GALNT16
polypeptide N-acetylgalactosaminyltransferase 16
Summary
Enables polypeptide N-acetylgalactosaminyltransferase activity. Involved in protein O-linked glycosylation via serine and protein O-linked glycosylation via threonine. Predicted to be located in Golgi membrane. Predicted to be active in Golgi apparatus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs970107609 | 14:69,727,119 | C/T | — | uncertain significance |
| rs1245161409 | 14:69,727,120 | G/A | — | uncertain significance |
| rs749129208 | 14:69,727,134 | G/T | — | uncertain significance |
| rs79805373 | 14:69,736,557 | G/A | intron variant | — |
| rs7150195 | 14:69,740,483 | T/G | intron variant | — |
| rs7141058 | 14:69,751,819 | A/G | intron variant | — |
| rs267604038 | 14:69,787,435 | G/A | — | uncertain significance |
| rs984809988 | 14:69,787,444 | C/T | — | uncertain significance |
| rs1448796873 | 14:69,787,457 | T/A | — | uncertain significance |
| rs775973077 | 14:69,787,474 | C/T | — | uncertain significance |
| rs754723049 | 14:69,787,534 | A/C | — | uncertain significance |
| rs778518465 | 14:69,787,543 | A/T | — | uncertain significance |
| rs1273242900 | 14:69,787,557 | C/T | — | uncertain significance |
| rs775681302 | 14:69,787,569 | G/A | — | uncertain significance |
| rs762619892 | 14:69,791,471 | A/G | — | uncertain significance |
| rs761614171 | 14:69,791,479 | C/T | — | uncertain significance |
| rs2503623126 | 14:69,791,503 | A/G | — | uncertain significance |
| rs774434799 | 14:69,792,679 | C/T | — | uncertain significance |
| rs138742665 | 14:69,792,727 | G/A | — | uncertain significance |
| rs991910123 | 14:69,795,253 | G/A | — | uncertain significance |
| rs61746597 | 14:69,795,270 | G/T | — | uncertain significance |
| rs543194043 | 14:69,798,190 | C/T | — | uncertain significance |
| rs2503645594 | 14:69,798,209 | T/C | — | uncertain significance |
| rs2503650672 | 14:69,799,843 | C/G | — | uncertain significance |
| rs772987286 | 14:69,799,861 | C/T | — | uncertain significance |
| rs2045444687 | 14:69,805,383 | T/C | — | uncertain significance |
| rs2503666008 | 14:69,805,397 | G/A | — | uncertain significance |
| rs2503666394 | 14:69,805,467 | C/G | — | uncertain significance |
| rs1249446889 | 14:69,806,288 | A/C | — | uncertain significance |
| rs2503669365 | 14:69,806,299 | G/A | — | uncertain significance |
| rs371505126 | 14:69,808,406 | C/T | — | uncertain significance |
| rs143736198 | 14:69,808,415 | A/T | — | uncertain significance |
| rs754157094 | 14:69,813,759 | T/G | — | uncertain significance |
| rs1243201366 | 14:69,813,761 | C/T | — | uncertain significance |
| rs144096232 | 14:69,813,764 | G/A | — | uncertain significance |
| rs759999006 | 14:69,813,774 | C/T | — | likely benign |
| rs760810166 | 14:69,813,885 | C/T | — | uncertain significance |
| rs2045587382 | 14:69,814,594 | G/T | — | uncertain significance |
| rs201756553 | 14:69,814,612 | C/T | — | uncertain significance |
| rs769803181 | 14:69,814,655 | C/T | — | uncertain significance |
| rs773637812 | 14:69,814,685 | T/C | — | uncertain significance |
| rs2503692418 | 14:69,814,712 | G/A | — | uncertain significance |
| rs144512254 | 14:69,818,847 | G/A | — | uncertain significance |
| rs7144886 | 14:69,831,037 | A/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.