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Aia1 QTL Detail
Summary
  • Symbol
    Aia1
  • Name
    autoimmune hemolytic anemia 1
  • Synonyms
    Aia-1
  • Feature Type
    QTL
  • IDs
    MGI:87973
    NCBI Gene: 110113
Location &
Maps
more
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 4, cM position of peak correlated region/marker: Syntenic
  • Mapping Data
    2 experiments
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    1 phenotype from 2 alleles in 1 genetic background
    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.
Aia1 and Aia2 are postulated to explain the occurrence of autoimmune hemolytic anemia in the NZB strain. The dominant allele of Aia1 determines occurrence of anemia in the NZB strain; the recessive allele determines absence of anemia in the NZC strain and probably most other strains.
Sequences &
Gene Models
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Other
Accession IDs
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MGD-MRK-1233, MGD-MRK-1235
References
more
  • Summaries
    All 3
    Phenotypes 1
  • Earliest
    J:6517 Knight JG, et al., Genes determining autoimmune disease in New Zealand mice. J Clin Lab Immunol. 1981 May;5(3):165-70

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
12/10/2024
MGI 6.24
The Jackson Laboratory