Mapping Data

Experiment

• Experiment
  CROSS
• Chromosome
  4
• Reference
  J:41514 Roderick TH, et al., A new dominant retinal degeneration (Rd4) associated with a chromosomal inversion in the mouse. Genomics. 1997 Jun 15;42(3):393-6
• ID
  MGI:1095322

Genes

Gene	Assay Type
Pgm1	electrophoretic
In(4)56Rk	visible phenotype

Notes

• Reference
  These data have been submitted with MGD under accession numbers MGD-CREX- 621, 622, 623, and 624. Authors indicate that Rd4 may map with either the proximal or diatal inversion breakpoint in the In(4)56Rk Chromosome.
• Experiment
  In represents the breakpoint in In(4)56Rk.Offspring types indicate alleles inherited from F1 parent.
  

CROSS

• Type
  Backcross, sexes unspecified or combined
• Female Parent
  + a/+ a
• Strain
  Not Specified
• Male Parent
  In a/+ b
• Strain
  Not Specified

CROSS Data

MC #mice	Pgm1	In(4)56Rk
7	In	a
6	+	b
1	In	b
3	+	a

Statistics

Marker 1	Marker 2	# Recombinants	Total	% Recombinants	Std Error
Pgm1	In(4)56Rk	17	17	100.000	0.000