Gm15317 Gene Detail

Summary

• Symbol
  Gm15317
• Name
  predicted gene 15317

• Feature Type
  antisense lncRNA gene
• IDs
  MGI:3705262
• Alliance
  gene page

Location &
Maps

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

• Genetic Map
  Chromosome 16, 56.84 cM

Human Diseases

• References
  3 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  35 phenotype references
  

• All Mutations and Alleles
  4
• Targeted
  4
• Genomic Mutations
  4 involving Gm15317
• Find Mice (IMSR)
  0 strains or lines available

Gene Ontology
(GO)
Classifications

References

• Summaries
  All 38

  Diseases 3

  Phenotypes 35
• Earliest
  J:93223 Olson LE, et al., A chromosome 21 critical region does not cause specific down syndrome phenotypes. Science. 2004 Oct 22;306(5696):687-90
• Latest
  J:361105 Tateossian H, et al., DYRK1A kinase triplication is the major cause of Otitis Media in Down Syndrome. Elife. 2025;