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sau Gene Detail
Summary
  • Symbol
    sau
  • Name
    sauron
  • Synonyms
    1239
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:3607718
  • Alliance
    gene page
Location &
Maps
more
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 13, Syntenic
  • Mapping Data
    1 experiment
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    5 phenotypes from multigenic genotypes
    1 phenotype reference
Most embryos hemizygous (opposite the Del(13)36H on the homologous chromosome) for the mutation die by embryonic day E16.5. Holoprocencephaly is observed among embryonic and surviving neonatal hemizygotes. Heterozygous mice exhibit elevated anxiety.
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
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Send questions and comments to User Support. 		last database update
05/28/2024
MGI 6.13 		The Jackson Laboratory