Phenotypes Associated with This Genotype

Genotype
MGI:5754843

• Allelic Composition: Grm6^nob7/Grm6^nob7
• Genetic Background: C57BL/6J-Grm6^nob7

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

vision/eye

decreased b-wave amplitude ( J:229885 )

• electroretinography has no b wave component under dark or light adapted conditions

abnormal cone electrophysiology ( J:229885 )

• photopic b waves are absent and cone ERGs are electronegative

abnormal rod electrophysiology ( J:229885 )

• 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