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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
  • 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
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 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
04/16/2024
MGI 6.23 		The Jackson Laboratory