Del(18Ctxn3-Ccdc192)1Kcl Cytogenetic Marker Detail

Summary

• Symbol
  Del(18Ctxn3-Ccdc192)1Kcl
• Name
  deletion, Chr 18, King's College London 1

• Feature Type
  chromosomal deletion
• IDs
  MGI:6473455

Location &
Maps

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

• Genetic Map
  Chromosome 18, Syntenic

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  1 phenotype reference
  

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

References

• Summaries
  All 2

  Phenotypes 1
• Earliest
  J:327181 Lewis MA, et al., Identification and characterisation of spontaneous mutations causing deafness from a targeted knockout programme. BMC Biol. 2022 Mar 17;20(1):67