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Phenotypes Associated with This Genotype
Genotype
MGI:3028003
Allelic
Composition
Pde6batrd3/Pde6brd1
Genetic
Background
involves: BALB/cAnN * C3H/HeN
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pde6batrd3 mutation (2 available); any Pde6b mutation (117 available)
Pde6brd1 mutation (88 available); any Pde6b mutation (117 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• slow onset of degeneration; the visual tracking response persists until several weeks of age in contrast to Pde6brd1 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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last database update
02/16/2021
MGI 6.16
The Jackson Laboratory