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shsn Gene Detail
Summary
  • Symbol
    shsn
  • Name
    short snout
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:3812132
  • Alliance
Location &
Maps
less
  • Sequence Map
    Genome coordinates not available
  • Genetic Map
    Chromosome Unknown
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    6 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
immune system
integument
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
neoplasm
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
vision/eye

Click cells to view annotations.
Homozygotes for this spontaneous mutation have shortened, squared snouts, lower than normal bone mineral density, body mass and percent body fat, and develop lens spots and photosensitivity.
References
more
  • Summaries
    All 1
    Phenotypes 1
  • Earliest
    J:183310 Curtain MM, et al., A mutation causing short snout and lens spots that maps to Chromosome 4. MGI Direct Data Submission. 2012;

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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last database update
07/07/2020
MGI 6.15
The Jackson Laboratory