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Phenotypes Associated with This Genotype
Genotype
MGI:5431492
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 (40 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


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
02/16/2021
MGI 6.16
The Jackson Laboratory