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spc Gene Detail
Summary
  • Symbol
    spc
  • Name
    sparse coat
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:98374
    NCBI Gene: 20693
  • Alliance
    gene page
Location &
Maps
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  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 14, Syntenic
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    6 phenotypes from 1 allele in 1 genetic background
    1 images
    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.
Mutations in this gene affect hair growth, viability and fertility.
Sequences &
Gene Models
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Other
Accession IDs
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MGD-MRK-14515
References
more
  • Summaries
    All 5
    Phenotypes 3
  • Earliest
    J:100664 Baden HP, et al., Targeted deletion of the sciellin gene resulted in normal development and maturation. Genesis. 2005 Aug;42(4):219-28
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
12/10/2024
MGI 6.24 		The Jackson Laboratory