DDX3X Chromosome X

DEAD-box helicase 3 X-linked
289 variants 1 Drug Response 288 Health Risk

Upload your DNA to see your personal genotypes for variants in DDX3X.

What This Gene Does
The protein encoded by this gene is a member of the large DEAD-box protein family, that is defined by the presence of the conserved Asp-Glu-Ala-Asp (DEAD) motif, and has ATP-dependent RNA helicase activity. This protein has been reported to display a high level of RNA-independent ATPase activity, and unlike most DEAD-box helicases, the ATPase activity is thought to be stimulated by both RNA and DNA. This protein has multiple conserved domains and is thought to play roles in both the nucleus and cytoplasm. Nuclear roles include transcriptional regulation, mRNP assembly, pre-mRNA splicing, and mRNA export. In the cytoplasm, this protein is thought to be involved in translation, cellular signaling, and viral replication. Misregulation of this gene has been implicated in tumorigenesis. This gene has a paralog located in the nonrecombining region of the Y chromosome. Pseudogenes sharing similarity to both this gene and the DDX3Y paralog are found on chromosome 4 and the X chromosome. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014]
Gene Info
Gene Group
DEAD-box helicases
Locus Type
gene with protein product
Location
Xp11.4
Ensembl
ENSG00000215301
Associated Conditions (33)
Poly (ADP-Ribose) polymerase inhibitor response
Inborn genetic diseases
DDX3X-related X-linked intellectual disability
Intellectual disability
X-linked 102
X-linked syndromic intellectual disability
Lymphoma
DDX3X-related disorder
Nonpapillary renal cell carcinoma
Medulloblastoma WNT activated
Neurodevelopmental delay
Medulloblastoma
Marfanoid habitus and intellectual disability
Rare genetic intellectual disability
Thyroid cancer
nonmedullary
1
See cases
DDX3X-Related Neurodevelopmental Disorder
EBV-positive nodal T- and NK-cell lymphoma
+13 more conditions
Key Variants
RS1555951992
drug response
Poly (ADP-Ribose) polymerase inhibitor response, Poly (ADP-Ribose) polymerase inhibitor response
Drug Response
RS1057523822
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1064794993
Conflicting classifications of pathogenicity
DDX3X-related X-linked intellectual disability, DDX3X-related X-linked intellectual disability
Health Risk
RS1064795323
Conflicting classifications of pathogenicity
Intellectual disability, X-linked 102, Intellectual disability
Health Risk
RS1188370836
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1302694358
Conflicting classifications of pathogenicity
Health Risk
RS1307578363
Conflicting classifications of pathogenicity
X-linked syndromic intellectual disability, X-linked syndromic intellectual disability
Health Risk
RS1555953527
Conflicting classifications of pathogenicity
Inborn genetic diseases, Intellectual disability, X-linked 102
Health Risk
RS2063889864
Conflicting classifications of pathogenicity
Intellectual disability, X-linked 102, Intellectual disability
Health Risk
RS2063923789
Conflicting classifications of pathogenicity
Intellectual disability, X-linked 102, Intellectual disability
Health Risk
RS2063940085
Conflicting classifications of pathogenicity
Health Risk
RS2147356713
Conflicting classifications of pathogenicity
Intellectual disability, X-linked 102, Intellectual disability
Health Risk
All Variants (289)
RSID Category Clinical Significance Conditions
RS1555951992 Drug Response drug response Poly (ADP-Ribose) polymerase inhibitor response, Poly (ADP-Ribose) polymerase inhibitor response
RS1057523822 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1064794993 Health Risk Conflicting classifications of pathogenicity DDX3X-related X-linked intellectual disability, DDX3X-related X-linked intellectual disability
RS1064795323 Health Risk Conflicting classifications of pathogenicity Intellectual disability, X-linked 102, Intellectual disability
RS1188370836 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1302694358 Health Risk Conflicting classifications of pathogenicity
