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Rpgrip1tvrm111
Chemically induced Allele Detail
Nomenclature
Symbol: Rpgrip1tvrm111
Name: retinitis pigmentosa GTPase regulator interacting protein 1; translational research vision model 111
MGI ID: MGI:5810760
Gene: Rpgrip1  Location: Chr14:52110704-52163546 bp, + strand  Genetic Position: Chr14, 26.81 cM
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Chemically induced (ENU) (Not Specified)
Mutation:    Single point mutation
 
Mutation detailsThis ENU induced c.813+1G>A point transition in a splice acceptor results in the generation of multiple isoforms that lead to premature termination or transcripts with an in-frame deletion of an early exon. (J:243745)
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 structures
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 Rpgrip1 Mutation:  14 strains or lines available
References
Original:  J:243745 Krebs MP, et al., Mouse models of human ocular disease for translational research. PLoS One. 2017;12(8):e0183837
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
02/11/2020
MGI 6.14
The Jackson Laboratory