GALNT18
polypeptide N-acetylgalactosaminyltransferase 18
Summary
Enables polypeptide N-acetylgalactosaminyltransferase activity. Involved in protein O-linked glycosylation. Predicted to be located in Golgi membrane. Predicted to be active in Golgi apparatus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs146661446 | 11:11,292,698 | G/A | — | uncertain significance |
| rs748319190 | 11:11,292,699 | C/T | — | uncertain significance |
| rs756823960 | 11:11,292,716 | T/C | — | uncertain significance |
| rs1227443446 | 11:11,292,719 | G/C | — | uncertain significance |
| rs774695210 | 11:11,292,749 | T/C | — | uncertain significance |
| rs202042081 | 11:11,292,768 | C/T | — | uncertain significance |
| rs200063803 | 11:11,292,780 | C/T | — | uncertain significance |
| rs1848821153 | 11:11,292,823 | C/G | — | uncertain significance |
| rs2539727998 | 11:11,292,824 | T/A | — | uncertain significance |
| rs16909324 | 11:11,306,686 | C/T | intron variant | — |
| rs1157398145 | 11:11,314,585 | C/A | — | uncertain significance |
| rs781639055 | 11:11,314,644 | G/A | — | uncertain significance |
| rs150701186 | 11:11,314,653 | C/T | — | uncertain significance |
| rs779735158 | 11:11,314,667 | C/T | — | uncertain significance |
| rs2539752484 | 11:11,314,676 | T/C | — | uncertain significance |
| rs116436785 | 11:11,348,721 | T/C | — | uncertain significance |
| rs779912079 | 11:11,354,261 | C/T | — | uncertain significance |
| rs372293544 | 11:11,354,305 | C/T | — | uncertain significance |
| rs1850042195 | 11:11,354,369 | T/C | — | uncertain significance |
| rs150122075 | 11:11,362,448 | C/T | — | uncertain significance |
| rs2538803536 | 11:11,362,476 | A/T | — | uncertain significance |
| rs2538803564 | 11:11,362,502 | G/T | — | uncertain significance |
| rs780515661 | 11:11,362,508 | C/T | — | uncertain significance |
| rs184216160 | 11:11,385,773 | A/G | intron variant | — |
| rs541834542 | 11:11,390,086 | T/C | — | — |
| rs201734768 | 11:11,398,885 | C/T | — | uncertain significance |
| rs777463455 | 11:11,398,891 | C/T | — | uncertain significance |
| rs768928094 | 11:11,400,637 | T/C | — | uncertain significance |
| rs375573422 | 11:11,400,652 | G/T | — | uncertain significance |
| rs368911998 | 11:11,400,740 | C/T | — | uncertain significance |
| rs1855294513 | 11:11,454,185 | T/C | — | uncertain significance |
| rs754112703 | 11:11,454,224 | C/T | — | uncertain significance |
| rs12278731 | 11:11,466,613 | C/T | intron variant | — |
| rs9988868 | 11:11,469,752 | G/T | intron variant | — |
| rs2538982441 | 11:11,470,382 | C/T | — | uncertain significance |
| rs747627683 | 11:11,470,385 | C/T | — | uncertain significance |
| rs561448006 | 11:11,472,425 | G/A | — | — |
| rs7940423 | 11:11,504,228 | G/A | intron variant | — |
| rs7105429 | 11:11,598,591 | G/A | — | — |
| rs57250050 | 11:11,606,095 | T/C | regulatory region variant | — |
| rs748134086 | 11:11,643,005 | G/T | — | uncertain significance |
| rs763235928 | 11:11,643,014 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.