sau Gene Detail

Summary

• Symbol
  sau
• Name
  sauron
• Synonyms
  1239

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:3607718
• Alliance
  gene page

Location &
Maps

• Sequence Map
  Genome coordinates not available from the current reference assembly.

• Genetic Map
  Chromosome 13, Syntenic
• Mapping Data
  1 experiment

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  5 phenotypes from multigenic genotypes
  1 phenotype reference
  

• All Mutations and Alleles
  1
• Chemically induced (ENU)
  1
• Find Mice (IMSR)
  2 strains or lines available

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

• 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