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Mapping Data
Experiment
  • Experiment
    TEXT-Genetic Cross
  • Chromosome
    19
  • Reference
    J:89093 Rhodes CR, et al., The homeobox gene Emx2 underlies middle ear and inner ear defects in the deaf mouse mutant pardon. J Neurocytol. 2003 Nov;32(9):1143-54
  • ID
    MGI:3574848
Genes
GeneAlleleAssay TypeDescription
D19Mgc5
Emx2 Emx2Pdo visible phenotype
D19Mit71
Notes
  • Experiment
    C3H/HeN-BALB/cN3-Pdo/+ x C3H/HeN outcross and ( M.m. castaneus x C3H/HeN-BALB/cN3-Pdo/+)F1 x C3H/HeN backcross mice were informative in mapping the Pdo mutation to an 800 kb region of mouse Chromosome 19 flanked by D19Mit71 and D19Mgc5. This 800 kb region included the Emx2 gene. Pdo was determined to be a mutant form of Emx2.

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
04/30/2024
MGI 6.23
The Jackson Laboratory