Del(13)36H
Radiation induced Allele Detail

Summary

• Symbol: Del(13)36H
• Name: deletion, Chr 13, Harwell 36
• MGI ID: MGI:3607783
• Synonyms: Del(13)Svea36H, Del36H
• Gene: Del(13)36H Location: unknown Genetic Position: Chr13, cytoband A3.3-A5

Mutation origin

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

Mutation description

• Allele Type: Radiation induced
• Mutation: Intergenic deletion
• Del(13)36H involves 467 genes/genome features (A530084C06Rik, n-TMcat2, n-TAagc7 ...) View all
• Mutation details: This deletion, induced by X-irradiation of a (C3H/HeH x101/H)F1 female mouse, encompasses 12.66 Mb representing approximately 20% of mouse Chr 13 including bands A3.1 through A4. The deleted segment shares synteny with regions of human 6p25 and 6p22 associated with 6p deletion syndromes and 6p associated disorders. (J:94183, J:101156)

Find Mice (IMSR)

• Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
• Carrying this Mutation: Mouse Strains: 0 strains available Cell Lines: 0 lines available
• Carrying any Del(13)36H Mutation: 0 strains or lines available

References

• Original: J:16316 Tease C, et al., Cytogenetic detection of four new, viable deletions in the progeny of X-irradiated females. Mouse Genome. 1993;91(4):855
• All: 5 reference(s)