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Summary Expression Phenotypes Gene Literature (3) GO Terms (19) Nucleotides (92) Proteins (45) Interactants (71) Wiki
XB-GENEPAGE-989254
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 oca2

???displayGene.name???: 
oculocutaneous albinism II

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LOC108708435 ( Nomenclature history )

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Sodium sulfate symporter and related arsenite permeases

AI Protein Function :
The gene oca2 encodes a transporter protein localized to melanosomes and functions in melanin synthesis within melanophores, iridophores, and retinal pigment epithelium.


InterPro :
Cit transptr-like dom, Diverse Ion Transporter

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Diseases: 


Disease Ontology:
oculocutaneous albinism [+]

MIM:
ALBINISM, OCULOCUTANEOUS, TYPE II; OCA2 [+]

External Links:
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???displayGene.expression???                  Development Stages                                               Embryonic Tissues                                                                Adult Tissues
More Information
Xenbase Expression Details In situ images Single cell data at SPRING In situ: RNA-Seq:


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