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Oca2p-39DSD
Radiation induced Allele Detail
Summary
Symbol: Oca2p-39DSD
Name: oculocutaneous albinism II; pink-eyed dilution 39DSD
MGI ID: MGI:1857924
Synonyms: Herc2p-39DSD, Oca2p-75R, p39DSD
Gene: Oca2  Location: Chr7:55889508-56186266 bp, + strand  Genetic Position: Chr7, 33.44 cM
Alliance: Oca2p-39DSD page
Mutation
origin
Strain of Origin:  (101/Rl x C3H/Rl)F1
Mutation
description
Allele Type:    Radiation induced
Mutation:    Other
 
Mutation detailsThis mutation involves a rearrangement detected at nucleotide ~7000 using a cDNA clone isolated from a mouse cerebellum library with a human HERC2 probe. (J:56827, J:100221)
Inheritance:    Not Specified
Phenotypes
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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
Notes
This mutation is associated with mottled pigmentation and a mild juvenile development and fertility phenotype (jdf2; J:56827).
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:  4 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)
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory