Phenotypes Associated with This Genotype

Genotype
MGI:2178344

• Allelic Composition: Pde6b^rd1/Pde6b^rd1
• Genetic Background: Not Specified

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

vision/eye

impaired pupillary reflex ( J:81500 )

• substantial loss of constriction in response to light

absent retina rod cells ( J:24999 )

behavior/neurological

impaired pupillary reflex ( J:81500 )

• substantial loss of constriction in response to light

nervous system

absent retina rod cells ( J:24999 )

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
congenital stationary night blindness autosomal dominant 2		DOID:0110863	OMIM:163500	J:24999