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nma Gene Detail
Summary
  • Symbol
    nma
  • Name
    neuromuscular ataxia
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:1855684
    NCBI Gene: 117226
  • Alliance
    gene page
Location &
Maps
more
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 12, Syntenic
  • Mapping Data
    1 experiment
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    13 phenotypes from 1 allele in 1 genetic background
    1 images
    1 phenotype reference
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.
Homozygotes for a spontaneous mutation exhibit small size, uncoordinated gait, dysmetria, dystonia, general weakness, decreased blood glucose levels and premature death.
Sequences &
Gene Models
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References
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  • Summaries
    All 2
    Phenotypes 1
  • Earliest
    J:60439 Ward-Bailey PF, et al., Neuromuscular ataxia: a new spontaneous mutation in the mouse. Mamm Genome. 2000 Oct;11(10):820-3
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