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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Gpr179nob5
no b wave 5
MGI:5431477
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Gpr179nob5/Gpr179nob5 involves: C3H MGI:5431492
cx2
Gpr179nob5/Gpr179+
Grm6nob3/Grm6+
involves: C3H * C57BL/10 MGI:5568985


Genotype
MGI:5431492
hm1
Allelic
Composition
Gpr179nob5/Gpr179nob5
Genetic
Background
involves: C3H
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gpr179nob5 mutation (0 available); any Gpr179 mutation (71 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
N
• mice exhibit normal retinal morphology
• no b waves under photopic conditions
• no b waves under scotopic conditions
• however, a waves are normal

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
congenital stationary night blindness 1E DOID:0110869 OMIM:614565
J:185567




Genotype
MGI:5568985
cx2
Allelic
Composition
Gpr179nob5/Gpr179+
Grm6nob3/Grm6+
Genetic
Background
involves: C3H * C57BL/10
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gpr179nob5 mutation (0 available); any Gpr179 mutation (71 available)
Grm6nob3 mutation (1 available); any Grm6 mutation (53 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• reduced b-wave in dark-adapted mice





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
11/19/2024
MGI 6.24
The Jackson Laboratory