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rd26
Spontaneous Allele Detail
Summary
Symbol: rd26
Name: retinal degeneration 26
MGI ID: MGI:7662983
Gene: rd26  Location: unknown  Genetic Position: ChrUN, Syntenic
Alliance: rd26 page
Retinal degeneration in homozygous rd26 mice

Show the 1 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  STOCK Terctm1Rdp Dmdmdx/J
Mutation
description
Allele Type:    Spontaneous (Not Specified)
Mutation:    Undefined
 
Mutation detailsThis spontaneous mutation, which causes late-onset progressive retinal degeneration, has not been mapped. (J:350383)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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: 1 strain available      Cell Lines: 0 lines available
Carrying any rd26 Mutation:  1 strain or line available
References
Original:  J:350383 Chang B, The retinal degeneration 26 (rd26) mutation. MGI Direct Data Submission. 2024;
All:  1 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
09/17/2024
MGI 6.24
The Jackson Laboratory