Summary | Mutation origin | Mutation description | Phenotypes | Find Mice (IMSR) | References

Symbol:	Oca2p-87H
Name:	oculocutaneous albinism II; pink-eyed dilution 87 Harwell
MGI ID:	MGI:1856314
Synonyms:	p87H
Gene:	Oca2  Location: Chr7:55889508-56186266 bp, + strand  Genetic Position: Chr7, 33.44 cM
Alliance:	Oca2p-87H page

Strain of Origin:

(C3H/HeH x 101/H)F1

Allele Type:    Radiation induced Mutation:    Deletion   Oca2p-87H involves 1 genes/genome features (Oca2) View all   Mutation details: The mutation was identified as an allele of Oca2 by its failure to complement Oca2p. (J:2108) Inheritance:    Recessive

View phenotypes and curated references for all genotypes (concatenated display).

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Oca2 Mutation:	67 strains or lines available

Original:	J:2108 Lyon MF, et al., Genetic and molecular analysis of recessive alleles at the pink-eyed dilution (p) locus of the mouse. Proc Natl Acad Sci U S A. 1992 Aug 1;89(15):6968-72
All:	1 reference(s)