NDST4
N-deacetylase and N-sulfotransferase 4
Summary
Predicted to enable deacetylase activity and heparan sulfate N-sulfotransferase activity. Predicted to be involved in heparan sulfate proteoglycan biosynthetic process and heparin proteoglycan biosynthetic process. Predicted to be located in Golgi membrane. Predicted to be active in Golgi apparatus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants52 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs990269402 | 4:115,749,071 | A/C | — | uncertain significance |
| rs771184078 | 4:115,749,084 | G/A | — | uncertain significance |
| rs148745383 | 4:115,750,971 | C/T | — | uncertain significance |
| rs200457179 | 4:115,751,002 | T/C | — | uncertain significance |
| rs140482377 | 4:115,754,831 | G/A | — | uncertain significance |
| rs774392218 | 4:115,760,553 | G/T | — | uncertain significance |
| rs1446583230 | 4:115,760,587 | C/T | — | uncertain significance |
| rs200463704 | 4:115,760,640 | C/T | — | uncertain significance |
| rs960873160 | 4:115,760,644 | T/C | — | likely benign |
| rs2476753505 | 4:115,767,017 | G/A | — | uncertain significance |
| rs565794015 | 4:115,767,019 | A/G | — | uncertain significance |
| rs777081214 | 4:115,767,029 | T/A | — | uncertain significance |
| rs369719779 | 4:115,767,053 | C/A | — | uncertain significance |
| rs760252865 | 4:115,767,059 | G/A | — | uncertain significance |
| rs1723596110 | 4:115,769,375 | C/G | — | uncertain significance |
| rs781538417 | 4:115,769,438 | G/A | — | uncertain significance |
| rs148854444 | 4:115,769,450 | T/C | — | uncertain significance |
| rs775011469 | 4:115,769,458 | G/C | — | uncertain significance |
| rs146949694 | 4:115,769,478 | A/G | — | likely benign |
| rs2476758067 | 4:115,769,482 | A/G | — | uncertain significance |
| rs183643524 | 4:115,769,485 | G/A | — | uncertain significance |
| rs2126196806 | 4:115,791,953 | A/C | — | uncertain significance |
| rs201752251 | 4:115,792,064 | G/A | — | uncertain significance |
| rs187967316 | 4:115,834,521 | T/C | intron variant | — |
| rs2476928259 | 4:115,856,489 | A/T | — | uncertain significance |
| rs1725655623 | 4:115,858,650 | T/C | — | uncertain significance |
| rs1303093395 | 4:115,880,164 | T/A | — | — |
| rs200191868 | 4:115,891,701 | C/T | — | uncertain significance |
| rs1015339872 | 4:115,898,395 | C/G | — | uncertain significance |
| rs2477064483 | 4:115,898,405 | A/C | — | uncertain significance |
| rs13150562 | 4:115,957,593 | T/C | — | — |
| rs516638 | 4:115,979,468 | T/G | — | — |
| rs533950 | 4:115,981,549 | G/A | — | — |
| rs1284729229 | 4:115,997,271 | T/C | — | uncertain significance |
| rs138579687 | 4:115,997,346 | T/C | — | likely benign |
| rs2477386359 | 4:115,997,349 | G/A | — | uncertain significance |
| rs1056444301 | 4:115,997,385 | G/A | — | uncertain significance |
| rs367584567 | 4:115,997,459 | G/A | — | uncertain significance |
| rs774731806 | 4:115,997,519 | T/C | — | uncertain significance |
| rs764114208 | 4:115,997,690 | T/C | — | uncertain significance |
| rs200476917 | 4:115,997,706 | C/T | — | uncertain significance |
| rs1327129332 | 4:115,997,753 | C/T | — | uncertain significance |
| rs1483243590 | 4:115,997,823 | C/T | — | uncertain significance |
| rs778348193 | 4:115,997,843 | A/G | — | uncertain significance |
| rs145767700 | 4:115,997,847 | C/A | — | uncertain significance |
| rs750499631 | 4:115,997,886 | G/C | — | uncertain significance |
| rs766300712 | 4:115,997,981 | A/G | — | uncertain significance |
| rs781089432 | 4:115,998,039 | A/G | — | uncertain significance |
| rs139617299 | 4:115,998,083 | T/C | — | uncertain significance |
| rs142820981 | 4:115,998,150 | T/C | — | uncertain significance |
| rs372475983 | 4:115,998,170 | C/T | — | uncertain significance |
| rs72667319 | 4:116,001,098 | T/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.