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OCA2 gene

OCA2 melanosomal transmembrane protein

Key facts

Official symbol
OCA2
Full name
OCA2
Chromosome
15
Map location
15q12-q13.1
Organism
Homo sapiens
NCBI Gene ID
4948
Also known as
BEY, BEY1, BEY2, BOCA, D15S12, EYCL

Function summary

This gene encodes the human homolog of the mouse p (pink-eyed dilution) gene. The encoded protein is believed to be an integral membrane protein involved in small molecule transport, specifically tyrosine, which is a precursor to melanin synthesis. It is involved in mammalian pigmentation, where it may control skin color variation and act as a determinant of brown or blue eye color. Mutations in this gene result in type 2 oculocutaneous albinism. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014].

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Data source: NCBI Gene · alsesAI Gene Library