Mapping Data

Experiment

• Experiment
  TEXT-Physical Mapping
• Chromosome
  18
• Reference
  J:79322 Wilson SM, et al., Synaptic defects in ataxia mice result from a mutation in Usp14, encoding a ubiquitin-specific protease. Nat Genet. 2002 Nov;32(3):420-5
• ID
  MGI:2429774

Genes

Gene	Assay Type
D18Fcr15	overlapping clones
D18Fcr14	overlapping clones
D18Fcr16	overlapping clones
D18Fcr17	overlapping clones
D18Fcr18	overlapping clones
D18Fcr19	overlapping clones
D18Fcr23	overlapping clones
D18Fcr20	overlapping clones
D18Fcr21	overlapping clones
D18Fcr13	overlapping clones
D18Fcr22	overlapping clones
Usp14	overlapping clones

Notes

• Experiment
  Overlapping BACs with 1 YAC clone covering approximately 1.0 Mb to 1.5 Mb of gneomic DNA were informative to provide the following order of markers on mouse Chromosome 18: D18Fcr15 - D18Fcr14 - D18Fcr16 - D18Fcr17 - D18Fcr18 - D18Fcr19 - D18Fcr23 - D18Fcr20 - D18Fcr21 - D18Fcr13 - D18Fcr22. The Usp14 ataxia region lies between markers D18Fcr14 to D18Fcr21 and segregated without recombination in a genetic cross with D18Fcr23.