Phenotypes Associated with This Genotype

Genotype
MGI:5431492

• Allelic Composition: Gpr179^nob5/Gpr179^nob5
• Genetic Background: involves: C3H

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

vision/eye

vision/eye phenotype ( J:185567 )

N • mice exhibit normal retinal morphology

abnormal cone electrophysiology ( J:185567 )

• no b waves under photopic conditions

abnormal rod electrophysiology ( J:185567 )

• 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