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| Nomenclature |
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Symbol:
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Wfs1tm1Yoka
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Name:
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Wolfram syndrome 1 homolog (human);
targeted mutation 1, Yoshitomo Oka
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MGI ID: |
MGI:3044175 |
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Synonyms: |
wfs1- |
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Gene:
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Wfs1
Location:
Chr5:36966104-36988982 bp, - strand
Genetic Position: Chr5,
19.46 cM
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Mutation origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:90420
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Parent Cell Line:
| Not Specified (ES Cell) |
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Strain of Origin:
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129/Sv
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Mutation description |
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Allele
Type: | |
Targeted (knock-out) |
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Mutation: | |
Insertion |
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Mutation details: A neomycin-resistance gene was inserted into the second exon, which contains the initial ATG codon. Western blot indicated absence of protein in mutant brains. (J:90420)
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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 Wfs1 Mutation:
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6 strains or lines available |
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| References |
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Original: |
J:90420
Ishihara H et al.,
"Disruption of the WFS1 gene in mice causes progressive beta-cell loss and impaired stimulus-secretion coupling in insulin secretion."
Hum Mol Genet 2004 Jun 1;13(11):1159-70
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All: |
6 reference(s)
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