Mapping Data

Experiment

• Experiment
  TEXT
• Chromosome
  10
• Reference
  J:69028 Wada T, et al., A point mutation in a cadherin gene, Cdh23, causes deafness in a novel mutant, Waltzer mouse niigata. Biochem Biophys Res Commun. 2001 Apr 27;283(1):113-7
• ID
  MGI:2152725

Genes

Gene	Assay Type
D10Mit59	PCR amplified length variant
536R	PCR amplified length variant
536F	PCR amplified length variant
49R	PCR amplified length variant
189R	PCR amplified length variant
573F	PCR amplified length variant
57F	PCR amplified length variant
D10Mit258	PCR amplified length variant
D10Mit172	PCR amplified length variant
D10Mit48	PCR amplified length variant
Cdh23	reported elsewhere

Notes

• Experiment
  1648 (ICR-v^ngt/v^ngt x MSM)F1 x ICR-v^ngt/v^ngt backross animals were used to map the v^ngt mutation. v^ngt segregated with 49R and there were no recombinations between v^ngt and 49R. v^ngt is an allele of Cdh23.