A new spontaneous mutation in the mouse Ames waltzer gene, Pcdh15

Lori L. Hampton, Charles G. Wright, Kumar N. Alagramam, James F. Battey, Konrad Noben-Trauth

Research output: Contribution to journalArticlepeer-review

20 Scopus citations


A recessive deafness mutation in the mouse arose spontaneously and was identified in a colony segregating a null allele of the gastrin-releasing peptide receptor (Grpr) locus. Auditory-evoked brain stem response measurements revealed deafness in 7-week-old affected mice. By linkage analyses, the mutant phenotype was mapped near marker D10Mit186 and the protocadherin gene Pcdh15. As shown by complementation testing, the new mutation is allelic with Ames waltzer (Pcdh15av). Sequencing mutant-derived brain Pcdh15 cDNAs identified the insertion of a cytosine residue at nucleotide position c2099 (2099insC), which results in a frame-shift and premature stop codon. Abnormal stereocilia on inner and outer hair cells of the organ of Corti were identified by scanning electron microscopy as early as postnatal day 0 and cross-sectional histology revealed severe neuroepithelial degeneration in cochleas of 30-50-day-old mutants. The new allele of Ames waltzer, designated Pcdh15av-Jfb, may aid in studying the histopathology associated with Usher syndrome type 1F, which is caused by a functional null allele of PCDH15.

Original languageEnglish (US)
Pages (from-to)67-75
Number of pages9
JournalHearing Research
Issue number1-2
StatePublished - Jun 2003


  • Ames waltzer
  • Deafness
  • Protocadherin 15 (Pcdh15)

ASJC Scopus subject areas

  • Sensory Systems


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