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Oca2p-2Btlr
Chemically induced Allele Detail
Summary
Symbol: Oca2p-2Btlr
Name: oculocutaneous albinism II; pink-eyed dilution 2 Bruce Beutler
MGI ID: MGI:3783461
Synonyms: Oca2m2Btlr, whitemouse
Gene: Oca2  Location: Chr7:55889508-56186266 bp, + strand  Genetic Position: Chr7, 33.44 cM
Alliance: Oca2p-2Btlr page
Mutation
origin
Strain of Origin:  C57BL/6J
Project Collection: Beutler Mutagenetix
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsThe whitemouse mutation corresponds to a T-to-C transition at nucleotide position 2303, in the 21st of 24 total exons, resulting in replacement of tryptophan by arginine at amino acid position 725 of the protein (W725R), in the tenth transmembrane domain. (J:133622)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
Find Mice (IMSR)
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:  69 strains or lines available
References
Original:  J:133622 Rutschmann S, et al., Whitemouse is an allele of Oca2 and displays pigmentation defects. MGI Direct Data Submission. 2008;
All:  1 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
04/23/2024
MGI 6.23
The Jackson Laboratory