About   Help   FAQ
elap Gene Detail
Summary
  • Symbol
    elap
  • Name
    eye lens aplasia
  • Synonyms
    lap
  • Feature Type
    heritable phenotypic marker
  • IDs
    MGI:105916
    NCBI Gene: 13708
  • Alliance
    gene page
Location &
Maps
more
  • Sequence Map
    Genome coordinates not available from the current reference assembly.
  • Genetic Map
    Chromosome 2, Syntenic
  • Mapping Data
    1 experiment
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    3 phenotype references
Homozygotes for a spontaneous mutation exhibit eye defects including microphthalmia, aphakia, absence of the anterior chamber, dystrophy of the cornea and vitreous body, and retinal disorganization.
Sequences &
Gene Models
less
Other
Accession IDs
less
MGD-MRK-33296, MGD-MRK-33593
References
more
  • Summaries
    All 7
    Phenotypes 3
  • Earliest
    J:23892 Aso S, et al., Lens aplasia: a new mutation producing lens abnormality in the mouse. Lab Anim Sci. 1995 Feb;45(1):41-6
  • Latest
    J:238745 Nishikii H, et al., DR3 signaling modulates the function of Foxp3+ regulatory T cells and the severity of acute graft-versus-host disease. Blood. 2016 Dec 15;128(24):2846-2858
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
04/16/2024
MGI 6.23 		The Jackson Laboratory