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Gene : TYRP1 Homo sapiens

Name  ? tyrosinase related protein 1 Cytological Location  9p23
Brief Description  tyrosinase related protein 1
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. [provided by RefSeq, Mar 2009]
  • synonyms:
  • b-PROTEIN,
  • uc003zkv.5,
  • TRP1,
  • GP75,
  • OCA3,
  • CAS2,
  • TYRP1,
  • HGNC:12450,
  • TRP,
  • NM_000550,
  • OCA3,
  • TYRP,
  • TYRP,
  • TRP,
  • CATB,
  • CATB,
  • b-PROTEIN,
  • L33830,
  • GP75,
  • OTTHUMG00000021034,
  • CAS2
  • identifiers:
  • 7306,
  • ENSG00000107165,
  • TYRP1

Genome feature

Region: gene ? Length: 16892  
Location: 9:12693375-12710266 Cyto location: 9p23


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Function

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Gene --> GO terms.

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

2 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Gene --> Physical and Genetic Interactions

Expression

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.

 

Other

305 SN Ps

5 Cross References

19 Data Sets

14 Homologues

0 Located Features

90 Rna Seq Results