Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5189
Gene Symbol: PEX1
PEX1 		0.100 Biomarker phenotype HPO
Entrez Id: 2592
Gene Symbol: GALT
GALT 		0.100 Biomarker phenotype HPO
Entrez Id: 10630
Gene Symbol: PDPN
PDPN 		0.200 Biomarker phenotype RGD Albuminuria developed starting at 6 wk of age and coincided with focal and segmental loss of podoplanin, increased expression of desmin, entrapment of albumin in affected podocytes, and focal and segmental foot process effacement at the ultrastructural level. 18199599 2008
Entrez Id: 118
Gene Symbol: ADD1
ADD1 		0.010 GeneticVariation phenotype LHGDN ADD1 polymorphisms per se were not associated with albuminuria. 16612256 2006
Entrez Id: 183
Gene Symbol: AGT
AGT 		0.300 Biomarker phenotype CTD_human A nonpeptide, piperidine renin inhibitor provides renal and cardiac protection in double-transgenic mice expressing human renin and angiotensinogen genes. 18679781 2008
Entrez Id: 5972
Gene Symbol: REN
REN 		0.300 Biomarker phenotype CTD_human A nonpeptide, piperidine renin inhibitor provides renal and cardiac protection in double-transgenic mice expressing human renin and angiotensinogen genes. 18679781 2008
Entrez Id: 2776
Gene Symbol: GNAQ
GNAQ 		0.300 Biomarker phenotype CTD_human Activation of Galpha q-coupled signaling pathways in glomerular podocytes promotes renal injury. 16267159 2005
Entrez Id: 1584
Gene Symbol: CYP11B1
CYP11B1 		0.200 Biomarker phenotype RGD Aldosterone synthase inhibitor ameliorates angiotensin II-induced organ damage. 15939810 2005
Entrez Id: 85480
Gene Symbol: TSLP
TSLP 		0.300 Biomarker phenotype CTD_human All-trans-retinoic acid aggravates cryoglobulin-associated membranoproliferative glomerulonephritis in mice. 17686814 2007
Entrez Id: 1636
Gene Symbol: ACE
ACE 		0.510 GeneticVariation phenotype LHGDN Alpha-adducin and angiotensin-converting enzyme polymorphisms in hypertension: evidence for a joint influence on albuminuria. 16612256 2006
Entrez Id: 1636
Gene Symbol: ACE
ACE 		0.510 Biomarker phenotype CTD_human Angiotensin-converting enzyme inhibition and angiotensin AT1 receptor blockade downregulate angiotensin-converting enzyme expression and attenuate renal injury in streptozotocin-induced diabetic rats. 23733546 2013
Entrez Id: 1636
Gene Symbol: ACE
ACE 		0.510 Therapeutic phenotype RGD Beneficial effect of TGFbeta antagonism in treating diabetic nephropathy depends on when treatment is started. 16902320 2006
Entrez Id: 3953
Gene Symbol: LEPR
LEPR 		0.300 Biomarker phenotype CTD_human Coagonist of glucagon-like peptide-1 and glucagon receptors ameliorates kidney injury in murine models of obesity and diabetes mellitus. 29988851 2018
Entrez Id: 2262
Gene Symbol: GPC5
GPC5 		0.300 Therapeutic phenotype CTD_human Common variation in GPC5 is associated with acquired nephrotic syndrome. 21441931 2011
Entrez Id: 8029
Gene Symbol: CUBN
CUBN 		0.100 GeneticVariation phenotype GWASCAT CUBN is a gene locus for albuminuria. 21355061 2011
Entrez Id: 8029
Gene Symbol: CUBN
CUBN 		0.100 GeneticVariation phenotype GWASDB CUBN is a gene locus for albuminuria. 21355061 2011
Entrez Id: 177
Gene Symbol: AGER
AGER 		0.200 Therapeutic phenotype RGD Effects of atorvastatin on progression of diabetic nephropathy and local RAGE and soluble RAGE expressions in rats. 21796806 2011
Entrez Id: 1286
Gene Symbol: COL4A4
COL4A4 		0.100 GeneticVariation phenotype GWASCAT Genetic Association of Albuminuria with Cardiometabolic Disease and Blood Pressure. 30220432 2018
Entrez Id: 57597
Gene Symbol: BAHCC1
BAHCC1 		0.100 GeneticVariation phenotype GWASCAT Genetic Association of Albuminuria with Cardiometabolic Disease and Blood Pressure. 30220432 2018
Entrez Id: 2523
Gene Symbol: FUT1
FUT1 		0.100 GeneticVariation phenotype GWASCAT Genetic Association of Albuminuria with Cardiometabolic Disease and Blood Pressure. 30220432 2018
Entrez Id: 9960
Gene Symbol: USP3
USP3 		0.100 GeneticVariation phenotype GWASCAT Genetic Association of Albuminuria with Cardiometabolic Disease and Blood Pressure. 30220432 2018
Entrez Id: 81846
Gene Symbol: SBF2
SBF2 		0.100 GeneticVariation phenotype GWASCAT Genetic Association of Albuminuria with Cardiometabolic Disease and Blood Pressure. 30220432 2018
Entrez Id: 23005
Gene Symbol: MAPKBP1
MAPKBP1 		0.100 GeneticVariation phenotype GWASCAT Genetic Association of Albuminuria with Cardiometabolic Disease and Blood Pressure. 30220432 2018
Entrez Id: 55636
Gene Symbol: CHD7
CHD7 		0.100 GeneticVariation phenotype GWASCAT Genetic Association of Albuminuria with Cardiometabolic Disease and Blood Pressure. 30220432 2018
Entrez Id: 364
Gene Symbol: AQP7
AQP7 		0.100 GeneticVariation phenotype GWASCAT Genetic Association of Albuminuria with Cardiometabolic Disease and Blood Pressure. 30220432 2018