Phenotypes for Pde6b MGI:3028003 MGI Mouse

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Phenotypes Associated with This Genotype

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

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pde6b^atrd3 mutation (2 available); any Pde6b mutation (122 available)
Pde6b^rd1 mutation (41 available); any Pde6b mutation (122 available)

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

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

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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