A novel splice site mutation of the EXT2 gene in a Finnish hereditary multiple exostoses family. Mutations in brief no. 197. Online

Hum Mutat. 1998;12(5):362. doi: 10.1002/(sici)1098-1004(1998)12:5<304::aid-humu3>3.3.co;2-y.

Abstract

Hereditary multiple exostoses is a dominantly inherited disease characterized by multiple benign osteochondromas. The affected individuals have an increased risk of developing sarcoma. A large Finnish family with hereditary multiple exostosis was analyzed to find the disease-causing mutation. Blood samples were obtained from 35 family members, including 21 affected and 14 unaffected individuals. Using 2-point linkage analysis the EXT phenotype was shown to be linked to the recently cloned EXT2 gene on chromosome 11p11. The coding region of the gene was sequenced and a previously unreported splice site mutation found. This G to T transversion within a 5-prime splice donor site following exon 6 was shown to cause aberrant splicing of RNA. The described change is considered to be a novel disease-causing mutation in the EXT2 gene.

MeSH terms

  • Alternative Splicing / genetics*
  • Chromosomes, Human, Pair 11 / genetics
  • Exostoses, Multiple Hereditary / genetics*
  • Humans
  • N-Acetylglucosaminyltransferases*
  • Point Mutation / genetics*
  • Proteins / genetics*

Substances

  • Proteins
  • N-Acetylglucosaminyltransferases
  • exostosin-2