All Phenotypes Pde6b<rd1-4H> MGI Mouse

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Phenotypes associated with this allele

Allele Symbol
Allele Name
Allele ID

Pde6b^rd1-4H
retinal degeneration 1, 4 Harwell
MGI:2178320

Summary

2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Pde6b^rd1-4H/Pde6b^rd1-4H	involves: BALB/cAnN * C3H/HeN	MGI:3028389
ht2	Pde6b^rd1-4H/Pde6b^rd1	involves: BALB/cAnN * C3H/HeN	MGI:3028383

Allelic Composition	Pde6b^rd1-4H/Pde6b^rd1-4H
Genetic Background	involves: BALB/cAnN * C3H/HeN

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pde6b^rd1-4H mutation (2 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

Allelic Composition	Pde6b^rd1-4H/Pde6b^rd1
Genetic Background	involves: BALB/cAnN * C3H/HeN

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pde6b^rd1 mutation (41 available); any Pde6b mutation (122 available)
Pde6b^rd1-4H mutation (2 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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