Mapping Data

Experiment

• Experiment
  CROSS
• Chromosome
  7
• Reference
  J:61187 Gwynn B, et al., Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3-independent mechanism. Blood. 2000 Dec 15;96(13):4227-35
• ID
  MGI:1929249

Genes

Gene	Assay Type	Description
D7Xrf229
Prc1
Ap3s2	Southern analysis	IMAGE 43481
Furin
Il16
Tyr

Notes

• Experiment
  Detailed mapping data from 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>/<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>
• Strain
  SPRET/EiJ
• Mapping Panel
  JAX (BSS)
• Allele 1
  b from C57BL/6JEiJ
• Allele 2
  s from SPRET/EiJ