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| Nomenclature |
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Symbol:
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Pde6anmf282
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Name:
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phosphodiesterase 6A, cGMP-specific, rod, alpha;
neuroscience mutagenesis facility, 282
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MGI ID: |
MGI:3611307 |
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Synonyms: |
nmf-282, NMF282 |
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Gene:
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Pde6a
Location:
Chr18:61220482-61289924 bp, + strand
Genetic Position: Chr18,
34.41 cM
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Mutation
origin |
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Strain of Origin:
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A.B6-Tyr+/J
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Mutation
description |
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Allele
Type: | |
Chemically induced (ENU) |
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Mutation: | |
Single point mutation |
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Mutation details: This 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)
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Inheritance: | |
Recessive |
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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Disease models
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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| References |
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Original: |
J:87349
JAX Neuroscience Mutagenesis Facility,
"Heritable mouse mutants from JAX NMF ENU Mutagenesis Program"
MGI Direct Data Submission 2004-7;():
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All: |
4 reference(s)
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Analysis Tools
