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Pde6atvrm58
Chemically induced Allele Detail
Summary
Symbol: Pde6atvrm58
Name: phosphodiesterase 6A, cGMP-specific, rod, alpha; translational vision research model 58
MGI ID: MGI:4867884
Gene: Pde6a  Location: Chr18:61353387-61422995 bp, + strand  Genetic Position: Chr18, 34.41 cM
Alliance: Pde6atvrm58 page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsENU induced a point mutation (T to C) that results in the amino acid substitution of proline for leucine at position 638 (L638P) within the conserved metal dependent phosphohydrolase HD domain. (J:166679, J:214072)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 3 anatomical structure(s)
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 Pde6a Mutation:  52 strains or lines available
References
Original:  J:166679 Won J, et al., Mouse model resources for vision research. J Ophthalmol. 2011;2011:391384
All:  3 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
04/23/2024
MGI 6.23
The Jackson Laboratory