Symbol Name ID |
Oca2
oculocutaneous albinism II MGI:97454 |
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 |
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Availability | Mouse Genotype | ||||
Oca2p-2Btlr/Oca2p-2Btlr | |||||
Oca2p-3Btlr/Oca2p-3Btlr | |||||
Oca2p-4Btlr/Oca2p-4Btlr | |||||
Oca2p-5Btlr/Oca2p-5Btlr | |||||
Oca2p-6Btlr/Oca2p-6Btlr | |||||
Oca2p-7Btlr/Oca2p-7Btlr | |||||
Oca2p-7R/Oca2p-7R | |||||
Oca2p-9J/Oca2p-9J | |||||
Oca2p-15J/Oca2p-15J | |||||
Oca2p-18J/Oca2p-18J | |||||
Oca2p-65H/Oca2p-65H | |||||
Oca2p-103G/Oca2p-103G | |||||
Oca2p-Btlr/Oca2p-Btlr | |||||
Oca2p-cas/Oca2p-cas | |||||
Oca2p-d/Oca2p-d | |||||
Oca2p-dn/Oca2p-dn | |||||
Oca2p-s/Oca2p-s | |||||
Oca2p-un+2J/Oca2p-un+2J | |||||
Oca2p-un+3J/Oca2p-un+3J | |||||
Oca2p-un+J/Oca2p-un+J | |||||
Oca2p-un/Oca2p-un | |||||
Oca2p-x/Oca2p-x | |||||
Oca2p/Oca2p | |||||
Oca2p-65H/Oca2p | |||||
Oca2p-66H/Oca2p | |||||
Oca2p-86H/Oca2p | |||||
Oca2p-88H/Oca2p | |||||
Oca2p-un/Oca2p-un+J | |||||
Oca2p/Oca2p-7R | |||||
Oca2p/Oca2p-8FDFoD | |||||
Oca2p/Oca2p-80K | |||||
Oca2p/Oca2p-103G |
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 09/03/2024 MGI 6.24 |
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