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Allele : Oca2<p-18CoS> oculocutaneous albinism II; pink-eyed dilution 18CoS

Primary Identifier  MGI:3612248 Allele Type  Radiation induced
Gene  Oca2 Inheritance Mode  Not Specified
Strain of Origin  (101/Rl x C3H/Rl)F1 Is Recombinase  false
Is Wild Type  false
molecularNote  This mutation is associated with mottled pigmentation and a mild juvenile development and fertility phenotype (jdf2). Herc2 cDNA sequences and regional P1 end-probes did not detect DNA rearrangements in this allele.
  • mutations:
  • Deletion
  • synonyms:
  • p<16Cos>,
  • p<16Cos>,
  • p<18CoS>,
  • Oca2<p-29R>,
  • p<18CoS>,
  • Oca2<p-29R>
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

4 Publication categories