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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Pde6brd1-3H
retinal degeneration 1, 3 Harwell
MGI:2178319
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Pde6brd1-3H/Pde6brd1-3H involves: BALB/cAnN * C3H/HeN MGI:3028388
ht2
Pde6brd1-3H/Pde6brd1 involves: BALB/cAnN * C3H/HeN MGI:3028382


Genotype
MGI:3028388
hm1
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 (144 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




Genotype
MGI:3028382
ht2
Allelic
Composition
Pde6brd1-3H/Pde6brd1
Genetic
Background
involves: BALB/cAnN * C3H/HeN
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pde6brd1 mutation (92 available); any Pde6b mutation (144 available)
Pde6brd1-3H mutation (2 available); any Pde6b mutation (144 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





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last database update
12/05/2017
MGI 6.11
The Jackson Laboratory