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TYRP1

Official Full Name
tyrosinase related protein 1
Organism
Homo sapiens
GeneID
7306
Background
This gene encodes a melanosomal enzyme that belongs to the tyrosinase family and plays an important role in the melanin biosynthetic pathway. Defects in this gene are the cause of rufous oculocutaneous albinism and oculocutaneous albinism type III. [provided by RefSeq, Mar 2009]
Synonyms
TRP; CAS2; CATB; GP75; OCA3; TRP1; TYRP; b-PROTEIN;

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