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Mapping Data
Experiment
  • Experiment
    TEXT-Genetic Cross
  • Chromosome
    7
  • Reference
    J:93998 Rhodes CR, et al., A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment. Mamm Genome. 2004 Sep;15(9):686-97
  • ID
    MGI:3511987
Genes
GeneAlleleAssay TypeDescription
D7Mit191
D7Mit40
D7Mit32a
Myo7a
Myo7a
Notes
  • Experiment
    A mapping cross between (C3Heb/FeJ x C57BL/6J)F1-Hdb/+ x C57BL/6J was informative in mapping the Hdb mutation between D7Mit191 and D7Mit40. A further refinement of this location showed the Hdb phenotype segregating with Myo7a distal of D7Mit32. The authors could not determin with certainty that a mutation in the Myo7a locus caused Hdb.

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
06/12/2024
MGI 6.13
The Jackson Laboratory