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Has lost the ability to synthesize Forssman glycolipid antigen (FORS1/FG. Might have acquired an alternative function in glycosphingolipid metabolism, but it remains to be established. It appears to have drifted more slowly than confirmed pseudogenes in the glycosyltransferase 6 family, suggesting that it has remained under evolutionary pressure.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Forssman glycolipid synthase; Forssman glycolipid synthase-like protein; forssman glycolipid synthetase; Forssman glycolipid synthetase (FS); Globoside alpha-1,3-N-acetylgalactosaminyltransferase 1; similar to globoside alpha-1,3-N-acetylgalactosaminyltransferase 1
Gene Aliases: A3GALNT; Fgs; FS; GBGT1; UNQ2513; UNQ2513/PRO6002
UniProt ID: (Human) Q8N5D6, (Mouse) Q8VI38
Entrez Gene ID: (Human) 26301, (Mouse) 227671, (Rat) 499764
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