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T(7;18)50H
Radiation induced Allele Detail
Nomenclature
Symbol: T(7;18)50H
Name: reciprocal translocation, Chr 7 and 18, Harwell 50
MGI ID: MGI:3029990
Gene: T(7;18)50H  Location: unknown  Genetic Position: Chr18, cytoband B2
T(7;18)50H homozygous female: FISH to metaphase chromosomes

Show the 3 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  (C3H/HeH x 101/H)F1
Mutation
description
Allele Type:    Radiation induced
Mutation:    Translocation
    The chromosomal breakpoints for this reciprocal translocation are at 7E2 and 18B2. (J:148604)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 6 anatomical structures
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any T(7;18)50H Mutation:  2 strains or lines available
References
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
All:  9 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
05/15/2018
MGI 6.12
The Jackson Laboratory