GAL3ST4
galactose-3-O-sulfotransferase 4
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 to the C-3' position of galactose residues in O-linked glycoproteins. This enzyme is highly specific for core 1 structures, with asialofetuin, Gal-beta-1,3-GalNAc and Gal-beta-1,3 (GlcNAc-beta-1,6)GalNAc being good substrates. [provided by RefSeq, Jul 2008]
Known Variants53 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs149961692 | 7:99,757,598 | G/C | — | uncertain significance |
| rs765114251 | 7:99,757,608 | C/A | — | uncertain significance |
| rs144461733 | 7:99,757,654 | C/T | — | uncertain significance |
| rs200159207 | 7:99,757,739 | G/T | — | uncertain significance |
| rs754074041 | 7:99,757,781 | C/T | — | uncertain significance |
| rs1456158446 | 7:99,757,829 | C/T | — | uncertain significance |
| rs776755474 | 7:99,757,840 | G/A | — | uncertain significance |
| rs762070602 | 7:99,757,849 | C/T | — | uncertain significance |
| rs766932470 | 7:99,757,859 | C/T | — | uncertain significance |
| rs755375291 | 7:99,757,880 | A/G | — | uncertain significance |
| rs1364763696 | 7:99,757,930 | G/C | — | uncertain significance |
| rs138298556 | 7:99,757,939 | C/T | — | uncertain significance |
| rs3800952 | 7:99,757,954 | C/T | — | benign |
| rs112880621 | 7:99,757,955 | G/A | — | benign |
| rs757897746 | 7:99,758,033 | C/T | — | uncertain significance |
| rs140652132 | 7:99,758,040 | G/A | — | benign |
| rs2484671491 | 7:99,758,107 | A/G | — | uncertain significance |
| rs750043430 | 7:99,758,129 | C/G | — | uncertain significance |
| rs2484671621 | 7:99,758,131 | A/G | — | uncertain significance |
| rs147809354 | 7:99,758,145 | C/T | — | likely benign |
| rs149908309 | 7:99,758,158 | G/T | — | uncertain significance |
| rs144870417 | 7:99,758,174 | C/T | — | uncertain significance |
| rs2484671837 | 7:99,758,215 | A/G | — | uncertain significance |
| rs775899842 | 7:99,758,276 | C/G | — | uncertain significance |
| rs149033197 | 7:99,758,299 | G/C | — | likely benign |
| rs748647653 | 7:99,758,304 | G/T | — | uncertain significance |
| rs770433938 | 7:99,758,323 | T/A | — | uncertain significance |
| rs200053288 | 7:99,758,396 | C/T | — | uncertain significance |
| rs368643591 | 7:99,758,400 | G/C | — | uncertain significance |
| rs768637210 | 7:99,758,405 | C/T | — | uncertain significance |
| rs774937557 | 7:99,758,434 | C/T | — | uncertain significance |
| rs374392589 | 7:99,758,474 | G/A | — | uncertain significance |
| rs550951408 | 7:99,758,527 | G/A | — | uncertain significance |
| rs1429891844 | 7:99,758,569 | A/G | — | uncertain significance |
| rs1918352 | 7:99,763,439 | G/A | downstream gene variant | — |
| rs149092760 | 7:99,764,116 | A/T | — | benign |
| rs777894947 | 7:99,764,133 | G/T | — | uncertain significance |
| rs2484679215 | 7:99,764,192 | G/A | — | uncertain significance |
| rs763411487 | 7:99,764,195 | C/T | — | likely benign |
| rs201437336 | 7:99,764,237 | C/T | — | uncertain significance |
| rs142988850 | 7:99,764,240 | A/G | — | likely benign |
| rs200571320 | 7:99,764,249 | C/T | — | uncertain significance |
| rs115841575 | 7:99,764,274 | C/T | — | benign |
| rs760360297 | 7:99,764,281 | G/T | — | uncertain significance |
| rs373254633 | 7:99,764,291 | C/T | — | uncertain significance |
| rs376538136 | 7:99,764,292 | G/A | — | uncertain significance |
| rs1415973188 | 7:99,764,303 | C/T | — | likely benign |
| rs777963100 | 7:99,764,330 | T/G | — | uncertain significance |
| rs368429546 | 7:99,764,372 | G/T | — | uncertain significance |
| rs779838710 | 7:99,764,384 | C/T | — | uncertain significance |
| rs760276260 | 7:99,764,399 | G/A | — | likely benign |
| rs1799085397 | 7:99,764,622 | G/A | — | uncertain significance |
| rs752372982 | 7:99,764,687 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.