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

• Sequence Map
  Genome coordinates not available from the current reference assembly.

• Genetic Map
  Chromosome 11, Syntenic
• Mapping Data
  3 experiments

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  5 phenotypes from 1 allele in 1 genetic background
  1 images
  4 phenotype references
  

• All Mutations and Alleles
  1
• Spontaneous
  1
• Find Mice (IMSR)
  0 strains or lines available

Mutations in the gene interfere with normal eye development resulting in blindness.

Sequences &
Gene Models

• NCBI Gene
  14722

Other
Accession IDs

MGD-MRK-10217

References

• 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