Del(13)80H
Radiation induced Allele Detail

Summary

• Symbol: Del(13)80H
• Name: deletion, Chr 13, Harwell 80
• MGI ID: MGI:5304931
• Synonyms: Del80H
• Gene: Del(13)80H Location: unknown Genetic Position: Chr13, cytoband A5-B1

Mutation origin

• Strain of Origin: (C3H/HeH x 101/H)F1

Mutation description

• Allele Type: Radiation induced
• Mutation: Intergenic deletion
• Radiation induced a deletion encompassing cytoband A5 through B1 of chromosome 13.
• Inheritance: Dominant

Expression

In Structures Affected by this Mutation:

1 anatomical structure(s)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 2 strains available Cell Lines: 0 lines available
• Carrying any Del(13)80H Mutation: 2 strains or lines available

Notes

The satin locus (Foxq1 MGI:1298228) is known to lie within the region deleted. Generated by irradiation with 2 Gy X-rays.

References

• Original: J:179962 Medical Research Council (MRC) Harwell, Direct Data Submission 2012/02/02. MGI Direct Data Submission. 2012
• All: 1 reference(s)