| Gene Symbol | ALG12 | 
| Entrez Gene ID | 79087 | 
| Full Name | ALG12, alpha-1,6-mannosyltransferase | 
| Synonyms | CDG1G,ECM39,PP14673,hALG12 | 
| General protein information | 
 | 
| Gene Type | protein-coding | 
| Organism | Homo sapiens(human) | 
| Genome | |
| Summary | This gene encodes a member of the glycosyltransferase 22 family. The encoded protein catalyzes the addition of the eighth mannose residue in an alpha-1,6 linkage onto the dolichol-PP-oligosaccharide precursor (dolichol-PP-Man(7)GlcNAc(2)) required for protein glycosylation. Mutations in this gene have been associated with congenital disorder of glycosylation type Ig (CDG-Ig)characterized by abnormal N-glycosylation. [provided by RefSeq, Jul 2008]. | 
| Disorder MIM: | |
| Disorder Html: | Congenital disorder of glycosylation, type Ig, 607143 (3) | 
 
                   
                 
                   
 
                   
                     
                   
                 
                   
                     
                     
                       
                     
                     
                       
                       
                         
			 
			 
			 
			 
			 
			 
			 
			 
			 
			 
             
                     
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
               
                                     
                                         
                                         User Manual
User Manual
 
                                                                         
       
       
        