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rd24
Spontaneous Allele Detail
Summary
Symbol: rd24
Name: retinal degeneration 24
MGI ID: MGI:7643884
Gene: rd24  Location: unknown  Genetic Position: Chr5, Syntenic
Alliance: rd24 page
Mutation
origin
Strain of Origin:  NOD.Cg-Rag1tm1Mom Il2rgtm1Wjl/SzJ
Mutation
description
Allele Type:    Spontaneous (Not Specified)
Mutation:    Undefined
 
Mutation detailsThis spontaneous heritable phenotypic mutation has been mapped to Chromosome 5 closely linked to D5Mit356 with no crossovers in 100 F2 mice. Sequence characterization has not been done but the most likely candidate gene is Cnga1. (J:348730)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 4 strains available      Cell Lines: 0 lines available
Carrying any rd24 Mutation:  4 strains or lines available
References
Original:  J:348730 Chang B, The retinal degeneration 24 (rd24) mutation. 2024;
All:  3 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory