Gm26895 Gene Detail

Summary

• Symbol
  Gm26895
• Name
  predicted gene, 26895

• Feature Type
  lncRNA gene
• IDs
  MGI:5477389
• Alliance
  gene page

Location &
Maps

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

• Genetic Map
  Chromosome 4, Syntenic
• Mapping Data
  1 experiment

Human Diseases

• References
  1 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  4 phenotype references
  

• All Mutations and Alleles
  1
• Spontaneous
  1
• Genomic Mutations
  1 involving Gm26895
• Find Mice (IMSR)
  0 strains or lines available

References

• Summaries
  All 5

  Diseases 1

  Phenotypes 4
• Earliest
  J:144929 Cook SA, et al., A Mouse Model for Meckel Syndrome Type 3. J Am Soc Nephrol. 2009 Apr;20(4):753-64
• Latest
  J:282558 Collin GB, et al., Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss. Cells. 2020 Apr 10;9(4):931