Del(5Gtf2i-Limk1)1Uta Cytogenetic Marker Detail

Summary

• Symbol
  Del(5Gtf2i-Limk1)1Uta
• Name
  deletion, Chr 5, Uta Francke 1

• Feature Type
  chromosomal deletion
• IDs
  MGI:5317137

Location &
Maps

• Sequence Map
  Chr5:134266688-134717452 bp

  From MGI annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 5, Syntenic

Human Diseases

• Mutations/Alleles
  1 with disease annotations

• References
  1 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  15 phenotypes from 1 allele in 1 genetic background
  21 phenotypes from multigenic genotypes
  5 phenotype references
  

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

References

• Summaries
  All 6

  Diseases 1

  Phenotypes 5
• Earliest
  J:182796 Li HH, et al., Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice. EMBO Mol Med. 2009 Apr;1(1):50-65
• Latest
  J:334324 Davenport CM, et al., Innate frequency-discrimination hyperacuity in Williams-Beuren syndrome mice. Cell. 2022 Oct 13;185(21):3877-3895.e21