Gm23587 Gene Detail

Summary

• Symbol
  Gm23587
• Name
  predicted gene, 23587

• Feature Type
  snRNA gene
• IDs
  MGI:5453364
• Alliance
  gene page

Location &
Maps

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

• Genetic Map
  Chromosome 16, Syntenic
• Mapping Data
  1 experiment

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  5 phenotype references
  

• All Mutations and Alleles
  2
• Targeted
  2
• Genomic Mutations
  2 involving Gm23587
• Find Mice (IMSR)
  0 strains or lines available

References

• Summaries
  All 6

  Phenotypes 5
• Earliest
  J:185269 Raveau M, et al., The app-runx1 region is critical for birth defects and electrocardiographic dysfunctions observed in a down syndrome mouse model. PLoS Genet. 2012 May;8(5):e1002724
• Latest
  J:335294 Redhead Y, et al., Craniofacial dysmorphology in Down syndrome is caused by increased dosage of Dyrk1a and at least three other genes. Development. 2023 Apr 15;150(8):dev201077