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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.
Protein class

Disease related genes, Human disease related genes, Metabolic proteins

Predicted location

Intracellular, Membrane (different isoforms)

Single cell type specificity

Cell type enriched (Melanocytes)

Immune cell specificity

Not detected in immune cells

Cell line specificity

Cell line enriched (SK-MEL-30)

Interaction

Monomer (PubMed:28661582). Interacts with ATP7A (By similarity).

Molecular function

Monooxygenase, Oxidoreductase

More Types Infomation

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For Research Use Only. Not For Clinical Use.

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