GAL3ST2
galactose-3-O-sulfotransferase 2
Summary
This gene encodes a member of the galactose-3-O-sulfotransferase protein family. The product of this gene catalyzes sulfonation by transferring a sulfate group to the hydroxyl at C-3 of nonreducing beta-galactosyl residues, and it can act on both type 1 and type 2 (Galbeta 1-3/1-4GlcNAc-R) oligosaccharides with similar efficiencies, and on core 1 glycans. This enzyme has been implicated in tumor metastasis processes. This gene is different from the GAL3ST3 gene located on chromosome 11, which has also been referred to as GAL3ST2 and encodes a related enzyme with distinct tissue distribution and substrate specificities, compared to galactose-3-O-sulfotransferase 2. [provided by RefSeq, Jul 2008]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs200875314 | 2:242,716,384 | T/A | — | uncertain significance |
| rs78620448 | 2:242,716,400 | G/A | — | conflicting classifications of pathogenicity |
| rs62193063 | 2:242,728,098 | C/T | regulatory region variant | — |
| rs62193069 | 2:242,730,565 | G/A | intron variant | — |
| rs62193070 | 2:242,730,588 | A/T | — | — |
| rs137862503 | 2:242,738,488 | G/A | — | likely benign |
| rs756214263 | 2:242,738,548 | C/T | — | uncertain significance |
| rs1004576024 | 2:242,741,249 | A/C | — | uncertain significance |
| rs372108744 | 2:242,741,273 | C/T | missense variant | pathogenic |
| rs1411413266 | 2:242,741,276 | T/C | — | uncertain significance |
| rs202108971 | 2:242,741,377 | C/T | — | uncertain significance |
| rs369237199 | 2:242,741,392 | G/A | — | uncertain significance |
| rs922557666 | 2:242,742,766 | A/G | — | uncertain significance |
| rs141828605 | 2:242,742,812 | C/T | missense variant | — |
| rs371281574 | 2:242,742,826 | G/A | — | uncertain significance |
| rs139344622 | 2:242,742,842 | A/G | missense variant | — |
| rs939445638 | 2:242,742,857 | C/T | — | likely benign |
| rs1466780364 | 2:242,742,934 | C/G | — | uncertain significance |
| rs200606493 | 2:242,743,007 | G/C | — | uncertain significance |
| rs775193067 | 2:242,743,066 | G/A | — | uncertain significance |
| rs1442940687 | 2:242,743,082 | C/G | — | uncertain significance |
| rs891728138 | 2:242,743,102 | C/T | — | uncertain significance |
| rs1209450044 | 2:242,743,112 | G/T | — | uncertain significance |
| rs2469669264 | 2:242,743,177 | T/G | — | likely benign |
| rs961001870 | 2:242,743,183 | G/A | — | uncertain significance |
| rs753837152 | 2:242,743,297 | G/T | — | uncertain significance |
| rs771805845 | 2:242,743,316 | G/T | — | uncertain significance |
| rs1433252490 | 2:242,743,322 | G/A | — | uncertain significance |
| rs1252814383 | 2:242,743,346 | G/A | — | uncertain significance |
| rs1433386502 | 2:242,743,366 | C/T | — | uncertain significance |
| rs1455726008 | 2:242,743,376 | A/C | — | uncertain significance |
| rs961245190 | 2:242,743,382 | A/T | — | uncertain significance |
| rs145527407 | 2:242,743,424 | C/T | — | uncertain significance |
| rs773556478 | 2:242,743,443 | C/A | — | uncertain significance |
| rs2469670135 | 2:242,743,508 | A/G | — | uncertain significance |
| rs756952557 | 2:242,743,513 | A/C | — | uncertain significance |
| rs373185622 | 2:242,743,541 | C/G | — | uncertain significance |
| rs376663386 | 2:242,743,547 | A/C | — | uncertain significance |
| rs1427596228 | 2:242,743,565 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.