All Phenotypes Oca2<p-8FDFoD> MGI Mouse

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Phenotypes associated with this allele

Allele Symbol
Allele Name
Allele ID

Oca2^p-8FDFoD
pink-eyed dilution 8FDFoD
MGI:3798907

Summary

3 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Oca2^p-8FDFoD/Oca2^p-8FDFoD	involves: 101/Rl * C3H/Rl	MGI:3849884
ht2	Oca2^p-4THO-II/Oca2^p-8FDFoD	involves: 101/Rl * C3H/Rl	MGI:3799478
ht3	Oca2^p/Oca2^p-8FDFoD	involves: 101/Rl * C3H/Rl	MGI:3849885

Allelic Composition	Oca2^p-8FDFoD/Oca2^p-8FDFoD
Genetic Background	involves: 101/Rl * C3H/Rl

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Oca2^p-8FDFoD mutation (1 available); any Oca2 mutation (69 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

mortality/aging

prenatal lethality, complete penetrance ( J:100221 )

Allelic Composition	Oca2^p-4THO-II/Oca2^p-8FDFoD
Genetic Background	involves: 101/Rl * C3H/Rl

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Oca2^p-4THO-II mutation (4 available); any Oca2 mutation (69 available)
Oca2^p-8FDFoD mutation (1 available); any Oca2 mutation (69 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

mortality/aging

neonatal lethality ( J:12553 )

craniofacial

cleft palate ( J:12553 )

digestive/alimentary system

cleft palate ( J:12553 )

growth/size/body

cleft palate ( J:12553 )

Allelic Composition	Oca2^p/Oca2^p-8FDFoD
Genetic Background	involves: 101/Rl * C3H/Rl

Find Mice

Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Oca2^p mutation (11 available); any Oca2 mutation (69 available)
Oca2^p-8FDFoD mutation (1 available); any Oca2 mutation (69 available)

♀	phenotype observed in females
♂	phenotype observed in males
N	normal phenotype

pigmentation

abnormal coat/hair pigmentation ( J:100221 )

• reduced eumelanin pigmentation in hair

absent eye pigmentation ( J:100221 )

vision/eye

absent eye pigmentation ( J:100221 )

integument

abnormal coat/hair pigmentation ( J:100221 )

• reduced eumelanin pigmentation in hair

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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