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nd Gene Detail
Summary
  • Symbol
    nd
  • Name
    nodding
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:97289
    NCBI Gene: 17983
  • Alliance
    gene page
Location &
Maps
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  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome Unknown
Strain
Comparison
more
  • RFLP
    2
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    15 phenotypes from 1 allele in 1 genetic background
    3 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.
Mutations in this gene cause mice to be ataxic with continuous head-bobbing.
Sequences &
Gene Models
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Other
Accession IDs
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MGD-MRK-12798
References
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  • Summaries
    All 6
    Phenotypes 3
  • Earliest
    J:24834 Sotelo C, et al., Nodding, a new mutant of the mouse with cerebellar abnormalities. Neurosci Lett. 1983;14(Suppl):S353 (Abstr.)
  • Latest
    J:232403 Lachaud C, et al., Karyomegalic interstitial nephritis and DNA damage-induced polyploidy in Fan1 nuclease-defective knock-in mice. Genes Dev. 2016 Mar 15;30(6):639-44
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
12/10/2024
MGI 6.24 		The Jackson Laboratory