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oe Gene Detail
Summary
  • Symbol
    oe
  • Name
    open eyelids
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:97425
    NCBI Gene: 18287
  • Alliance
    gene page
Location &
Maps
more
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 11, Syntenic
  • Mapping Data
    10 experiments
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    10 phenotypes from 1 allele in 1 genetic background
    4 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.
Homozygotes for a spontaneous mutation exhibit open eyelids at birth, microphthalmia, and opaque corneas in adults.
Sequences &
Gene Models
less
Other
Accession IDs
less
MGD-MRK-13017
References
more
  • Summaries
    All 10
    Phenotypes 4
  • Earliest
    J:13074 Mackensen JA, "Open eyelids" in newborn mice. J Hered. 1960;51(4):188-190
  • Latest
    J:7160 Juriloff DM, et al., The lidgap defect in mice: update and hypotheses. Can J Genet Cytol. 1983 Jun;25(3):246-54
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)
Citing These Resources
Funding Information
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Send questions and comments to User Support. 		last database update
04/23/2024
MGI 6.23 		The Jackson Laboratory