The protein encoded by this gene is a type II transmembrane protein that resides in the golgi. It participates in O-mannosyl glycosylation, and is specific for alpha linked terminal mannose. Mutations in this gene are associated with muscle-eye-brain (MEB) disease. Alternatively spliced transcript variants have been found for this gene.
POMGNT1; protein O-linked mannose beta1,2-N-acetylglucosaminyltransferase; protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1; FLJ20277; MGAT1.2; protein O mannose beta 1; 2 N acetylglucosaminyltransferase; UDP-GlcNAc:alpha-D-mannoside be; UDP-GlcNAc:alpha-D-mannoside beta-1,2-N-acetylglucosaminyltransferase I.2; MEB; GNTI.2; MDDGA3; MDDGB3; MDDGC3; GnT I.2; gnT-I.2; DKFZp761B182; RP11-322N21.3, DKFZp761B182, FLJ20277, GNTI.2, GnT I.2, MDDGA3, MDDGB3, MDDGC3, MEB, MGAT1.2, gnT-I.2, POMGNT1; protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-); zPOMGnT1; im:7151461; zgc:158130; Protein O-Mannose beta-1,2-N-acetylglucosaminyltransferase 1; protein O