mwfh QTL Detail

Summary

• Symbol
  mwfh
• Name
  modifier of white forlock hypopigmentation

• Feature Type
  QTL
• IDs
  MGI:1344358
  NCBI Gene: 23951

Location &
Maps

• Sequence Map
  Chr10:100017003-100017136 bp

  From MGI annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 10, cM position of peak correlated region/marker: Syntenic
• Mapping Data
  1 experiment

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  1 phenotype from multigenic genotypes
  1 phenotype reference
  

• All Mutations and Alleles
  2
• QTL
  2
• Find Mice (IMSR)
  0 strains or lines available

Sequences &
Gene Models

• NCBI Gene
  23951

References

• Summaries
  All 2

  Phenotypes 1
• Earliest
  J:53978 Southard-Smith EM, et al., The Sox10(Dom) mouse: modeling the genetic variation of Waardenburg-Shah (WS4) syndrome. Genome Res. 1999 Mar;9(3):215-25