T(7;18)50H
Radiation induced Allele Detail

Summary

• 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)

Disease models

Expression

In Structures Affected by this Mutation:

4 anatomical structure(s)

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(3):448-467
• All: 9 reference(s)