Mapping Data

Experiment

• Experiment
  CROSS
• Chromosome
  19
• Reference
  J:11111 Sweet HO, et al., Osteochondrodystrophy (ocd): a new autosomal recessive mutation in the mouse. J Hered. 1991 Mar-Apr;82(2):140-4
• ID
  MGI:40576

Genes

Gene	Assay Type
Tbx10	visible phenotype
ocd	visible phenotype
Scd1	visible phenotype

Notes

• Experiment
  The absence of Dc and odc phenotypes in the offspring classes is due to a low penetrance of Dc and a reduced viability of ocd.

CROSS

• Type
  Backcross, male
• Female Parent
  + ocd ab<J>/+ ocd ab<J>
• Strain
  Not Specified
• Male Parent
  Dc + +/+ ocd ab<J>
• Strain
  Not Specified

CROSS Data

MC #mice	Tbx10	ocd	Scd1
50	+	ocd	ab<J>
61	Dc	+	+
0	Dc	ocd	ab<J>
20	+	+	+
7	+	ocd	+
17	Dc	+	ab<J>
19	+	+	ab<J>
0	Dc	ocd	+

Statistics

Marker 1	Marker 2	# Recombinants	Total	% Recombinants	Std Error
Tbx10	ocd	39	174	22.414	3.161
ocd	Scd1	43	174	24.713	3.270