The protein encoded by this gene is a lysosomal enzyme involved in the degradation of fucose-containing glycoproteins and glycolipids. Mutations in this gene are associated with fucosidosis (FUCA1D), which is an autosomal recessive lysosomal storage disease. A pseudogene of this locus is present on chr 2.[provided by RefSeq, Oct 2009].
Latest Publications for our Fucosidase, alpha-L- 1, Tissue 抗体
Nandakumar, Hsu, Lin, Lo, Lo, Lin: "Detection of Human ?-L-Fucosidases by a Quinone Methide-Generating Probe: Enhanced Activities in Response to Helicobacter pylori Infection." in: Chembiochem : a European journal of chemical biology, Vol. 16, Issue 11, pp. 1555-9, (2015) (PubMed).
Gustafson, Shepherd, Miller, Jayachandran: "Age- and sex-specific differences in blood-borne microvesicles from apparently healthy humans." in: Biology of sex differences, Vol. 6, pp. 10, (2015) (PubMed).