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Pde6brd1-4H
Chemically induced Allele Detail
Summary
Symbol: Pde6brd1-4H
Name: phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide; retinal degeneration 1, 4 Harwell
MGI ID: MGI:2178320
Synonyms: Gena366, GENA 366
Gene: Pde6b  Location: Chr5:108536239-108579609 bp, + strand  Genetic Position: Chr5, 53.07 cM
Alliance: Pde6brd1-4H page
Mutation
origin
Strain of Origin:  (C3H/HeN x BALB/cAnN)F1
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
    A T2067A mutation in exon 17 changed the tyrosine at position 689 to a premature stop codon. (J:75964)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 2 strains available      Cell Lines: 0 lines available
Carrying any Pde6b Mutation:  119 strains or lines available
References
Original:  J:75964 Thaung C, et al., Novel ENU-induced eye mutations in the mouse: models for human eye disease. Hum Mol Genet. 2002 Apr 1;11(7):755-67
All:  2 reference(s)

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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory