MPO, myeloperoxidase, 4353

N. diseases: 653; N. variants: 25
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs119469014
rs119469014
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C0398595
Disease:
Myeloperoxidase Deficiency
A 0.700 CausalMutation CLINVAR
dbSNP: rs28730837
rs28730837
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C0398595
Disease:
Myeloperoxidase Deficiency
A 0.700 CausalMutation CLINVAR
dbSNP: rs536522394
rs536522394
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C0398595
Disease:
Myeloperoxidase Deficiency
G 0.700 CausalMutation CLINVAR
dbSNP: rs762688992
rs762688992
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C0009402
Disease:
Colorectal Carcinoma
0.700 GeneticVariation UNIPROT
dbSNP: rs2333227
rs2333227
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C0006826
Disease:
Malignant Neoplasms
0.030 GeneticVariation BEFREE Taken together, our findings indicate that <i>MPO</i> SNP rs2333227 serves as a marker of enhanced risk for development of colorectal cancer.<b>Significance:</b> MPO polymorphisms are a guide for high risk and poor prognosis in patients colorectal cancer.<i>Cancer Res; 78(10); 2760-9.©2018 AACR</i>. 29540402 2018
dbSNP: rs2333227
rs2333227
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C0006826
Disease:
Malignant Neoplasms
0.030 GeneticVariation BEFREE The myeloperoxidase (MPO) -463G>A (rs2333227) polymorphism has been linked with increased susceptibility to the development of various malignancies. 27197583 2016
dbSNP: rs2333227
rs2333227
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C0006826
Disease:
Malignant Neoplasms
0.030 GeneticVariation BEFREE We suggest that rs2333227 (MPO_ -463G/A) and rs854560 polymorphisms have a great predictive significance; they could probably be utilized as cancer predictors in the future. 23167629 2012
dbSNP: rs2333227
rs2333227
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C1306459
Disease:
Primary malignant neoplasm
0.020 GeneticVariation BEFREE Taken together, our findings indicate that <i>MPO</i> SNP rs2333227 serves as a marker of enhanced risk for development of colorectal cancer.<b>Significance:</b> MPO polymorphisms are a guide for high risk and poor prognosis in patients colorectal cancer.<i>Cancer Res; 78(10); 2760-9.©2018 AACR</i>. 29540402 2018
dbSNP: rs2333227
rs2333227
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C0600139
Disease:
Prostate carcinoma
0.020 GeneticVariation BEFREE The authors investigated associations of serum phospholipid n-3 and n-6 polyunsaturated fatty acids (PUFAs) and trans-fatty acids with prostate cancer risk, and whether myeloperoxidase G-463A (rs2333227) modified the associations in the Carotene and Retinol Efficacy Trial (CARET) (Seattle, Washington; Irvine, California; New Haven, Connecticut; San Francisco, California; Baltimore, Maryland; and Portland, Oregon, 1985-2003). 23535901 2013
dbSNP: rs2333227
rs2333227
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C0376358
Disease:
Malignant neoplasm of prostate
0.020 GeneticVariation BEFREE The authors investigated associations of serum phospholipid n-3 and n-6 polyunsaturated fatty acids (PUFAs) and trans-fatty acids with prostate cancer risk, and whether myeloperoxidase G-463A (rs2333227) modified the associations in the Carotene and Retinol Efficacy Trial (CARET) (Seattle, Washington; Irvine, California; New Haven, Connecticut; San Francisco, California; Baltimore, Maryland; and Portland, Oregon, 1985-2003). 23535901 2013
dbSNP: rs2333227
rs2333227
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C1306459
Disease:
Primary malignant neoplasm
0.020 GeneticVariation BEFREE We suggest that rs2333227 (MPO_ -463G/A) and rs854560 polymorphisms have a great predictive significance; they could probably be utilized as cancer predictors in the future. 23167629 2012
dbSNP: rs376373278
rs376373278
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C0023890
Disease:
Liver Cirrhosis
0.020 GeneticVariation BEFREE We assessed the role of the G(-463)A-MPO, T(-262)C-CAT, Ala16Val-SOD2, and Pro198Leu-GPx1 variants in modulating HCC development in patients with HCV-induced cirrhosis. 21907168 2012
dbSNP: rs376373278
rs376373278
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C1623038
Disease:
Cirrhosis
0.020 GeneticVariation BEFREE We assessed the role of the G(-463)A-MPO, T(-262)C-CAT, Ala16Val-SOD2, and Pro198Leu-GPx1 variants in modulating HCC development in patients with HCV-induced cirrhosis. 21907168 2012
dbSNP: rs972427414
rs972427414
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C0023890
Disease:
Liver Cirrhosis
0.020 GeneticVariation BEFREE We assessed the role of the G(-463)A-MPO, T(-262)C-CAT, Ala16Val-SOD2, and Pro198Leu-GPx1 variants in modulating HCC development in patients with HCV-induced cirrhosis. 21907168 2012
dbSNP: rs972427414
rs972427414
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C1623038
Disease:
Cirrhosis
