Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

XB-GENEPAGE-989254
???displayGene.symbol???:
 oca2

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

???displayGene.synonyms???
LOC108708435 ( Nomenclature history )

???displayGene.geneFunction???
Sodium sulfate symporter and related arsenite permeases

AI Protein Function :
oca2 is a melanosomal membrane protein that functions as an ion transporter regulating melanosome pH, thereby influencing melanin synthesis and pigment granule formation; it is essential for normal col...[+]



???displayGene.geneInteractants???
Loading ...

Diseases: 


Disease Ontology:
oculocutaneous albinism [+]

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

External Links:
Loading gene data...
Please wait while we fetch the latest information
???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:


Symbol legend: Blast sequence    View sequence    Literature or expression images   Hover cursor for info