Mapping Data

Experiment

• Experiment
  CROSS
• Chromosome
  7
• Reference
  J:43448 MacDonald HR, et al., The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse. Hum Mol Genet. 1997 Oct;6(11):1873-8
• ID
  MGI:1195373

Genes

Gene	Assay Type	Description
Ldhc	reported elsewhere
Snrpn	reported elsewhere
Ndn	restriction analysis	Nec9F, Nec10R
Tjp1	reported elsewhere
D7Bir11	reported elsewhere

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>/<s> <s> <s> <s> <s>
• Strain
  (C57BL/6JEi x SPRET/Ei)F1
• Male Parent
  <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