QuickView for TYRP1 (gene)

Gene Symbol:

TYRP1 Homo sapiens

Full name:

tyrosinase related protein 1

Synonyms:

CAS2, CATB, GP75, OCA3, TRP, TRP1, TYRP, b-PROTEIN, 5,6-dihydroxyindole-2-carboxylic acid oxidase, DHICA oxidase, catalase B, glycoprotein 75, melanoma antigen gp75

Genomic Location:

Chr 9: 12683449-12700258

Description:

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.

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.

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Orthologs:

Mus musculus ,  Rattus norvegicus ,  Macaca mulatta ,  Bos taurus ,  Gallus gallus ,  Canis lupus familiaris ,  Danio rerio ,  Pan troglodytes

External Links:

Entrez Gene

Transcription Factor
Binding Sites:

ZIC1_01 ,  MYCMAX_02 ,  GGATTA_PITX2_Q2 ,  CTTTAAR_UNKNOWN ,  TGCTTTG_MIR330 ,  CRX_Q4

miRNA binding sites
(Source: TargetScan):

Predicted Gene Targets for miR-330

Cytogenetic Map:

9p23

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