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Mapping Data
Experiment
  • Experiment
    TEXT-Genetic Cross
  • Chromosome
    2
  • Reference
    J:38773 Gwynn B, et al., The gene encoding protein 4.2 is distinct from the mouse platelet storage pool deficiency mutation pallid. Genomics. 1997 Jun 15;42(3):532-5
  • ID
    MGI:1095303
Genes
GeneAlleleAssay TypeDescription
Epb42 Southern analysis Epb4.2 cDNA3
Bloc1s6 visible phenotype
Notes
  • Experiment
    Analysis of an F2 intercross was informative in showing that Stx13bp1pa and Epb4.2 recombined on mouse Chromosome 2. In an attempt to substantiate that these loci are in fact separate loci, a recombinant mouse pa Epb4.2c/pa Epb4.2b was mated with apa Epb4.2b/pa pa Epb4.2b mouse. In 10 pallid offspring (all pa/pa), 5 inherited the Epb4.2b allele and 5 inherited the Epb4.2c confirming the separation observed in the recombinant mouse.

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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
12/10/2024
MGI 6.24
The Jackson Laboratory