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pf Gene Detail
Summary
  • Symbol
    pf
  • Name
    pupoid fetus
  • Synonyms
    pd
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:97544
    NCBI Gene: 18635
  • Alliance
    gene page
Location &
Maps
more
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 4, Syntenic
  • Mapping Data
    1 experiment
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    13 phenotypes from 1 allele in 1 genetic background
    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 abnormal epidermal growth, keratinization failure, and neonatal death.
Sequences &
Gene Models
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Other
Accession IDs
less
MGD-MRK-13204, MGD-MRK-13242
References
more
  • Summaries
    All 9
    Phenotypes 7
  • Earliest
    J:7379 Fisher C, et al., Abnormal keratinization in the pupoid fetus (pf/pf) mutant mouse epidermis. Dev Biol. 1984 Apr;102(2):290-9
  • Latest
    J:65526 Fisher C, IKKalpha-/- mice share phenotype with pupoid fetus (pf/pf) and repeated epilation (Er/Er) mutant mice. Trends Genet. 2000 Nov;16(11):482-4
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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Send questions and comments to User Support. 		last database update
11/19/2024
MGI 6.24 		The Jackson Laboratory