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Rpe65rd12-2J
Spontaneous Allele Detail
Summary
Symbol: Rpe65rd12-2J
Name: retinal pigment epithelium 65; retinal degeneration 12, 2 Jackson
MGI ID: MGI:7614412
Gene: Rpe65  Location: Chr3:159304812-159330958 bp, + strand  Genetic Position: Chr3, 82.52 cM, cytoband H4
Alliance: Rpe65rd12-2J page
Show the 1 phenotype image(s) involving this allele.
Mutation
origin
Mutation
description
Allele Type:    Spontaneous (Not Specified)
Mutation:    Undefined
 
Mutation detailsThis spontaneous mutation was proven an allele of Rep65 by failed complementation testing with the rd12 allele. cDNA sequencing has not identified a mutation in the coding region of this gene. (J:346129)
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 Rpe65 Mutation:  52 strains or lines available
References
Original:  J:346129 Chang B, The Rpe65 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
11/12/2024
MGI 6.24
The Jackson Laboratory