Gm23962 Gene Detail

Summary

• Symbol
  Gm23962
• Name
  predicted gene, 23962

• Feature Type
  miRNA gene
• IDs
  MGI:5453739
• Alliance
  gene page

Location &
Maps

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

• Genetic Map
  Chromosome 7, Syntenic
• Mapping Data
  1 experiment

Human Diseases

• References
  4 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  24 phenotype references
  

• All Mutations and Alleles
  2
• Targeted
  1
• Transgenic
  1
• Genomic Mutations
  2 involving Gm23962
• Find Mice (IMSR)
  0 strains or lines available

References

• Summaries
  All 25

  Diseases 4

  Phenotypes 24
• Earliest
  J:56614 Gabriel JM, et al., A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and angelman syndromes. Proc Natl Acad Sci U S A. 1999 Aug 3;96(16):9258-63
• Latest
  J:335224 Nakai N, et al., Virtual reality-based real-time imaging reveals abnormal cortical dynamics during behavioral transitions in a mouse model of autism. Cell Rep. 2023 Mar 24;:112258