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rd25
Spontaneous Allele Detail
Summary
Symbol: rd25
Name: retinal degeneration 25
MGI ID: MGI:7660543
Gene: rd25  Location: unknown  
Alliance: rd25 page
Show the 1 phenotype image(s) involving this allele.
Mutation
origin
Strain of Origin:  B6.129S2(Cg)-Ramp1tm1.1Tsuj/WkinJ
Mutation
description
Allele Type:    Spontaneous (Not Specified)
Mutation:    Undefined
 
Mutation detailsThis spontaneous mutation maps to Chr 14 between D14Mit62 and D14Mit234 where Rpgrip1 is the best candidate gene given the phenotype (J:349874)
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: 2 strains available      Cell Lines: 0 lines available
Carrying any rd25 Mutation:  2 strains or lines available
References
Original:  J:349874 Chang B, The retinal degeneration 25 (rd25) mutation. MGI Direct Data Submission. 2024;
All:  2 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
12/10/2024
MGI 6.24
The Jackson Laboratory