Tyr^c-25H
Radiation induced Allele Detail

Summary

• Symbol: Tyr^c-25H
• Name: tyrosinase; albino 25 Harwell
• MGI ID: MGI:1856306
• Synonyms: c^25H, Del(7)c-25H
• Gene: Tyr Location: Chr7:87073979-87142637 bp, - strand Genetic Position: Chr7, 49.01 cM
• Alliance: Tyr^c-25H page

Mutation origin

• Strain of Origin: Not Specified

Mutation description

• Allele Type: Radiation induced
• Mutation: Intergenic deletion
• Mutation details: This allele comprises a cytologically visible intergenic deletion estimated to be less than 6 cM. Minimally Tyr and Mod2 are deleted. (J:5520)
• Inheritance: Recessive

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 Tyr Mutation: 375 strains or lines available

References

• Original: J:5435 Gluecksohn-Waelsch S, et al., Complementation studies of lethal alleles in the mouse causing deficiencies of glucose-6-phosphatase, tyrosine aminotransferase, and serine dehydratase. Proc Natl Acad Sci U S A. 1974 Mar;71(3):825-9
• All: 6 reference(s)