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Chromosomal localization of the gene for human glucosamine-6-sulphatase to 12q14

✍ Scribed by Daniel A. Robertson; David F. Callen; Elizabeth G. Baker; C. Phillip Morris; John J. Hopwood


Publisher
Springer
Year
1988
Tongue
English
Weight
505 KB
Volume
79
Category
Article
ISSN
0340-6717

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✦ Synopsis


Glucosamine-6-sulphatase (G6S), a lysosomal enzyme found in all cells, is involved in the catabolism of heparin, heparan sulphate, and keratan sulphate. Deficiency of G6S results in the accumulation of undegraded substrate and the lysosomal storage disorder mucopolysaccharidosis type IIID (Sanfilippo D syndrome). Regional mapping by in situ hybridization of a 3H-labelled human G6S cDNA probe to human metaphase chromosomes indicated that the G6S gene is localized to chromosome 12 at q14. The localization of the G6S gene to chromosome 12 was confirmed using the G6S cDNA clone in Southern blot hybridization analysis of DNA from human x mouse hybrid cell lines.


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