Mapping Data

Experiment

• Experiment
  CROSS
• Chromosome
  X
• Reference
  J:46361 Dal Zotto L, et al., The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region. Hum Mol Genet. 1998 Mar;7(3):489-99
• ID
  MGI:1328086

Genes

Gene	Assay Type	Description
Mid1	Southern analysis	ME10.2, ME5A

Notes

• Reference
  Mid1 spans the pseudoautosomal region (PAR) boundary in some mouse species, while it lies entirely within the non-recombining region of the X chromosome in others. Because only the X chromosome version of Mid1 is functional, Mid1 has been assigned to the X chromosome. Please note that varying portions of this gene reside within the PAR in different mouse strains.
• 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>/<s>
• Strain
  (C57BL/6JEi x SPRET/Ei)F1
• Male Parent
  <s>/<s>
• Strain
  SPRET/EiJ
• Mapping Panel
  JAX (BSS)
• Allele 1
  b from C57BL/6JEiJ
• Allele 2
  s from SPRET/EiJ