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Pde6anmf282
Chemically induced Allele Detail
Nomenclature
Symbol: Pde6anmf282
Name: phosphodiesterase 6A, cGMP-specific, rod, alpha; neuroscience mutagenesis facility, 282
MGI ID: MGI:3611307
Synonyms: nmf-282, NMF282
Gene: Pde6a  Location: Chr18:61220482-61289924 bp, + strand  Genetic Position: Chr18, 34.41 cM
Mutation
origin
Strain of Origin:  A.B6-Tyr+/J
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsThis phenotypic mutation was identified in an ENU mutagenesis screen. The molecular mutation is a single nucleotide G to A missense transition in exon 16, predicted to cause an amino acid change from valine to methionine (V685M). (J:142108)
Inheritance:    Recessive
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: 3 anatomical structures
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:  29 strains or lines available
References
Original:  J:87349 JAX Neuroscience Mutagenesis Facility, Heritable mouse mutants from JAX NMF ENU Mutagenesis Program. MGI Direct Data Submission. 2004-7;
All:  6 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
05/15/2018
MGI 6.12
The Jackson Laboratory