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M1073b Gene Detail
Summary
  • Symbol
    M1073b
  • Name
    mutant 1073b
  • Synonyms
    line 1073
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:5515454
  • Alliance
Location &
Maps
less
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 13, Syntenic
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    12 phenotypes from multigenic genotypes
    1 phenotype reference
Mice hemizygous for this mutation exhibit craniofacial and neurological defects. Mice heterozygous for this mutation exhibit decreased anxiety-related response.
References
more
  • Summaries
    All 2
    Phenotypes 1
  • Earliest
    J:101156 Bogani D, et al., Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen. Proc Natl Acad Sci U S A. 2005 Aug 30;102(35):12477-82

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
11/19/2024
MGI 6.24
The Jackson Laboratory