lg Gene Detail

Summary

• Symbol
  lg
• Name
  lid gap

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:96775
  NCBI Gene: 16851
• Alliance
  gene page

Location &
Maps

• Sequence Map
  Chr13:110699804-112898424 bp

  From MGI annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 13, Syntenic
• Mapping Data
  4 experiments

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  11 phenotypes from 4 alleles in 3 genetic backgrounds
  10 phenotype references
  

• All Mutations and Alleles
  4
• Spontaneous
  4
• Find Mice (IMSR)
  0 strains or lines available

Homozygotes for spontaneous mutations exhibit open eyelids at birth with variable penetrance depending on genetic background. Mutants may develop vacuolization of the lens, as well as corneal and retinal defects.

Sequences &
Gene Models

• NCBI Gene
  16851

Other
Accession IDs

MGD-MRK-11793

References

• Summaries
  All 15

  Phenotypes 10
• Earliest
  J:27504 Strong LC, The inheritance of cataract and allied eye defects in the house mouse. Proc Sixth Int Cong Genet. 1932;2:195 (Abstr.)
• Latest
  J:95944 Juriloff DM, et al., The open-eyelid mutation, lidgap-Gates, is an eight-exon deletion in the mouse Map3k1 gene. Genomics. 2005 Jan;85(1):139-42