RS1307578363 Health Risk Conflicting classifications of pathogenicity X-linked syndromic intellectual disability, X-linked syndromic intellectual disability
RS1555953527 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Intellectual disability, X-linked 102
RS2063889864 Health Risk Conflicting classifications of pathogenicity Intellectual disability, X-linked 102, Intellectual disability
RS2063923789 Health Risk Conflicting classifications of pathogenicity Intellectual disability, X-linked 102, Intellectual disability
RS2063940085 Health Risk Conflicting classifications of pathogenicity
RS2147356713 Health Risk Conflicting classifications of pathogenicity Intellectual disability, X-linked 102, Intellectual disability
RS2519514556 Health Risk Conflicting classifications of pathogenicity Intellectual disability, X-linked 102, Lymphoma
RS2519519335 Health Risk Conflicting classifications of pathogenicity
RS2519525946 Health Risk Conflicting classifications of pathogenicity Intellectual disability, X-linked 102, DDX3X-related disorder
RS2519527570 Health Risk Conflicting classifications of pathogenicity
RS368731454 Health Risk Conflicting classifications of pathogenicity
RS745429365 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS751868529 Health Risk Conflicting classifications of pathogenicity
RS779721240 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS796052224 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS797045026 Health Risk Conflicting classifications of pathogenicity Intellectual disability, X-linked 102, Inborn genetic diseases
RS867967504 Health Risk Conflicting classifications of pathogenicity Intellectual disability, X-linked 102, Intellectual disability
RS892274119 Health Risk Conflicting classifications of pathogenicity DDX3X-related disorder, Inborn genetic diseases, DDX3X-related disorder
RS942326584 Health Risk Conflicting classifications of pathogenicity Intellectual disability, X-linked 102, Intellectual disability
RS1017583398 Health Risk Likely pathogenic
RS1057518255 Health Risk Likely pathogenic
RS1057518707 Health Risk Likely pathogenic Intellectual disability, X-linked 102, Intellectual disability
RS1057521603 Health Risk Likely pathogenic Medulloblastoma WNT activated, Medulloblastoma WNT activated
RS1064793858 Health Risk Likely pathogenic Neurodevelopmental delay, Intellectual disability, X-linked 102
RS1064796924 Health Risk Likely pathogenic
RS1131691769 Health Risk Likely pathogenic Intellectual disability, X-linked 102, Intellectual disability
RS1267519974 Health Risk Likely pathogenic Intellectual disability, X-linked 102, Intellectual disability
RS1463769342 Health Risk Likely pathogenic
RS1555952659 Health Risk Likely pathogenic
RS1555953158 Health Risk Likely pathogenic
RS1555953550 Health Risk Likely pathogenic
RS1555953796 Health Risk Likely pathogenic Medulloblastoma, Intellectual disability, X-linked 102
RS1555954154 Health Risk Likely pathogenic Intellectual disability, X-linked 102, Intellectual disability
RS1569238251 Health Risk Likely pathogenic
RS1569240261 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1602122138 Health Risk Likely pathogenic Intellectual disability, X-linked 102, Intellectual disability
RS1602122237 Health Risk Likely pathogenic Marfanoid habitus and intellectual disability, Marfanoid habitus and intellectual disability
RS1602131872 Health Risk Likely pathogenic Intellectual disability, X-linked 102, Intellectual disability
RS1602132216 Health Risk Likely pathogenic Intellectual disability, X-linked 102, Intellectual disability
RS1602134468 Health Risk Likely pathogenic Intellectual disability, X-linked 102, Intellectual disability
RS1602135832 Health Risk Likely pathogenic Rare genetic intellectual disability, Rare genetic intellectual disability
RS1602136369 Health Risk Likely pathogenic Intellectual disability, X-linked 102, Intellectual disability
RS2063786541 Health Risk Likely pathogenic
RS2063866799 Health Risk Likely pathogenic
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