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Oca2p-23DFiOD
Radiation induced Allele Detail
Nomenclature
Symbol: Oca2p-23DFiOD
Name: oculocutaneous albinism II; pink-eyed dilution 23DFiOD
MGI ID: MGI:3043517
Synonyms: Oca2p-52R, p23DFiOD
Gene: Oca2  Location: Chr7:56239760-56536518 bp, + strand  Genetic Position: Chr7, 33.44 cM
Mutation
origin
Strain of Origin:  (101/Rl x C3H/Rl)F1
Mutation
description
Allele Type:    Radiation induced
Mutation:    Deletion
  Oca2p-23DFiOD involves 5 genes/genome features (Oca2, Gabrg3, Gabra5 ...) View all
 
Mutation detailsThis deletion region extends distally from the p locus past Gabrb3 to between D7Mit198 and D7Mit84. Included in the deletion region is Atp10a. (J:29904, J:66645, J:100221)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 4 anatomical structures
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:  59 strains or lines available
Notes
Phenotypes related to obesity may be the consequence of disruption of Atp10a at the distal end of this deletion J:89922 .
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:  6 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
12/03/2019
MGI 6.14
The Jackson Laboratory