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Wt Gene Detail
Summary
  • Symbol
    Wt
  • Name
    waltzer-type
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:98967
    NCBI Gene: 103986
  • Alliance
    gene page
Location &
Maps
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  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome Unknown
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    33 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 die at embryonic day 11. Heterozygotes have abnormal behavior ranging from nervousness to intense circling, are poor swimmers and females may not raise their young. All carriers have posterior and lateral semicircular canal defects.
Sequences &
Gene Models
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Other
Accession IDs
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MGD-MRK-15462
References
more
  • Summaries
    All 6
    Phenotypes 4
  • Earliest
    J:304 STEIN KF, et al., Morphology and behavior of Waltzertype mice. J Morphol. 1960 Mar;106:197-203
  • Latest
    J:17092 Bartolomei MS, The search for imprinted genes [news]. Nat Genet. 1994 Mar;6(3):220-1
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
04/30/2024
MGI 6.23 		The Jackson Laboratory