DHX58

DExH-box helicase 58

Summary

Enables several functions, including ATP hydrolysis activity; RNA binding activity; and zinc ion binding activity. Involved in negative regulation of type I interferon production and regulation of innate immune response. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants60 total

rsidPosition (GRCh37)AllelesClassClinVar
rs78184923617:40,253,787G/Cuncertain significance
rs90878575817:40,253,793G/Auncertain significance
rs78218642017:40,253,906C/Tuncertain significance
rs14544510817:40,254,239C/Auncertain significance
rs139588080317:40,254,257T/Auncertain significance
rs13996388617:40,254,262C/Auncertain significance
rs118207129217:40,254,269G/Cuncertain significance
rs127245011817:40,254,290T/Cuncertain significance
rs143968449017:40,255,738G/Tuncertain significance
rs37125220617:40,255,749C/Tlikely benign
rs78231105217:40,255,754G/Tuncertain significance
rs78214685217:40,255,761C/Tuncertain significance
rs20211207617:40,255,779G/Auncertain significance
rs78213507017:40,256,786T/Guncertain significance
rs78204077717:40,256,798C/Tuncertain significance
rs14562681817:40,256,808C/Auncertain significance
rs14542021217:40,256,834G/Cuncertain significance
rs254404543817:40,256,836T/Cuncertain significance
rs36777864817:40,256,884C/Tuncertain significance
rs103038432617:40,256,899G/Auncertain significance
rs19995823017:40,256,909C/Tuncertain significance
rs78241404917:40,257,080C/Tuncertain significance
rs14102347817:40,257,098T/Auncertain significance
rs119900642117:40,257,121C/Tuncertain significance
rs57216989017:40,257,124G/Tuncertain significance
rs205403637317:40,257,146T/Cuncertain significance
rs207415817:40,257,163T/Cbenign
rs14955188217:40,257,785C/Tuncertain significance
rs20123559817:40,257,809C/Guncertain significance
rs37448337517:40,257,810G/Auncertain significance
rs13808821817:40,257,875C/Tuncertain significance
rs20081586517:40,257,876G/Auncertain significance
rs78270876317:40,257,882G/Auncertain significance
rs254404798517:40,257,983A/Guncertain significance
rs78190578017:40,258,004C/Tlikely benign
rs57022090017:40,259,664G/Cuncertain significance
rs254405111417:40,259,677G/Tuncertain significance
rs37260338817:40,259,680C/Auncertain significance
rs78273527917:40,259,690T/Cuncertain significance
rs254405119017:40,259,708G/Auncertain significance
rs91258342517:40,259,789T/Clikely benign
rs13998042217:40,261,295C/Tuncertain significance
rs14402324417:40,262,767C/Tuncertain significance
rs14313612317:40,262,782C/Tuncertain significance
rs14886372817:40,262,830G/Alikely benign
rs15038553717:40,262,881C/Tuncertain significance
rs13868768417:40,262,893G/Auncertain significance
rs14302437817:40,262,895G/Auncertain significance
rs137397896717:40,263,320G/Auncertain significance
rs155566411217:40,263,321C/Guncertain significance
rs14877732117:40,263,409T/Cuncertain significance
rs205415073117:40,263,419C/Guncertain significance
rs78241756217:40,263,466C/Tuncertain significance
rs78270229117:40,263,479G/Tuncertain significance
rs97228527917:40,263,487T/Guncertain significance
rs205415376617:40,263,502G/Cuncertain significance
rs37187480917:40,263,793G/Auncertain significance
rs36864410217:40,263,816C/Tuncertain significance
rs96020260217:40,263,844A/Guncertain significance
rs37305871717:40,263,891T/Auncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.