About   Help   FAQ
sho Gene Detail
Summary
  • Symbol
    sho
  • Name
    shorthead
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:98300
    NCBI Gene: 20428
  • Alliance
    gene page
Location &
Maps
less
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome Unknown
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    38 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.
Homozygotes for a spontaneous mutation exhibit small size, disproportionate shortening of the head and limbs, cleft palate, reduced mandible, and closed nares. Newborns die soon after birth.
Sequences &
Gene Models
less
Other
Accession IDs
less
MGD-MRK-14407
References
more
  • Summaries
    All 4
    Phenotypes 3
  • Earliest
    J:255 FITCH N, A mutation in mice producing dwarfism, brachycephaly, cleft palate and micromelia. J Morphol. 1961 Sep;109:141-9
  • Latest
    J:285676 Suzuki A, et al., Genes and microRNAs associated with mouse cleft palate: A systematic review and bioinformatics analysis. Mech Dev. 2018 Apr;150:21-27
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
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
04/30/2024
MGI 6.23 		The Jackson Laboratory