1. Gene
  2. PRDX6 - peroxiredoxin 6 Gene

PRDX6 - peroxiredoxin 6 Gene

Homo sapiens

Also known as PRX; p29; AOP2; 1-Cys; NSGPx; aiPLA2; LPCAT-5; HEL-S-128m

Gene ID: 9588 | Gene type: protein coding

About PRDX6

Cytogenetic location: 1q25.1 Genomic coordinates (GRCh38): 1:173,477,335-173,488,815 (from NCBI)

This gene has 3 transcripts (splice variants), 184 orthologues and 4 paralogues. Ubiquitous expression in fat (RPKM 236.1), liver (RPKM 127.7) and 25 other tissues.

Summary

The protein encoded by this gene is a member of the thiol-specific antioxidant protein family. This protein is a bifunctional Enzyme with two distinct active sites. It is involved in redox regulation of the cell; it can reduce H(2)O(2) and short chain organic, fatty acid, and phospholipid hydroperoxides. It may play a role in the regulation of phospholipid turnover as well as in protection against oxidative injury. [provided by RefSeq, Jul 2008]

PRDX6 Products(1)

mRNA Protein Name
NM_004905.3 NP_004896.1 peroxiredoxin-6

PRDX6 Protein Structure

AhpC-TSA

AhpC-TSA: AhpC/TSA family (7 - 144)

1-cysPrx_C

1-cysPrx_C: C-terminal domain of 1-Cys peroxiredoxin (166 - 205)

  • 0
  • 100
  • 200
  • 224 a.a.
Protein Preferred Names Protein Names

peroxiredoxin-6

1-Cys PRX

Recombinant PRDX6 Proteins

Cat. No. Product Name Accession Purity
HY-P71145 PRDX6 Protein, Human (His) P30041 (M1-P224) ≥95%

Related Diseases

Diseases Alias
Gnathomiasis

Gnathostomiasis

Infectious Disease By Gnathostoma

Gnathostomosis

Wandering Swelling

Fuchs' Endothelial Dystrophy

Fuchs Endothelial Corneal Dystrophy

Fuchs Endothelial Dystrophy

Fuchs Dystrophy

Fced

Fuchs' Corneal Dystrophy

Fuchs' Endothelial Corneal Dystrophy

Fuchs Atrophy

Fuchs Corneal Dystrophy

Endoepithelial Corneal Dystrophy

Fecd

Late Hereditary Endothelial Dystrophy

Corneal Dystrophy, Fuchs Endothelial

Dystrophy, Corneal, Fuchs Endothelial

Corneal Dystrophy, Fuchs' Endothelial, 1

Diabetic Cataract

Cataract - Diabetic

Small Intestine Leiomyosarcoma

Leiomyosarcoma Of The Small Bowel

Smooth Muscle Connective Tissue Tumor

Leiomyosarcoma Of Small Intestine

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Macaca mulatta PRDX6 VGNC VGNC:76267
Felis catus PRDX6 VGNC VGNC:107925
Bos taurus PRDX6 VGNC VGNC:33304
Mus musculus PRDX6 MGD MGI:894320
Canis familiaris PRDX6 VGNC VGNC:44953
Rattus norvegicus PRDX6 RGD RGD:71005
Others PRDX6 NCBI