Species Human Entrez 3423 | Human Mouse Ensembl ENSG00000010404 | |
External IDs OMIM: 300823 MGI: 96417 HomoloGene: 169 GeneCards: IDS |
Iduronate 2-sulfatase (IDS) is a sulfatase enzyme associated with Hunter syndrome.
Function
Iduronate 2-sulfatase is required for the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations in this X-chromosome gene that result in enzymatic deficiency lead to the sex-linked mucopolysaccharidosis type II, also known as Hunter syndrome. Iduronate-2-sulfatase has a strong sequence homology with human arylsulfatases A, B, and C, and human glucosamine-6-sulfatase. A splice variant of this gene has been described.
References
Iduronate-2-sulfatase Wikipedia(Text) CC BY-SA