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:1095321

Genes

Gene	Allele	Assay Type
Tyrp1	Tyrp1^b	visible phenotype
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
  + b/+ b
• Strain
  Not Specified
• Male Parent
  In b/+ +
• Strain
  Not Specified

CROSS Data

MC #mice	Tyrp1	In(4)56Rk
7	In	b
6	+	+
1	In	+
3	+	b

Statistics

Marker 1	Marker 2	# Recombinants	Total	% Recombinants	Std Error
Tyrp1	In(4)56Rk	4	17	23.529	10.288