0.020 GeneticVariation BEFREE We assessed the role of the G(-463)A-MPO, T(-262)C-CAT, Ala16Val-SOD2, and Pro198Leu-GPx1 variants in modulating HCC development in patients with HCV-induced cirrhosis. 21907168 2012
dbSNP: rs376373278
rs376373278
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C1623038
Disease:
Cirrhosis
0.020 GeneticVariation BEFREE We assessed the influence of Ala16Val-superoxide dismutase 2, Pro198Leu-glutathione peroxidase 1, and -463G/A-myeloperoxidase genotypes (high activity for the Ala, Pro, and G alleles, respectively) on the risks of cirrhosis and hepatocellular carcinoma (HCC) in patients homozygous for the C282Y-hemochromatosis (HFE) gene mutation. 20673159 2011
dbSNP: rs376373278
rs376373278
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C0023890
Disease:
Liver Cirrhosis
0.020 GeneticVariation BEFREE We assessed the influence of Ala16Val-superoxide dismutase 2, Pro198Leu-glutathione peroxidase 1, and -463G/A-myeloperoxidase genotypes (high activity for the Ala, Pro, and G alleles, respectively) on the risks of cirrhosis and hepatocellular carcinoma (HCC) in patients homozygous for the C282Y-hemochromatosis (HFE) gene mutation. 20673159 2011
dbSNP: rs972427414
rs972427414
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C0023890
Disease:
Liver Cirrhosis
0.020 GeneticVariation BEFREE We assessed the influence of Ala16Val-superoxide dismutase 2, Pro198Leu-glutathione peroxidase 1, and -463G/A-myeloperoxidase genotypes (high activity for the Ala, Pro, and G alleles, respectively) on the risks of cirrhosis and hepatocellular carcinoma (HCC) in patients homozygous for the C282Y-hemochromatosis (HFE) gene mutation. 20673159 2011
dbSNP: rs972427414
rs972427414
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C1623038
Disease:
Cirrhosis
0.020 GeneticVariation BEFREE We assessed the influence of Ala16Val-superoxide dismutase 2, Pro198Leu-glutathione peroxidase 1, and -463G/A-myeloperoxidase genotypes (high activity for the Ala, Pro, and G alleles, respectively) on the risks of cirrhosis and hepatocellular carcinoma (HCC) in patients homozygous for the C282Y-hemochromatosis (HFE) gene mutation. 20673159 2011
dbSNP: rs2333227
rs2333227
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C0600139
Disease:
Prostate carcinoma
0.020 GeneticVariation BEFREE Associations between MPO -463 G to A genotype (rs2333227) and prostate cancer risk were only noted among men with aggressive cancer, with more than a 2-fold risk reduction among men with AA genotypes (OR = 0.4, 95% CI = 0.2-1.0); MnSOD was not associated with risk overall, but the MnSOD T to C (Val-9Ala, rs4880) polymorphism modified associations between risk of clinically aggressive prostate cancer and dietary iron intake (P for interaction = 0.02). 18296681 2008
dbSNP: rs2333227
rs2333227
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C0376358
Disease:
Malignant neoplasm of prostate
0.020 GeneticVariation BEFREE Associations between MPO -463 G to A genotype (rs2333227) and prostate cancer risk were only noted among men with aggressive cancer, with more than a 2-fold risk reduction among men with AA genotypes (OR = 0.4, 95% CI = 0.2-1.0); MnSOD was not associated with risk overall, but the MnSOD T to C (Val-9Ala, rs4880) polymorphism modified associations between risk of clinically aggressive prostate cancer and dietary iron intake (P for interaction = 0.02). 18296681 2008
dbSNP: rs2107545
rs2107545
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE We found one single-nucleotide polymorphism in the MPO gene was associated with type 2 diabetes mellitus susceptibility [rs2107545: odds ratio = 1.563 (1.166-2.096); p = 0.003], after adjusting for covariates. 29383971 2018
dbSNP: rs2333227
rs2333227
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C4048328
Disease:
cervical cancer
0.010 GeneticVariation BEFREE The possible association between the presence of an MPO -463 G > A (rs2333227) polymorphism and cervical cancer risk. 29937309 2018
dbSNP: rs2333227
rs2333227
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C1561643
Disease:
Chronic Kidney Diseases
0.010 GeneticVariation BEFREE Previous studies have shown that MPO -463G > A (rs2333227) might be associated with chronic kidney disease (CKD) susceptibility, but sample sizes of those studies are relatively small. 30278820 2018
dbSNP: rs2333227
rs2333227
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C1269955
Disease:
Tumor Cell Invasion
0.010 GeneticVariation BEFREE Colorectal cancer cells with the rs2333227 TT genotype exhibited enhanced proliferation, migration, and invasion capacity <i>in vitro</i> and <i>in vivo</i> Mechanistically, we found that <i>MPO</i> SNP rs2333227 C to T mutation altered the binding affinity of the transcription factors AP-2α to the rs2333227 mutation region, sequentially enhancing expression levels of <i>MPO</i> and activating further IL23A-MMP9 axis-mediated oncogenic signaling. 29540402 2018