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Radiation induced Allele Detail
Symbol: Tyrc-26DVT
Name: tyrosinase; albino deletion 26DVT, Oak Ridge
MGI ID: MGI:2153742
Synonyms: c26DVT, cFp1, Df(c Mod-2 sh-1)26DVT, Tyrc-49R, Tyrc-Fp1
Gene: Tyr  Location: Chr7:87427405-87493411 bp, - strand  Genetic Position: Chr7, 49.01 cM
Strain of Origin:  (101/Rl x C3H/Rl)F1
Allele Type:    Radiation induced
Mutation:    Deletion
Mutation detailsThis 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
View phenotypes for all genotypes (concatenated display).
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:  347 strains or lines available
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)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.01
The Jackson Laboratory