mix Gene Detail

Summary

• Symbol
  mix
• Name
  inner ear dysfuntion, Malou Hultcrantz

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:3054790
• 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
  16 phenotypes from 1 allele in 1 genetic background
  1 phenotype reference
  

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

Heterozygous mutant mice display congenital deafness, male infertility, degeneration of the cochlea, circling, head tossing, and impaired swimming, righting response, position change reflex, and acceleration reflex.

References

• Summaries
  All 1

  Phenotypes 1
• Earliest
  J:92589 Erichsen S, et al., Cochlear distribution of Na,K-ATPase and corticosteroid receptors in two mouse strains with congenital hearing disorders. Acta Otolaryngol. 2001 Oct;121(7):794-802