Puneet Varma (Editor)

Iduronate 2 sulfatase

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Species
  
Human

Entrez
  
3423

Human
  
Mouse

Ensembl
  
ENSG00000010404

Aliases
  
IDS, MPS2, Siduronate 2-sulfatase

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