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amd QTL Detail
Summary
  • Symbol
    amd
  • Name
    autoimmune myocardial disease
  • Feature Type
    QTL
  • IDs
    MGI:88003
    NCBI Gene: 11700
Location &
Maps
more
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 14, cM position of peak correlated region/marker: Syntenic
  • Mapping Data
    6 experiments
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    1 phenotype from 2 alleles in 2 genetic backgrounds
    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.
Homozygous mutant animals are susceptibility to Coxsackievirus B3-induced myocarditis.
Sequences &
Gene Models
less
Other
Accession IDs
less
MGD-MRK-1292
References
more
  • Summaries
    All 3
    Phenotypes 1
  • Earliest
    J:2843 Traystman MD, et al., Genetic control of Coxsackievirus B3-induced heart-specific autoantibodies associated with chronic myocarditis. Clin Exp Immunol. 1991 Nov;86(2):291-8
  • Latest
    J:11025 Traystman MD, et al., Susceptibility to Coxsackievirus B3-induced chronic myocarditis maps near the murine Tcr alpha and Myhc alpha loci on chromosome 14. Am J Pathol. 1991 Mar;138(3):721-6

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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory