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wh Gene Detail
Summary
  • Symbol
    wh
  • Name
    writher
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:98949
    NCBI Gene: 22394
  • Alliance
Location &
Maps
less
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 6, Syntenic
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    1 phenotype reference
Homozygous mutants exhibit progressive muscular weakness, with convulsions at later stages, and die prior to weaning.
Sequences &
Gene Models
less
Other
Accession IDs
less
MGD-MRK-15433
References
more
  • Summaries
    All 2
    Phenotypes 1
  • Earliest
    J:26647 Kelly EM, New mutant: Writher (wh). Mouse News Lett. 1953;8(Research News Suppl):15
  • Latest
    J:63103 Mouse Genome Database and National Center for Biotechnology Information, Entrez Gene Load. Database Release. 2000;

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)
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Funding Information
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last database update
06/12/2024
MGI 6.13
The Jackson Laboratory