Mapping Data

Experiment

• Experiment
  CROSS
• Chromosome
  11
• Reference
  J:62514 Juriloff DM, et al., Gaping lids, gp, a mutation on centromeric chromosome 11 that causes defective eyelid development in mice. Mamm Genome. 2000 Jun;11(6):440-7
• ID
  MGI:1860095

Genes

Gene	Assay Type	Description
gp	visible phenotype
Gck	PCR amplified length variant	D11Bc1-pA, pB
D11Mit62	PCR amplified length variant

Notes

• Experiment
  Authors identified Gck using SSLP marker D11Bc1 (L41631).Offspring types indicate alleles inherited from F1 parent.
  

CROSS

• Type
  Backcross, sexes unspecified or combined
• Female Parent
  <g> <g> <g>/<c> <c> <c>
• Strain
  (GP/Bc x CBA/J)F1
• Male Parent
  <g> <g> <g>/<g> <g> <g>
• Strain
  GP/Bc
• Allele 1
  g from GP/Bc
• Allele 2
  c from CBA/J

CROSS Data

MC #mice	gp	Gck	D11Mit62
59	g	g	g
54	c	c	c
2	g	c	c
2	c	g	g
2	g	g	c
1	c	c	g

Statistics

Marker 1	Marker 2	# Recombinants	Total	% Recombinants	Std Error
gp	Gck	4	120	3.333	1.639
Gck	D11Mit62	3	120	2.500	1.425