Igs13 Other Genome Feature Detail

Summary

• Symbol
  Igs13
• Name
  intergenic site 13

• Feature Type
  unclassified other genome feature
• IDs
  MGI:5569494

Location &
Maps

• Sequence Map
  Genome coordinates not available from the current reference assembly.
• The insertion site is 1165 bp centromeric (transcriptionally downstream) of the last Coro1a exon.

• Genetic Map
  Chromosome 7, Syntenic

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  1 phenotype from multigenic genotypes
  4 phenotype references
  

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

References

• Summaries
  All 5

  Phenotypes 4
• Earliest
  J:210018 Portmann T, et al., Behavioral abnormalities and circuit defects in the Basal Ganglia of a mouse model of 16p11.2 deletion syndrome. Cell Rep. 2014 May 22;7(4):1077-92
• Latest
  J:335872 Beland-Millar A, et al., 16p11.2 haploinsufficiency reduces mitochondrial biogenesis in brain endothelial cells and alters brain metabolism in adult mice. Cell Rep. 2023 May 6;42(5):112485