Mapping Data

Experiment

• Experiment
  TEXT
• Chromosome
  12
• Reference
  J:48268 Kasarskis A, et al., A phenotype-based screen for embryonic lethal mutations in the mouse. Proc Natl Acad Sci U S A. 1998 Jun 23;95(13):7485-90
• ID
  MGI:1276143

Genes

Gene	Assay Type
Hectd1	visible phenotype
D12Mit69	PCR amplified length variant

Notes

• Experiment
  Mutagenesis using ENU was informative in identifying recessive mutations that disrupt midgestation development in embryonic mice. One such locus opm, mapped to mouse Chromosome 12 with the nearest marker being D12Mit69 at cM 28.0 and a range between 6.0- 28.0 cMs.