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| Nomenclature |
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Symbol:
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Lrrc17tm1Nik
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Name:
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leucine rich repeat containing 17;
targeted mutation 1, Nigel Killeen
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MGI ID: |
MGI:4460700 |
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Gene:
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Lrrc17
Location:
Chr5:21543527-21575900 bp, + strand
Genetic Position: Chr5,
9.89 cM
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Mutation
origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:161558
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Parent Cell Line:
| E14 (ES Cell) |
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Strain of Origin:
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129P2/OlaHsd
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Mutation
description |
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Allele
Type: | |
Targeted (other) |
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Mutation: | |
Insertion |
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A loxP site, neo cassette, and 5'Hprt minigene was inserted into the locus. (J:161558)
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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 Lrrc17 Mutation:
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2 strains or lines available |
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| References |
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Original: |
J:161558
Wong JC et al.,
"Use of chromosome engineering to model a segmental deletion of chromosome band 7q22 found in myeloid malignancies."
Blood 2010 Jun 3;115(22):4524-32
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All: |
1 reference(s)
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Analysis Tools
