HS6ST2
heparan sulfate 6-O-sulfotransferase 2
Summary
Heparan sulfate proteoglycans are ubiquitous components of the cell surface, extracellular matrix, and basement membranes, and interact with various ligands to influence cell growth, differentiation, adhesion, and migration. This gene encodes a member of the heparan sulfate (HS) sulfotransferase gene family, which catalyze the transfer of sulfate to HS. Different family members and isoforms are thought to synthesize heparan sulfates with tissue-specific structures and functions. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Known Variants64 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs760879396 | X:131,762,311 | C/T | — | likely benign |
| rs1425420882 | X:131,762,336 | G/A | — | likely benign |
| rs1379425881 | X:131,762,345 | C/T | — | uncertain significance |
| rs374128505 | X:131,762,346 | G/A | — | uncertain significance |
| rs2523291901 | X:131,762,401 | G/C | — | uncertain significance |
| rs367714566 | X:131,762,447 | G/A | — | uncertain significance |
| rs2063494024 | X:131,762,465 | T/C | — | uncertain significance |
| rs755385990 | X:131,762,497 | C/G | — | uncertain significance |
| rs202245508 | X:131,762,508 | G/T | — | uncertain significance |
| rs2063494629 | X:131,762,523 | C/T | — | uncertain significance |
| rs267606357 | X:131,762,534 | C/T | — | uncertain significance |
| rs201186035 | X:131,762,541 | C/A | — | likely benign |
| rs368413228 | X:131,762,549 | T/G | — | uncertain significance |
| rs2523292739 | X:131,762,570 | T/C | — | uncertain significance |
| rs2523292887 | X:131,762,614 | C/A | — | uncertain significance |
| rs1190798652 | X:131,762,651 | A/G | — | uncertain significance |
| rs145272508 | X:131,762,658 | C/T | — | benign |
| rs762429850 | X:131,762,708 | G/A | — | uncertain significance |
| rs966651728 | X:131,762,783 | G/A | — | uncertain significance |
| rs758915436 | X:131,762,850 | C/G | — | conflicting classifications of pathogenicity |
| rs764683533 | X:131,762,858 | T/C | — | uncertain significance |
| rs748100852 | X:131,762,948 | G/T | — | conflicting classifications of pathogenicity |
| rs772058407 | X:131,762,963 | T/C | — | uncertain significance |
| rs2523294167 | X:131,762,969 | C/T | — | uncertain significance |
| rs1448659572 | X:131,763,007 | C/G | — | uncertain significance |
| rs183103 | X:131,768,905 | T/C | intron variant | — |
| rs243466 | X:131,802,339 | G/A | coding sequence variant | — |
| rs762311620 | X:131,803,144 | C/T | — | uncertain significance |
| rs767217888 | X:131,803,150 | T/C | — | uncertain significance |
| rs761023821 | X:131,803,163 | G/A | — | uncertain significance |
| rs369708094 | X:131,803,197 | G/A | — | likely benign |
| rs2523375602 | X:131,803,214 | C/A | — | uncertain significance |
| rs761216951 | X:131,803,216 | C/T | — | uncertain significance |
| rs143752287 | X:131,842,495 | T/C | — | likely benign |
| rs62599022 | X:131,890,506 | C/A | — | — |
| rs5977755 | X:131,940,440 | G/C | intron variant | — |
| rs7892161 | X:132,024,504 | C/G | — | — |
| rs1198179034 | X:132,090,842 | G/C | — | uncertain significance |
| rs868295125 | X:132,090,866 | C/G | — | uncertain significance |
| rs866919041 | X:132,090,867 | C/G | — | pathogenic |
| rs2524055434 | X:132,090,878 | G/A | — | uncertain significance |
| rs2524055806 | X:132,090,947 | G/C | — | uncertain significance |
| rs2524056624 | X:132,091,056 | C/T | — | uncertain significance |
| rs369040064 | X:132,091,096 | G/C | — | uncertain significance |
| rs746316980 | X:132,091,131 | T/G | — | uncertain significance |
| rs1032518524 | X:132,091,140 | G/C | — | uncertain significance |
| rs2067086898 | X:132,091,179 | C/A | — | uncertain significance |
| rs1245417639 | X:132,091,211 | G/C | — | likely benign |
| rs2524057897 | X:132,091,215 | C/T | — | likely benign |
| rs2067089167 | X:132,091,247 | T/C | — | uncertain significance |
| rs917762811 | X:132,092,247 | G/C | — | uncertain significance |
| rs2524063680 | X:132,092,278 | C/T | — | uncertain significance |
| rs1314814300 | X:132,092,309 | C/T | — | uncertain significance |
| rs201640022 | X:132,092,310 | C/A | — | benign |
| rs763422749 | X:132,092,377 | G/A | — | uncertain significance |
| rs1384043599 | X:132,092,394 | C/T | — | likely benign |
| rs1343137006 | X:132,092,476 | G/A | — | uncertain significance |
| rs202179309 | X:132,092,479 | C/A | — | benign |
| rs181526961 | X:132,092,485 | G/A | — | benign |
| rs769385715 | X:132,092,542 | C/A | — | conflicting classifications of pathogenicity |
| rs1276990594 | X:132,092,564 | C/A | — | uncertain significance |
| rs1292550156 | X:132,092,613 | A/T | — | uncertain significance |
| rs1199392308 | X:132,092,615 | A/G | — | uncertain significance |
| rs2524066109 | X:132,092,617 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.