Del(10)1H
Radiation induced Allele Detail

Summary

• Symbol: Del(10)1H
• Name: deletion, Chr 10, Harwell 1
• MGI ID: MGI:1856365
• Synonyms: Del(10)Sl¹²1H, Kitl^Sl-12H, SCF, steel 12 Harwell
• Gene: Del(10)1H Location: unknown Genetic Position: Chr10, cytoband D1

Mutation origin

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

Mutation description

• Allele Type: Radiation induced
• Mutation: Deletion
• Del(10)1H involves 1 genes/genome features (Kitl) View all
• Mutation details: This X-ray-induced deletion encompasses about 10% of Chr 10, including the Kitl locus (J:5931). Southern analyses of genomic DNA indicate that there is a 13 kb deletion of sequence present in wild-type DNA and presence of a 7 kb fragment that is not present in wild-type DNA (J:10750). (J:5931, J:10750)
• Inheritance: Semidominant

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(10)1H Mutation: 0 strains or lines available

References

• Original: J:18279 Cattanach BM, et al., A new steel allele with pre-implantation homozygous lethality. Mouse News Lett. 1988;80:156-57
• All: 6 reference(s)