Mos3 Gene Detail

Summary

• Symbol
  Mos3
• Name
  modifier of Sox10 3

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:3822489
• Alliance
  gene page

Location &
Maps

• Sequence Map
  Chr3:30447355-50639447 bp

  From MGI annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 3, Syntenic
• Mapping Data
  1 experiment

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  1 phenotype from multigenic genotypes
  1 phenotype reference
  

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

This locus intensifies the white spotting (hypopigmentation) phenotype associated with Sox10 haploinsufficiency.

References

• Summaries
  All 2

  Phenotypes 1
• Earliest
  J:136642 Matera I, et al., A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy. Hum Mol Genet. 2008 Jul 15;17(14):2118-31