hm1

Pde6b^rd1-3H/Pde6b^rd1-3H
involves: BALB/cAnN * C3H/HeN

Key:
♀	phenotype observed in females	WTSI	Wellcome Trust Sanger Institute
♂	phenotype observed in males	EuPh	Europhenome
N	normal phenotype

vision/eye

retinal degeneration ( J:75964 )

• rapid onset of degeneration

Mouse Models of Human Disease		OMIM ID	Ref(s)
Night Blindness, Congenital Stationary, Autosomal Dominant 2; CSNBAD2		163500	J:75964

ht2

Pde6b^rd1-3H/Pde6b^rd1
involves: BALB/cAnN * C3H/HeN

Key:
♀	phenotype observed in females	WTSI	Wellcome Trust Sanger Institute
♂	phenotype observed in males	EuPh	Europhenome
N	normal phenotype

vision/eye

retinal degeneration ( J:75964 )

• rapid onset of degeneration

Mouse Models of Human Disease		OMIM ID	Ref(s)
Night Blindness, Congenital Stationary, Autosomal Dominant 2; CSNBAD2		163500	J:75964