This gene encodes a member of the N-terminal nucleophile (Ntn) hydrolase family of proteins. The encoded preproprotein is proteolytically processed to generate alpha and beta chains that comprise the mature enzyme. This enzyme is involved in the catabolism of N-linked oligosaccharides of glycoproteins. It cleaves asparagine from N-acetylglucosamines as one of the final steps in the lysosomal breakdown of glycoproteins. Mutations in this gene are associated with the lysosomal storage disease aspartylglycosaminuria that results in progressive neurodegeneration. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is subject to proteolytic processing. [provided by RefSeq, Nov 2015]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| AGABA-20-REGO | 20 (40 μL) | 200 μL |
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| AGABA-20-REGR | 20 (40 μL) | 200 μL |
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| AGABA-20-ORGR | 20 (40 μL) | 200 μL |
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| AGABA-20-GOGR | 20 (40 μL) | 200 μL |
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| AGABA-20-GRRE | 20 (40 μL) | 200 μL |
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| AGABA-20-GROR | 20 (40 μL) | 200 μL |
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| AGABA-20-GRGO | 20 (40 μL) | 200 μL |
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| AGABA-20-AQOR | 20 (40 μL) | 200 μL |
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This gene encodes a member of the N-terminal nucleophile (Ntn) hydrolase family of proteins. The encoded preproprotein is proteolytically processed to generate alpha and beta chains that comprise the mature enzyme. This enzyme is involved in the catabolism of N-linked oligosaccharides of glycoproteins. It cleaves asparagine from N-acetylglucosamines as one of the final steps in the lysosomal breakdown of glycoproteins. Mutations in this gene are associated with the lysosomal storage disease aspartylglycosaminuria that results in progressive neurodegeneration. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is subject to proteolytic processing. [provided by RefSeq, Nov 2015]
Gene Symbol : AGA
Gene Name : Aspartylglucosaminidase
Chromosome : CHR 4: 177,442,502-177,430,773
Locus : 4q34.3
Alt. Genes : HIPK3
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