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NCBI Description of TYRP1 |
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. |
Community Annotation of TYRP1 Add / Edit TYRP1: Annotations
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Figure notes
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Data details