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Allele : Oca2<p-46DfiOD> oculocutaneous albinism II; pink-eyed dilution 46DfiOD

Primary Identifier	MGI:1857914	Allele Type	Radiation induced
Gene	Oca2	Inheritance Mode	Recessive
Strain of Origin	(101/Rl x C3H/Rl)F1 x p STOCK	Is Recombinase	false
Is Wild Type	false

molecularNote

This mutation includes a large deletion removing all of Herc2 and p.

mutations:
Intergenic deletion

synonyms:
p<46DfiOD>,
p<46DfiOD>,
Oca2<p-88R>,
Herc2<p-46DfiOD>,
Herc2<p-46DfiOD>,
Oca2<p-88R>

earliestPublication:
Culiat CT, et al. (1993) Concordance between isolated cleft palate in mice and alterations within a region including the gene encoding the beta 3 subunit of the type A gamma-aminobutyric acid receptor. Proc Natl Acad Sci U S A 90(11):5105-9

1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

Other

0 Carried By

0 Driven By

9 Publication categories

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