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Pde6brd1-2J
Chemically induced Allele Detail
Nomenclature
Symbol: Pde6brd1-2J
Name: phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide; retinal degeneration 1, 2 Jackson
MGI ID: MGI:2665102
Synonyms: neuroscience mutagenesis facility, 137, nmf137, NMF137, Pde6b2J, Pde6bnmf137
Gene: Pde6b  Location: Chr5:108388391-108432397 bp, + strand  Genetic Position: Chr5, 53.07 cM
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Nucleotide substitutions
 
Mutation details
Inheritance:    Recessive
Phenotypes
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View phenotypes for all genotypes (concatenated display).
Disease models
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Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Pde6b Mutation:  104 strains or lines available
References
Original:  J:122722 Chang B, et al., Two mouse retinal degenerations caused by missense mutations in the beta-subunit of rod cGMP phosphodiesterase gene. Vision Res. 2007 Mar;47(5):624-33
All:  4 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
12/09/2014
MGI 5.20
The Jackson Laboratory