About   Help   FAQ
Oca2p-18CoS
Radiation induced Allele Detail
Summary
Symbol: Oca2p-18CoS
Name: oculocutaneous albinism II; pink-eyed dilution 18CoS
MGI ID: MGI:3612248
Synonyms: Oca2p-29R, p16Cos, p18CoS
Gene: Oca2  Location: Chr7:55889508-56186266 bp, + strand  Genetic Position: Chr7, 33.44 cM
Alliance: Oca2p-18CoS page
Mutation
origin
Strain of Origin:  (101/Rl x C3H/Rl)F1
Mutation
description
Allele Type:    Radiation induced
Mutation:    Deletion
 
Mutation detailsThis 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. (J:56827, J:100221)
Inheritance:    Not Specified
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
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:  70 strains or lines available
References
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:  3 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory