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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
GeneAlleleAssay TypeDescription
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
  • Allele 1
    b from C57BL/6JEiJ
  • Allele 2
    s from SPRET/EiJ

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory