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Allele : Tyr<c-17UThc> tyrosinase; albino deletion 17UThc, Oak Ridge

Primary Identifier	MGI:2153722	Allele Type	Radiation induced
Gene	Tyr	Inheritance Mode	Recessive
Strain of Origin	(101/Rl x C3H/Rl)F1	Is Recombinase	false
Is Wild Type	false

molecularNote

Intragenic mutation.

mutations:
Intragenic deletion

synonyms:
c<17UThc>,
c<17UThc>

earliestPublication:
Rinchik EM, et al. (1993) Molecular analysis of viable spontaneous and radiation-induced albino (c)-locus mutations in the mouse. Mutat Res 286(2):199-207

1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

Other

0 Carried By

0 Driven By

3 Publication categories

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