Aliases for GPX1 Gene
External Ids for GPX1 Gene
This gene encodes a member of the glutathione peroxidase family. Glutathione peroxidase functions in the detoxification of hydrogen peroxide, and is one of the most important antioxidant enzymes in humans. This protein is one of only a few proteins known in higher vertebrates to contain selenocysteine, which occurs at the active site of glutathione peroxidase and is coded by UGA, that normally functions as a translation termination codon. In addition, this protein is characterized in a polyalanine sequence polymorphism in the N-terminal region, which includes three alleles with five, six or seven alanine (ALA) repeats in this sequence. The allele with five ALA repeats is significantly associated with breast cancer risk. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
GeneCards Summary for GPX1 Gene
GPX1 (Glutathione Peroxidase 1) is a Protein Coding gene. Diseases associated with GPX1 include hemolytic anemia due to glutathione peroxidase deficiency and keshan disease. Among its related pathways are Metabolism and Metabolism. GO annotations related to this gene include SH3 domain binding and glutathione peroxidase activity. An important paralog of this gene is GPX4.
UniProtKB/Swiss-Prot for GPX1 Gene
Protects the hemoglobin in erythrocytes from oxidative breakdown