Gene Gene information from NCBI Gene database.
Entrez ID 5052
Gene name Peroxiredoxin 1
Gene symbol PRDX1
Synonyms (NCBI Gene)
MSP23NKEF-ANKEFAPAGPAGAPAGBPRX1PRXITDPX2
Chromosome 1
Chromosome location 1p34.1
Summary This gene encodes a member of the peroxiredoxin family of antioxidant enzymes, which reduce hydrogen peroxide and alkyl hydroperoxides. The encoded protein may play an antioxidant protective role in cells, and may contribute to the antiviral activity of C
miRNA miRNA information provided by mirtarbase database.
82
miRTarBase ID miRNA Experiments Reference
MIRT019836 hsa-miR-375 Microarray 20215506
MIRT025797 hsa-miR-7-5p Sequencing 20371350
MIRT048535 hsa-miR-100-5p CLASH 23622248
MIRT046315 hsa-miR-23b-3p CLASH 23622248
MIRT041864 hsa-miR-484 CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
41
GO ID Ontology Definition Evidence Reference
GO:0000302 Process Response to reactive oxygen species IEA
GO:0001501 Process Skeletal system development TAS 8089076
GO:0003723 Function RNA binding HDA 22658674, 22681889
GO:0004601 Function Peroxidase activity IDA 11986303
GO:0004601 Function Peroxidase activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
176763 9352 ENSG00000117450
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q06830
Protein name Peroxiredoxin-1 (EC 1.11.1.24) (Natural killer cell-enhancing factor A) (NKEF-A) (Proliferation-associated gene protein) (PAG) (Thioredoxin peroxidase 2) (Thioredoxin-dependent peroxide reductase 2) (Thioredoxin-dependent peroxiredoxin 1)
Protein function Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides and as sensor of hydrog
PDB 2RII , 3HY2 , 4XCS , 7LJ1 , 7WET , 7WEU , 8X71 , 8X73 , 8Z54 , 8Z55 , 8Z56 , 8Z57 , 8Z58 , 9B7A
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00578 AhpC-TSA 8 142 AhpC/TSA family Domain
PF10417 1-cysPrx_C 162 197 C-terminal domain of 1-Cys peroxiredoxin Domain
Sequence
Sequence length 199
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Peroxisome
Cobalamin transport and metabolism
Amoebiasis
  Detoxification of Reactive Oxygen Species
TP53 Regulates Metabolic Genes
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
9
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA, cblC TYPE, DIGENIC Pathogenic rs1379672870 RCV000585793
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Cholangiocarcinoma Benign rs2356560 RCV005921535
Cobalamin C disease Benign rs2356559 RCV001789462
Hepatocellular carcinoma Benign rs2356560 RCV005921531
Malignant lymphoma, large B-cell, diffuse Benign rs2356560 RCV005921532
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma Associate 23065574
Adenocarcinoma of Lung Associate 37620336, 38213773
Adenoma Associate 34409853
Altitude Sickness Associate 39173139
Alzheimer Disease Associate 33049317
Anemia Hemolytic Associate 30521599
Aortic Aneurysm Abdominal Stimulate 21273562
Astrocytoma Associate 20307276
Autistic Disorder Associate 22051046
beta Thalassemia Associate 30521599