVariation
group
CLINVAR
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
24267886
2013
×
Entrez Id:
1654
Gene Symbol:
DDX3X
DDX3X
0.110
CausalMutation
group
CLINVAR
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
24267886
2013
×
Entrez Id:
1654
Gene Symbol:
DDX3X
DDX3X
0.110
CausalMutation
group
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
0.110
GeneticVariation
group
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
0.110
CausalMutation
group
CLINVAR
Novel mutations target distinct subgroups of medulloblastoma.
22722829
2012
×
Entrez Id:
1654
Gene Symbol:
DDX3X
DDX3X
0.110
GeneticVariation
group
CLINVAR
Novel mutations target distinct subgroups of medulloblastoma.
22722829
2012
×
Entrez Id:
1654
Gene Symbol:
DDX3X
DDX3X
0.110
GeneticVariation
group
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
0.110
CausalMutation
group
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
0.110
CausalMutation
group
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
0.110
GeneticVariation
group
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
0.110
CausalMutation
group
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
0.110
GeneticVariation
group
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