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Pt Gene Detail
Summary
  • Symbol
    Pt
  • Name
    pintail
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:97790
    NCBI Gene: 109555
  • Alliance
Location &
Maps
more
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 4, Syntenic
  • Mapping Data
    38 experiments
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    12 phenotypes from 1 allele in 2 genetic backgrounds
    1 phenotype from multigenic genotypes
    1 images
    7 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.
Mutations in this gene result in caudal vertebrae defects. Homozygous mice are small and few survive.
Sequences &
Gene Models
less
Other
Accession IDs
less
MGD-MRK-13657
References
more
  • Summaries
    All 28
    Phenotypes 7
  • Earliest
    J:15 Hollander WF, et al., Pintail, a dominant mutation linked with brown in the house mouse. J Hered. 1951;42(4):179-182
  • Latest
    J:292269 Tsubosaka Y, et al., Hematopoietic prostaglandin D synthase-derived prostaglandin D2 ameliorates adjuvant-induced joint inflammation in mice. FASEB J. 2019 Jun;33(6):6829-6837

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
04/09/2024
MGI 6.23
The Jackson Laboratory