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]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TYRP1-20-RE | 20 (40 μL) | 200 μL |  |
Request Pricing |
| TYRP1-20-OR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| TYRP1-20-GO | 20 (40 μL) | 200 μL |  |
Request Pricing |
| TYRP1-20-GR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| TYRP1-20-AQ | 20 (40 μL) | 200 μL |  |
Request Pricing |
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]
Gene Symbol : TYRP1
Gene Name : Tyrosinase related protein 1
Chromosome : CHR 9: 126,933,84-127,102,65
Locus : 9p23
Alt. Genes : LRPPRC
Lorem Ipsum is simply dummy text of the printing and typesetting industry.
Lorem Ipsum is simply dummy text of the printing and typesetting industry.