Mapping Data

Experiment

• Experiment
  CROSS
• Chromosome
  8
• Reference
  J:39060 Chang B, et al., Improved genetic map for the mnd gene, using the retinal degeneration aspect of the phenotype. MGI Direct Data Submission. 1998;
• ID
  MGI:1201360

Genes

Gene	Assay Type
D8Mit124	PCR amplified length variant
Cln8	visible phenotype
D8Mit94	PCR amplified length variant
D8Mit4	PCR amplified length variant
Gsr	electrophoretic
Ces1c	electrophoretic
Got2	electrophoretic

Notes

• Experiment
  Authors demonstrate that retinal degeneration is a pleiotropic effect of mnd by demonstrating that the phenotype segregates with the mnd locus.Offspring types indicate alleles inherited from F1 parent.
  

CROSS

• Type
  Backcross, female
• Female Parent
  <b> <b> <b> <b> <b> <b> <b>/<s> <s> <s> <s> <s> <s> <s>
• Strain
  (C57BL/6J-Cln8 x SWR/J)F1
• Male Parent
  <b> <b> <b> <b> <b> <b> <b>/<b> <b> <b> <b> <b> <b> <b>
• Strain
  C57BL/6J-Cln8
• Allele 1
  b from Not Specified
• Allele 2
  s from SWR/J

CROSS Data

MC #mice	D8Mit124	Cln8	D8Mit94	D8Mit4	Gsr	Ces1c	Got2
55	b	b	b	b	b	b	b
64	s	s	s	s	s	s	s
8	b	b	s	s	s	s	s
8	s	s	b	b	b	b	b
4	b	b	b	b	b	b	s
3	s	s	s	s	s	s	b
2	b	b	s	s	s	b	b

Statistics

Marker 1	Marker 2	# Recombinants	Total	% Recombinants	Std Error
D8Mit124	Cln8	0	144	0.000	0.000
Cln8	D8Mit94	18	144	12.500	2.756
D8Mit94	D8Mit4	0	144	0.000	0.000
D8Mit4	Gsr	0	144	0.000	0.000
Gsr	Ces1c	2	144	1.389	0.975
Ces1c	Got2	7	144	4.861	1.792