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| Nomenclature |
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Symbol:
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T(7;18)50H
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Name:
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reciprocal translocation, Chr 7 and 18, Harwell 50
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MGI ID: |
MGI:3029992 |
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Gene:
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T(7;18)50H
Location:
unknown
Genetic Position: Chr7,
cytoband E2
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Mutation
origin |
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Strain of Origin:
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(C3H/HeH x 101/H)F1
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Mutation
description |
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Allele
Type: | |
Radiation induced |
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Mutation: | |
Translocation |
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The chromosomal breakpoints for this reciprocal translocation are at 7E2 and 18B2. (J:148604)
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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 T(7;18)50H Mutation:
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0 strains or lines available |
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| References |
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Original: |
J:12947
Lyon MF et al.,
"The overall rates of dominant and recessive lethal and visible mutation induced by spermatogonial X-irradiation of mice."
Genet Res 1964;5():448-467
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All: |
8 reference(s)
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Analysis Tools
