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Mnm Gene Detail
Summary
  • Symbol
    Mnm
  • Name
    modifier of neuromuscular degeneration
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:1332551
    NCBI Gene: 110525
  • Alliance
Location &
Maps
more
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 13, Syntenic
  • Mapping Data
    1 experiment
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    17 phenotypes from multigenic genotypes
    3 phenotype references
Sequences &
Gene Models
less
References
more
  • Summaries
    All 4
    Phenotypes 3
  • Earliest
    J:51890 Cox GA, et al., Identification of the mouse neuromuscular degeneration gene and mapping of a second site suppressor allele. Neuron. 1998 Dec;21(6):1327-37
  • Latest
    J:148546 de Planell-Saguer M, et al., Biochemical and genetic evidence for a role of IGHMBP2 in the translational machinery. Hum Mol Genet. 2009 Jun 15;18(12):2115-26

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
10/01/2024
MGI 6.24
The Jackson Laboratory