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dm Gene Detail
Summary
  • Symbol
    dm
  • Name
    diminutive
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:94905
    NCBI Gene: 13399
  • Alliance
    gene page
Location &
Maps
more
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 2, Syntenic
  • Mapping Data
    1 experiment
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    15 phenotypes from 1 allele in 1 genetic background
    4 phenotype references
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
Homozygous mutants have low viability, are smaller than normal, have macrocytic anemia and display various skeletal abnormalities.
Sequences &
Gene Models
less
Other
Accession IDs
less
MGD-MRK-8865
References
more
  • Summaries
    All 6
    Phenotypes 4
  • Earliest
    J:2479 Stevens LC, et al., The inheritance and expression of a mutation in the mouse affecting blood formation, the axial skeleton, and body size. J Hered. 1958;49(4):153-160
  • Latest
    J:5439 Bannerman RM, et al., Hereditary disorders of the red cell in animals. Prog Hematol. 1973;8:131-79
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