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

Symbol:	Oca2p-17FATWb
Name:	oculocutaneous albinism II; pink-eyed dilution 17FATWb
MGI ID:	MGI:1857918
Synonyms:	Herc2p-17FATWb, Oca2p-27R, p17FATWb
Gene:	Oca2  Location: Chr7:55889508-56186266 bp, + strand  Genetic Position: Chr7, 33.44 cM
Alliance:	Oca2p-17FATWb page

Strain of Origin:

(101/Rl x C3H/Rl)F1 x p STOCK

Allele Type:    Radiation induced Mutation:    Deletion   Oca2p-17FATWb involves 1 genes/genome features (Herc2) View all   Mutation details: This mutation includes a deletion from Herc2 at nucleotide ~2600 ending before the 5-prime end of p, and possibly an inversion. (J:56827, J:100221) Inheritance:    Not Specified

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: 1 strain available      Cell Lines: 0 lines available
Carrying any Oca2 Mutation:	69 strains or lines available

Original:	J:29903 Russell LB, et al., Complementation analyses for 45 mutations encompassing the pink-eyed dilution (p) locus of the mouse. Genetics. 1995 Dec;141(4):1547-62
All:	4 reference(s)