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mwfh QTL Detail
Summary
  • Symbol
    mwfh
  • Name
    modifier of white forlock hypopigmentation
  • Feature Type
    QTL
  • IDs
    MGI:1344358
    NCBI Gene: 23951
Location & Maps
more
  • Genetic Map
    Chromosome 10, cM position of peak correlated region/marker: Syntenic
  • Mapping Data
    1 experiment
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    1 phenotype from multigenic genotypes
    1 phenotype reference
Sequences &
Gene Models
less
References
more
  • 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

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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last database update
03/21/2017
MGI 6.08
The Jackson Laboratory