Mapping Data

Experiment

• Experiment
  CROSS
• Chromosome
  12
• Reference
  J:32083 Burmeister M, et al., Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation. Nat Genet. 1996 Apr;12(4):376-84
• ID
  MGI:46346

Genes

Gene	Assay Type
D12Mit91	PCR amplified length variant
Vsx2	visible phenotype
D12Mit6	PCR amplified length variant

CROSS

• Type
  Backcross, sexes unspecified or combined
• Female Parent
  <s> <s> <s> <s>/<c> <c> <c> <c>
• Strain
  (129S/Sv-Vsx2 x CASA/Rk)F1
• Male Parent
  <s> <s> <s> <s>/<s> <s> <s> <s>
• Strain
  129/Sv-Vsx2
• Allele 1
  s from 129/Sv-Vsx2
• Allele 2
  c from CASA/RkJ

2x2 Data Reported

Marker 1	Marker 2	# Recombinants	# Parentals
D12Mit91	Vsx2	21	131
Vsx2	D12Mit6	7	160

Statistics

Marker 1	Marker 2	# Recombinants	Total	% Recombinants	Std Error
D12Mit91	Vsx2	21	152	13.816	2.799
Vsx2	D12Mit6	7	167	4.192	1.551