This gene encodes an enzyme that hydrolyzes the terminal alpha-L-iduronic acid residues of two glycosaminoglycans, dermatan sulfate and heparan sulfate. This hydrolysis is required for the lysosomal degradation of these glycosaminoglycans. Mutations in this gene that result in enzymatic deficiency lead to the autosomal recessive disease mucopolysaccharidosis type I (MPS I). [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| IDUABA-20-REGO | 20 (40 μL) | 200 μL |
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| IDUABA-20-REGR | 20 (40 μL) | 200 μL |
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| IDUABA-20-ORGR | 20 (40 μL) | 200 μL |
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| IDUABA-20-GOGR | 20 (40 μL) | 200 μL |
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| IDUABA-20-GRRE | 20 (40 μL) | 200 μL |
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| IDUABA-20-GROR | 20 (40 μL) | 200 μL |
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| IDUABA-20-GRGO | 20 (40 μL) | 200 μL |
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| IDUABA-20-AQOR | 20 (40 μL) | 200 μL |
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This gene encodes an enzyme that hydrolyzes the terminal alpha-L-iduronic acid residues of two glycosaminoglycans, dermatan sulfate and heparan sulfate. This hydrolysis is required for the lysosomal degradation of these glycosaminoglycans. Mutations in this gene that result in enzymatic deficiency lead to the autosomal recessive disease mucopolysaccharidosis type I (MPS I). [provided by RefSeq, Jul 2008]
Gene Symbol : IDUA
Gene Name : Iduronidase, alpha-L-
Chromosome : CHR 4: 986,996-100,455,6
Locus : 4p16.3
Alt. Genes : ZNF263
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