Del(1)3H
Radiation induced Allele Detail

Summary

• Symbol: Del(1)3H
• Name: deletion, Chr 1, Harwell 3
• MGI ID: MGI:1856175
• Synonyms: Pax3^Sp-r, retarded splotch, Sp-3H
• Gene: Del(1)3H Location: unknown Genetic Position: Chr1, cytoband C5

Mutation origin

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

Mutation description

• Allele Type: Radiation induced
• Mutation: Intergenic deletion
• Del(1)3H involves 66 genes/genome features (Gm25035, Gm27943, Gm27507 ...) View all
• Mutation details: Maternal X-irradiation produced this a deletion of multiple genes. The distal breakpoint maps to a location within D1mit79 and D1mit134 and a proximal endpoint maps between Tnp1 and Vil. (J:28990, J:41878, J:179727)
• Inheritance: Semidominant

Expression

In Structures Affected by this Mutation:

2 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(1)3H Mutation: 2 strains or lines available

References

• Original: J:14096 Beechey CV, et al., Mutations at the Sp locus. Mouse News Lett. 1986;75:28
• All: 5 reference(s)