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| Nomenclature |
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Symbol:
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Pde6anmf363
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Name:
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phosphodiesterase 6A, cGMP-specific, rod, alpha;
neuroscience mutagenesis facility, 363
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MGI ID: |
MGI:3828520 |
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Synonyms: |
NMF363 |
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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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C57BL/6J
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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: ENU mutagenesis was used to create an A to G transition that results in an amino acid substitution of glycine for aspartic acid at position 670 (D670G). (J:142108)
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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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Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available |
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Carrying any Pde6a Mutation:
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7 strains or lines available |
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| References |
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Original: |
J:142108
Sakamoto K et al.,
"New mouse models for recessive retinitis pigmentosa caused by mutations in the Pde6a gene."
Hum Mol Genet 2009 Jan 1;18(1):178-92
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All: |
3 reference(s)
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Analysis Tools
