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Oca2p-55H
Radiation induced Allele Detail
Summary
Symbol: Oca2p-55H
Name: oculocutaneous albinism II; pink-eyed dilution 55 Harwell
MGI ID: MGI:5301923
Gene: Oca2  Location: Chr7:55889508-56186266 bp, + strand  Genetic Position: Chr7, 33.44 cM
Alliance: Oca2p-55H page
Mutation
origin
Strain of Origin:  C3H/HeH x 101/H
Mutation
description
Allele Type:    Radiation induced
Mutation:    Undefined
 
Mutation detailsThe mutation was identified as an allele of Oca2 by its failure to complement Oca2p.
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:  67 strains or lines available
References
Original:  J:179354 Medical Research Council (MRC) Harwell, Direct Data Submission 2012/01/19. MGI Direct Data Submission. 2012;
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
03/19/2024
MGI 6.23
The Jackson Laboratory