Human | NPHP4 | 261734 | nephronophthisis 4 | INFERRED, Score=800, UMLKSK CUI: C0403447 |
Human | CEP290 | 80184 | centrosomal protein 290kDa | INFERRED, Score=800, UMLKSK CUI: C0403447 |
Human | RETN | 56729 | resistin | circulating resistin levels are strongly associated with both GFR and inflammatory biomarkers in chronic kidney disease (CKD); resistin is not a likely mediator of insulin resistance in patients with CKD |
Human | AHI1 | 54806 | Abelson helper integration site 1 | INFERRED, Score=800, UMLKSK CUI: C0403447 |
Human | NAMPT | 10135 | nicotinamide phosphoribosyltransferase | Circulating levels of visfatin and adiponectin are associated with endothelial dysfunction in all stages of chronic kidney disease, independently of inflammation and insulin resistance Circulating levels of the cytokine visfatin/PBEF-1 are influenced by renal function, but are not associated with fat mass or surrogate markers of insulin resistance in patients with chronic kidney disease |
Human | IQCB1 | 9657 | IQ motif containing B1 | INFERRED, Score=800, UMLKSK CUI: C0403447 |
Human | ADIPOQ | 9370 | adiponectin, C1Q and collagen domain containing | this adipocyte protein may serve to mitigate endothelial damage triggered by dyslipidemia and other risk factors in patients with chronic renal diseases |
Human | SLC7A7 | 9056 | solute carrier family 7 (amino acid transporter light chain, y+L system), member 7 | INFERRED, Score=800, UMLKSK CUI: C0403447 |
Human | PROZ | 8858 | protein Z, vitamin K-dependent plasma glycoprotein | Protien Z levels were reduced in patients with chronic kidney disease, and not elevated in patients on haemodialysis |
Human | FGF23 | 8074 | fibroblast growth factor 23 | Association between FGF23 and parathyroid hormone levels in chronic kidney disease may suggest a co-regulation that remains to be further elucidated Circulating FGF-23 was significantly elevated in patients with chronic kidney disease and its concentration correlated with renal creatinine clearance |
Human | NPHS2 | 7827 | nephrosis 2, idiopathic, steroid-resistant (podocin) | NPHS2 gene mutations are not a major cause of chronic renal insufficiency caused by sporadic SRNS or heavy proteinuria in Japanese children |
Human | XDH | 7498 | xanthine dehydrogenase | Genetic variations in xanthine dehydrogenase contribute partly to hypertension and its complications, including atherosclerosis and chronic kidney disease |
Human | WT1 | 7490 | Wilms tumor 1 | INFERRED, Score=800, UMLKSK CUI: C0403447 |
Human | VEGFA | 7422 | vascular endothelial growth factor A | free plasma VEGF levels are high in chronic renal impairment; may contribute to the endothelial dysfunction of uraemia |
Human | TNF | 7124 | tumor necrosis factor | Involved in prevalence of hyperinsulinemia and insulin resistance in pediatric patients with chronic kidney disease in children the anemia of chronic kidney disease was associated with up regulation of TNF-alpha, and possibly IL-6 and IL-8 along with increased levels of these proinflammatory cytokines in patients treated with epoetin |
Human | TLR4 | 7099 | toll-like receptor 4 | The capacity of monocytes to synthesize proinflammatory cytokines was significantly reduced in infection prone chronic renal insufficiency patients, and this may possibly be due to the reduced monocyte expression of TLR4 |
Human | TGFB1 | 7040 | transforming growth factor, beta 1 | TGF-beta1 polymorphisms are associated with end-stage renal disease, particularly in patients with associated clinical cardiovascular disease, and could be useful as genetic markers of chronic renal disease and higher cardiovascular risk |
Human | HNF1B | 6928 | HNF1 homeobox B | INFERRED, Score=800, UMLKSK CUI: C0403447 |
Human | SLC9A1 | 6548 | solute carrier family 9, subfamily A (NHE1, cation proton antiporter 1), member 1 | critical for countering renal tubular atrophy and chronic renal disease progression |
Human | PLAUR | 5329 | plasminogen activator, urokinase receptor | Role of the serine protease urokinase-type plasminogen activator and its high affinity receptor uPAR/CD87 in chronic kidney disease [REVIEW] |
Human | ABCB1 | 5243 | ATP-binding cassette, sub-family B (MDR/TAP), member 1 | No pharmacogenomic associations are found between the most common ABCB1 haplotypes and acute kidney injury or chronic kidney disease following myeloablative allogeneic hematopoietic cell transplantation |
Human | PAX2 | 5076 | paired box 2 | INFERRED, Score=800, UMLKSK CUI: C0403447 |
Human | TNFRSF11B | 4982 | tumor necrosis factor receptor superfamily, member 11b | polymorphism OPG-223 (C/T) was not associated with chronic kidney disease or periodontal disease in a Brazilian population |
Human | SLC11A2 | 4891 | solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2 | DMT1 (NRAMP2/DCT1) genetic variability and resistance to recombinant human erythropoietin therapy in chronic kidney disease patients under haemodialysis |
Human | NPPB | 4879 | natriuretic peptide B | Report BNP/NT-proBNP levels in chronic kidney disease |