SLC35B3

solute carrier family 35 member B3

Summary

This gene is a member of the solute carrier family. The encoded protein is involved in the transport of 3-prime phosphoadenosine 5-prime phosphosulfate (PAPS) from the nucleus or the cytosol to the Golgi lumen. This gene has been reported to be expressed preferentially in the human colon tissues. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]

Known Variants20 total

rsidPosition (GRCh37)AllelesClassClinVar
rs7492083486:8,413,817C/T—uncertain significance
rs9088111796:8,413,822A/G—uncertain significance
rs24803604906:8,413,849G/A—uncertain significance
rs7492980116:8,413,919C/G—uncertain significance
rs10025818206:8,415,153G/A—uncertain significance
rs24804160766:8,417,637T/C—uncertain significance
rs2004303596:8,417,717G/A—uncertain significance
rs3743801646:8,419,842T/C—uncertain significance
rs7500439296:8,419,872C/T—uncertain significance
rs7533095216:8,419,895G/A—uncertain significance
rs7590292456:8,420,986T/G—uncertain significance
rs12234855576:8,421,020T/C—uncertain significance
rs7586139466:8,421,026T/C—likely benign
rs1502898936:8,428,109C/Tintron variant—
rs7714866856:8,428,246G/A—uncertain significance
rs1382042926:8,428,266A/G—uncertain significance
rs7546322766:8,428,276C/A—uncertain significance
rs2021291686:8,430,155T/C—uncertain significance
rs8664361166:8,430,162G/A—uncertain significance
rs1419644636:8,430,201C/T—likely benign

Gene information from NCBI Gene. Variant classifications from ClinVar.