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Pde6brd1
Spontaneous Allele Detail
Nomenclature
Symbol: Pde6brd1
Name: phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide; retinal degeneration 1
MGI ID: MGI:1856373
Synonyms: Pdebrd1, rd, rd1, rd-1, rodless retina
Gene: Pde6b  Location: Chr5:108388391-108432397 bp, + strand  Genetic Position: Chr5, 53.07 cM
Retinal degeneration in Pde6brd1/Pde6brd1, and Pde6brd1/Pde6brd1 Cry1tm1Asn/Cry1tm1Asn Cry2tm1Asn/Cry2tm1Asn mouse retinas

Show the 1 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  various
Mutation
description
Allele Type:    Spontaneous
Mutations:    Single point mutation, Viral insertion
 
Mutation details
Inheritance:    Recessive
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Disease models
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Expression
In Mice Carrying this Mutation: 3 assay results
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 78 strains available      Cell Lines: 2 lines available
Carrying any Pde6b Mutation:  104 strains or lines available
Notes
The following inbred strains are known to be homozygous for Pde6b: C3H sublines, CBA/J, FVB/NJ, PL/J, SB, SJL/J, and SWR/J.

References
Original:  J:24999 Keeler CE, The inheritance of a retinal abnormality in white mice. Proc Natl Acad Sci U S A. 1924 Jul;10(7):329-33
All:  249 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
07/23/2014
MGI 5.19
The Jackson Laboratory