Phenotypes associated with this allele

• Allele Symbol: Pde6b^atrd3
• Allele Name: atypical retinal degeneration 3
• Allele ID: MGI:2178316
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Pde6b^atrd3/Pde6b^atrd3	involves: BALB/cAnN * C3H/HeN	MGI:3028004
ht2	Pde6b^atrd3/Pde6b^rd1	involves: BALB/cAnN * C3H/HeN	MGI:3028003

Genotype
MGI:3028004

hm1

• Allelic Composition: Pde6b^atrd3/Pde6b^atrd3
• Genetic Background: involves: BALB/cAnN * C3H/HeN

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

vision/eye

abnormal optic disk morphology ( J:101336 )

• pale by 10 weeks of age

thin retina outer nuclear layer ( J:101336 )

• unexpectedly mild decrease in thickness at 3.5 weeks of age

retina degeneration ( J:75964 , J:101336 )

• slow onset of degeneration; the visual tracking response persists until several weeks of age in contrast to Pde6b^rd1 homozygous mice (J:75964)

• onset is later than in Pde6b^rd1 (J:101336)

decreased visual acuity ( J:101336 )

• at 3.5 weeks of age all but 1 mouse fail to respond in a visual tracking drum assay; on subsequent days all mice fail to respond

nervous system

abnormal optic disk morphology ( J:101336 )

• pale by 10 weeks of age

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
congenital stationary night blindness autosomal dominant 2		DOID:0110863	OMIM:163500	J:75964
retinitis pigmentosa 40		DOID:0110375	OMIM:613801	J:101336

Genotype
MGI:3028003

ht2

• Allelic Composition: Pde6b^atrd3/Pde6b^rd1
• Genetic Background: involves: BALB/cAnN * C3H/HeN

vision/eye

retina degeneration ( J:75964 )

• slow onset of degeneration; the visual tracking response persists until several weeks of age in contrast to Pde6b^rd1 homozygous mice

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
congenital stationary night blindness autosomal dominant 2		DOID:0110863	OMIM:163500	J:75964