rs180984980

This variant is located in the IDUA gene.

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ClinVar annotation

Conflicting Classifications
6 submitters6 publications

Mucopolysaccharidosis type 1; Inborn genetic diseases; not provided

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About IDUA

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]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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