A novel single basepair insertion in exon 6 of the Bruton's tyrosine kinase (Btk) gene from a Japanese X-linked agammaglobulinemia patient with growth hormone insufficiency

Hum Mutat. 1998;11(4):336.

Abstract

A novel insertion mutation in exon 6 of the Btk gene was detected in a 17 year-old XLA patient with GH insufficiency. We synthesized cDNA from leukocyte total RNA and amplified every region of the Btk-coding sequence. Sequencing of cDNA fragments revealed a single basepair insertion mutation at codon 157 in exon 6 (CAG-->CAAG) which leads to premature termination at codon 193 in exon 7. To confirm the results, we also performed a PCR-DdeI digestion analysis using leukocyte genomic DNA. The PCR product from the patient's genomic DNA was uncleaved with DdeI, as expected. PCR-DdeI digestion analysis of the family members showed that the mother and elder sister were carriers with the mutation and that the younger sister did not carry the mutation.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Agammaglobulinaemia Tyrosine Kinase
  • Agammaglobulinemia / genetics*
  • Agammaglobulinemia / physiopathology
  • Base Sequence
  • Codon, Terminator / genetics
  • DNA Primers / genetics
  • Exons
  • Female
  • Frameshift Mutation
  • Genetic Linkage
  • Human Growth Hormone / deficiency*
  • Humans
  • Male
  • Mutation*
  • Polymerase Chain Reaction
  • Protein-Tyrosine Kinases / genetics*
  • X Chromosome / genetics

Substances

  • Codon, Terminator
  • DNA Primers
  • Human Growth Hormone
  • Protein-Tyrosine Kinases
  • Agammaglobulinaemia Tyrosine Kinase
  • BTK protein, human