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Symbol
Name
ID

Oca2
oculocutaneous albinism II
MGI:97454

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Blue irides	Hypoplasia of the fovea	Hypopigmentation of the fundus	Strabismus	Exotropia	Nystagmus	Myopia	Visual impairment	Reduced visual acuity
Disease(s) Associated with OCA2
oculocutaneous albinism type II

Mouse Phenotypes		abnormal eye pigmentation	absent eye pigmentation	ocular albinism	decreased eye pigmentation
Availability	Mouse Genotype	abnormal eye pigmentation	absent eye pigmentation	ocular albinism	decreased eye pigmentation
	Oca2^p-2Btlr/Oca2^p-2Btlr
	Oca2^p-3Btlr/Oca2^p-3Btlr
	Oca2^p-4Btlr/Oca2^p-4Btlr
	Oca2^p-5Btlr/Oca2^p-5Btlr
	Oca2^p-6Btlr/Oca2^p-6Btlr
	Oca2^p-7Btlr/Oca2^p-7Btlr
	Oca2^p-7R/Oca2^p-7R
	Oca2^p-9J/Oca2^p-9J
	Oca2^p-15J/Oca2^p-15J
	Oca2^p-18J/Oca2^p-18J
	Oca2^p-65H/Oca2^p-65H
	Oca2^p-103G/Oca2^p-103G
	Oca2^p-Btlr/Oca2^p-Btlr
	Oca2^p-cas/Oca2^p-cas
	Oca2^p-d/Oca2^p-d
	Oca2^p-dn/Oca2^p-dn
	Oca2^p-s/Oca2^p-s
	Oca2^p-un+2J/Oca2^p-un+2J
	Oca2^p-un+3J/Oca2^p-un+3J
	Oca2^p-un+J/Oca2^p-un+J
	Oca2^p-un/Oca2^p-un
	Oca2^p-x/Oca2^p-x
	Oca2^p/Oca2^p
	Oca2^p-65H/Oca2^p
	Oca2^p-66H/Oca2^p
	Oca2^p-86H/Oca2^p
	Oca2^p-88H/Oca2^p
	Oca2^p-un/Oca2^p-un+J
	Oca2^p/Oca2^p-7R
	Oca2^p/Oca2^p-8FDFoD
	Oca2^p/Oca2^p-80K
	Oca2^p/Oca2^p-103G

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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