MANBA 抗体
(Mannosidase, beta A, Lysosomal (MANBA))
This gene encodes a member of the glycosyl hydrolase 2 family. The encoded protein localizes to the lysosome where it is the final exoglycosidase in the pathway for N-linked glycoprotein oligosaccharide catabolism. Mutations in this gene are associated with beta-mannosidosis, a lysosomal storage disease that has a wide spectrum of neurological involvement. [provided by RefSeq, Jul 2008].
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Latest Publications for our MANBA 抗体
: "A MANBA mutation resulting in residual beta-mannosidase activity associated with severe leukoencephalopathy: a possible pseudodeficiency variant." in: BMC medical genetics, Vol. 10, pp. 84, (2009) (PubMed).Aliases for MANBA 抗体
mannosidase, beta A, lysosomal (manba) 抗体mannosidase beta (MANBA) 抗体
mannosidase, beta A, lysosomal L homeolog (manba.L) 抗体
Probable beta-mannosidase (C33G3.4) 抗体
beta-mannosidase (SCO6232) 抗体
beta-mannosidase (bmnA) 抗体
beta-mannosidase (THAPSDRAFT_262343) 抗体
Beta-mannosidase (Jden_1756) 抗体
beta-mannosidase (PAAG_08337) 抗体
Beta-mannosidase (Ndas_4827) 抗体
Beta-mannosidase (Spirs_1196) 抗体
beta-mannosidase (VDBG_07992) 抗体
Beta-mannosidase (RBRH_03524) 抗体
mannosidase, beta A, lysosomal (Manba) 抗体
mannosidase beta (Manba) 抗体
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