Mapping Data

Experiment

• Experiment
  TEXT
• Chromosome
  16
• 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:1276144

Genes

Gene	Assay Type
Poglut1	visible phenotype
D16Mit59	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 wsnp, mapped to mouse Chromosome 16 with the nearest marker being D16Mit59 at cM 27.8 and a range between 21.5 - 32.0 cMs.