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Phenotypes Associated with This Genotype
Genotype
MGI:3028388
Allelic
Composition
Pde6brd1-3H/Pde6brd1-3H
Genetic
Background
involves: BALB/cAnN * C3H/HeN
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pde6brd1-3H mutation (2 available); any Pde6b mutation (117 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• rapid onset of degeneration

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