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SGSH

Official Full Name
N-sulfoglucosamine sulfohydrolase
Organism
Homo sapiens
GeneID
6448
Background
This gene encodes the enzyme sulfamidase; one of several enzymes involved in the lysosomal degradation of heparan sulfate. Mutations in this gene are associated with the lysosomal storage disease mucopolysaccaridosis IIIA, also known as Sanfilippo syndrome A, which results from impaired degradation of heparan sulfate. Transcripts of varying sizes have been reported but their biological validity has not been determined. [provided by RefSeq, Jun 2017]
Synonyms
HSS; SFMD; MPS3A;

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