Mapping Data

Experiment

• Experiment
  TEXT
• Chromosome
  7
• Reference
  J:67045 Aponte JL, et al., Point mutations in the murine fumarylacetoacetate hydrolase gene: Animal models for the human genetic disorder hereditary tyrosinemia type 1. Proc Natl Acad Sci U S A. 2001 Jan 16;98(2):641-5
• ID
  MGI:2152359

Genes

Gene	Assay Type
Fes	Deletion Mapping
Fah	Deletion Mapping
D7Cwr18	Deletion Mapping
Tyr	Deletion Mapping
Emv23	Deletion Mapping
Mod2	Deletion Mapping
D7Cwr11D	Deletion Mapping
Myo7a	Deletion Mapping

Notes

• Experiment
  Two ENU induced mutations were mapped to an interval on mouse Chromosome 7 containing the Fah gene via a series of overlapping albino (Tyr) deletion mutants. The order of the markers spanning the deletion map is as follows: centromere - Fes - Fah - D7Cwr18 - Tyr - Emv23 - Mod2 - D7Cwr11D - Myo7a.