Mapping Data

Experiment

• Experiment
  CROSS
• Chromosome
  5
• Reference
  J:52002 Paperna T, et al., Genes for the CPE receptor (CPETR1) and the human homolog of RVP1 (CPETR2) are localized within the Williams-Beuren syndrome deletion. Genomics. 1998 Dec 15;54(3):453-9
• ID
  MGI:1336111

Genes

Gene	Assay Type	Description
Asl
Gtf2i
Cldn4	PCR amplified length variant	411F, 411G
Cldn3	PCR amplified length variant	mRIV1G, mRVP1H
Hip1
Zp3
D5Mit46

Notes

• Experiment
  Detailed mapping data for markers segregating in this cross are 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