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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| MANBA-20-RE | 20 (40 μL) | 200 μL |  |
Request Pricing |
| MANBA-20-OR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| MANBA-20-GO | 20 (40 μL) | 200 μL |  |
Request Pricing |
| MANBA-20-GR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| MANBA-20-AQ | 20 (40 μL) | 200 μL |  |
Request Pricing |
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]
Gene Symbol : MANBA
Gene Name : Mannosidase beta
Chromosome : CHR 4: 102,760,997-102,631,485
Locus : 4q24
Alt. Genes : OPTN
Lorem Ipsum is simply dummy text of the printing and typesetting industry.
Lorem Ipsum is simply dummy text of the printing and typesetting industry.