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Scs Gene Detail
Summary
  • Symbol
    Scs
  • Name
    semi-dominant compacted skeleton
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:5517546
  • Alliance
Location &
Maps
less
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 5, Syntenic
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    15 phenotypes from 1 allele in 4 genetic backgrounds
    2 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
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.
With compressed, misaligned, and fused vertebrae, missing or herniated intervertebral discs, and fused or bifurcated ribs, heterozygotes for this semi-dominant spontaneous mutation have a shortened tail and compressed axial skeleton and these phenotypes are more severe in the homozygotes
References
more
  • Summaries
    All 1
    Phenotypes 1
  • Earliest
    J:202091 Harris BS, et al., A new skeletal mutation named semi-dominant compacted skeleton that maps to Chromosome 5. MGI Direct Data Submission. 2013;

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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Funding Information
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory