Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4010
Gene Symbol: LMX1B
LMX1B 		0.600 Biomarker phenotype GENOMICS_ENGLAND LMX1B mutation with residual transcriptional activity as a cause of isolated glomerulopathy. 24042019 2014
Entrez Id: 4010
Gene Symbol: LMX1B
LMX1B 		0.600 Biomarker phenotype CTD_human Nail-patella syndrome with an emphasis on the risk of renal and ocular findings. 20199424 2010
Entrez Id: 4010
Gene Symbol: LMX1B
LMX1B 		0.600 Biomarker phenotype CTD_human Nail-patella syndrome, infantile nephrotic syndrome: complete remission with antiproteinuric treatment. 19147669 2009
Entrez Id: 4010
Gene Symbol: LMX1B
LMX1B 		0.600 Biomarker phenotype HPO
Entrez Id: 7040
Gene Symbol: TGFB1
TGFB1 		0.500 Biomarker phenotype RGD Heterozygous knockout of transforming growth factor-β1 protects Dahl S rats against high salt-induced renal injury. 23249995 2013
Entrez Id: 185
Gene Symbol: AGTR1
AGTR1 		0.500 Biomarker phenotype RGD Angiotensin type 2 receptor actions contribute to angiotensin type 1 receptor blocker effects on kidney fibrosis. 20042458 2010
Entrez Id: 26762
Gene Symbol: HAVCR1
HAVCR1 		0.500 Biomarker phenotype CTD_human Reduction of proteinuria in adriamycin-induced nephropathy is associated with reduction of renal kidney injury molecule (Kim-1) over time. 19225054 2009
Entrez Id: 26762
Gene Symbol: HAVCR1
HAVCR1 		0.500 Biomarker phenotype RGD Tubular kidney injury molecule-1 in protein-overload nephropathy. 16467126 2006
Entrez Id: 185
Gene Symbol: AGTR1
AGTR1 		0.500 Biomarker phenotype CTD_human Estradiol increases proteinuria and angiotensin II type 1 receptor in kidneys of rats receiving L-NAME and angiotensin II. 17021606 2006
Entrez Id: 7040
Gene Symbol: TGFB1
TGFB1 		0.500 Biomarker phenotype CTD_human Antiproteinuric efficacy of losartan in comparison with amlodipine in non-diabetic proteinuric renal diseases: a double-blind, randomized clinical trial. 12937228 2003
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1 		0.410 Biomarker phenotype CTD_human p21-activated kinases regulate actin remodeling in glomerular podocytes. 20071462 2010
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1 		0.410 Therapeutic phenotype CTD_human p21-activated kinases regulate actin remodeling in glomerular podocytes. 20071462 2010
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1 		0.410 Biomarker phenotype CTD_human Transcriptional regulation of nephrin gene by peroxisome proliferator-activated receptor-gamma agonist: molecular mechanism of the antiproteinuric effect of pioglitazone. 16687628 2006
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1 		0.410 Therapeutic phenotype CTD_human Transcriptional regulation of nephrin gene by peroxisome proliferator-activated receptor-gamma agonist: molecular mechanism of the antiproteinuric effect of pioglitazone. 16687628 2006
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1 		0.410 AlteredExpression phenotype LHGDN Expression of human nephrin mRNA in diabetic nephropathy. 14736962 2004
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1 		0.410 Biomarker phenotype CTD_human mAb 5-1-6 nephropathy and nephrin. 12012391 2002
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1 		0.410 Therapeutic phenotype CTD_human mAb 5-1-6 nephropathy and nephrin. 12012391 2002
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1 		0.410 CausalMutation phenotype CLINVAR
Entrez Id: 4868
Gene Symbol: NPHS1
NPHS1 		0.410 Biomarker phenotype HPO
Entrez Id: 1287
Gene Symbol: COL4A5
COL4A5 		0.400 Biomarker phenotype GENOMICS_ENGLAND Natural History and Genotype-Phenotype Correlation in Female X-Linked Alport Syndrome. 29270492 2017
Entrez Id: 64423
Gene Symbol: INF2
INF2 		0.400 Biomarker phenotype GENOMICS_ENGLAND Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathy. 25165188 2014
Entrez Id: 4627
Gene Symbol: MYH9
MYH9 		0.400 Biomarker phenotype GENOMICS_ENGLAND MYH9-related disorders: report on a patient of Greek origin presenting with macroscopic hematuria and presenile cataract, caused by an R1165C mutation. 22627578 2012
Entrez Id: 348
Gene Symbol: APOE
APOE 		0.400 Biomarker phenotype CTD_human Successful treatment of lipoprotein glomerulopathy in a daughter and a mother using niceritrol. 20842518 2010
Entrez Id: 7225
Gene Symbol: TRPC6
TRPC6 		0.400 Biomarker phenotype GENOMICS_ENGLAND A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis. 15879175 2005
Entrez Id: 6696
Gene Symbol: SPP1
SPP1 		0.400 Biomarker phenotype CTD_human Phenotypic changes and cell cycle activation in early tubulointerstitial injury of rat adriamycin nephrosis. 11972865 2002