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| Nomenclature |
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Symbol:
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Pde6brd1-2H
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Name:
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phosphodiesterase 6B, cGMP, rod receptor, beta polypeptide;
retinal degeneration 1, 2 Harwell
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MGI ID: |
MGI:2178318 |
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Synonyms: |
GENA 308 |
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Gene:
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Pde6b
Location:
Chr5:108388391-108432397 bp, + strand
Genetic Position: Chr5,
53.07 cM
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Mutation
origin |
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Strain of Origin:
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(C3H/HeN x BALB/cAnN)F1
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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: A nonsense mutation in exon 21 (C2395T) caused a premature stop codon at the arginine at position 799.
(J:75964)
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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: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
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All: |
1 reference(s)
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Analysis Tools
