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

Symbol:	Oca2p-4THO-II
Name:	oculocutaneous albinism II; pink-eyed dilution 4THO-II
MGI ID:	MGI:2673989
Synonyms:	Oca2p-95R, p4THO-II
Gene:	Oca2  Location: Chr7:55889508-56186266 bp, + strand  Genetic Position: Chr7, 33.44 cM
Alliance:	Oca2p-4THO-II page

Strain of Origin:

(C3H/Rl x 101/Rl)F1

Allele Type:    Radiation induced Mutation:    Deletion   Oca2p-4THO-II involves 4 genes/genome features (Oca2, Gabra5, Mir6389 ...) View all   Mutation details: This deletion is known to encompass the Gabrb3 and the Gabra5 loci. The proximal breakpoint lies within Oca2. (J:29904, J:100221) Inheritance:    Recessive

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

In Mice Carrying this Mutation:

7 assay results

Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:	Mouse Strains: 4 strains available      Cell Lines: 0 lines available
Carrying any Oca2 Mutation:	67 strains or lines available

Original:	J:4101 Nicholls RD, et al., Evaluation of potential models for imprinted and nonimprinted components of human chromosome 15q11-q13 syndromes by fine-structure homology mapping in the mouse. Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):2050-4
All:	11 reference(s)