The mutational spectrum in Treacher Collins syndrome reveals a predominance of mutations that create a premature-termination codon

Am J Hum Genet. 1997 Mar;60(3):515-24.


Treacher Collins syndrome (TCS) is an autosomal dominant disorder of craniofacial development, the features of which include conductive hearing loss and cleft palate. The TCS locus has been mapped to human chromosome 5q31.3-32 and the mutated gene identified. In the current investigation, 25 previously undescribed mutations, which are spread throughout the gene, are presented. This brings the total reported to date to 35, which represents a detection rate of 60%. Of the mutations that have been reported to date, all but one result in the introduction of a premature-termination codon into the predicted protein, treacle. Moreover, the mutations are largely family specific, although a common 5 bp deletion in exon 24 (seven different families) and a recurrent splicing mutation in intron 3 (two different families) have been identified. This mutational spectrum supports the hypothesis that TCS results from haploinsufficiency.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosomes, Human, Pair 5
  • Codon, Terminator / genetics*
  • Female
  • Humans
  • Male
  • Mandibulofacial Dysostosis / genetics*
  • Mutation*
  • Nuclear Proteins / genetics
  • Pedigree
  • Phosphoproteins / genetics
  • Polymorphism, Single-Stranded Conformational
  • RNA Splicing


  • Codon, Terminator
  • Nuclear Proteins
  • Phosphoproteins
  • TCOF1 protein, human