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st Gene Detail
Summary
  • Symbol
    st
  • Name
    shaker-short
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:98426
    NCBI Gene: 20837
  • Alliance
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
    16 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.
Mice homozygous for this spontaneous mutation are sterile and display absent or short tails, decreased survivor rate, impaired balance and coordination, erratic choreic movements, circling, deafness, abnormal brain and otic vesicle development, cerebral hernias and cranial dysmorphology.
Sequences &
Gene Models
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Other
Accession IDs
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MGD-MRK-14614
References
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  • Summaries
    All 4
    Phenotypes 3
  • Earliest
    J:240 Dunn LC, A New Gene Affecting Behavior and Skeleton in the House Mouse. Proc Natl Acad Sci U S A. 1934 Apr;20(4):230-2
  • Latest
    J:15089 Bonnevie K, Abortive differentiation of the ear vesicles following a hereditary brain-anomaly in the short- tailed waltzing mice. Genetica. 1936;18:105-125

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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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory