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Galactose-1-phosphate uridyl transferase (GALT) catalyzes the second step of the Leloir pathway of galactose metabolism, namely the conversion of UDP-glucose + galactose-1-phosphate to glucose-1-phosphate + UDP-galactose. The absence of this enzyme results in classic galactosemia in humans and can be fatal in the newborn period if lactose is not removed from the diet. The pathophysiology of galactosemia has not been clearly defined.
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Protein Aliases: Gal-1-P uridylyltransferase; galactose-1-phosphate uridyl transferase; Galactose-1-phosphate uridylyltransferase; UDP-glucose--hexose-1-phosphate uridylyltransferase
Gene Aliases: GALT
UniProt ID: (Human) Q53XK1
Entrez Gene ID: (Human) 2592
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