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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID 		Pde6brd1-2H
retinal degeneration 1, 2 Harwell
MGI:2178318
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
 		Pde6brd1-2H/Pde6brd1-2H involves: BALB/cAnN * C3H/HeN MGI:3028386
ht2
 		Pde6brd1-2H/Pde6brd1 involves: BALB/cAnN * C3H/HeN MGI:3028381


Genotype
MGI:3028386
hm1
Allelic
Composition		 Pde6brd1-2H/Pde6brd1-2H
Genetic
Background		 involves: BALB/cAnN * C3H/HeN
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pde6brd1-2H mutation (3 available); any Pde6b mutation (122 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
vision/eye
retina degeneration ( J:75964 )
• rapid onset of degeneration




Genotype
MGI:3028381
ht2
Allelic
Composition		 Pde6brd1-2H/Pde6brd1
Genetic
Background		 involves: BALB/cAnN * C3H/HeN
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pde6brd1 mutation (41 available); any Pde6b mutation (122 available)
Pde6brd1-2H mutation (3 available); any Pde6b mutation (122 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
vision/eye
retina degeneration ( J:75964 )
• 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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Send questions and comments to User Support. 		last database update
11/05/2024
MGI 6.24 		The Jackson Laboratory