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Oca2+
Allele Detail

Nomenclature
Symbol: Oca2+
Name: oculocutaneous albinism II; wild type
MGI ID: MGI:2383978
Gene: Oca2   Location: Chr7:63495130-63791887 bp, + strand    Genetic Position: Chr7, 28.0 cM
Mutation
description
Allele Type: Not Specified
Find Mice (IMSR) Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation: Mouse Strains: 5 strains available      Cell Lines: 0 lines available
Carrying any Oca2 Mutation: 166 strains or lines available
Expression
In Mice Carrying this Mutation: 11 assay results
Phenotype
summary
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Phenotype Summary by Mammalian Phenotype terms

(show or hide all annotated terms)

Genotypes are listed in the next section.

      Key:  
hm homozygous ht heterozygous
cn conditional genotype  cx complex: > 1 genome feature
tg involves transgenes ot other: hemizygous, indeterminate,...
N normal phenotype expected model not found
Affected SystemsGenotypes:
 
ht1
 
cx2
 
cx3
  
pigmentation          
  
  
reproductive system          
  
  
skin/coat/nails          
  
Phenotypic
data by
genotype
Phenotypic Data by Genotype

(show or hide all phenotypic details)

GenotypeAllelic CompositionGenetic Background
  
 ht1   
Oca2p-25H/Oca2+ Not Specified
  
 cx2   
A/a
Myo5ad/Myo5a+
Oca2p/Oca2+
Tyrp1B-lt/Tyrp1+
involves: C58 * CT/Ch
  
 cx3   
Oca2p-Nem/Oca2+
TNem/T+
KDT/NemOdaRbrc
References
All: 1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
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last database update
11/20/2009
MGI_4.31
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The Jackson Laboratory