Structure and sequence of the human sulphamidase gene

DNA Res. 1996 Aug 31;3(4):269-71. doi: 10.1093/dnares/3.4.269.

Abstract

Sanfilippo A syndrome (MPS-IIIA) is a mucopolysaccharide lysosomal storage disorder caused by a deficiency in the lysosomal enzyme, sulphamidase (EC 3.10.1.1), which is required for the degradation of heparan sulphate. A genomic clone containing the entire sulphamidase gene was isolated from a chromosome 17-specific gridded cosmid library. The structure of the gene and the sequence of the exon/intron boundaries and the 5' promoter region were determined. The sulphamidase gene is split into 8 exons spanning approximately 11 kb.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Blotting, Northern
  • DNA, Complementary
  • Humans
  • Hydrolases / genetics*
  • Molecular Sequence Data

Substances

  • DNA, Complementary
  • Hydrolases
  • N-sulfoglucosamine sulfohydrolase

Associated data

  • GENBANK/U60107
  • GENBANK/U60108
  • GENBANK/U60109
  • GENBANK/U60110
  • GENBANK/U60111