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Rp1tvrm64
Chemically induced Allele Detail
Summary
Symbol: Rp1tvrm64
Name: retinitis pigmentosa 1 (human); translational vision research model 64
MGI ID: MGI:4867393
Gene: Rp1  Location: Chr1:4185896-4479508 bp, - strand  Genetic Position: Chr1, 1.65 cM
Alliance: Rp1tvrm64 page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsA T-to-A transversion mutation at nucleotide 1769 results in a nonsense mutation in which codon 522 is altered from one encoding arginine to a termination codon. (J:166679)
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 Rp1 Mutation:  121 strains or lines available
References
Original:  J:166679 Won J, et al., Mouse model resources for vision research. J Ophthalmol. 2011;2011:391384
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
04/23/2024
MGI 6.23
The Jackson Laboratory