Del(7)Tyr^c-6H
Radiation induced Allele Detail

Summary

• Symbol: Del(7)Tyr^c-6H
• Name: deletion, Chr 7, albino 6 Harwell
• MGI ID: MGI:1856305
• Synonyms: c^6H, Tyr^c-6H
• Gene: Del(7)Tyr^c-6H Location: unknown Genetic Position: Chr7, Syntenic

Mutation origin

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

Mutation description

• Allele Type: Radiation induced
• Mutation: Intergenic deletion
• Mutation details: This chromosomal aberration comprises a deletion of at least 1 cM in length that affects these loci: Tyr, jdf, Mod2, Eed, and exed. (J:2961, J:5437)
• Inheritance: Recessive

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: 1 strain available Cell Lines: 0 lines available
• Carrying any Del(7)Tyr c-6H Mutation: 0 strains or lines available

References

• Original: J:157682 Searle AG, Mutants c^3H, c^6H. Mouse News Lett. 1970;43:28
• All: 13 reference(s)