mrs1 Gene Detail

Summary

• Symbol
  mrs1
• Name
  mouse retinoschisis 1

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:7464299
• Alliance
  gene page

Location &
Maps

• Sequence Map
  Genome coordinates not available from the current reference assembly.
• mrs1 mapped to Chromosome X between DxMit155 and DXMit186

• Genetic Map
  Chromosome X, Syntenic

Human Diseases

• Diseases
  1 with mrs1 mouse models

Human Disease

Mouse Models

retinoschisis

IDs

retinoschisis      

DOID:8465
ICD10CM:H33.10
ICD9CM:361.10
MESH:D041441
NCI:C85046
UMLS_CUI:C0152439

View 1 model

Mouse Models

Human Disease Modeled: retinoschisis

Allelic Composition	Genetic Background	Reference	Phenotypes
mrs1/Y	B6.Cg-mrs1/BocJ	J:334762	View

Click on a disease name to see all genes associated with that disease.

• Mutations/Alleles
  1 with disease annotations

• References
  1 with disease annotations

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  3 phenotypes from 1 allele in 1 genetic background
  1 phenotype reference
  

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

References

• Summaries
  All 2

  Diseases 1

  Phenotypes 1
• Earliest
  J:23000 MGD Nomenclature Committee, Nomenclature Committee Use. 1995-02-14;
• Latest
  J:334762 Chang B, Mouse Retinoschisis 1. MGI Direct Data Submission. 2023;