| ALG2 | 
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| Identifiers | 
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| Aliases | ALG2, CDGIi, NET38, hALPG2, CMS14, CMSTA3, alpha-1,3/1,6-mannosyltransferase, CDG1I, ALG2 alpha-1,3/1,6-mannosyltransferase | 
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| External IDs | OMIM: 607905; MGI: 1914731; HomoloGene: 5930; GeneCards: ALG2; OMA:ALG2 - orthologs | 
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| | Gene location (Mouse) | 
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 |  |  | Chr. | Chromosome 4 (mouse) | 
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 |  |  | Band | 4|4 B1 | Start | 47,465,067 bp | 
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 | End | 47,474,333 bp | 
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| | RNA expression pattern | 
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 | Bgee | | Human | Mouse (ortholog) | 
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 | | Top expressed in |  | pancreatic epithelial cell
 corpus epididymis
 caput epididymis
 secondary oocyte
 germinal epithelium
 tibia
 islet of Langerhans
 body of pancreas
 visceral pleura
 parietal pleura
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 | | Top expressed in |  | median eminence
 dorsomedial hypothalamic nucleus
 paraventricular nucleus of hypothalamus
 supraoptic nucleus
 arcuate nucleus
 dorsal tegmental nucleus
 ventral tegmental area
 suprachiasmatic nucleus
 habenula
 lateral hypothalamus
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 |  | More reference expression data | 
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 | BioGPS |  | 
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| Wikidata | 
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Alpha-1,3/1,6-mannosyltransferase ALG2 is an enzyme that is encoded by the ALG2 gene.  Mutations in the human gene are associated with congenital defects in glycosylation  The protein encoded by the ALG2 gene belongs to two classes of enzymes: GDP-Man:Man1GlcNAc2-PP-dolichol alpha-1,3-mannosyltransferase (EC 2.4.1.132) and GDP-Man:Man2GlcNAc2-PP-dolichol alpha-1,6-mannosyltransferase (EC 2.4.1.257).