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| Nomenclature |
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Symbol:
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Npm1tm1Ppp
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Name:
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nucleophosmin 1;
targeted mutation 1, Pier Paolo Pandolfi
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MGI ID: |
MGI:3604807 |
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Synonyms: |
Npm- |
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Gene:
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Npm1
Location:
Chr11:33152287-33163206 bp, - strand
Genetic Position: Chr11,
19.21 cM
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Mutation origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:101494
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Parent Cell Line:
| CJ7 (ES Cell) |
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Strain of Origin:
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129S1/Sv-Oca2+ Tyr+ Kitl+
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Mutation description |
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Allele
Type: | |
Targeted (Reporter) |
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Mutations: | |
Insertion, Intragenic deletion |
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Mutation details: A targeting vector containing GFP was inserted in-frame with exon 2 at the upstream end, with a modified ACN cassette containing a self-excising neo, resulting in the removal of exons 2-7. GFP was demonstrated to express in the same manner as the endogenous protein. (J:101494)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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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 Npm1 Mutation:
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17 strains or lines available |
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Notes |
Heterozygous mice exhibit phenotypic similarity to human myelodysplastic syndromes (MDS).
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| References |
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Original: |
J:101494
Grisendi S et al.,
"Role of nucleophosmin in embryonic development and tumorigenesis."
Nature 2005 Sep 1;437(7055):147-53
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All: |
4 reference(s)
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