cosa Gene Detail

Summary

• Symbol
  cosa
• Name
  cochleo-saccular defects

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:3665146
• Alliance
  gene page

Location &
Maps

• Sequence Map
  Genome coordinates not available from the current reference assembly.

• Genetic Map
  Chromosome Unknown

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  13 phenotypes from 1 allele in 1 genetic background
  1 phenotype reference
  

• All Mutations and Alleles
  1
• Spontaneous
  1
• Find Mice (IMSR)
  1 strains or lines available

Mice homozygous for this mutation are hyperactive, exhibit head shaking and circling behavior, lack startle response to sound, cannot swim, and have abnormal cochlear morphology.

References

• Summaries
  All 1

  Phenotypes 1
• Earliest
  J:113137 Oda S, et al., A new mouse model with cochleo-saccular type inner ear defects. Exp Anim. 2001 Oct;50(5):417-21