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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Grm6nob7
no b wave 7
MGI:5754842
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Grm6nob7/Grm6nob7 C57BL/6J-Grm6nob7 MGI:5754843
ht2
Grm6nob3/Grm6nob7 involves: C57BL/6J * C57BL/10J MGI:5755378


Genotype
MGI:5754843
hm1
Allelic
Composition
Grm6nob7/Grm6nob7
Genetic
Background
C57BL/6J-Grm6nob7
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Grm6nob7 mutation (0 available); any Grm6 mutation (51 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• electroretinography has no b wave component under dark or light adapted conditions
• photopic b waves are absent and cone ERGs are electronegative
• scotopic b waves are absent, and the a wave is followed by a negative component, slow PIII

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
congenital stationary night blindness 1B DOID:0110865 OMIM:257270
J:229885




Genotype
MGI:5755378
ht2
Allelic
Composition
Grm6nob3/Grm6nob7
Genetic
Background
involves: C57BL/6J * C57BL/10J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Grm6nob3 mutation (1 available); any Grm6 mutation (51 available)
Grm6nob7 mutation (0 available); any Grm6 mutation (51 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• electroretinography has no b wave component under dark or light adapted conditions
• photopic b waves are absent and cone ERGs are electronegative
• scotopic b waves are absent, and the a wave is followed by a negative component, slow PIII





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
05/07/2024
MGI 6.23
The Jackson Laboratory