SPP1, secreted phosphoprotein 1, 6696

N. diseases: 824; N. variants: 13
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.100 GeneticVariation disease GWASDB Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. 20884846 2010
CUI: C0003868
Disease: Arthritis, Gouty
Arthritis, Gouty
0.100 GeneticVariation disease GWASDB Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. 23263486 2013
CUI: C0018099
Disease: Gout
Gout
0.100 GeneticVariation disease GWASDB Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. 23263486 2013
CUI: C0018099
Disease: Gout
Gout
0.100 GeneticVariation disease GWASDB Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. 20884846 2010
CUI: C0017638
Disease: Glioma
Glioma
0.600 Biomarker disease RGD Based on these findings, we conclude that OPN overexpression in ENU-induced gliomas occurs within a specific subset of intratumoral glial fibrillary acidic protein-positive cells and becomes evident at the stage of tumor progression. 16651633 2006
CUI: C0022650
Disease: Kidney Calculi
Kidney Calculi
0.600 Biomarker disease RGD Effect of NADPH oxidase inhibition on the expression of kidney injury molecule and calcium oxalate crystal deposition in hydroxy-L-proline-induced hyperoxaluria in the male Sprague-Dawley rats. 21378157 2011
CUI: C0555198
Disease: Malignant Glioma
Malignant Glioma
0.560 Biomarker disease RGD Osteopontin expression in intratumoral astrocytes marks tumor progression in gliomas induced by prenatal exposure to N-ethyl-N-nitrosourea. 16651633 2006
CUI: C0006663
Disease: Calcinosis
Calcinosis
0.500 Biomarker phenotype RGD Uraemic hyperparathyroidism causes a reversible inflammatory process of aortic valve calcification in rats. 18390899 2008
CUI: C0014070
Disease: Encephalomyelitis
Encephalomyelitis
0.270 Biomarker disease RGD The influence of the proinflammatory cytokine, osteopontin, on autoimmune demyelinating disease. 11721059 2001
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.230 Biomarker disease RGD These findings suggest that osteopontin expression and macrophage accumulation may play a role in the tubulointerstitial injury in diabetic nephropathy, and that inhibition of osteopontin expression may be one of the mechanisms by which blockade of the renin-angiotensin system confers a renoprotective effect. 12032186 2002
CUI: C0017658
Disease: Glomerulonephritis
Glomerulonephritis
0.210 ModifyingMutation disease RGD Blockade of osteopontin inhibits glomerular fibrosis in a model of anti-glomerular basement membrane glomerulonephritis. 20720406 2010
CUI: C0017658
Disease: Glomerulonephritis
Glomerulonephritis
0.210 Biomarker disease RGD Aldosterone/salt induces renal inflammation and fibrosis in hypertensive rats. 12675855 2003
CUI: C0027059
Disease: Myocarditis
Myocarditis
0.210 Biomarker disease RGD Increased expression of osteopontin in the heart tissue of Lewis rats with experimental autoimmune myocarditis. 16679731 2006
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.200 Biomarker phenotype RGD Taken together, these results indicate that Opn plays an important role in the development of albuminuria, possibly by modulating podocyte signaling and motility. 18443355 2008
CUI: C0011853
Disease: Diabetes Mellitus, Experimental
Diabetes Mellitus, Experimental
0.200 Biomarker disease RGD Upregulation of osteopontin gene expression in diabetic rat proximal tubular cells revealed by microarray profiling. 16528250 2006
CUI: C0020545
Disease: Hypertension, Renovascular
Hypertension, Renovascular
0.200 Biomarker disease RGD Differential regulation of osteopontin expression in the clipped and nonclipped kidney of two-kidney, one-clip hypertensive rats. 12620700 2003
CUI: C0022680
Disease: Polycystic Kidney Diseases
Polycystic Kidney Diseases
0.200 Biomarker group RGD Global gene expression profiling in early-stage polycystic kidney disease in the Han:SPRD Cy rat identifies a role for RXR signaling. 20926632 2011
CUI: C0023893
Disease: Liver Cirrhosis, Experimental
Liver Cirrhosis, Experimental
0.200 Biomarker disease RGD Osteopontin expression in normal and fibrotic liver. altered liver healing in osteopontin-deficient mice. 16221502 2006
CUI: C0027814
Disease: Neuritis, Autoimmune, Experimental
Neuritis, Autoimmune, Experimental
0.200 Biomarker disease RGD Upregulation of osteopontin in Schwann cells of the sciatic nerves of Lewis rats with experimental autoimmune neuritis. 15531104 2004
CUI: C0178664
Disease: Glomerulosclerosis (disorder)
Glomerulosclerosis (disorder)
0.200 Biomarker disease RGD Aldosterone/salt induces renal inflammation and fibrosis in hypertensive rats. 12675855 2003
CUI: C0270824
Disease: Visual seizure
Visual seizure
0.200 Biomarker disease RGD Osteopontin in kainic acid-induced microglial reactions in the rat brain. 12132583 2002
CUI: C0700594
Disease: Radiculopathy
Radiculopathy
0.200 Biomarker disease RGD Spinal root avulsion-induced upregulation of osteopontin expression in the adult rat spinal cord. 14513263 2004
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.500 SusceptibilityMutation disease ORPHANET The present study evaluates association between SPP1 polymorphisms and SLE in a large cohort of 1141 unrelated SLE patients [707 European-American (EA) and 434 African-American (AA)], and 2009 unrelated controls (1309 EA and 700 AA). 18335026 2008
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.500 SusceptibilityMutation disease ORPHANET We can speculate that these sequence variants (or others in perfect linkage disequilibrium) create a predisposition to high production of OPN, and that this in turn may confer susceptibility to SLE. 15692970 2005
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.500 SusceptibilityMutation disease ORPHANET A silent polymorphism (707C>T, rs1126616) of osteopontin was significantly associated with SLE. 11933203 2002