| Name | POMT1 |
| Reaction | Ser/Thr + Dol-P-Man = Man(a1-)Ser/Thr + Dol-P |
| Description | O-mannosyltransferase 1 |
| EC | EC 2.4.1.109 |
| DB | NCBI/Gene Swissprot/TrEMBL CAZy:GT39 |
| Gene deficient organisms | |
| Comment | |
| |
| Name | POMT2 |
| Reaction | Ser/Thr + Dol-P-Man = Man(a1-)Ser/Thr + Dol-P |
| Description | O-mannosyltransferase 2 |
| EC | EC 2.4.1.109 |
| DB | NCBI/Gene Swissprot/TrEMBL CAZy:GT39 |
| Gene deficient organisms | |
| Comment | |
| |
| Name | POMGnT1 |
| Reaction | Man(a1-)Ser/Thr + UDP-GlcNAc = GlcNAc(b1-2)Man(a1-)Ser/Thr + UDP |
| Description | protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase |
| EC | EC 2.4.1.- |
| DB | NCBI/Gene Swissprot/TrEMBL |
| Gene deficient organisms | |
| Comment | Muscular dystrophy and neuronal migration disorder are caused by mutations in a glycosyltransferase, POMGnT1.[7] |
| |
| Name | GalT |
| Reaction | GlcNAc(b1-2)Man(a1-)Ser/Thr + UDP-Gal = Gal(b1-4)GlcNAc(b1-2)Man(a1-)Ser/Thr + UDP |
| Description | |
| EC | |
| DB | NCBI/Gene Swissprot/TrEMBL |
| Gene deficient organisms | |
| Comment | |
| |
