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HGSNAT

Official Full Name
heparan-alpha-glucosaminide N-acetyltransferase
Organism
Homo sapiens
GeneID
138050
Background
This gene encodes a lysosomal acetyltransferase, which is one of several enzymes involved in the lysosomal degradation of heparin sulfate. Mutations in this gene are associated with Sanfilippo syndrome C, one type of the lysosomal storage disease mucopolysaccaridosis III, which results from impaired degradation of heparan sulfate. [provided by RefSeq, Jan 2009]
Synonyms
RP73; HGNAT; MPS3C; TMEM76;

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