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Oca2p-x
Spontaneous Allele Detail
Summary
Symbol: Oca2p-x
Name: oculocutaneous albinism II; pink-eyed dilution extra dark
MGI ID: MGI:1856124
Synonyms: px
Gene: Oca2  Location: Chr7:55889508-56186266 bp, + strand  Genetic Position: Chr7, 33.44 cM
Alliance: Oca2p-x page
Mutation
origin
Strain of Origin:  C3H/HeH
Mutation
description
Allele Type:    Spontaneous
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 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:  70 strains or lines available
References
Original:  J:15082 Phillips RJS, Description of the phenotypes of p-alleles (other than p) held at Harwell. Mouse News Lett. 1977;56:38
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)
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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory