Mapping Data

Experiment

• Experiment
  CROSS
• Chromosome
  19
• Reference
  J:37055 Favor J, et al., The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney. Proc Natl Acad Sci U S A. 1996 Nov 26;93(24):13870-5
• ID
  MGI:47833

Genes

Gene	Allele	Assay Type
D19Mit61		PCR amplified length variant
D19Mit11.1		PCR amplified length variant
Pax2	Pax2^1Neu	visible phenotype
D19Mit91		PCR amplified length variant
D19Mit1		PCR amplified length variant

Notes

• Experiment
  Mutant K289 is a mutant allele at the Pax2 locus designated Pax2^1Neu.Offspring types indicate alleles inherited from F1 parent.
  

CROSS

• Type
  Unspecified
• Female Parent
  <c> <c> <c> <c> <c>/<b> <b> <b> <b> <b>
• Strain
  (C3H x C57BL/6 K289/+)F1
• Male Parent
  <b> <b> <b> <b> <b>/<b> <b> <b> <b> <b>
• Strain
  C57BL/6
• Allele 1
  c from C3H
• Allele 2
  b from C57BL/6

CROSS Data

MC #mice	D19Mit61	D19Mit11.1	Pax2	D19Mit91	D19Mit1
33	c	c	c	c	c
37	b	b	b	b	b
8	c	b	b	b	b
16	b	c	c	c	c
1	c	c	b	b	b
1	c	c	c	b	b
1	b	b	b	c	c
2	b	b	b	b	c