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ap Gene Detail
Summary
  • Symbol
    ap
  • Name
    alopecia periodica
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:88037
    NCBI Gene: 11763
  • Alliance
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
    16 phenotypes from 1 allele 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.
Animals homozygous for this mutation have hair and skin abnormalities.
Sequences &
Gene Models
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Other
Accession IDs
less
MGD-MRK-1344
References
more
  • Summaries
    All 3
    Phenotypes 1
  • Earliest
    J:30747 Tutikawa K, Studies on an apparently new mutant, alopecia periodica, found in the mouse. Annu Rep Natl Inst Genet Jpn. 1952;3:9-10
  • Latest
    J:30749 Tutikawa K, Test for allelism of alopecia periodica and furless in the house mouse. Annu Rep Natl Inst Genet Jpn. 1954;5:16

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