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

• Sequence Map
  Genome coordinates not available from the current reference assembly.

• Genetic Map
  Chromosome Unknown

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  15 phenotypes from 1 allele in 1 genetic background
  2 phenotype references
  

• All Mutations and Alleles
  1
• Spontaneous
  1
• Find Mice (IMSR)
  0 strains or lines available

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

• NCBI Gene
  12281

Other
Accession IDs

MGD-MRK-1718

References

• 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