Mapping Data

Experiment

• Experiment
  CROSS
• Chromosome
  13
• Reference
  J:60236 Pasteris NG, et al., Isolation, characterization, and mapping of the mouse Fgd3 gene, a new Faciogenital Dysplasia (FGD1; Aarskog Syndrome) gene homologue. Gene. 2000 Jan 25;242(1-2):237-47
• ID
  MGI:1354899

Genes

Gene	Assay Type	Description
D13Mit9
Atxn1
D13Mit91
D13Mit10
Fgd3	SSCP	Fgd3-pA, Fgd3-pB
D13Bir13
Fancc

Notes

• Experiment
  Detailed mapping data for markers segregating in this cross is associated with the JAX (BSS) mapping panel, accessible by clicking on the JAX link highlighted below.Offspring types indicate alleles inherited from F1 parent.
  F1 direction known.
  

CROSS

• Type
  Backcross, female
• Female Parent
  <b> <b> <b> <b> <b> <b> <b>/<s> <s> <s> <s> <s> <s> <s>
• Strain
  (C57BL/6JEi x SPRET/Ei)F1
• Male Parent
  <s> <s> <s> <s> <s> <s> <s>/<s> <s> <s> <s> <s> <s> <s>
• Strain
  SPRET/EiJ
• Mapping Panel
  JAX (BSS)
• Allele 1
  b from C57BL/6JEiJ
• Allele 2
  s from SPRET/EiJ