rd24 Gene Detail

Summary

• Symbol
  rd24
• Name
  retinal degeneration 24

• Feature Type
  heritable phenotypic marker
• IDs
  MGI:6794095
• Alliance
  genome feature page

Location &
Maps

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

• Genetic Map
  Chromosome 5, Syntenic

Human Diseases

• Diseases
  1 with rd24 mouse models

Human Disease

Mouse Models

retinitis pigmentosa 49

IDs

retinitis pigmentosa 49      

DOID:0110377
ICD10CM:H35.5
OMIM:613756

View 1 model

Mouse Models

Human Disease Modeled: retinitis pigmentosa 49

Allelic Composition	Genetic Background	Reference	Phenotypes
rd24/rd24	B6.NOD(Cg)-rd24/BocJ	J:348730	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
  5 phenotypes from 1 allele in 1 genetic background
  10 phenotype references
  

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

References

• Summaries
  All 10

  Diseases 1

  Phenotypes 10
• Earliest
  J:392617 Rothe K, et al., Integrin-Linked Kinase Mediates Therapeutic Resistance of Quiescent CML Stem Cells to Tyrosine Kinase Inhibitors. Cell Stem Cell. 2020 Jul 2;27(1):110-124.e9
• Latest
  J:391905 Wu BX, et al., SCLC humanized mice identify T cell infiltration phenotypes in response to combination immune-radiation therapies. iScience. 2026 Aug 21;29(8):116864