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| Nomenclature |
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Symbol:
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Sh3bp2tm1Bjro
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Name:
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SH3-domain binding protein 2;
targeted mutation 1, Bjorn R Olsen
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MGI ID: |
MGI:3698401 |
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Gene:
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Sh3bp2
Location:
Chr5:34525838-34563625 bp, + strand
Genetic Position: Chr5,
17.89 cM
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Mutation origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:117880
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Parent Cell Line:
| J1 (ES Cell) |
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Strain of Origin:
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129S4/SvJae
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Mutation description |
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Allele
Type: | |
Targeted (knock-in) |
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Mutations: | |
Insertion, Nucleotide substitutions |
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Mutation details: A proline to arginine mutation was inserted into exon 9. A floxed neo included in the vector was subsequently removed from the locus. (J:117880)
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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 Sh3bp2 Mutation:
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2 strains or lines available |
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| References |
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Original: |
J:117880
Ueki Y et al.,
"Increased myeloid cell responses to M-CSF and RANKL cause bone loss and inflammation in SH3BP2 'cherubism' mice."
Cell 2007 Jan 12;128(1):71-83
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All: |
5 reference(s)
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