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| Nomenclature |
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Symbol:
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Recql4tm1Glu
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Name:
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RecQ protein-like 4;
targeted mutation 1, Guangbin Luo
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MGI ID: |
MGI:3045113 |
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Synonyms: |
Recql4- |
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Gene:
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Recql4
Location:
Chr15:76703553-76710559 bp, - strand
Genetic Position: Chr15,
36.28 cM, cytoband D3
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Mutation origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:97101
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Parent Cell Line:
| AB2.2 (ES Cell) |
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Strain of Origin:
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129S7/SvEvBrd-Hprtb-m2
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Mutation description |
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Allele
Type: | |
Targeted (knock-out) |
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Mutations: | |
Insertion, Intragenic deletion |
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Mutation details: The targted mutation replaces a 1075bp genomic fragment encompassing part of exon 9 through exon 13 of the Recql4 gene with a PGKhprt-mini gene cassette. (J:97101)
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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 Recql4 Mutation:
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3 strains or lines available |
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| References |
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Original: |
J:97101
Mann MB et al.,
"Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome."
Hum Mol Genet 2005 Mar 15;14(6):813-25
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All: |
1 reference(s)
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