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Mapping Data
Experiment
  • Experiment
    CROSS
  • Chromosome
    8
  • 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:1929251
Genes
GeneAlleleAssay TypeDescription
D8Bir3
Sox1
Ap3s1-ps2 Southern analysis IMAGE 585789
D8Bir6
Ap3m2 Southern analysis IMAGE 737067
Adam5
D8Hun2
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> <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
  • 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
10/29/2024
MGI 6.24
The Jackson Laboratory