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sps Gene Detail
Summary
  • Symbol
    sps
  • Name
    spontaneous seizure
  • Synonyms
    dd
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:98390
    NCBI Gene: 20767
  • Alliance
    gene page
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
    8 phenotypes from 1 allele in 1 genetic background
    7 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 result in neurological and convulsive behaviors resulting in early death.
Sequences &
Gene Models
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Other
Accession IDs
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MGD-MRK-14546, MGD-MRK-8817
References
more
  • Summaries
    All 9
    Phenotypes 7
  • Earliest
    J:6937 Maxson SC, et al., A mutant for spontaneous seizures in C57BL/10Bg mice. Epilepsia. 1983 Feb;24(1):15-24
  • Latest
    J:22266 Cordero ML, et al., Altered GABAergic and glutamatergic transmission in audiogenic seizure-susceptible mice. Mol Neurobiol. 1994 Aug-Dec;9(1-3):253-8
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
11/19/2024
MGI 6.24 		The Jackson Laboratory