ARSG

arylsulfatase G

Summary

The protein encoded by this gene belongs to the sulfatase enzyme family. Sulfatases hydrolyze sulfate esters from sulfated steroids, carbohydrates, proteoglycans, and glycolipids. They are involved in hormone biosynthesis, modulation of cell signaling, and degradation of macromolecules. This protein displays arylsulfatase activity at acidic pH, as is typical of lysosomal sulfatases, and has been shown to localize in the lysosomes. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jun 2012]

Known Variants346 total

rsidPosition (GRCh37)AllelesClassClinVar
rs201838217:66,299,023G/Aregulatory region variant—
rs207664982017:66,303,638G/T—uncertain significance
rs251005704717:66,303,643G/C—uncertain significance
rs78266271417:66,303,649T/C—likely benign
rs36792143517:66,303,655G/A—likely benign
rs78185714817:66,303,657T/C—uncertain significance
rs807480617:66,303,666C/T—benign
rs129316449317:66,303,671G/T—uncertain significance
rs78235915017:66,303,680T/C—uncertain significance
rs155576472717:66,303,682A/G—likely benign
rs130412890317:66,303,693A/T—uncertain significance
rs14407399417:66,303,697T/A—benign
rs6173494917:66,303,721G/A—likely benign
rs125709258617:66,303,732G/A—uncertain significance
rs207665469017:66,303,734C/T—pathogenic
rs78233409617:66,303,763C/T—likely benign
rs19956695017:66,303,764G/A—conflicting classifications of pathogenicity
rs156844589317:66,303,767G/T—pathogenic
rs36864296717:66,303,769C/T—likely benign
rs207665707417:66,303,771T/C—uncertain significance
rs134079490617:66,303,772G/A—uncertain significance
rs91560390517:66,303,774G/A—uncertain significance
rs168992206217:66,303,780G/A—uncertain significance
rs131446874617:66,303,797T/C—uncertain significance
rs251006004817:66,303,810A/T—uncertain significance
rs78264612817:66,303,814C/T—likely benign
rs78182551517:66,303,820C/A—likely benign
rs207666014817:66,303,823C/T—likely benign
rs13863567917:66,303,829T/A—uncertain significance
rs136935024217:66,303,840C/T—uncertain significance
rs37273817617:66,303,841G/A—likely benign
rs78254214017:66,303,851A/G—uncertain significance
rs94710814817:66,303,853G/A—likely pathogenic
rs155576496017:66,303,854T/C—likely pathogenic
rs214559158017:66,303,866T/C—likely benign
rs7783970617:66,303,916A/T—benign
rs57726035117:66,308,872G/A——
rs5931336617:66,339,572A/G—benign
rs37532220917:66,339,728C/T—likely benign
rs75941857717:66,339,757C/T—likely benign
rs251052261917:66,339,759A/G—uncertain significance
rs14174884517:66,339,779T/C—likely pathogenic
rs76061574717:66,339,789G/A—uncertain significance
rs14626395717:66,339,793T/A—likely benign
rs20068591617:66,339,801T/C—pathogenic
rs76467562717:66,339,804C/T—uncertain significance
rs20086328217:66,339,805C/T—likely benign
rs19990835017:66,339,806G/A—uncertain significance
rs207837439917:66,339,807G/A—uncertain significance
rs101659436117:66,339,809C/T—pathogenic
rs36931569717:66,339,810G/A—uncertain significance
rs78155532717:66,339,812C/G—uncertain significance
rs74835289317:66,339,816G/A—uncertain significance
rs251052470817:66,339,820T/G—likely benign
rs117993687117:66,339,821C/T—uncertain significance
rs75631441617:66,339,822G/A—uncertain significance
rs20086941917:66,339,824A/G—uncertain significance
rs74942647717:66,339,826T/C—likely benign
rs20152192917:66,339,833A/C—uncertain significance
rs13942465317:66,339,837G/A—uncertain significance
rs76149067117:66,339,857G/A—uncertain significance
rs14140604517:66,339,860G/A—uncertain significance
rs124471864717:66,339,864G/A—pathogenic
rs125189605817:66,339,865C/G—likely benign
rs75206744817:66,339,870C/T—uncertain significance
rs75544023717:66,339,877C/T—likely benign
rs76779635317:66,339,886C/T—likely benign
rs20103058417:66,339,909C/T—uncertain significance
rs75640692017:66,339,916C/A—pathogenic
rs77812817317:66,339,917G/A—uncertain significance
rs15083201417:66,339,922T/A—likely benign
rs251052911817:66,339,923G/A—uncertain significance
rs77639786517:66,339,941G/A—likely benign
rs92681910517:66,339,944C/A—likely benign
rs76946258017:66,339,947C/T—likely benign
rs991125517:66,339,948G/A—likely benign
rs6144287517:66,343,182A/G—benign
rs76561719817:66,343,251T/C—likely benign
rs251061453917:66,343,264A/C—likely pathogenic
rs37503078517:66,343,267C/G—likely benign
rs251061479917:66,343,274C/A—uncertain significance
rs77993014217:66,343,285C/T—likely benign
rs55473157517:66,343,288C/T—likely benign
rs36763271717:66,343,289G/A—uncertain significance
rs251061498517:66,343,291C/T—likely benign
rs141064100417:66,343,297T/C—likely benign
rs94481036917:66,343,300C/T—likely benign
rs91330593517:66,343,304A/T—uncertain significance
rs96613949317:66,343,306C/T—likely benign
rs77859926317:66,343,309C/G—uncertain significance
rs13930485217:66,343,310C/T—uncertain significance
rs57719095017:66,343,311G/A—uncertain significance
rs214630925417:66,343,314G/T—pathogenic
rs251061586217:66,343,322T/G—likely benign
rs119803650317:66,343,330G/A—likely benign
rs37587442517:66,347,698C/T—likely benign
rs74656428217:66,347,699G/A—likely benign
rs7520965417:66,347,700A/G—benign
rs77031223617:66,347,716G/C—uncertain significance
rs123962934517:66,347,731T/A—uncertain significance

Showing 100 of 346 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.