Phenotypes Associated with This Genotype

Genotype
MGI:7620520

• Allelic Composition: Trpm1^nob11/Trpm1^nob11
• Genetic Background: B6.Cg-Trpm1^nob11/BocJ

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

vision/eye

retina spots ( J:347037 )

• some retinal white spots at

abnormal electroretinogram waveform feature ( J:347037 )

absent b-wave ( J:347037 )

abnormal eye electrophysiology ( J:347037 )

• at 4 weeks of age there is no rod ERG b-wave and a greatly diminished cone ERG

abnormal cone electrophysiology ( J:347037 )

abnormal rod electrophysiology ( J:347037 )

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
congenital stationary night blindness 1C		DOID:0110867	OMIM:613216	J:347037