About   Help   FAQ
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
05/28/2024
MGI 6.13
The Jackson Laboratory