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Dp(16Mis18a-Runx1)2TybEmcf Cytogenetic Marker Detail
Summary
  • Symbol
    Dp(16Mis18a-Runx1)2TybEmcf
  • Name
    duplication, Chr 16, Victor Tybulewicz and Elizabeth M C Fisher 2
  • Feature Type
    cytogenetic marker
  • IDs
    MGI:5703854
Location &
Maps
less
  • Sequence Map
    Genome coordinates not available
  • Genetic Map
    Chromosome 16, Syntenic
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    1 phenotype from 1 allele in 1 genetic background
    2 phenotype references
References
more
  • Summaries
    All 2
    Phenotypes 2
  • Earliest
    J:227899 Lana-Elola E, et al., Genetic dissection of Down syndrome-associated congenital heart defects using a new mouse mapping panel. Elife. 2016 Jan 14;5
  • Latest
    J:262380 Watson-Scales S, et al., Analysis of motor dysfunction in Down Syndrome reveals motor neuron degeneration. PLoS Genet. 2018 May;14(5):e1007383

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)
Citing These Resources
Funding Information
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last database update
09/10/2019
MGI 6.14
The Jackson Laboratory