GALNTL6
polypeptide N-acetylgalactosaminyltransferase like 6
Summary
Enables polypeptide N-acetylgalactosaminyltransferase activity. Involved in 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 |
|---|---|---|---|---|
| rs1491617 | 4:173,033,976 | C/T | intron variant | — |
| rs6815512 | 4:173,075,232 | A/T | — | — |
| rs6852117 | 4:173,076,888 | C/G | intron variant | — |
| rs6811532 | 4:173,086,492 | A/G | intron variant | — |
| rs973599 | 4:173,141,903 | A/G | intron variant | — |
| rs749051811 | 4:173,150,880 | A/T | — | uncertain significance |
| rs761483452 | 4:173,232,810 | A/G | — | uncertain significance |
| rs746294876 | 4:173,232,893 | C/T | — | uncertain significance |
| rs143943063 | 4:173,238,414 | T/C | intron variant | — |
| rs333414 | 4:173,261,630 | T/C | intron variant | — |
| rs143545755 | 4:173,269,681 | C/T | — | uncertain significance |
| rs1450015829 | 4:173,269,738 | G/C | — | uncertain significance |
| rs187766040 | 4:173,291,230 | C/T | intron variant | — |
| rs143791481 | 4:173,385,102 | G/A | intron variant | — |
| rs756771238 | 4:173,392,198 | A/G | — | — |
| rs1455126 | 4:173,467,522 | C/A | — | — |
| rs7696322 | 4:173,502,461 | T/C | intron variant | — |
| rs35980999 | 4:173,505,231 | A/G | — | — |
| rs12505030 | 4:173,515,224 | G/A | intron variant | — |
| rs6831785 | 4:173,520,551 | C/T | intron variant | — |
| rs4695878 | 4:173,521,023 | G/A | intron variant | — |
| rs181972414 | 4:173,587,687 | C/T | intron variant | — |
| rs891843933 | 4:173,730,548 | G/A | — | uncertain significance |
| rs146548110 | 4:173,730,599 | G/A | — | uncertain significance |
| rs189797609 | 4:173,730,605 | G/A | — | uncertain significance |
| rs760911328 | 4:173,734,751 | A/G | — | uncertain significance |
| rs375298105 | 4:173,734,795 | G/A | — | uncertain significance |
| rs1220760916 | 4:173,734,852 | G/A | — | uncertain significance |
| rs752243982 | 4:173,803,979 | G/A | — | uncertain significance |
| rs760406869 | 4:173,803,981 | A/G | — | uncertain significance |
| rs774850813 | 4:173,852,381 | G/A | — | uncertain significance |
| rs1466953930 | 4:173,873,322 | G/T | — | uncertain significance |
| rs755470500 | 4:173,873,371 | T/C | — | uncertain significance |
| rs1296628437 | 4:173,873,380 | G/A | — | uncertain significance |
| rs377199176 | 4:173,873,390 | C/T | — | uncertain significance |
| rs137921635 | 4:173,930,380 | G/A | — | uncertain significance |
| rs201835999 | 4:173,930,407 | G/A | — | uncertain significance |
| rs201464822 | 4:173,942,658 | G/A | — | uncertain significance |
| rs143941607 | 4:173,942,720 | G/A | — | uncertain significance |
| rs1431682391 | 4:173,961,130 | A/G | — | uncertain significance |
| rs745423532 | 4:173,961,142 | A/G | — | uncertain significance |
| rs1753840928 | 4:173,961,145 | A/T | — | uncertain significance |
| rs377273020 | 4:173,961,154 | T/C | — | uncertain significance |
| rs765257084 | 4:173,961,157 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.