PAX3

Summary

Gene Symbol: PAX3
Description: paired box 3
Alias: paired box gene 3 (Waardenburg syndrome 1), paired-box 3 protein
Species: dog

Publications

  1. Assignment of the canine paired-box 3 (PAX3) gene to chromosome 37q16-->q17 by in situ hybridization
    A Krempler
    Institute of Veterinary Medicine, University of Göttingen, Germany
    Cytogenet Cell Genet 90:66-7
  2. Analysis of the 5' region of the canine PAX3 gene and exclusion as a candidate for Dalmatian deafness
    B Brenig
    Institute of Veterinary Medicine, University of Goettingen, Goettingen, Germany
    Anim Genet 34:47-50
  3. Linkage mapping of the primary disease locus for collie eye anomaly
    Jennifer K Lowe
    Division of Human Biology, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue North, D4 100, Seattle, WA 98109 1024, USA
    Genomics 82:86-95

Scientific Experts

  • B Brenig
  • Jennifer K Lowe
  • A Krempler
  • Ewen F Kirkness
  • Gustavo D Aguirre
  • Gregory M Acland
  • Anna V Kukekova
  • Elaine A Ostrander
  • Mariela C Langlois
  • M Breen

Detail Information

Publications3

  1. Assignment of the canine paired-box 3 (PAX3) gene to chromosome 37q16-->q17 by in situ hybridization
    A Krempler
    Institute of Veterinary Medicine, University of Göttingen, Germany
    Cytogenet Cell Genet 90:66-7
  2. Analysis of the 5' region of the canine PAX3 gene and exclusion as a candidate for Dalmatian deafness
    B Brenig
    Institute of Veterinary Medicine, University of Goettingen, Goettingen, Germany
    Anim Genet 34:47-50
    ..in melanocyte migration and differentiation as integral component of the inner ear, we hypothesized that the canine PAX3 (paired box homeotic gene 3) gene could be a candidate for Dalmatian deafness...
  3. Linkage mapping of the primary disease locus for collie eye anomaly
    Jennifer K Lowe
    Division of Human Biology, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue North, D4 100, Seattle, WA 98109 1024, USA
    Genomics 82:86-95
    ..076), in a region corresponding to human chromosome 2q35. These results suggest the presence of a developmental regulatory gene important in ocular embryogenesis, with potential implications for other disorders of ocular vascularization...