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Gpr179nob5
Spontaneous Allele Detail
Summary
Symbol: Gpr179nob5
Name: G protein-coupled receptor 179; no b wave 5
MGI ID: MGI:5431477
Gene: Gpr179  Location: Chr11:97222935-97242903 bp, - strand  Genetic Position: Chr11, 60.95 cM
Alliance: Gpr179nob5 page
Mutation
origin
Strain of Origin:  C3H
Mutation
description
Allele Type:    Spontaneous
Mutation:    Transposon insertion
 
Mutation detailsThe ERV2 retroviral transposon inserted into intron 1. RT-PCR confirmed reduced transcript expression in the retina. (J:185567)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Gpr179 Mutation:  71 strains or lines available
Notes
This mutation has been found in C3H/HeN, but is absent from C3H/HeJ, C3H/HeOuJ, C3HeB/FeJ, C3H/HeSnJ (J:224435) and C3H/HeH (J:211946).
References
Original:  J:185567 Peachey NS, et al., GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness. Am J Hum Genet. 2012 Feb 10;90(2):331-9
All:  15 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
03/12/2024
MGI 6.23
The Jackson Laboratory