Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residues

Eur J Hum Genet. 1999 Jul;7(5):615-9. doi: 10.1038/sj.ejhg.5200341.

Abstract

Thirty newly detected mutations in the PHEX gene are reported, and pooled with all the previously published mutations. The spectrum of mutations displayed 16% deletions, 8% insertions, 34% missense, 27% nonsense, and 15% splice site mutations, with two peaks in exon 15, and 17. Since 32.8% of PHEX amino acids were conserved in the endopeptidases family, the number of missense mutations detected at non-conserved residues was smaller than expected, whereas the number of nonsense mutations observed at non-conserved residues was very close to the expected number. Compared with conserved amino acids, the changes in non-conserved amino acids may result in benign polymorphisms or possibly mild disease that may go undiagnosed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Exons
  • Female
  • Genotype
  • Humans
  • Male
  • Mutation*
  • Open Reading Frames
  • PHEX Phosphate Regulating Neutral Endopeptidase
  • Phenotype
  • Proteins / genetics*

Substances

  • Proteins
  • PHEX Phosphate Regulating Neutral Endopeptidase
  • PHEX protein, human