DDX3Y

DEAD-box helicase 3 Y-linked

Summary

The protein encoded by this gene is a member of the DEAD-box RNA helicase family, characterized by nine conserved motifs, included the conserved Asp-Glu-Ala-Asp (DEAD) motif. These motifs are thought to be involved in ATP binding, hydrolysis, RNA binding, and in the formation of intramolecular interactions. This protein shares high similarity to DDX3X, on the X chromosome, but a deletion of this gene is not complemented by DDX3X. Mutations in this gene result in male infertility, a reduction in germ cell numbers, and can result in Sertoli-cell only sydrome. Pseudogenes sharing similarity to both this gene and the DDX3X paralog are found on chromosome 4 and the X chromosome. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Oct 2014]

Known Variants37 total

rsidPosition (GRCh37)AllelesClassClinVar
rs2032662Y:15,014,262C/T——
rs2032677Y:15,014,550T/C——
rs9306836Y:15,016,438G/C——
rs2032680Y:15,016,536A/G——
rs9341285Y:15,017,505C/T——
rs8179022Y:15,018,459G/A——
rs8179021Y:15,018,582C/Tintron variant—
rs9341286Y:15,019,092T/C——
rs9341287Y:15,019,124A/C——
rs2032590Y:15,019,613T/G——
rs9341289Y:15,020,304T/G——
rs9341290Y:15,020,578T/C——
rs9341292Y:15,021,104A/G——
rs9786025Y:15,021,522G/A——
rs9341294Y:15,022,370A/G——
rs13447365Y:15,022,465T/C——
rs9341296Y:15,022,707C/Tintron variant—
rs9341298Y:15,022,939C/T——
rs113287778Y:15,023,205T/C——
rs9341301Y:15,023,364T/C——
rs9341303Y:15,025,506G/A——
rs2032610Y:15,025,598T/Cintron variant—
rs796483281Y:15,026,395T/A——
rs2032624Y:15,026,424A/Cintron variant—
rs34812786Y:15,026,633C/T——
rs72625304Y:15,027,507A/Gintron variant—
rs2032636Y:15,027,529T/Gintron variant—
rs201495354Y:15,027,638C/Tsynonymous variantlikely benign
rs72625359Y:15,028,176G/Cmissense variant—
rs2032649Y:15,029,492T/Gintron variant—
rs3212294Y:15,030,650C/A——
rs2032591Y:15,030,682C/G——
rs2020857Y:15,030,752C/T——
rs13447374Y:15,030,767T/G——
rs13447375Y:15,030,878C/T——
rs2032592Y:15,031,385A/G——
rs2032593Y:15,031,416G/A——

Gene information from NCBI Gene. Variant classifications from ClinVar.