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Alpha-L-fucosidase (EC 3.2.1.51) is a lysosomal enzyme involved in the degradation of fucose-containing glycoproteins and glycolipids (Occhiodoro et al., 1989 [PubMed 2803312]). At least 2 separate polymorphic alpha-L-fucosidases are recognized in man: that in tissues, FUCA1, which is deficient in fucosidosis (MIM 230000), and that in plasma, FUCA2 (MIM 136820).[supplied by OMIM].
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: A L fucosidase I; A L fucoside fucohydrolase 1; Alpha-L-fucosidase 1; Alpha-L-fucosidase I; Alpha-L-fucoside fucohydrolase 1; EC 3.2.1; EC 3.2.1.51; Fucosidase alpha-L-1 tissue; Fucosidase, alpha-L-1, tissue; Tissue alpha-L-fucosidase; Tissue α L fucosidase; α L fucosidase 1; α L fucosidase I; α L fucoside fucohydrolase 1
Gene Aliases: 0610006A03Rik; 9530055J05Rik; Afuc; Fuca; Fuca1
UniProt ID: (Rat) P17164, (Mouse) Q99LJ1
Entrez Gene ID: (Rat) 24375, (Mouse) 71665
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