SLC22A2, solute carrier family 22 member 2, 6582

N. diseases: 98; N. variants: 16
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.300 GeneticVariation disease GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.300 Biomarker disease RGD Down-regulation of rat organic cation transporter rOCT2 by 5/6 nephrectomy. 12110012 2002
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.300 Biomarker disease RGD Protein and mRNA expression levels of Oat1, Oat 3, Oct1, and Oct2 were significantly decreased in adenine-induced CRF rats. 23280877 2013
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic
0.300 GeneticVariation disease GWASCAT New loci associated with kidney function and chronic kidney disease. 20383146 2010
CUI: C0028754
Disease: Obesity
Obesity
0.300 Biomarker disease CTD_human Similarly, OCT2 (∼2-fold) and OCT3 (∼3-fold) showed increased protein expression in the kidneys of obese patients compared with those of nonobese individuals. 27401566 2016
CUI: C0740394
Disease: Hyperuricemia
Hyperuricemia
0.210 Biomarker disease BEFREE Changes of drug pharmacokinetics mediated by downregulation of kidney organic cation transporters Mate1 and Oct2 in a rat model of hyperuricemia. 30951542 2019
CUI: C0740394
Disease: Hyperuricemia
Hyperuricemia
0.210 Biomarker disease RGD Restored expression and activity of organic ion transporters rOAT1, rOAT3 and rOCT2 after hyperuricemia in the rat kidney. 15748710 2005
CUI: C0005398
Disease: Cholestasis, Extrahepatic
Cholestasis, Extrahepatic
0.200 Biomarker disease RGD Elevated systemic elimination of cimetidine in rats with acute biliary obstruction: the role of renal organic cation transporter OCT2. 20814153 2010
CUI: C0008372
Disease: Intrahepatic Cholestasis
Intrahepatic Cholestasis
0.200 Biomarker disease RGD Reduced antidiabetic effect of metformin and down-regulation of hepatic Oct1 in rats with ethynylestradiol-induced cholestasis. 19002567 2009
CUI: C0011853
Disease: Diabetes Mellitus, Experimental
Diabetes Mellitus, Experimental
0.200 Biomarker disease RGD Renal and hepatic transporter expression in type 2 diabetic rats. 19356064 2008
CUI: C0035078
Disease: Kidney Failure
Kidney Failure
0.200 Biomarker disease RGD Aristolochic acid-induced destruction of organic ion transporters and fatty acid metabolic disorder in the kidney of rats. 21167265 2011
CUI: C2316810
Disease: Chronic kidney disease stage 5
Chronic kidney disease stage 5
0.200 Biomarker disease RGD Down-regulation of rat organic cation transporter rOCT2 by 5/6 nephrectomy. 12110012 2002
CUI: C2316810
Disease: Chronic kidney disease stage 5
Chronic kidney disease stage 5
0.200 Biomarker disease RGD Renal uptake of substrates for organic anion transporters Oat1 and Oat3 and organic cation transporters Oct1 and Oct2 is altered in rats with adenine-induced chronic renal failure. 23280877 2013
CUI: C2609414
Disease: Acute kidney injury
Acute kidney injury
0.200 Biomarker disease RGD Regulation of renal organic ion transporters in cisplatin-induced acute kidney injury and uremia in rats. 18612803 2008
CUI: C2609414
Disease: Acute kidney injury
Acute kidney injury
0.200 Therapeutic disease RGD Regulation of renal organic anion and cation transporters by thymoquinone in cisplatin induced kidney injury. 22414646 2012
CUI: C0011847
Disease: Diabetes
Diabetes
0.100 GeneticVariation disease GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708 2019
Diabetes Mellitus, Non-Insulin-Dependent
0.060 GeneticVariation disease BEFREE The SLC22A2 single nucleotide polymorphism (SNP) 808G/T was genotyped in 400 T2DM patients, including a metformin-treated group (n=200) and a non-metformin-treated group (n=200). 20139901 2010
Diabetes Mellitus, Non-Insulin-Dependent
0.060 GeneticVariation disease BEFREE Single nucleotide polymorphisms in the intergenic region between metformin transporter OCT2 and OCT3 coding genes are associated with short-term response to metformin monotherapy in type 2 diabetes mellitus patients. 27609360 2016
Diabetes Mellitus, Non-Insulin-Dependent
0.060 GeneticVariation disease BEFREE In this study, we examined the role of OCT2-T201M (602 C>T) variant in insulin resistance in patients with type 2 diabetes (T2D) who were treated with metformin. 25662675 2015
Diabetes Mellitus, Non-Insulin-Dependent
0.060 GeneticVariation disease BEFREE As well as gender, the glucose-lowering efficiency of metformin can be enhanced by SLC22A2 808G > T variants through the delay of its transportation and CLr in Chinese type 2 diabetes populations. 25573751 2015
Diabetes Mellitus, Non-Insulin-Dependent
0.060 GeneticVariation disease BEFREE The aim of this study was to evaluate whether genetic variations in the SLC22A1, SLC22A2, and SLC47A1 genes could be associated with an altered response to metformin in patients with type 2 diabetes mellitus. 31012983 2019
Diabetes Mellitus, Non-Insulin-Dependent
0.060 Biomarker disease BEFREE The aim of this study was to investigate possible associations of the variants in genes encoding organic cationic transporters-solute carrier family 22, members A1, A2 (SLC22A1, SLC22A2) and solute carrier family 47, member A1 (SLC47A1) with response to metformin in type 2 diabetes. 22882994 2013
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.040 Biomarker disease BEFREE Down-regulation of BOB.1/OBF.1 and Oct2 in classical Hodgkin disease but not in lymphocyte predominant Hodgkin disease correlates with immunoglobulin transcription. 11154228 2001
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.040 Biomarker disease BEFREE To check the genomic status of PU.1, BOB1, and OCT2 in HL, we performed metaphase fluorescence in situ hybridization (FISH) analysis of 10 HL cases using locus-specific bacterial artificial chromosome clones. 15796964 2005
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
0.040 AlteredExpression disease BEFREE Seven different cell lines derived from patients with Hodgkin's disease (HD), as well as primary H/Reed-Sternberg (RS) cells isolated from the pericardial fluid of a patient with HD, were compared with a number of hematopoietic and nonhematopoietic cell lines for the expression of Oct-2, a tissue-specific transcription factor normally restricted to B cells, and nuclear factor kappa B (NF-kappa B), an inducible transcription factor. 8639794 1996