Mapping Data

Experiment

• Experiment
  CROSS
• Chromosome
  13
• Reference
  J:50233 Mjaatvedt CH, et al., The Cspg2 gene, disrupted in the hdf mutant, is required for right cardiac chamber and endocardial cushion formation. Dev Biol. 1998 Oct 1;202(1):56-66
• ID
  MGI:1338574

Genes

Gene
D13Bir16
D13Mit27
Vcan
Dhfr
D13Mit160

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. Cspg2 was mapped using a molecular segment from a mouse Chromosome 13 transgene insertion causing the hdf (heart defect) mutation.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