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D13Cwr32 DNA Segment Detail
Summary
  • Symbol
    D13Cwr32
  • Name
    DNA segment, Chr. 13, Case Western Reserve 32
  • Feature Type
    DNA segment
  • IDs
    MGI:1341103
Location &
Maps
more
  • Sequence Map
    Genome coordinates not available
  • Genetic Map
    Chromosome 13, Syntenic
  • Mapping Data
    2 experiments
Molecular
Reagents
less
  • All nucleic 2
    Genomic 1
    Primer pair 1
References
more
  • Summaries
    All 2
  • Earliest
    J:54407 Hong HK, et al., Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcriptionfactor gene. Hum Mol Genet. 1999 Apr;8(4):625-37

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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Funding Information
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last database update
10/08/2019
MGI 6.14
The Jackson Laboratory