Tyr^c-26DVT
Radiation induced Allele Detail

Summary

• Symbol: Tyr^c-26DVT
• Name: tyrosinase; albino deletion 26DVT, Oak Ridge
• MGI ID: MGI:2153742
• Synonyms: c^26DVT, c^Fp1, Df(c Mod-2 sh-1)^26DVT, Tyr^c-49R, Tyr^c-Fp1
• Gene: Tyr Location: Chr7:87073979-87142637 bp, - strand Genetic Position: Chr7, 49.01 cM
• Alliance: Tyr^c-26DVT page

Mutation origin

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

Mutation description

• Allele Type: Radiation induced
• Mutation: Deletion
• Tyr^c-26DVT involves 139 genes/genome features (Fah, Zfand6, 2610206C17Rik ...) View all
• Mutation details: This multi-locus deletion, induced by X-ray irradiation of a male mouse, encompasses G-bands 7D3-7E3 and includes, proximally, Fah (fumarylacetoacetate hydrolase) and distally, Aqp11 (aquaporin 11; formerly sjds). The deletion is flanked proximally by Mesdc2, mesoderm development candidate 2, and distally by Hbb, the hemoglobin beta chain complex. (J:54592, J:100221)
• Inheritance: Recessive

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 Tyr Mutation: 379 strains or lines available

References

• Original: J:23420 Russell LB, et al., Analysis of the albino-locus region of the mouse: IV. Characterization of 34 deficiencies. Genetics. 1982 Mar;100(3):427-53
• All: 13 reference(s)