Gene Gene information from NCBI Gene database.
Entrez ID 5445
Gene name Paraoxonase 2
Gene symbol PON2
Synonyms (NCBI Gene)
-
Chromosome 7
Chromosome location 7q21.3
Summary This gene encodes a member of the paraoxonase gene family, which includes three known members located adjacent to each other on the long arm of chromosome 7. The encoded protein is ubiquitously expressed in human tissues, membrane-bound, and may act as a
miRNA miRNA information provided by mirtarbase database.
59
miRTarBase ID miRNA Experiments Reference
MIRT020479 hsa-miR-106b-5p Microarray 17242205
MIRT021086 hsa-miR-186-5p Sequencing 20371350
MIRT027891 hsa-miR-96-5p Sequencing 20371350
MIRT031391 hsa-miR-16-5p Proteomics 18668040
MIRT050663 hsa-miR-18a-5p CLASH 23622248
Transcription factors Transcription factors information provided by TRRUST V2 database.
2
Transcription factor Regulation Reference
NFKBIA Activation 19401157
SREBF2 Activation 19497963
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
16
GO ID Ontology Definition Evidence Reference
GO:0004064 Function Arylesterase activity IBA
GO:0004064 Function Arylesterase activity IEA
GO:0004064 Function Arylesterase activity TAS 8661009
GO:0005515 Function Protein binding IPI 33961781
GO:0005576 Component Extracellular region IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
602447 9205 ENSG00000105854
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q15165
Protein name Serum paraoxonase/arylesterase 2 (PON 2) (EC 3.1.1.2) (EC 3.1.1.81) (Aromatic esterase 2) (A-esterase 2) (Serum aryldialkylphosphatase 2)
Protein function Capable of hydrolyzing lactones and a number of aromatic carboxylic acid esters. Has antioxidant activity. Is not associated with high density lipoprotein. Prevents LDL lipid peroxidation, reverses the oxidation of mildly oxidized LDL, and inhib
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01731 Arylesterase 167 252 Arylesterase Family
Tissue specificity TISSUE SPECIFICITY: Widely expressed with highest expression in liver, lung, placenta, testis and heart. {ECO:0000269|PubMed:11579088}.
Sequence
MGRLVAVGLLGIALALLGERLLALRNRLKASREVESVDLPHCHLIKGIEAGSEDIDILPN
GLAFFSVGLKFPGLHSFAPDKPGGILMMDLKEEKPRARELRISRGFDLASFNPHGISTFI
DNDDTVYLFVVNHPEFKNTVEIFKFEEAENSLLHLKTVKHELLPSVNDITAVGPAHFYAT
NDHYFSDPFLKYLETYLNLHWANVVYYSPNEVKVVAEGFDSANGINISPDDKYIYVADIL
AHEIHVLEKHTN
MNLTQLKVLELDTLVDNLSIDPSSGDIWVGCHPNGQKLFVYDPNNPPS
SEVLRIQNILSEKPTVTTVYANNGSVLQGSSVASVYDGKLLIGTLYHRALYCEL
Sequence length 354
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Synthesis of 5-eicosatetraenoic acids
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
6
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
PARAOXONASE 2 POLYMORPHISM Benign rs7493, rs12026 RCV000007500
RCV000007501
PON2-related disorder Likely benign; Benign rs1183901052, rs116397066, rs747794096, rs17876183 RCV003897176
RCV003914471
RCV003968985
RCV003980066
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Associate 18842138, 24088404, 34714861
Amyotrophic Lateral Sclerosis Associate 18618303
Asthma Associate 24895604
Atherosclerosis Inhibit 20530481, 21368884
Atherosclerosis Associate 21836061, 26169365, 34714861
Blood Coagulation Disorders Associate 33259846
Carcinogenesis Associate 21368884
Cardiovascular Diseases Associate 16141008, 34714861, 36840500
Cerebral Infarction Associate 36076661
Communicable Diseases Associate 35092416