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/Tuncertain significance
rs9088111796:8,413,822A/Guncertain significance
rs24803604906:8,413,849G/Auncertain significance
rs7492980116:8,413,919C/Guncertain significance
rs10025818206:8,415,153G/Auncertain significance
rs24804160766:8,417,637T/Cuncertain significance
rs2004303596:8,417,717G/Auncertain significance
rs3743801646:8,419,842T/Cuncertain significance
rs7500439296:8,419,872C/Tuncertain significance
rs7533095216:8,419,895G/Auncertain significance
rs7590292456:8,420,986T/Guncertain significance
rs12234855576:8,421,020T/Cuncertain significance
rs7586139466:8,421,026T/Clikely benign
rs1502898936:8,428,109C/Tintron variant
rs7714866856:8,428,246G/Auncertain significance
rs1382042926:8,428,266A/Guncertain significance
rs7546322766:8,428,276C/Auncertain significance
rs2021291686:8,430,155T/Cuncertain significance
rs8664361166:8,430,162G/Auncertain significance
rs1419644636:8,430,201C/Tlikely benign

Gene information from NCBI Gene. Variant classifications from ClinVar.