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cab Gene Detail
Summary
  • Symbol
    cab
  • Name
    cardiac abnormality
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:88239
    NCBI Gene: 12281
  • 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
    15 phenotypes from 1 allele in 1 genetic background
    2 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 have no detectable glycogen in liver, lung, heart or skeletal muscle, spontaneous movements are greatly decreased in late stage fetuses, and die perinataly.
Sequences &
Gene Models
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Other
Accession IDs
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MGD-MRK-1718
References
more
  • Summaries
    All 3
    Phenotypes 2
  • Earliest
    J:6195 Essien FB, A lethal mutation (cab) affecting heart function in the mouse. Genet Res. 1979 Feb;33(1):57-9
  • Latest
    J:7797 Tyson FL, et al., Prenatal expression of a lethal genetic defect in carbohydrate metabolism in mice. Proc Natl Acad Sci U S A. 1985 Apr;82(7):2101-5
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
07/02/2024
MGI 6.13 		The Jackson Laboratory