Mapping Data

Experiment

• Experiment
  CROSS
• Chromosome
  X
• Reference
  J:10593 Herman GE, et al., Close linkage of the murine locus bare patches to the X-linked visual pigment gene: implications for mapping human X-linked dominant chondrodysplasia punctata. Genomics. 1990 Jul;7(3):307-12
• ID
  MGI:39290

Genes

Gene	Assay Type	Description
Otc	Southern analysis	pOTC
Hprt1	Southern analysis	pHPT5
DXHXS144E	Southern analysis	C11
F9	Southern analysis	F9
Nsdhl	visible phenotype
Opn1mw	Southern analysis	hs-7
Dmd	Southern analysis	pXD4, pXD1
Pgk1	Southern analysis	pCAB17
Gla	Southern analysis	R989

Notes

• Experiment
  Offspring types indicate alleles inherited from F1 parent.
  

CROSS

• Type
  Backcross, sexes unspecified or combined
• Female Parent
  <b> <b> <b> <b> <b> <b> <b> <b>/<s> <s> <s> <s> <s> <s> <s> <s> <s>
• Strain
  (B6CB-A/A Nsdhl x M. spretus)F1
• Male Parent
  <b> <b> <b> <b> <b> <b> <b> <b> <b>/Y
• Strain
  (C57BL/6J-A x CBA)F1
• Allele 1
  b from C57BL/6J or CBA
• Allele 2
  s from M. spretus

CROSS Data

MC #mice	Otc	Hprt1	DXHXS144E	F9	Nsdhl	Opn1mw	Dmd	Pgk1	Gla
2	b	b	b	b	b	b	b	b	b
8	s	s	s	s	s	s	s	s	s
4	b	s	s	s	s	s	s	s	s
1	b	b	b	s	s	s	s	s	s
1	s	s	s	b	b	b	b	b	b
1	b	b	b	b	s	s	s	s	s
1	s	s	s	s	b	b	b	b	b
3	s	s	s	s	s	s	s	b	b
1	s	s	s	s	s	s	s	s	b

Statistics

Marker 1	Marker 2	# Recombinants	Total	% Recombinants	Std Error
Otc	Hprt1	4	22	18.182	8.223
Hprt1	DXHXS144E	0	22	0.000	0.000
DXHXS144E	F9	2	22	9.091	6.129
F9	Nsdhl	2	22	9.091	6.129
Nsdhl	Opn1mw	0	22	0.000	0.000
Opn1mw	Dmd	0	22	0.000	0.000
Dmd	Pgk1	3	22	13.636	7.317
Pgk1	Gla	1	22	4.545	4.441