About   Help   FAQ
gp Gene Detail
Summary
  • Symbol
    gp
  • Name
    gaping lids
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:95793
    NCBI Gene: 14722
  • Alliance
    gene page
Location &
Maps
more
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 11, Syntenic
  • Mapping Data
    3 experiments
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    5 phenotypes from 1 allele in 1 genetic background
    1 images
    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.
Mutations in the gene interfere with normal eye development resulting in blindness.
Sequences &
Gene Models
less
Other
Accession IDs
less
MGD-MRK-10217
References
more
  • Summaries
    All 5
    Phenotypes 4
  • Earliest
    J:211 Kelton DE, et al., Gaping, a new open eyelid mutation in the house mouse. Genetics. 1964;50(2):261-2 (Abstr.)
  • Latest
    J:62514 Juriloff DM, et al., Gaping lids, gp, a mutation on centromeric chromosome 11 that causes defective eyelid development in mice. Mamm Genome. 2000 Jun;11(6):440-7
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
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
05/28/2024
MGI 6.13 		The Jackson Laboratory